Extended, high dose VEGF antagonist regimens for treatment of angiogenic eye disorders

Abstract

The present invention relates to a method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, comprising administering to an eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose.

Description

(19) *EP004647125A2* (11) EP 4 647 125 A2 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: 12.11.2025 Bulletin 2025 / 46 (21) Application number: 25189523.1 (22) Date of filing: 16.05.2022 (51) International Patent Classification (IPC): A61P 27 / 02 (2006.01) (52) Cooperative Patent Classification (CPC): A61K 38 / 179; A61P 27 / 02 (84) Designated Contracting States: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR Designated Extension States: BA ME Designated Validation States: KH MA MD TN (30) Priority: 17.05.2021 US 202163189541 P 20.08.2021 US 202163235398 P 07.01.2022 US 202263297420 P 03.02.2022 US 202263306315 P (62) Document number(s) of the earlier application(s) in accordance with Art. 76 EPC: 22728724.0 / 4 185 318 (71) Applicants: • Regeneron Pharmaceuticals, Inc. Tarrytown, NY 10591 (US) • Bayer Healthcare LLC Whippany, NJ 07981 (US) (72) Inventors: • VITTI, Robert L. Tarrytown, 10591 (US) • BERLINER, Alyson J. Tarrytown, 10591 (US) • CHU, Karen Tarrytown, 10591 (US) • ASMUS, Friedrich 14129 Berlin (DE) • DA SILVA LEAL, Sergio Casimiro 4153 Reinach (CH) • EISSING, Thomas 40764 Langenfeld (DE) • RITTENHOUSE, Kay D. Randolph, NJ 07869 (US) (74) Representative: J A Kemp LLP 80 Turnmill Street London EC1M 5QU (GB) Remarks: •The complete document including Reference Table(s) and the Sequence Listing(s) can be downloaded from the EPO website •This application was filed on 15‑07‑2025 as a divisional application to the application mentioned under INID code 62. •Claims filed after the date of receipt of the application (Rule 68(4) EPC). (54) EXTENDED, HIGH DOSE VEGF ANTAGONIST REGIMENS FOR TREATMENT OF ANGIOGENIC EYE DISORDERS (57) The present invention relates to a method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, comprising administering to an eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. EP 4 64 7 12 5 A 2 Processed by Luminess, 75001 PARIS (FR) Description

[0001] This application claims the benefit of U.S. Provisional Patent Application No. 63 / 189,541, filed May 17, 2021; U.S. Provisional Patent Application No. 63 / 235,398, filed August 20, 2021; U.S. Provisional Patent Application No. 63 / 297,420, filed January 7, 2022; andU.S.ProvisionalPatentApplicationNo. 63 / 306,315, filedFebruary 3, 2022; eachof which is herein incorporated by reference for all purposes. REFERENCE TO A SEQUENCE LISTING

[0002] Thesequence listingof thepresent application is submittedelectronically asanASCII formattedsequence listing with a file name "10861WO01-Sequence", creation date of May 16, 2022, and a size of 6,006 bytes. This sequence listing submitted is part of the specification and is herein incorporated by reference in its entirety. FIELD OF THE INVENTION

[0003] The field of the present invention relates to methods for treating or preventing angiogenic eye disorders by administering a VEGF antagonist. BACKGROUND OF THE INVENTION

[0004] Neovascular (wet) AMD (nAMD) is amajor health issue in aging populations globally. Vision loss in nAMD results from the abnormal growth and leakage of blood vessels in the macula. In elderly patients affected by nAMD, vision loss frequently has an even greater impact, as it substantially reduces the visual compensation of functional impairment by other age-related comorbidities, such as arthritis and osteoporosis.

[0005] Intravitreally (IVT) administered anti-vascular endothelial growth factor (VEGF) therapies like EYLEA® inhibit neovascular vessel growth and leakage in the retina, and they are currently the standard-of-care for patients with nAMD. Theynotonlymaintain visual functionbutalsoprovideclinicallymeaningful visual gains.Treatmentof nAMD ischronicand life-long inmost patients to suppress retinal edema and recurrences of choroidal neovascularization (CNV). Although the currently approved IVT anti-VEGF therapies are efficacious and well-tolerated, the need for IVT injections every 4 to 8 weeks, specifically in the initial phase and duringmaintenance of treatment, represents a significant burden to physicians, patients, and caregivers. While the procedure is straightforward and relatively easy to perform, capacity issues for ensuringanappropriate injection frequency inorder toachievepatientoutcomessimilar to thoseseen in thepivotal studies represent an increasing challenge to individual practices and the healthcare system, overall. Moreover, high frequency dosing leads to increased burdenson patients, e.g., to find transportation andmisswork. A secondary effect of this burden is a lower probability of non-compliance with the prescribed treatment regimen.

[0006] While the efficacy and safety of currently approved VEGF antagonist therapies have been established for the treatment of nAMD, there remains an unmet medical need for the development of therapies with the potential to reduce treatment burden while providing at least similar or even improved visual outcomes over currently available standard-of- care.

[0007] EYLEA (2 mg dose, administered at a concentration of 40 mg / mL, also called intravitreal aflibercept injection [IAI]) is currently approved in the United States (US) for the treatment of nAMD, and is also approved for the treatment of macular edema following retinal vein occlusion (RVO), diabetic macular edema (DME), and diabetic retinopathy (DR). SUMMARY OF THE INVENTION

[0008] Thepresent invention providesamethod for treatingor preventinganangiogenic eyedisorder (e.g., neovascular age-related macular edema (nAMD), diabetic macular edema (DME), diabetic retinopathy (DR), macular edema (ME) secondary to retinal vein occlusion (RVO) (ME-RVO), in a subject in need thereof, comprising administering to an eye of the subject (e.g., by intravitreal injection), e.g., in about 70 µl, a single initial dose of about 8 mg or more of a VEGF antagonist (e.g., aflibercept) to an eye of the subject, followed by one or more secondary doses of the VEGF antagonist, followed by one ormore tertiary doses of theVEGFantagonist; wherein each secondary dose is administered about 2 to 4 or 3 to 5 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose.

[0009] In an embodiment of the invention, wherein, e.g., while receiving such a regimen: (i) with respect to visual acuity or best corrected visual acuity (BCVA), the subject achieves: no loss in visual acuity or BCVA; a gain in visual acuity or BCVA; no loss of visual acuity or BCVA by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according toETDRSor theSnellen equivalent; no loss of visual acuity or BCVAof about 5 ormore, about10ormore, or about15ormore lettersbyaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40or44, following the 2 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 initial dosewherein visual acuity orBCVA is according toETDRSor theSnellen equivalent; a gain in visual acuity orBCVA, of about 5 or more, about 10 or more or about 15 or more letters, by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose, wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; and / or a gain in visual acuity or BCVA of about 6 or 7 or 8 letters by about week 8 andmaintaining a gain of about 6 or 7 or 8 letters until at least about week 44 wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; (ii) with respect to central retinal thickness (CRT), the subject achieves: a decrease in central retinal thickness; a decrease in central retinal thickness by at least about 123, 125, 131, 142, 147, 149, 150, 151, 156, 157, 158, 159, 161, 162, 166, 167, 168, 172, 173, 175, 177, 178 or 183micrometers (µm)by aboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40or 44 following the initial dose; a decrease in central retinal thickness of about 47 micrometers from about week 12 to about week 20 following the initial dose; a decrease in central retinal thickness of about 17 micrometers from about week 24 to about week 32 following the initial dose; a decrease in central retinal thickness of about 18micrometers fromaboutweek 36 to aboutweek 44 following the initial dose; a decrease in central retinal thickness of about 123, 131161micrometers by about week 4, 8, 12, 16 or 20 following the initial dose and maintaining the decrease until at least about week 44 following the initial dose; and / or a reduction inCRTofabout159, 160, 161or162micrometersbyaboutweek4or8or12andmaintaininga reductionof about 159, 160, 161 or 162 micrometers until at least about week 44; (iii) with respect to retinal fluid, the subject achieves: a dry retinahavingno intraretinal fluidandnosubretinal fluid; or no intraretinal fluid; or nosubretinal fluid; in the center subfieldor macula as measured by spectral domain optical coherence tomography; a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield asmeasured by spectral domain optical coherence tomography byaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose; noSRFand IRF in themacula asmeasured bySD-OCTbyweek 16 orweek 44 following the initial dose; no sub-retinal pigment epithelium (RPE) fluid until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or maintenance of a dry retina once achieved until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or (iv) the subject achieves: a reduction in total choroidal neovascularization (CNV) lesion size by at least about 3.2 or 3.3µmbyaboutweek 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40or 44 following the initial dose; no significant increase in intraocular pressure frombaselinebyaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40or 44or later following the initial dose; and / or no significant increase in systolic (S) and / or diastolic (D) blood pressure frombaseline by aboutweek 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later following the initial dose. The scope of the present invention also encompasses methods for achieving any of such achievements in a subject in need thereof who is suffering from an angiogenic eye disorder, by administering the dosing regimen set forth above. For example, in an embodiment of the invention, the method for treating or preventing an angiogenic eye disorder (e.g., neovascular age-relatedmacularedema,diabetic retinopathy, diabeticmacular edemaormacularedema following retinal veinocclusion (RVO) ) includesadministeringasingle initial doseofVEGFantagonist (e.g., aflibercept), followedbyoneor more secondary doses of the VEGF antagonist, followed by one or more tertiary doses of the VEGF antagonist; wherein eachsecondarydose is administeredabout 4weeksafter the immediately precedingdose; andwherein each tertiary dose is administered about 4, 8 or 12weeksafter the immediately preceding dose. In anembodiment of the invention, relative to asubject receiving suchadosing regimen, except that only 2mgofVEGFantagonist is administered, the subject receiving 8mgof VEGFantagonist exhibits a greater decrease in central retinal thickness after 4, 8, 12, 16 ormoreweeks; a greater improvement in best corrected visual acuity after 4, 8, 12, 16 or more weeks; and / or a greater likelihood of having a dry retina (e.g., lacks intraretinal fluid and / or subretinal fluid) after 4, 8, 12, 16 or more weeks. In an embodiment of the invention, 2‑4weeks is 2, 3or 4weeks.Thepresent invention further providesamethod for improvingbest correctedvisual acuity, decreasing central retinal thickness and / or achieving a dry retina, in the eye of a subject (e.g., suffering from neovascular age-relatedmacularedema,diabetic retinopathy, diabeticmacular edemaormacularedema following retinal vein occlusion (RVO)) in need thereof, comprisingadministering to theeyeof the subject, a single initial doseof about 8mg or more of a VEGF antagonist (e.g., aflibercept) to an eye of the subject, followed by one or more secondary doses of the VEGF antagonist, followed by one or more tertiary doses of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. Also provided by the present invention is a method for promoting retinal drying, in the eye of a subject suffering from an angiogenic eye disorder (e.g., neovascular age-related macular edema, diabetic retinopathy, diabetic macular edema or macular edema following retinal vein occlusion (RVO)), comprising administering to the eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose; for example, wherein retinal drying is characterized by no intraretinal fluid (IRF) and / or no subretinal fluid (SRF) in the eye of the subject, e.g., after the subject has received the three monthly doses of the VEGF antagonist. In an embodiment of the invention, the VEGF antagonist is: (i) aVEGF receptor fusion protein, for example, comprising twopolypeptides that comprise (1) aVEGFR1component 3 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 comprising amino acids 27 to 129 of SEQ ID NO: 2; (2) a VEGFR2 component comprising amino acids 130‑231 of SEQ ID NO: 2; and (3) a multimerization component comprising amino acids 232‑457 of SEQ ID NO: 2; (ii) a VEGF receptor fusion protein comprising two polypeptides that comprise immunoglobin-like (Ig) domain 2 of a VEGFR1 and Ig domain 3 of VEGFR2, and a multimerizing component; (iii) a VEGF receptor fusion protein comprising two polypeptides that comprise an immunoglobin-like (Ig) domain 2 of VEGFR1, an Ig domain 3 of VEGFR2, an Ig domain 4 of said VEGFR2; and a multimerizing component; (iv) a VEGF receptor fusion protein comprising two VEGFR1R2-FcΔC1(a) polypeptides encoded by the nucleic acid sequence of SEQ ID NO: 1; or (v) selected from the group consisting of: aflibercept, conbercept, bevacizumab, ranibizumab, pegaptanib, broluci- zumab, an anti-VEGFDARPin, abicipar pegol, faricimab, an anti-VEGFantibody or antigen-binding fragment thereof or biopolymer conjugate thereof (e.g., KSI‑301), bevacizumab, ranibizumab and a bispecific anti-VEGF / ANG2 antibody.

[0010] In an embodiment of the invention, the VEGF antagonist is administered to the eye of the subject in a pharmaceutical formulation, for example, which is selected from the group consisting of A-KKKK as so designated herein. In an embodiment of the invention, the VEGFantagonist is administered to the eye froma syringe, e.g., a pre-filled syringe, (e.g., which is glass, plastic and / or sterile). In an embodiment of the invention, the syringe is characterized by the ornamental design as set forth in International Design Registration No. DM / 212 509; which is herein incorporated by reference.

[0011] In an embodiment of the invention, a dosage of about 8 mg or more is a dose of about 9, 9.3, 9.33, 9.7, 9.8, 9.9, 9.7‑9.9mg or more and such a dosage amount may vary within a given range, e.g.,± about 0.5, or± about 0.51mg. The volume in which a dose is delivered can be, for example, about 70, 81, 82, 81.7, 85, 86, 87, 85‑87 microliters and the volume may vary within a given range, e.g., ± about 4, 4.45, 4.5, or 5 microliters. Doses may be delivered with a dose delivery device (DDD) which is a syringe.

[0012] Highly precise doses of VEGF antagonist (e.g., aflibercept) may be delivered, for example, in a volume that is device-determined. In an embodiment of the invention, a dose is delivered with a syringe by a method that includes the steps: (a) withdrawing a plunger rod of the syringe to fill the syringe with the formulation; (b) priming the syringe, thereby removing air from the syringe and, thus avoiding injection of air into the eye, by advancing the plunger rod by a predetermined distance into the syringe body until advancement of the plunger rod is resisted by a stop; (c) rotating the plunger rod about a longitudinal axis; and (d) actuating the plunger rod to dispense a predetermined (device- determined) volume (e.g., about 70, 81, 82, 81.7, 85, 86, 87, 85‑87microliters,± about 4, 4.45, 4.5, or 5microliters) of the formulation. BRIEF DESCRIPTION OF THE FIGURES

[0013] Figure 1: Summary of CANDELA Clinical Trial Plan and Dosing Schedule. Figure 2: Baseline Demographics of Patients in CANDELA trial (IAI dosing group, HD dosing group and All patients (all patients with data reported as of data cut-off (IAI n=27; HD n=28))) at week 16. Figure3:ContinuedBaselineDemographicsofPatients inCANDELATrial at (all patientswithdata reportedasofdata cut-off (IAI n=27; HD n=28))) at week 16. Figure 4:BaselineBloodPressures of IAI andHDDosingGroups inCANDELA trial (all patientswith data reported as of data cut-off (IAI n=27; HD n=28))) at week 16. Figure 5: Mean Change in Central Retinal Thickness (CRT) from Baseline (BL) in IAI and HD CANDELA Dosing Groups inPatientsCompletingWeek16.Completers are patientswithOCTvaluesat bothweeks12and16 (IAI n=22; HD n=27). Figure 6: Mean change in Best Corrected Visual Acuity (BCVA) (ETDRS letters) from Baseline (BL) in IAI and HD CANDELA Dosing Groups in Patients Completing to Week 16 (IAI n=22; HD n=27). Figure 7: Proportion of HD and IAI patients in CANDELACompleting toWeek 16 with a Dry Retina (no intraretinal or subretinal fluid) at Baseline and Weeks 4, 8, 12 and 16. Figure 8: Proportion of HD and IAI patients in CANDELA Completing to week 16 with a Retina that is Not Dry (intraretinal and / or subretinal fluid) at Baseline and Weeks 4, 8, 12 and 16. Figure 9: Proportion of HD and IAI Patients in CANDELA Completing to Week 16 with Intraretinal Fluid (IRF) at Baseline and Weeks 4, 8, 12 and 16. Figure 10: Proportion of HD and IAI Patients in CANDELA Completing to Week 16 with Subretinal fluid (SRF) at Baseline and Weeks 4, 8, 12 and 16. Figure11:Retinal Fluid statusof IAI patients (n=22) inCANDELACompleting toWeek16atBaseline andWeeks4, 8, 4 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 12 and 16. Figure 12: Retinal Fluid Status of HD Patients in CANDELA Completing to Week 16 at Baseline andWeeks 4, 8, 12 and 16. N=27 at Baseline, Week 8, 12 and 16; N=26 at Week 4. Figure 13: Summary of Treatment Exposure of IAI and HD Patients in CANDELA Trial. IAI n=27; HD n=28. Figure 14: Summary of Treatment Emergent Adverse Events (TEAE) of IAI and HD Patient Study Eye in CANDELA Trial. IAI n=27; HD n=27. Figure 15:ContinuedSummary of Treatment Emergent AdverseEvents (TEAE) of IAI andHDPatients inCANDELA Trial. IAI n=27; HD n=27. Figure 16: Intraocular Pressure (IOP) of HD and IAI Patients in CANDELA trial. IAI n=27; HD n=28. Figure 17: Summary of Non-Ocular Treatment Emergent Adverse Events (TEAE) of IAI and HD Patients in CANDELA trial. IAI n=27; HD n=28. Figure18:ContinuedSummaryofNon-Ocular TreatmentEmergentAdverseEvents (TEAE)of IAI andHDPatients in CANDELA Trial. IAI n=27; HD n=28. Figure 19: Summary of Non-Ocular Serious Adverse Events (SAES) of IAI and HD Patients in CANDELATrial. TIA- transient ischemic attack. IAI n=27; HD n=28. Figure 20: Summary of Hypertension Adverse Events of IAI and HD patients in CANDELATrial. IAI n=27; HD n=28. Figure 21: Mean Systolic Blood Pressure of IAI and HD Patients in CANDELA trial. Figure 22: Mean Diastolic Blood Pressure of IAI and HD Patients in CANDELA Trial. Figure 23: Mean Intraocular Pressure of IAI and HD Patients in CANDELA Trial. Figure 24: Change in Intraocular Pressure from Baseline of IAI and HD Patients in CANDELA Trial. Figures 25A, 25B and 25C: Precision Dose Delivery Device Analyses. (Fig. 25A) Delivered dose summary for REGN3-PFS‑0.5mL; (Fig. 25B)Delivereddosesummary for 1mLBDLuerLoksyringe; (Fig. 25C) Individual valueplot of doses delivered with REGN3-PFS‑0.5mL and 1mL BD Luer Lok syringe. Figure 26:Disposition and Exposure through week 16 in Patients treated with 8 mg Aflibercept High-Dose Regimen (HD) or 2 mg Aflibercept Regimen (IAI) or All Patients (Total) (analysis of additional patients reaching week 16: HD n=53; IAI n=53; All n=106). Figure 27: Baseline Demographics of in Patients treated with HD, IAI or All Patients (Total) (analysis of additional patients reaching week 16). HD n=53; IAI n=53; All n=106. Figure 28: Baseline Characteristics in Patients treated with HD, IAI or All Patients (analysis of additional patients reaching week 16). HD n=53; IAI n=53; All n=106. Figure 29: Baseline Blood Pressure and Medical History of Hypertension in All Patients treated with HD or IAI (analysis of additional patients reaching week 16; HD n=53; IAI n=53). Figure30:PrimaryEfficacyEndpoint -ProportionofPatients TreatedwithHDor IAIRegimenwithDryRetina atWeek 16 (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 31: Proportion of Patients Treated with HD or IAI Regimen without Intraretinal Fluid (IRF) and without Subretinal Fluid (SRF) at Week 16 (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 32: Median Change from Baseline in Central Retinal Thickness of Patients Treated with HD or IAI Regimen through Week 16 (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 33: Mean Change from Baseline in Central Retinal Thickness of Patients Treated with HD or IAI Regimen through Week 16 (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 34: Mean Change from Baseline to Week 12 in Choroidal Neovascular Size and Lesion Size of Patients Treated with HD or IAI Regimen. IAI n=44; HD n=46. Figure 35:MeanChange fromBaseline in Best CorrectedVisual Acuity (BCVA) throughWeek 16 in Patients Treated with HD or IAI Regimen (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 36:Changes in Vision atWeek 16 in Patients Treated with HD or IAI Regimen (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 37: Proportion of Patients Treated with HD or IAI Regimen Receiving Additional Treatment at Week 16 (analysis of additional patients reaching week 16; HD n=53; IAI n=53). Figures 38A, 38B and 38C: Summary of Treatment Emergent Adverse Events (TEAEs) in Patients Treated with HD or IAI Regimen, (Fig. 38A) Ocular TEAEs in Study Eye Occurring in ≥2% of Patients through Week 16, (Fig. 38B) OcularSeriousTEAEs in theStudyEye throughWeek16, (Fig. 38C) Intraocular InflammationTEAEs in theStudyEye through Week 16 (analysis of additional patients reaching week 16; HD n=53; IAI n=53). Figure 39: Mean Intraocular Pressure Change from Baseline in Patients Treated with HD or IAI Regimen through Week 16 (analysis of additional patients reaching week 16; number of patients analyzed is shown). Figure 40: Summary of Intraocular Pressure Events in Patients Treated with HD or IAI Regimen through Week 16 (analysis of additional patients reaching week 16; HD n=53; IAI n=53). Figure 41:Anti-Platelet Trialists’ Collaboration (APTC) Events or Deaths in Patients Treated with HD or IAI Regimen 5 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 through Week 16 (analysis of additional patients reaching week 16; HD n=53; IAI n=53). Figure 42: Hypertension Adverse Events in Patients Treated with HD or IAI Regimen through Week 16 (analysis of additional patients reaching week 16; HD n=53; IAI n=53). Figures 43A and 43B: Mean Change from Baseline in Blood Pressure (Fig. 43A: Systolic; Fig. 43B: Diastolic) in Patients Treatedwith HDor IAI Regimen throughWeek 16-All Patients (analysis of additional patients reachingweek 16; HD n=53; IAI n=53). Figures 44A and 44B: Mean Change from Baseline in Blood Pressure (Fig. 44A: Systolic; Fig. 44B: Diastolic) in PatientsTreatedwithHDor IAIRegimen throughWeek16-DensePharmacokinetic (PK)Sub-studyPatients (analysis of additional patients reaching week 16; HD n=15; IAI n=15). Figure 45: Patient Disposition as of study start, week 16 and week 44 of HD and IAI patient study groups and combined groups (All). Figure 46: Baseline Demographics (sex, ethnicity, race, age) of HD and IAI patient study groups and combined groups (All). Figure47:BaselineCharacteristicsof theStudyEyeofHDand IAI patient studygroupsandcombinedgroups (All). 58 ETDRS letters is about equivalent to 20 / 60‑20 / 70 Snellen visual acuity. SD=standard deviation; FA=fluorescein angiography. Figure 48: Treatment Exposure summary through Week 44 of HD and IAI patient study groups. Figure 49: Proportion of Eyes without Fluid in the Center Subfield (no intraretinal fluid (IRF) and no subretinal fluid (SRF) in the center subfield by SD-OCT (Spectral Domain Optical Coherence Tomography)) at Weeks 16 & 44. Percentages and number of patients out of 53 (n / 53) are shown. LOCF=last observation carried forward. FAS=full analysis set. At baseline, 9 / 53 (17.0%) and 10 / 53 (18.9%) of eyes in the aflibercept 2 mg and 8 mg groups, respectively, had no IRF or SRF in the center subfield. These eyes met criteria for inclusion due to presence of pigment epithelial detachment (PED) due to nAMD Figure 50:Proportion of Eyes without Fluid in the Macula (no IRF and no SRF in themacula on SD-OCT) at week 16 (difference of 17 (95% confidence interval: ‑0.9, 34.8)) and week 44 (difference of 17 (95% confidence interval: 1.1, 32.8)). Percentages and number of patients out of 53 (n / 53) are shown. Figure 51: Proportion of Eyes without Fluid in the Center Subfield (without fluid in the center subfield refers to no intraretinal fluid and no subretinal fluid in the center subfield on SD-OCT (Spectral Domain Optical Coherence Tomography)) at weeks 16, 20, 24 28, 32, 36, 40 and 44. Percentages and number of patients out of 53 (n / 53) are shown. Syringes on the X-axis indicate scheduled dose visits. Figure 52: Proportion of Eyes without Intraretinal Fluid (without intraretinal fluid is dry or with subretinal fluid only) in the Center Subfield at Weeks 16 and 44. Percentages and number of patients out of 53 (n / 53) are shown. Figure53:ProportionofEyeswithoutSubretinal Fluid (without subretinal fluid is dryorwith intraretinal fluidonly) in the Center Subfield at Weeks 16 and 44. The week 16 and 44 treatment effect was 18.9%. Percentages and number of patients out of 53 (n / 53) are shown. Figure 54: Mean Change from Baseline (BL) in Central Retinal Thickness (CRT; micrometers) over time through Week44.Syringeson theX-axis indicatescheduleddosevisits.Week16data forpatients receiving treatment atweek 16 are carried forward. LOCF:Patients receiving treatment at week16were considered not dry fromweek 16onward. Inset box shows changes in CRT between weeks 12 and 20; 24 and 32; or 36 and 44 in the HD and IAI groups. Figure 55: Median Change from Baseline (BL) in Central Retinal Thickness (CRT; micrometers) over time through Week 44. Syringes on the X-axis indicate scheduled dose visit. LOCF: Patients receiving treatment at week 16 were considered not dry from week 16 onward. Figure 56: Mean Change from Baseline (BL) in Best Corrected Visual Acuity (BCVA; ETDRS letters) over time throughWeek 44. Syringes on the X-axis indicate scheduled dose visit. LOCF: Patients receiving treatment at week 16 were considered not dry from week 16 onward. Figure 57: Proportion of Patients Losing and Gaining Vision (ETDRS letters) from Baseline (BL) at Week 44. Percentages and number of patients out of 53 (n / 53) are shown. Figure58:Ocular TreatmentEmergentAdverseEvents (TEAEs) in theStudyEyeOccurring in>2%ofPatients (Pts). Percentages and number of patients out of 53 (n / 53) in HD and IAI groups are shown. Figure 59:Ocular SeriousTreatment Emergent AdverseEvents (TEAEs) in theStudyEye. Percentages andnumber of patients out of 53 (n / 53) in HD and IAI groups are shown. Figure 60: Intraocular Inflammation Treatment Emergent Adverse Events (TEAEs) in the Study Eye. Percentages and number of patients out of 53 (n / 53) in HD and IAI groups are shown. Figure61:Summaryof IntraocularPressureEvents in theHDand IAIStudyGroups.Safetyanalysisset.Percentages are calculated based on N. Percentages and number of patients out of 53 (n / 53) in HD and IAI groups are shown. Figure 62: Mean Pre-Dose Intraocular Pressure, Change from Baseline in the HD and IAI study groups over time (mmHg). Safety analysis set. Figure 63: Non-Ocular Treatment Emergent Adverse Events (TEAEs) Occurring in ≥ 2% of Patients. Percentages 6 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 and number of patients out of 53 (n / 53) in HD and IAI groups are shown. Figure 64: Non-Ocular Serious Treatment Emergent Adverse Events (TEAEs) in the HD and IAI study groups. Percentages and number of patients out of 53 (n / 53) are shown. Figure 65:Hypertension TreatmentEmergent AdverseEvents (TEAEs) in theHDand IAI study groups. Percentages and number of patients out of 53 (n / 53) in HD and IAI groups are shown. Figure 66: Adjudicated Anti-Platelet Trialists’ Collaboration (APTC) Events and Deaths in the HD and IAI study groups. DETAILED DESCRIPTION OF THE INVENTION

[0014] Increasing themolar fraction of VEGF antagonist therapeutic protein in the dosing formulation is a potential way to bring further benefits to patients with chorioretinal vascular diseases, including nAMD. A higher dose of aflibercept administered IVT has the potential to prolong the drug’s therapeutic effects and for improvement in pharmacodynamics such as better drying. The resulting extension of treatment intervals early after the initiation of treatment to every 12weeks would reduce thenumberof injections in the first treatment year.Apotential decrease in injection-related treatment burden and safety events with fewer injections could be a significant contribution to patient care and healthcare services. The present invention provides, in part, a safe and effectivemethod for treating angiogenic eye disorders with an 8mg dose of aflibercept in a regimen calling formonthly loading doses before quarterlymaintenance doses. First, patients receiving an 8 mg dose, which is four times the dose approved for Eylea, (2 mg), were not observed in the CANDELA clinical trial (discussed herein) to develop any more hypertension treatment-emergent adverse events than patients receiving 2 mg (Figure 65). Systemic exposure to VEGF inhibitor is known to be associated with the risk of systemic blood pressure (BP) increases. Moreover, intravitreal injection of VEGF inhibitors has been associated with blood pressure effects. See, for example, Hanna et al., (2019) "Three patients with injection of intravitreal vascular endothelial growth factor inhibitors and subsequent exacerbation of chronic proteinuria and hypertension", Clinical Kidney Journal, 2019, vol. 12, no. 1, 92‑100 and Raiser et al., (2009) "The effect of intravitreal bevacizumab (Avastin) administration on systemic hypertension", Eye 23, 1714‑1718. In addition, in the CANDELA clinical trial, subjects receiving the 8 mg dose (HD) achieved numerically superior anatomical improvements in the eye as well as numerically superior improvements in vision relative to subjects receiving a 2mg dose (IAI). A higher proportion of eyes treated with aflibercept 8mg (HD) were dry (without intraretinal or subretinal fluid on OCT) in the center subfield versus aflibercept 2 mg (IAI). Treatment groups followed identical dosing regimens with the 8 mg group receiving slightly fewer PRN doses. A change from baseline in central retinal thickness (CRT) suggested better anatomic outcomes with aflibercept 8 mg versus aflibercept 2mg; and a change from baseline in BCVA favored aflibercept 8 mg (+7.9 vs +5.1 letters).

[0015] Theanatomical and visual improvements for theHDpatients that was observedwas also comparable to those of subjects in the VIEW1 and VIEW2 trials (VIEW1 / 2) that received a 2 mg dose every 8 weeks (following three monthly loading doses (2q8)). See e.g., Heier et al., Intravitreal Aflibercept (VEGF Trap-Eye) in Wet Age-related Macular Degeneration, Ophthalmology 2012;119:2537‑2548. The VIEW1 / 2 2q8 subjects achieved 8.1 letters of BCVA mean improvement at 44 weeks following the initial dose (Heier et al. (2012), Figure 3); whereas the CANDELA HD subjects hereinwere observed to achieve amean improvement of 7.9 letters at 44weeks (Figure 56).Moreover, the improvements in the central retinal thickness (CRT) that were observed to be achieved by CANDELA HD subjects were comparable to that observed in theVIEW1 / 22q8subjects. TheVIEW12q8subjectsachievedamean reductionof about125micrometers inCRTandVIEW22q8 subjects achieved about 150micrometersmean reduction inCRT, at 44weeks (Heieret al. (2012), Figure 4). The CANDELA HD subjects were observed to achieve a mean reduction of 159 micrometers and a median reductionof 162micrometersat 44weeks (Figure54&Figure55; andHeieret al. (2012), Figure4).While the2q8VIEW1 / 2 subjectsand theCANDELAHDsubjectswerenot evaluatedside-by-side in thesameclinical trial and theVIEWtrials hada greater number of participants, these data suggest that subjects can be administered 8 mg doses of aflibercept as infrequently as every 12 weeks yet achieve anatomic and visual outcomes comparable to that of patients dosed every 8 weeks (following threemonthly loading doses) with 2mg.While the VIEW1 / 2 subjects received only the scheduled doses within the first year, someof theCANDELAsubjects received additional dosespro re nataafterweek16 (Figure 1). Twenty eight out of 53 of the CANDELA HD subjects did not receive any additional doses (Figure 48). Moreover, time-domain optical coherence tomography was performed in VIEW1 / 2 to evaluated CRT whereas, a more sensitive spectral domain optical coherence tomography (SD-OCT) was used in CANDELA.

[0016] "Isolated" VEGF antagonists and VEGF receptor fusion proteins (e.g., aflibercept), polypeptides, polynucleo- tides and vectors, are at least partially free of other biological molecules from the cells or cell culture from which they are produced. Such biological molecules include nucleic acids, proteins, other VEGF antagonists and VEGF receptor fusion proteins, lipids, carbohydrates, or othermaterial such as cellular debris and growthmedium. An isolatedVEGFantagonist or VEGF receptor fusion proteinmay further be at least partially free of expression system components such as biological molecules from a host cell or of the growth medium thereof. Generally, the term "isolated" is not intended to refer to a complete absence of such biological molecules (e.g., minor or insignificant amounts of impurity may remain) or to an 7 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 absenceofwater, buffers, or salts or to componentsof apharmaceutical formulation that includes theVEGFantagonists or VEGF receptor fusion proteins.

[0017] A "subject" or "patient" is a mammal, for example a human, mouse, rabbit, monkey or non-human primate. A subject or patientmaybesaid to be "suffering from"anangiogenic eyedisorder suchasnAMD,DRorDME.Suchasubject has thedisorder inoneor botheyes. Inanembodiment of the invention, a subject or patient hasoneormoreof the following characteristics (at or before the start of treatment): 1. ≥50 years of age 2. Subfoveal CNV secondary to nAMD, e.g., including juxtafoveal lesions that affect the fovea in an eye. 3. Best Corrected Visual Acuity (BCVA) Early Treatment Diabetic Retinopathy Study (ETDRS) letter score of 78 to 24 (Snellen equivalent of 20 / 32 to 20 / 320) in an eye; or about 58±10, 58 ±14 or 58±12 ETDRS letters (or Snellen equivalent). 4. A central retinal thickness in aneyegreater thannormal,e.g., greater thanapproximately 130, 140, 150, 160, 170or 180 micrometers, e.g., as determined manually or by optical coherence tomography (OCT) mapping software, for example with a central retinal thickness of about 300, 400, 500 or 600 micrometers or more; or about 488.1±204.9, 516.2±175.64 or 502.1±190.6 micrometers. 5. Intraocular pressure of about 14.8±3.4 or 14.9±3.4 mmHg. 6. nAMD lesion size of about 7.9±6.21, 7.7±6.84 or 7.8±6.50 mm2. 7. Choroidal neovascularization lesion size of about 7.9±6.20, 7.5±6.86 or 7.7±6.51 mm2. 8. As per fluorescein angiography (FA), has occult choroidal neovascularization, minimally classic choroidal neovascularization or predominantly classic choroidal neovascularization. and / or, has or lacks any one or more of the following characteristics: 1. CNV (choroidal neovascularization) due to any cause other than nAMD in either eye. 2. Subretinal hemorrhage in an eye that is ≥50% of the total lesion area. 3. Intraocular pressure ≥25 mm Hg in an eye. 4. Evidence of infectious blepharitis, keratitis, scleritis, or conjunctivitis in an eye. 5. Any intraocular inflammation and / or ocular infection in an eye. 6. Any history of macular hole of stage 2 and above in an eye. 7. Iris neovascularization, vitreous hemorrhage, or tractional retinal detachment visible in an eye. 8. Uncontrolled blood-pressure (BP) (defined as systolic >140 mm Hg or diastolic >90 mm Hg). 9. Variation by more than 10% in the 3 pre-randomization BP measurements. 10. History of cerebrovascular accident / transient ischemic attack or myocardial infarction / acute coronary syndrome. 11. Renal failure, dialysis, or history of renal transplant. 12. Known sensitivity to aflibercept. 13. Any other intraocular surgery within 12 weeks (84 days). VEGF Antagonists

[0018] The present invention includes methods for using a VEGF antagonist for treating or preventing angiogenic eye disorders. VEGF antagonists include molecules which interfere with the interaction between VEGF and a natural VEGF receptor, e.g., moleculeswhich bind to VEGFor aVEGF receptor and prevent or otherwise hinder the interaction between VEGF and a VEGF receptor. Specific, exemplary VEGF antagonists include anti-VEGF antibodies, anti-VEGF receptor antibodies, and VEGF receptor fusion proteins.

[0019] For purposes herein, a "VEGF receptor fusion protein" refers to a molecule that comprises one or more VEGF receptors or domains thereof, fused to another polypeptide, which interferes with the interaction between VEGF and a naturalVEGFreceptor,e.g.,wherein twoof such fusionpolypeptidesareassociated thereby formingahomodimerorother multimer.SuchVEGFreceptor fusionproteinsmaybe referred toasa "VEGF-Trap"or "VEGFTrap".VEGFreceptor fusion proteins within the context of the present disclosure that fall within this definition include chimeric polypeptides which comprise two ormore immunoglobulin (Ig)‑like domains of a VEGF receptor such as VEGFR1 (also known as Flt1) and / or VEGFR2 (also known as Flk1 or KDR), and may also contain a multimerizing domain (for example, an Fc domain).

[0020] An exemplary VEGF receptor fusion protein is a molecule referred to as VEGF1R2-FcΔC1(a) which is encoded by the nucleic acid sequence of SEQ ID NO:1 or nucleotides 79‑1374 or 79‑1371 thereof.

[0021] VEGF1R2-FcΔC1(a) comprises three components: (1) a VEGFR1 component comprising amino acids 27 to 129 of SEQ ID NO:2; (2) a VEGFR2 component comprising amino acids 130 to 231 of SEQ ID NO:2; and 8 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 (3) a multimerization component ("FcΔC1(a)") comprising amino acids 232 to 457 of SEQ ID NO:2 (the C-terminal amino acids of SEQ ID NO:2, i.e., K458, may or may not be included in the VEGF receptor fusion proteins, see U.S. Patent No. 7,396,664 or 7,354,579, incorporated herein for all purposes). Note that amino acids 1 to 26 of SEQ ID NO:2 are the signal sequence.

[0022] If the multimerizing component (MC) of a VEGF receptor fusion protein is derived from an IgG (e.g., IgG1) Fc domain, then theMChasno fewer aminoacids thanare in aminoacids232 to457ofSEQ IDNO:2. Thus, the IgGof theMC cannot be truncated to be shorter than 226 amino acids.

[0023] In an embodiment of the invention, the VEGF receptor fusion protein comprises amino acids 27‑458 or 27‑457 of SEQ ID NO: 2. (SEQ ID NO: 2; signal sequence underscored-missing in mature, processed aflibercept; optionally, lacking C-terminal Lysine)

[0024] In an embodiment of the invention, aflibercept is N-glycosylated at any one or more of Asparagines 62, 94, 149, 222 and 308.

[0025] In an embodiment of the invention, the VEGF receptor fusion protein comprises 9 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 (1) an immunoglobin-like (Ig) domain 2 of a first VEGF receptor (e.g., VEGFR1), and (2) an Ig domain 3 of a second VEGF receptor (e.g., VEGFR2), (3) and, optionally, further including an Ig domain 4 of the second VEGF receptor (e.g., VEGFR2) and (4) a multimerizing component (e.g., Fc domain of IgG including the hinge, CH2 and CH3 domains).

[0026] Forexample, in anembodiment of the invention, theVEGF receptor fusionprotein has the followingarrangement of said domains: • [VEGFR1 Ig domain 2]‑[VEGFR2 Ig domain 3]‑[MC] (e.g., a homodimer thereof) or • [VEGFR1 Ig domain 2]‑[VEGFR2 Ig domain 3]‑[VEGFR2 Ig domain 4]‑[MC] (e.g., a homodimer thereof).

[0027] Note that the present disclosure also includes, within its scope, high concentration formulations including, instead of a VEGF receptor fusion protein, a VEGFbindingmolecule or anti-VEGF antibody or antigen-binding fragments thereof or biopolymer conjugate thereof (e.g., KSI‑301) and uses thereof as discussed, e.g., • bevacizumab (e.g., at a concentration of about 80‑90 or 88 mg / ml), • ranibizumab (e.g., at a concentration of about 20‑40 mg / ml, e.g., 21‑35, 21 or 35 mg / ml), • an anti-VEGF aptamer such as pegaptanib (e.g., pegaptanib sodium), • a single chain (e.g., VL‑VH) anti-VEGF antibody such as brolucizumab (e.g., at a concentration of about 200‑400 or 200, 210, 400 or 420 mg / ml), • ananti-VEGFDARPin suchas theAbiciparPegolDARPin (e.g., at a concentration of about 70‑140, 70or 140mg / ml), or • a bispecific anti-VEGFantibody, e.g., which also binds toANG2, such asRG7716 (faricimab) (e.g., at a concentration of about 100‑400, 100, 105, 400 or 420 mg / ml).

[0028] In order tominimize the repetitiveness of the embodiments discussed herein, it is contemplated that the scope of the present invention includes embodimentswherein any of the formulations discussed herein include, in place of aVEGF receptor fusion protein, an anti-VEGFantibody or antibody fragment or other VEGFbindingmolecule as discussed herein (e.g., substituted with an anti-VEGF DARPin) at any of the concentrations discussed herein. For example, the present invention includes a formulation having 35 or 80 mg / ml ranibizumab, a buffer, a thermal stabilizer, a viscosity reducing agent and a surfactant.

[0029] DARPins areDesignedAnkyrinRepeat Proteins. DARPins generally contain three to four tightly packed repeats of approximately 33 amino acid residues, with each repeat containing a β-turn and two anti-parallel α-helices. This rigid framework provides protein stability whilst enabling the presentation of variable regions, normally comprising six amino acid residues per repeat, for target recognition.

[0030] An "anti-VEGF" antibody or antigen-binding fragment of an antibody refers to an antibody or fragment that specifically binds to VEGF.

[0031] Illustrative VEGF receptor fusion proteins include aflibercept (EYLEA®, Regeneron Pharmaceuticals, Inc.) or conbercept (sold commercially by Chengdu Kanghong Biotechnology Co., Ltd.). See International patent application publication no. WO2005 / 121176 or WO2007 / 112675. The terms "aflibercept" and "conbercept" include biosimilar versions thereof. A biosimilar version of a reference product (e.g., aflibercept) generally refers to a product comprising the identical amino acid sequence but includes products which are biosimilar under the U.S. Biologics Price Competition and Innovation Act. Pharmaceutical Formulations

[0032] The present invention includes methods in which the VEGF antagonist (e.g., aflibercept) that is administered to the patient’s eye is contained within a pharmaceutical formulation. The pharmaceutical formulation includes a VEGF antagonist along with a pharmaceutically acceptable carrier. Other agents may be incorporated into the pharmaceutical formulation to provide improved transfer, delivery, tolerance, and the like. The term "pharmaceutically acceptable"means approvedbya regulatory agencyof theFederal or a stategovernment or listed in theU.S.Pharmacopeiaor other generally recognized pharmacopeia for use in animals, and more particularly, in humans. The term "carrier" refers to a diluent, adjuvant, excipient, or vehicle with which the VEGF antagonist is administered. A multitude of appropriate formulations can be found in the formulary known to all pharmaceutical chemists: Remington’s Pharmaceutical Sciences (15th ed, Mack Publishing Company, Easton, Pa., 1975), e.g., Chapter 87 by Blaug, Seymour, therein.

[0033] Pharmaceutical formulations for use in a method of the present invention can be "high concentration". High concentration pharmaceutical formulations of the present invention include VEGF antagonist, e.g., VEGF receptor fusion protein (e.g., aflibercept), at a concentration of greater than40mg / ml, at least 41mg / ml, of at least 80mg / ml, of at least 100 10 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 mg / ml, of at least 125mg / ml, of at least 140mg / ml, of at least 150mg / ml, of at least 175mg / ml, of at least 200mg / ml, of at least 225mg / ml, of at least 250mg / ml, or of at least 275mg / ml. "High concentration" can refer to formulations that includea concentration of VEGFantagonist of fromabout 140mg / ml to about 160mg / ml, at least about 140mg / ml but less than 160 mg / ml, from about 41mg / ml to about 275mg / ml, from about 70mg / ml to about 75mg / ml or from about 80mg / ml to about 250 mg / ml. In some aspects, the VEGF antagonist concentration in the formulation is about any of the following concentrations: 41 mg / ml; 42 mg / ml; 43 mg / ml; 44 mg / ml; 45 mg / ml; 46 mg / ml; 47 mg / ml; 48 mg / ml; 49 mg / ml; 50mg / ml; 51 mg / ml; 52 mg / ml; 53 mg / ml; 54 mg / ml; 55 mg / ml; 56 mg / ml; 57 mg / ml; 58 mg / ml; 59 mg / ml; 60 mg / ml; 61 mg / ml; 62 mg / ml; 63mg / ml; 64mg / ml; 65mg / ml; 66mg / ml; 67mg / ml; 68mg / ml; 69mg / ml; 70mg / ml; 71mg / ml; 72mg / ml; 73mg / ml; 74 mg / ml; 75 mg / ml; 76 mg / ml; 77 mg / ml; 78 mg / ml; 79 mg / ml; 80 mg / ml; 81 mg / ml; 82mg / ml; 83 mg / ml; 84 mg / ml; 85 mg / ml; 86mg / ml; 87mg / ml; 88mg / ml; 89mg / ml; 90mg / ml; 91mg / ml; 92mg / ml; 93mg / ml; 94mg / ml; 95mg / ml; 96mg / ml; 97 mg / ml; 98 mg / ml; 99 mg / ml; 100 mg / ml; 101 mg / ml; 102 mg / ml; 103 mg / ml; 104 mg / ml; 105 mg / ml; 106mg / ml; 107 mg / ml; 108mg / ml; 109mg / ml; 110mg / ml; 111mg / ml; 112mg / ml; 113mg / ml; 113.3mg / ml; 114mg / ml; 114.1mg / ml; 114.2 mg / ml; 114.3 mg / ml; 114.4 mg / ml; 114.5 mg / ml; 114.6 mg / ml, 114.7 mg / ml, 114.8 mg / ml; 114.9 mg / ml; 115 mg / ml; 116 mg / ml; 117 mg / ml; 118 mg / ml; 119 mg / ml; 120 mg / ml; 121 mg / ml; 122 mg / ml; 123 mg / ml; 124 mg / ml; 125 mg / ml; 126 mg / ml; 127mg / ml; 128mg / ml; 129mg / ml; 130mg / ml; 131mg / ml; 132mg / ml; 133mg / ml; 133.3 mg / ml; 133.4 mg / ml, 134 mg / ml; 135 mg / ml; 136 mg / ml; 137 mg / ml; 138 mg / ml; 139 mg / ml; 140 mg / ml; 141 mg / ml; 142 mg / ml; 143 mg / ml; 144 mg / ml; 145 mg / ml; 146 mg / ml; 147 mg / ml; 148 mg / ml; 149 mg / ml; 150 mg / ml; 151 mg / ml; 152 mg / ml; 153 mg / ml; 154mg / ml; 155mg / ml; 156mg / ml; 157mg / ml; 158mg / ml; 159mg / ml; 160mg / ml; 161mg / ml; 162mg / ml; 163mg / ml; 164 mg / ml; 165 mg / ml; 166 mg / ml; 167 mg / ml; 168 mg / ml; 169 mg / ml; 170 mg / ml; 171 mg / ml; 172 mg / ml; 173 mg / ml; 174 mg / ml; 175 mg / ml; 176 mg / ml; 177 mg / ml; 178 mg / ml; 179 mg / ml; 180 mg / ml; 181 mg / ml; 182 mg / ml; 183 mg / ml; 184 mg / ml; 185 mg / ml; 186 mg / ml; 187 mg / ml; 188 mg / ml; 189 mg / ml; 190 mg / ml; 191 mg / ml; 192 mg / ml; 193 mg / ml; 194 mg / ml; 195 mg / ml; 196 mg / ml; 197 mg / ml; 198 mg / ml; 199 mg / ml; 200 mg / ml; 201 mg / ml; 202 mg / ml; 203 mg / ml; 204 mg / ml; 205 mg / ml; 206 mg / ml; 207 mg / ml; 208 mg / ml; 209 mg / ml; 210 mg / ml; 211 mg / ml; 212 mg / ml; 213 mg / ml; 214 mg / ml; 215 mg / ml; 216 mg / ml; 217 mg / ml; 218 mg / ml; 219 mg / ml; 220 mg / ml; 221 mg / ml; 222 mg / ml; 223 mg / ml; 224 mg / ml; 225 mg / ml; 226 mg / ml; 227 mg / ml; 228 mg / ml; 229 mg / ml; 230 mg / ml; 231 mg / ml; 232 mg / ml; 233 mg / ml; 234 mg / ml; 235 mg / ml; 236 mg / ml; 237mg / ml; 238 mg / ml; 239 mg / ml; 240 mg / ml; 241 mg / ml; 242 mg / ml; 243 mg / ml; 244 mg / ml; 245 mg / ml; 246 mg / ml; 247 mg / ml; 248 mg / ml; 249 mg / ml; 250 mg / ml; 251 mg / ml; 252 mg / ml; 253 mg / ml; 254 mg / ml; 255 mg / ml; 256 mg / ml; 257 mg / ml; 258 mg / ml; 259 mg / ml; 260 mg / ml; 261 mg / ml; 262 mg / ml; 263 mg / ml; 264 mg / ml; 265 mg / ml; 266 mg / ml; 267 mg / ml; 268 mg / ml; 269 mg / ml; 270 mg / ml; 271 mg / ml; 272 mg / ml; 273 mg / ml; 274 mg / ml; or 275 mg / ml. Other VEGF antagonist concentrations are contemplated herein, as long as the concentration functions in accordance with embodiments herein.

[0034] In an embodiment of the invention, a pharmaceutical formulation for use in amethod of the present invention is of suchaconcentrationas to contain about 4, 6, 8, 10, 12, 14, 16, 18or 20mgVEGFreceptor fusionprotein (e.g., aflibercept), or the amount of such protein in any of the acceptable doses thereof which are discussed herein, in about 100 µl or less, about 75µl or less or about 70µl or less, e.g., about 50µl; 51µl; 52µl; 53µl; 54µl; 55µl; 56µl; 57µl; 58µl; 59µl; 60µl; 61 µl; 62µl; 63µl; 64µl; 65µl; 66µl; 67µl; 68µl; 69µl; 70µl; 71µl; 72µl; 73µl; 74µl; 75µl; 76µl; 77µl; 78µl; 79µl; 80µl; 81 µl; 82µl; 83µl; 84µl; 85µl; 86µl; 87µl; 88µl; 89µl; 90µl; 91µl; 92µl; 93µl; 94µl; 95µl; 96µl; 97µl; 98µl; 99µl; or 100µl.

[0035] The present invention includes methods of using (as discussed herein) any of the formulations set forth under "Illustrative Formulations" herein, but wherein the concentration of the VEGF receptor fusion protein (e.g., aflibercept) is substituted with a concentration which is set forth in this section ("VEGF Receptor Fusion Proteins and Other VEGF inhibitors").

[0036] Buffers for use in pharmaceutical formulations herein thatmay be used in amethod of the present invention refer to solutions that resist pH change by use of acid-base conjugates. Buffers are capable of maintaining pH in the range of fromabout 5.0 to about 6.8, andmore typically, fromabout 5.8 to about 6.5, andmost typically, fromabout 6.0 to about 6.5. In some cases, the pH of the formulation of the present invention is about 5.0, about 5.1, about 5.2, about 5.3, about 5.4, about 5.5, about 5.6, about 5.7, about 5.8, about 5.9, about 6.0, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, or about 6.8. Example buffers for inclusion in formulations herein include histidine-based buffers, for example, histidine, histidine hydrochloride, and histidine acetate. Buffers for inclusion in formulations herein can alternatively be phosphate-based buffers, for example, sodium phosphate, acetate-based buffers, for example, sodium acetate or acetic acid, or can be citrate-based, for example, sodium citrate or citric acid. It is also recognized that buffers can be a mix of the above, as long as the buffer functions to buffer the formulations in the above-described pH ranges. In some cases, the buffer is from about 5mM to about 25mM, or more typically, about 5 mM to about 15mM. Buffers can be about 5mM, about 6mM, about 7mM, about 8mM, about 9mM, about 10mM, about 11mM, about 12mM, about 13mM, about 14mM,about 15mM,about 16mM,about 17mM,about 18mM,about 19mM,about 20mM,about 21mM,about 22 mM, about 23 mM, about 24 mM, or about 25 mM.

[0037] In an embodiment of the invention, a histidine-based buffer is prepared using histidine and histidine mono- hydrochloride.

[0038] Surfactant for use herein refers to ingredients that protect the higher concentration of VEGF antagonist, e.g., 11 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 VEGF receptor fusion protein (e.g., aflibercept), from various surface and interfacial induced stresses. As such, surfactants can be used to limit or minimize VEGF receptor fusion protein aggregation and promote protein solubility. Suitable surfactants herein have been shown to be non-ionic, and can include surfactants that have a polyoxyethylene moiety. Illustrative surfactants in this category include: polysorbate 20, polysorbate 80, poloxamer 188, polyethylene glycol 3350, and mixtures thereof. Surfactants in the formulations can be present at from about 0.02% to about 0.1% weight per volume (w / v), and more typically, about 0.02% to about 0.04% (w / v). In some cases, the surfactant is about 0.02% (w / v), about 0.03% (w / v), about 0.04% (w / v), about 0.05% (w / v), about 0.06% (w / v), about 0.07% (w / v), about 0.08% (w / v), about 0.09% (w / v), or about 0.1% (w / v).

[0039] Thermal stabilizers for use in pharmaceutical formulations thatmay be used inmethods set forth herein refers to ingredients that provide thermal stability against thermal denaturation of theVEGFantagonist,e.g., VEGF receptor fusion protein (e.g., aflibercept), as well as protect against loss of VEGF receptor fusion protein potency or activity. Suitable thermal stabilizers include sugars, and can be sucrose, trehalose, sorbitol ormannitol, or can be amino acids, for example L-proline, L-arginine (e.g., L-arginine monohydrochloride), or taurine. Additionally, thermal stabilizers may also include substituted acrylamides or propane sulfonic acid, or may be compounds like glycerol.

[0040] In some cases, the pharmaceutical formulations for use in a method herein include both a sugar and taurine, a sugar and an amino acid, a sugar and propane sulfonic acid, a sugar and taurine, glycerol and taurine, glycerol and propane sulfonic acid, an aminoacid and taurine, or anaminoacid andpropane sulfonic acid. In addition, formulations can include a sugar, taurine andpropane sulfonic acid, glycerol, taurine andpropane sulfonic acid, aswell as L-proline, taurine and propane sulfonic acid.

[0041] Embodiments hereinmayhave thermal stabilizers present alone, each independently present at a concentration of, or present in combination at a total concentration of, from about 2% (w / v) to about 10% (w / v) or 4% (w / v) to about 10% (w / v), or about 4% (w / v) to about 9% (w / v), or about 5% (w / v) to about 8% (w / v). Thermal stabilizers in the formulation can beat a concentration of about 2% (w / v), about 2.5% (w / v), about 3% (w / v), about 4% (w / v), about 5% (w / v), about 6% (w / v), about 7% (w / v), about 8% (w / v), about 9% (w / v), about 10% (w / v) or about 20% (w / v).

[0042] With respect to taurine and propane sulfonic acid, in an embodiment of the invention, these thermal stabilizers can be present in the formulations at about from25mM to about 100mM, andmore typically fromabout 50mM to about 75 mM (as compared to the other thermal stabilizers).

[0043] Viscosity reducing agents typically are used to reduce or prevent protein aggregation. Viscosity reducing agents for inclusion herein include: sodium chloride, magnesium chloride, D‑ or L-arginine (e.g., L-argininemonohydrochloride), lysine, or mixtures thereof. When present herein, viscosity reducing agents can be present at from about 10 mM to about 100mM,andmore typically fromabout 30mM toabout 75mM,andevenmore typically fromabout 40mM toabout 70mM. In somecases, the viscosity reducingagent is present at about 10mM,about 15mM,about 20mM,about 25mM,about 30 mM, about 35 mM, about 40 mM, about 45 mM, about 50 mM, about 55 mM, about 60 mM, about 65 mM, about 70 mM, about 75 mM, about 80 mM, about 85 mM, about 90 mM, about 95 mM or about 100 mM.

[0044] Pharmaceutical formulations for use in amethodas set forth herein canalsohaveapharmaceutically acceptable viscosity for ocular administration, for example, intravitreal injection. Viscosity generally refers to the measure of resistance of a fluid which is being deformed by either shear stress or tensile stress (typically measured by techniques known in the art, viscometer or rheometer, for example). Typical viscosities of formulations for use in a method set forth hereinare fromabout 5.0 cP (centipoise) toabout15cP, fromabout 11cP toabout 14cP, fromabout 12cP toabout15cPor from about 11 cP to about 12 cP. As such, formulation viscosity herein can be about 5.0 cP, about 6.0, about 7.1 cP, about 7.2 cP, about7.3 cP,about 7.4 cP,about 7.5 cP, about7.6 cP,about 10cP,about 10.5cP, about11.0 cP, about11.5 cP, about 12.0cP,about12.5cP,about13.0cP,about13.5cP,about14.0cP,about14.5cP,orabout15.0cP (e.g.,whenmeasuredat 20°C).

[0045] Various embodiments herein do not require inclusion of an inorganic salt, or other viscosity reducing agent, to maintain thesehighlyuseful viscosities. Typically, high concentrationprotein solutions require viscosity reducingagents to avoid protein aggregation and higher viscosity, making the formulations difficult for intravitreal injection and reducing the potency of the VEGF receptor fusion protein. As such, embodiments herein include methods of using formulations that have had substantially no, or no added, sodium chloride (NaCl), magnesium chloride .(MgCl2), D‑ or L-arginine hydrochloride, lysine or other viscosity reducing agent.

[0046] Osmolality is a critical attribute for injectable pharmaceutical formulations for use in a method of the present invention. It is desirable to have products match physiological osmotic conditions. Furthermore, osmolality provides confirmation of soluble content in solution. In an embodiment of the invention, the osmolality of a formulation for use in a method of the present invention is less than or equal to about 506mmol / Kg or fromabout 250 to about 506mmol / Kg., e.g., about 250, 260, 270, 280, 290, 299, 300, 310, 314, 315, 316, 324, 343, 346, 349, 369, 384, 403, 426, 430 or 506mmol / Kg. In an embodiment of the invention, the osmolality is lower than about 250 mmol / Kg.

[0047] Illustrative pharmaceutical formulations for use in the methods of the present invention include the following: Formulation A: 80 mg / ml aflibercept, 10 mM histidine-based buffer, 5 % (w / v) sucrose, 0.03% (w / v) polysorbate 20, 12 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation B: 80mg / ml aflibercept, 10mMphosphate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation C: 80mg / ml aflibercept, 10mMcitrate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation D: 80 mg / ml aflibercept, 10 mM histidine-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 6.2. FormulationE: 80mg / ml aflibercept, 10mMphosphate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation F: 80mg / ml aflibercept, 10mMcitrate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation G: 80mg / ml aflibercept, 10 mM histidine-based buffer, 8 % (w / v) sucrose, and 0.03% (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. FormulationH: 80mg / ml aflibercept, 10mMphosphate-basedbuffer, 8%(w / v) sucrose, and0.03%(w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation I: 80 mg / ml aflibercept, 10mM citrate-based buffer, 8% (w / v) sucrose, and 0.0 3% (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation J: 80 mg / ml aflibercept, 10 mM histidine-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. FormulationK: 80mg / ml aflibercept, 10mMphosphate-basedbuffer, 8%(w / v) sucrose, and0.03% (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation L: 80mg / ml aflibercept, 10mMcitrate-based buffer, 8% (w / v) sucrose, and 0.03% (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. FormulationM: 150mg / ml aflibercept, 10mMhistidine-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation N: 150 mg / ml aflibercept, 10 mM phosphate-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation O: 150 mg / ml aflibercept, 10 mM citrate-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation P: 150mg / ml aflibercept, 10mM histidine-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 6.2. Formulation Q: 150 mg / ml aflibercept, 10 mM phosphate-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. FormulationR:150mg / mlaflibercept, 10mMcitrate-basedbuffer, 5%(w / v) sucrose, 0.03%(w / v)polysorbate80,and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation S: 150mg / ml aflibercept, 10mMhistidine-based buffer, 8% (w / v) sucrose, and 0.03% (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation T: 150 mg / ml aflibercept, 10 mM phosphate-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 20, with a pH of 5.8 to 6.2 (e.g., 6.2), and, optionally, specifically excluding a viscosity reducing agent. FormulationU:150mg / mlaflibercept, 10mMcitrate-basedbuffer, 8%(w / v) sucrose, and0.03%(w / v) polysorbate20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation V: 150mg / ml aflibercept, 10mMhistidine-based buffer, 8% (w / v) sucrose, and 0.03% (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation W: 150 mg / ml aflibercept, 10 mM phosphate-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. FormulationX: 150mg / mlaflibercept, 10mMcitrate-basedbuffer, 8%(w / v) sucrose, and0.03%(w / v) polysorbate80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation Y: 80 mg / ml conbercept, 10 mM histidine-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. FormulationZ: 80mg / ml conbercept, 10mMphosphate-basedbuffer, 5%(w / v) sucrose, 0.03% (w / v) polysorbate20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation AA: 80 mg / ml conbercept, 10 mM citrate-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. FormulationBB: 80mg / ml conbercept, 10mMhistidine-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 6.2. Formulation CC: 80mg / ml conbercept, 10mM phosphate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation DD: 80 mg / ml conbercept, 10 mM citrate-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 80, 13 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 and 40 mM sodium chloride, with a pH of 5.8 to 6.2. FormulationEE: 80mg / ml conbercept, 10mMhistidine-basedbuffer, 8%(w / v) sucrose, and0.03% (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation FF: 80 mg / ml conbercept, 10 mM phosphate-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation GG: 80mg / ml conbercept, 10mM citrate-based buffer, 8% (w / v) sucrose, and 0.03% (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. FormulationHH:80mg / ml conbercept, 10mMhistidine-basedbuffer, 8%(w / v) sucrose, and0.03%(w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation II: 80mg / ml conbercept, 10mMphosphate-basedbuffer, 8%(w / v) sucrose, and0.03%(w / v)polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation JJ: 80 mg / ml conbercept, 10 mM citrate-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation KK: 150 mg / ml conbercept, 10 mM histidine-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation LL: 150mg / ml conbercept, 10mMphosphate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. FormulationMM: 150mg / ml conbercept, 10mMcitrate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 20, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation NN: 150 mg / ml conbercept, 10 mM histidine-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 6.2. FormulationOO:150mg / ml conbercept, 10mMphosphate-basedbuffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation PP: 150mg / ml conbercept, 10mM citrate-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 80, and 40 mM sodium chloride, with a pH of 5.8 to 6.2. Formulation QQ: 150 mg / ml conbercept, 10 mM histidine-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation RR: 150 mg / ml conbercept, 10 mM phosphate-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation SS: 150mg / ml conbercept, 10mMcitrate-based buffer, 8% (w / v) sucrose, and 0.03% (w / v) polysorbate 20, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation TT: 150 mg / ml conbercept, 10 mM histidine-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation UU: 150 mg / ml conbercept, 10 mM phosphate-based buffer, 8 % (w / v) sucrose, and 0.03 % (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. Formulation VV: 150mg / ml conbercept, 10mMcitrate-based buffer, 8% (w / v) sucrose, and 0.03% (w / v) polysorbate 80, with a pH of 5.8 to 6.2, and, optionally, specifically excluding a viscosity reducing agent. FormulationWW:140mg / ml VEGF receptor fusion protein (e.g., aflibercept), 10mMhistidine-based buffer, 5% (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 50 mM taurine, with a pH of 5.8. Formulation XX: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept), 20 mM histidine-based buffer, 4 % (w / v) proline, 0.03 % (w / v) polysorbate 20, and 50 mM arginine hydrochloride, with a pH of 5.8. FormulationYY: 140mg / mlVEGF receptor fusion protein (e.g., aflibercept), 20mMhistidine-basedbuffer, 2.5% (w / v) sucrose, 2.0 % (w / v) proline, 0.03 % (w / v) polysorbate 20, and 50 mM taurine, with a pH of 5.8. FormulationZZ: 140mg / mlVEGF receptor fusion protein (e.g., aflibercept), 10mMhistidine-basedbuffer, 2.5% (w / v) sucrose, 2.0 % (w / v) proline, 0.03 % (w / v) polysorbate 20, and 50 mM arginine hydrochloride, with a pH of 5.8. FormulationAAA: 140mg / mlVEGF receptor fusion protein (e.g., aflibercept), 20mMhistidine-based buffer, 5% (w / v) sucrose, 0.03% (w / v) polysorbate 20, and 50 mM PSA, with a pH of 5.8. Formulation BBB: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept), 20 mM histidine-based buffer, 2.5 % (w / v) sucrose, 2.0 % (w / v) proline, 0.03 % (w / v) polysorbate 20, and 50 mM PSA, with a pH of 5.8. Formulation CCC: 80, 100, 120 or 140mg / ml VEGF receptor fusion protein (e.g., aflibercept), 20mMhistidine-based buffer, 5 % (w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 50 mM arginine hydrochloride, with a pH of 5.8. FormulationDDD:140mg / mlVEGF receptor fusionprotein (e.g., aflibercept), 10mMhistidine-basedbuffer, 4%(w / v) proline, 0.03 % (w / v) polysorbate 20, and 50 mM PSA, with a pH of 5.8. FormulationEEE: 140mg / mlVEGF receptor fusion protein (e.g., aflibercept), 20mMhistidine-based buffer, 5% (w / v) sucrose, and 0.03 % (w / v) polysorbate 20 and, optionally, no thermal stabilizer, with a pH of 5.8. Formulation FFF: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept), 10mM sodium phosphate, 5 % (w / v) sucrose and 0.03 % polysorbate 20 with a pH of 6.2. Formulation GGG: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5% sucrose; 14 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 0.03 % polysorbate 20; 50 mM sodium sulfate Formulation HHH: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5% sucrose; 0.03 % polysorbate 20; 50 mM sodium thiocyanate Formulation Ill: 140mg / mlVEGF receptor fusion protein (e.g., aflibercept); 20mMhistidine, pH5.8; 5%sucrose, 0.03 % polysorbate 20; 40 mM sodium citrate Formulation JJJ: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5% Sucrose, 0.03 % polysorbate 20; 50 mM glycine Formulation KKK: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5 % sucrose, 0.03 % polysorbate 20; 50 mM sodium chloride Formulation LLL: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5 % sucrose; 0.03 % polysorbate 20; 50 mM lysine FormulationMMM: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20mMhistidine, pH 5.8; 5% sucrose; 0.03% polysorbate 20; 50 mM sodium aspartate Formulation NNN: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5 % sucrose; 0.03 % polysorbate 20; 50 mM sodium glutamate Formulation OOO: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20mMhistidine, pH 5.8; 5% sucrose; 0.03% polysorbate 20; 50 mM sodium citrate; 50 mM arginine hydrochloride Formulation PPP: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5 % sucrose; 0.03% polysorbate 20; 50 mM glycine; 50 mM arginine hydrochloride Formulation QQQ: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20mMhistidine, pH 5.8; 5% sucrose; 0.03% polysorbate 20; 50 mM sodium aspartate; 50 mM arginine hydrochloride Formulation RRR: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20 mM histidine, pH 5.8; 5 % sucrose; 0.03% polysorbate 20; 50 mM sodium glutamate; 50 mM arginine hydrochloride FormulationSSS: 140mg / mlVEGF receptor fusion protein (e.g., aflibercept); 20mMHis, pH5.8; 5%sucrose; 0.03% polysorbate 20; 10 mM L-arginine hydrochloride Formulation TTT: 140mg / ml VEGF receptor fusion protein (e.g., aflibercept); 20mMHis, pH5.8; 5%sucrose; 0.03% polysorbate 20; 100 mM L-arginine hydrochloride FormulationUUU:30mg / mlVEGF receptor fusionprotein (e.g., aflibercept), 10%sucrose, 10mMphosphate, 0.03% polysorbate 20, pH 6.2 FormulationVVV: 30mg / mlVEGF receptor fusion protein (e.g., aflibercept), 20%sucrose, 10mMphosphate, 0.03% polysorbate 20, pH 6.2 FormulationWWW:60mg / ml VEGF receptor fusion protein (e.g., aflibercept), 10%sucrose, 10mMphosphate, 0.03 % polysorbate 20, pH 6.2 FormulationXXX: 60mg / mlVEGF receptor fusion protein (e.g., aflibercept), 20%sucrose, 10mMphosphate, 0.03% polysorbate 20, pH 6.2 Formulation YYY: 120mg / ml VEGF receptor fusion protein (e.g., aflibercept), 10% sucrose, 10mM phosphate, 0.03 % polysorbate 20, pH 6.2 Formulation ZZZ: 120mg / ml VEGF receptor fusion protein (e.g., aflibercept), 20% sucrose, 10 mM phosphate, 0.03 % polysorbate 20, pH 6.2 FormulationAAAA:120mg / mlVEGF receptor fusionprotein (e.g., aflibercept), 10%sucrose, 10mMphosphate, 0.03 % polysorbate 20, 50 mM NaCl, pH 6.2 FormulationBBBB:120mg / mlVEGF receptor fusionprotein (e.g., aflibercept), 20%sucrose, 10mMphosphate, 0.03 % polysorbate 20, 50 mM NaCl, pH 6.2 Formulation CCCC: 140 mg / ml VEGF receptor fusion protein (e.g., aflibercept), 10 mM sodium phosphate, 5 % sucrose, 40 mM sodium chloride, 0.03 % PS20, pH 6.2 FormulationDDDD:80mg / mlVEGFreceptor fusionprotein (e.g., aflibercept), 20mMhistidine-basedbuffer, 5%(w / v) sucrose, 0.03 % (w / v) polysorbate 20, and 50 mM L-arginine monohydrochloride, with a pH of 5.8. Formulation EEEE: 120.0mg / ml VEGF receptor fusion protein (e.g., aflibercept) (e.g.,± 12mg / ml), 20mMhistidine- based buffer (e.g.,± 2mM), 5% (w / v) sucrose (e.g.,± 0.5%), 0.03% (w / v) polysorbate 20 (e.g., 0.02‑0.04%), and 50 mM L-arginine monohydrochloride (e.g., ± 5 mM), with a pH of 5.8 (e.g., 5.6‑6.0 or 5.5‑6.1). Formulation FFFF: 113.3 mg / ml VEGF receptor fusion protein (e.g., aflibercept) (e.g., 102‑125 mg / ml), 20 mM histidine-based buffer (e.g., ± 2 mM), 5 % (w / v) sucrose (e.g., ± 0.5%), 0.03 % (w / v) polysorbate 20 (e.g., 0.02‑0.04%), and 50 mM L-arginine monohydrochloride (e.g., ± 5 mM), with a pH of 5.8 (e.g., 5.6‑6.0 or 5.5‑6.1). Formulation GGGG: 114.3 mg / ml VEGF receptor fusion protein (e.g., aflibercept) (e.g., 103‑126 mg / ml), 10 mM histidine-based buffer (e.g., ± 1 mM), 5 % (w / v) sucrose (e.g., ± 0.5%), 0.03 % (w / v) polysorbate 20 (e.g., 0.02‑0.04%), and 50 mM L-arginine (e.g., L-arginine monohydrochloride) (e.g., ± 5 mM), with a pH of 5.8 (e.g., 5.6‑6.0 or 5.5‑6.1). FormulationHHHH: 100.0mg / ml VEGF receptor fusion protein (e.g., aflibercept) (e.g.,± 10mg / ml), 20mMhistidine- 15 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 based buffer (e.g.,± 2mM), 5% (w / v) sucrose (e.g.,± 0.5%), 0.03% (w / v) polysorbate 20 (e.g., 0.02‑0.04%), and 50 mM L-arginine monohydrochloride (e.g., ± 5 mM), with a pH of 5.8 (e.g., 5.6‑6.0 or 5.5‑6.1). Formulation IIII: 133.3 mg / ml VEGF receptor fusion protein (e.g., aflibercept) (e.g., ± 13 mg / ml), 20 mM histidine- based buffer (e.g.,± 2mM), 5% (w / v) sucrose (e.g.,± 0.5%), 0.03% (w / v) polysorbate 20 (e.g., 0.02‑0.04%), and 50 mM L-arginine monohydrochloride (e.g., ± 5 mM), with a pH of 5.8 (e.g., 5.6‑6.0 or 5.5‑6.1). Formulation JJJJ: 150 mg / ml aflibercept (e.g., aflibercept) (e.g., ± 15 mg / ml), 10 mM sodium phosphate, 8% (w / v) sucrose (e.g.,± 0.8%), 0.03% (w / v) polysorbate 20 (e.g., 0.02‑0.04%) and 50 mM L-arginine hydrochloride, pH 6.2 (e.g., 6.0‑6.4 or 5.9‑6.5). Formulation KKKK: 114.3mg / ml VEGF receptor fusion protein (e.g., aflibercept) (e.g.,± 14mg / ml), 20mMhistidine- based buffer (e.g.,± 2mM), 5% (w / v) sucrose (e.g.,± 0.5%), 0.03% (w / v) polysorbate 20 (e.g., 0.02‑0.04%), and 50 mM L-arginine monohydrochloride (e.g., ± 5 mM), with a pH of 5.8 (e.g., 5.6‑6.0 or 5.5‑6.1).

[0048] In an embodiment of the invention the formulation that can be administered, e.g., intravitreally, to a subject is an aqueous pharmaceutical formulation comprising: at least about 100 mg / ml of a VEGF receptor fusion protein comprising two polypeptides that each comprises an immunoglobin-like (Ig) domain 2 of VEGFR1, an Ig domain 3 of VEGFR2, and a multimerizing component (e.g., aflibercept); about L-arginine (e.g., at a concentration of about 10‑100 mM); sucrose; a histidine-based buffer; and a surfactant; wherein the formulation has a pH of about 5.0 to about 6.8; wherein the VEGF receptor fusion protein has less than about 3.5%highmolecular weight species immediately aftermanufacture and purification and / or less than or equal to about 6% high molecular weight species after storage for about 24 months at about 2‑8°C.

[0049] See International Patent Application Publication No. WO2019 / 217927 and US Patent No. 11103552. Treatment and Administration

[0050] The present invention provides methods for treating angiogenic eye disorders by sequentially administering initial loadingdosesofgreater thanor equal to (≥) about8mg (e.g., about every2‑4or 3‑5weeks)ofVEGFantagonist (e.g., aflibercept) followed by additional doses of ≥ about 8 mg every 12 weeks of VEGF antagonist (e.g., aflibercept). For example, in an embodiment of the invention, the methods of the present invention include treating or preventing angiogenic eye disorders, such as diabetic retinopathy, diabetic macular edema or neovascular AMD, by administering, sequentially, oneormore (e.g., 3, 4or 5) doses (e.g.,≥about 8mg)about everymonth (or about every28days, 28±5days or about every 4 weeks), followed by one or more doses (e.g., ≥ about 8 mg) about every 12 weeks. For example, in an embodiment of the invention, about 8 mg is 7.2 mg, 8.8 mg or 7.2‑8.8 mg or 8 mg ± about 10%.

[0051] The terms "initial dose," "secondary doses," and "tertiary doses," refer to the temporal sequence of adminis- tration of theVEGFantagonist (e.g., aflibercept). Thus, the "initial dose" is the dosewhich is administered at the beginning of the treatment regimen (also referred to as the "baseline dose"); the "secondary doses" are the doses which are administered after the initial dose; and the "tertiary doses" are the doses which are administered after the secondary doses. The initial dose occurs onday 1 for the purposes of counting or numbering days thereafter (seee.g., Tables 1‑1and 1‑2 herein). The initial, secondary, and tertiary doses may all contain the same amount of VEGF antagonist, but will generally differ from one another in terms of frequency of administration. In certain embodiments, however, the amount of VEGF antagonist contained in the initial, secondary and / or tertiary doses will vary from one another (e.g., adjusted up or downasappropriate) during thecourseof treatment. Thus, adosing regimenof thepresent inventionmaybeexpressedas follows: a single initial dose (e.g.,≥about 8mg)of aVEGFantagonist (e.g., aflibercept), followedbyoneormore (e.g., 2, or 3or 4) secondary doses of the VEGF antagonist, followed by one or more tertiary doses of the VEGF antagonist; wherein each secondary dose is administered 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 12 weeks after the immediately preceding dose. The initial and secondary dosesadministeredbefore the tertiary dosesmaybe referred to, generally, as "loading" doses. The tertiary doses may be referred to as "maintenance" doses.

[0052] The present invention includes methods wherein one or more additional, non-scheduled, pro re nata (PRN) doses, in addition to any of the scheduled initial, secondary and / or tertiary doses of VEGFantagonist (e.g., aflibercept) are 16 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 administered to a subject. SuchPRNdosesare typically administeredat the discretion of the treating physician depending on the particular needs of the subject.

[0053] In an embodiment of the invention, - the method comprises administering the secondary doses to a subject who has received the initial dose - the method comprises administering the remaining secondary doses to a subject who has already received one or more secondary doses; - themethod comprises administering one ormore tertiary doses to a subject who has already received the secondary doses - the method comprises administering one or more tertiary doses to a subject who has already received one or more tertiary doses; optionally wherein the subject receives doses, earlier in the regimen, in one pharmaceutical formulation and additional doses, later in the regimen, in a different pharmaceutical formulation, for example, comprising a different buffer (e.g., wherein one ormore of the secondary doses are in one pharmaceutical formulation and the tertiary doses are in a different pharmaceutical formulation).

[0054] Dosing every "month" refers to dosing about every 28days, about every 4weeks, or about every 28±5days and may encompass up to every 5 weeks. Dosing every "4 weeks" refers to dosing about every 28 days, about everymonth or about every 28 ± 5 days, and may encompass up to every 5 weeks.

[0055] Dosing every "2‑4 weeks" refers to dosing about every 2 weeks, 3 weeks or 4 weeks. Dosing every "8 weeks" refers to dosing about every 2 months, about every 56 days, 56 ± 5 days.

[0056] Dosing every "12 weeks" refers to dosing about every 3 months, about every quarter year, about every 84, 90 days, 84 ± 5 days, or 90 ± 5 days.

[0057] Adoseof greater thanor equal to about 8mgor≥about 8mgVEGFantagonist (e.g., aflibercept) includes7.2mg; 7.2‑8.8mg; 8.0mg; 8.01mg; 8.1mg; 8.2mg; 8.3mg; 8.4mg; 8.5mg; 8.6mg; 8.7mg; 8.8mg; 8.9mg; 9mg; 9.1mg; 9.2mg; 9.3 mg; 9.4 mg; 9.5mg; 9.6 mg; 9.7 mg; 9.8 mg; 9.9 mg, 10.0mg, 10.1mg; 10.2mg; 10.3mg; 10.4mg; 10.5mg; 10.6mg; 10.7 mg; 10.8 mg; 10.9 mg; 11 mg; 11.1 mg; 11.2 mg; 11.3 mg; 11.4 mg; 11.5 mg; 11.6 mg; 11.7 mg; 11.8 mg; 11.9 mg; 12 mg; 12.1mg; 12.2mg; 12.3mg; 12.4mg; 12.5mg; 12.6mg; 12.7mg; 12.8mg; 12.9mg; 13mg; 13.1mg; 13.2mg; 13.3mg; 13.4mg;13.5mg;13.6mg;13.7mg;13.8mg;13.9mg;14mg;14.1mg;14.2mg;14.3mg;14.4mg;14.5mg;14.6mg;14.7 mg; 14.8mg; 14.9mg; 15mg; 15.1mg; 15.2mg; 15.3mg; 15.4mg; 15.5mg; 15.6mg; 15.7mg; 15.8mg; 15.9mg; 16mg; 16.1mg;16.2mg;16.3mg;16.4mg;16.5mg;16.6mg;16.7mg;16.8mg;16.9mg;17mg;17.1mg;17.2mg;17.3mg;17.4 mg; 17.5mg; 17.6mg; 17.7mg; 17.8mg; 17.9mg; 18mg; 18.1mg; 18.2mg; 18.3mg; 18.4mg; 18.5mg; 18.6mg; 18.7mg; 18.8mg; 18.9mg; 19mg; 19.1mg; 19.2mg; 19.3mg; 19.4mg; 19.5mg; 19.6mg; 19.7mg; 19.8mg; 19.9mg; or 20mg (± about 10%,±about 0.5, or±about 0.51mgof anyof the foregoing). In anembodiment of the invention, a dosageof≥8mg VEGF antagonist is administered in a dose having a volume of about 100 µl or less, about 75 µl or less or about 70 µl or less,e.g., about 50µl; 51µl; 52µl; 53µl; 54µl; 55µl; 56µl; 57µl; 58µl; 59µl; 60µl; 61µl; 62µl; 63µl; 64µl; 65µl; 66µl; 67 µl; 68µl; 69µl; 70µl; 71µl; 72µl; 73µl; 74µl; 75µl; 76µl; 77µl; 78µl; 79µl; 80µl; 81µl; 82µl; 83µl; 84µl; 85µl; 85‑87µl; 86µl; 87µl; 88µl; 89µl; 90µl; 91µl; 92µl; 93µl; 94µl; 95µl; 96µl; 97µl; 98µl; 99µl; or 100µl (± about 4, 4.45, 4.5, or 5 microliters).

[0058] Any dosing frequency specified herein may, in an embodiment of the invention, be expressed as the specific frequency "±5days" (e.g.,where "4weeks" is stated, thepresent inventionalso includesembodiments suchas4weeks± 5 days).

[0059] "Sequentially administering" means that each dose of VEGF antagonist (e.g., aflibercept) is administered to the eye of a patient at a different point in time, e.g., on different days separated by a predetermined interval (e.g., hours, days, weeks or months). The present invention includes methods which comprise sequentially administering, to the eye of a patient, a single initial dose of a VEGF antagonist, followed by one or more secondary doses of the VEGF antagonist, followed by one or more tertiary doses of the VEGF antagonist.

[0060] An effective or therapeutically effective dose of VEGF antagonist, e.g., aflibercept, for treating or preventing an angiogeniceyedisorder refers to theamountofVEGFantagonist sufficient toalleviateoneormoresignsand / or symptoms of the disease or condition in the treated subject, whether by inducing the regression or elimination of such signs and / or symptoms or by inhibiting the progression of such signs and / or symptoms. In an embodiment of the invention, an effective or therapeutically effective dose of VEGF antagonist is ≥ about 8 mg every month followed by once every 12 weeks.

[0061] An "angiogenic eye disorder" means any disease of the eye which is caused by or associated with the growth or proliferation of blood vessels or by blood vessel leakage. Non-limiting examples of angiogenic eye disorders that are treatable or preventable using the methods of the present invention include: • age-related macular degeneration (neovascular (nAMD)), • macular edema (ME), 17 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 • macular edema following retinal vein occlusion (ME-RVO), • retinal vein occlusion (RVO), • central retinal vein occlusion (CRVO), • branch retinal vein occlusion (BRVO), • diabetic macular edema (DME), • choroidal neovascularization (CNV), • iris neovascularization, • neovascular glaucoma, • post-surgical fibrosis in glaucoma, • proliferative vitreoretinopathy (PVR), • optic disc neovascularization, • corneal neovascularization, • retinal neovascularization, • vitreal neovascularization, • pannus, • pterygium, • vascular retinopathy, • diabetic retinopathies (DR) (e.g., non-proliferative diabetic retinopathy (e.g., characterized by aDiabetic Retinopathy Severity Scale (DRSS) level of about 47 or 53) or proliferative diabetic retinopathy; e.g., in a subject that does not suffer from DME), and • diabetic retinopathy in a patient who has diabetic macular edema (DME).

[0062] In an embodiment of the invention, a subject receiving a treatment for an angiogenic eye disorder as set forth herein (e.g., three monthly doses of about 8 mg aflibercept followed by doses of about 8 mg aflibercept every 12 weeks) achieves one or more of the following: • with respect to visual acuity (VA) or best corrected visual acuity (BCVA), achieving: ∘ No loss in visual acuity or BCVA or a gain in visual acuity or BCVA; ∘ no loss of visual acuity or BCVA, for example, by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose e.g., according to ETDRS (Early Treatment Diabetic Retinopathy Study) chart or Snellen equivalent (e.g., no loss of 5, 10, or 15 or more ETDRS letters (e.g., no loss of 5 (or more), 6 (or more), 7 (or more), 8 (ormore), 9 (ormore), 10 (ormore), 11 (ormore), 12 (ormore), 13 (ormore), 14 (ormore) or 15 (ormore) letters) or Snellen equivalent), ∘again in visual acuity orBCVA, forexample, byaboutweek4, 8, 9, 12, 16, 20,24, 28,32, 36, 40or44 following the initial dose,e.g., according toETDRSchart orSnellenequivalent (e.g., gaining5ormore,10ormoreor15ormore ETDRS letters (e.g., a gain of 5 (or more), 6 (or more), 7 (or more), 8 (or more), 9 (or more), 10 (or more), 11 (or more), 12 (or more), 13 (or more), 14 (or more) or 15 (or more) letters)); and / or ∘ a gain in BCVA of about 6 or 7 or 8 letters (or more) (e.g., according to ETDRS chart or Snellen equivalent) by week 8 and maintaining a gain of about 6 or 7 or 8 letters until at least about week 44; • with respect to central retinal thickness (CRT), achieving: o a decrease in central retinal thickness; o a decrease in central retinal thickness by at least about 123, 125, 131, 142, 147, 149, 150, 151, 156, 157, 158, 159, 161, 162, 166, 167, 168, 172, 173, 175, 177, 178 or 183micrometers (or more), for example, by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose, for example, wherein the baseline (prior to treatment) CRT, is about 488, 492, 497 or 516 micrometers; ∘ a decrease in CRTof about 47 micrometers (or more) from about week 12 to about week 20 following the initial dose, e.g., wherein the baseline CRT is about 516 micrometers; ∘ a decrease in CRTof about 17 micrometers (or more) from about week 24 to about week 32 following the initial dose, e.g., wherein the baseline CRT is about 516 micrometers; ∘ a decrease in CRTof about 18 micrometers (or more) from about week 36 to about week 44 following the initial dose, e.g., wherein the baseline CRT is about 516 micrometers; ∘ a decrease in central retinal thickness by at least about 4 or 24.3 micrometers (or more) from about week 12 to about week 16, for example, wherein the baseline CRT, prior to treatment, is about 516 micrometers; ∘ a decrease in CRTof about 123, 131 161 micrometers (or more) (e.g., by about week 4, 8, 12, 16 or 20) and maintaining the decrease until at least about week 44 following the initial dose; and / or 18 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 ∘ a reduction in CRT of about 159, 160, 161 or 162 micrometers (or more) by about week 4 or 8 or 12 and maintaining a reduction of about 159, 160, 161 or 162 micrometers (or more) until at least about week 44; • with respect to retinal fluid, achieving: ∘ a dry retina (e.g., no IRF and no SRF; or no IRF; or no SRF, e.g., in the center subfield or in the macula, e.g., on SD-OCT); ∘nofluid in the center subfield (e.g., no IRFandnoSRF;or no IRF; or noSRF)byaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose (e.g., as measured by SD-OCT); ∘ no sub-retinal pigment epithelium (RPE) fluid; e.g., by about week 16, e.g., until at least about week 44 following the initial dose (e.g., as measured by SD-OCT); ∘ no SRF and IRF in the macula, e.g., by SD-OCT, e.g., by week 16 or week 44 following the initial dose, and / or ∘maintenance of a dry retina, e.g., once achieved (e.g., at 16 weeks following the initial dose); until at least about week 44 (e.g., as measured by SD-OCT); • achieving: ∘ reduction in total lesion size by at least about 3.3µm; and / or choroidal neovascularization (CNV) size of at least about 3.2µm from baseline by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, e.g., wherein baseline total lesion size is about 7.7 µm and / or baseline CNV size is about 7.5 µm; ∘nosignificant increase in intraocular pressure frombaselinebyaboutweek4,8, 9, 12,16, 20, 24,28, 32, 36,40or 44 or later (e.g., by no more than about 0.2 or 0.5 mmHg); and / or ∘ no significant increase in blood pressure (e.g., systolic (S) or diastolic (D)) from baseline by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later (e.g., by nomore than about 0.1 (S) or 0.9 (S), 1.0 (D) or 1.4 (D)mmHg); e.g., wherein baseline systolic pressure is about 125 mmHg or 129 mmHg and / or baseline diastolic pressure is about 72 mmHg or 74 mmHg; and / or • with respect to efficacy or safety: ∘Efficacyand / or safety, in a subject suffering fromDRorDME, similar to or greater than that of afliberceptwhich is intravitreally dosed at 2 mg approximately every 4 weeks for the first 5 injections followed by 2mg approximately once every 8 weeks or once every 2months, e.g., wherein efficacy is measured as an increase in visual acuity or BCVA and / or a reduction in central retinal thickness, achievement of dry retina (e.g., no IRF and / or SRF), e.g., wherein safety is asmeasuredas the incidenceof adverseevents (treatment-emergent adverseeventsoccurring anytime within 30 days of any injection) such as intraocular inflammation, clinically significant blood pressure increase, clinically significant intraocular pressure increase, visual impairment, vitreous floaters, vitreous detachment, iris neovascularization and / or vitreous hemorrhage; and / or ∘ Efficacy and / or safety, in a subject suffering from nAMD, similar to or greater than that of aflibercept which is intravitreally dosed at 2 mg approximately every 4 weeks for the first 3 injections followed by 2mg approximately once every 8 weeks or once every 2months, e.g., wherein efficacy is measured as an increase in visual acuity or BCVA and / or a reduction in central retinal thickness, achievement of dry retina (e.g., no IRF and / or SRF), e.g., wherein safety is asmeasuredas the incidenceof adverseevents (treatment-emergent adverseeventsoccurring anytime within 30 days of any injection) such as intraocular inflammation, clinically significant blood pressure increase, clinically significant intraocular pressure increase, visual impairment, vitreous floaters, vitreous detachment, iris neovascularization and / or vitreous hemorrhage; for example, wherein such an effect (e.g., improvement of BCVA,CRTand / or retinal fluid) are achieved and / ormaintained for as long as the subject is receiving the treatment regimen.

[0063] The center subfield of the retina is a 1 mm diameter area around the macula. The macula itself is about 6 mm in diameter.

[0064] The present invention also includes methods for achieving any one or more of the foregoing in a subject (e.g., increase in VA or BCVA, or decrease in CRT) suffering from an angiogenic eye disorder, e.g., nAMD, DR or DME, comprising administering to an eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist (e.g., aflibercept), followed by one or more (e.g., 3, 4 or 5) secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 12 weeks after the immediately preceding dose. 19 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55

[0065] Thepresent invention includesmethods for treating or an angiogenic eye disorder (e.g., nAMD,DR,DMEorME- RVO), in a subject in need thereof, comprising administering to an eye of the subject, a single initial dose of about 8mg or moreof aVEGFantagonist (e.g., aflibercept), followedbyoneormoresecondarydosesofabout 8mgormoreof theVEGF antagonist, followedbyoneormore tertiary doses of about 8mgormoreof theVEGFantagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 12 weeks after the immediately preceding dose; wherein the subject achieves a change in central retinal thickness, from baseline at the initiation of treatment, as depicted in Figure 54 or Figure 55 (or a greater reduction), e.g., by the timepoint shown for such a change; and / or wherein the subject achieves a change in central retinal thickness, during the timeperiod as set forth in the inset boxof Figure 54 (or a greater reduction), and / or wherein the subject achieves a change in BCVA, from baseline at the initiation of treatment, as depicted in Figure 56 (or a greater increase), e.g., by the timepoint shown for such a change (such change in BCVA can be in terms of ETDRS letters gained or in the Snellen equivalent); and / or wherein the subject does not experience any one or more of the ocular TEAEs set forth in Figure 58, ocular serious TEAEs set forth in Figure 59, intraocular inflammation, any of the intraocular pressure events set forth in Figure 61, non-ocular TEAEs set forth in Figure 63, non-ocular serious TEAEs set forth in Figure 64, hypertension TEAEs set forth in Figure 65 and / or an APTC event. Best Corrected Visual Acuity (BCVA)

[0066] Best corrected visual acuity (BCVA) can bemeasured in variousmethods known in the art. First, determining the proper level of lens refraction needed to best correct the visual acuity (VA) of a subject is determined before testing best corrected visual acuity (BCVA) with a visual acuity chart.

[0067] Two separate VA charts used for testing the right and left eye (e.g., Sloan Letter ETDRSChart 1 andSloan Letter ETDRS Chart 2, respectively), and a third refraction chart is used for testing appropriate refraction (e.g., Sloan Letter ETDRSChart R). The features of the Sloan charts are high-contrast Sloan letters of equal difficulty, 5 letters in each of 14 rows, and a geometric progression of letter size (and, thus, an arithmetic progression of the logarithmofminimumangle of resolution [LogMAR]) from row to row. The charts have different letter sequences.

[0068] There are threebasic components to determining refraction according toETDRSprotocol-determining spherical power, determining cylindrical axis and determining cylindrical power usingmethods known by practitioners in the art. For assessing refraction, if the subject wears contact lenses and has glasses, he or she should be told not to wear the contact lenses on the day of the examination or remove them 30‑60 minutes before refraction is done. A trial frame is placed and adjusted on the subject’s face so that lens cells placed in the frame are parallel to the anterior plane of the orbits and centered in front of the pupils. (It is permissible to use a phoroptor for subjective refraction. However, for testing visual acuity, the lenses from the final phoroptor refraction must be placed in a frame, and the final sphere must be rechecked).

[0069] BCVA can be measured first in one eye with a visual acuity chart, and then in the other eye with another visual acuity chart (e.g., Charts 1 and 2 as discussed herein), wherein each chart remains hidden from view until the eye in question is ready for testing. Thedistance from thesubject’s eyes to the visual acuity chart is typically 4meters (13 feet and 1.5 inches, or 157.5 inches). The subject should be asked to read slowly (e.g., at a rate not faster than about one letter per second). Eyes reading 19 or fewer letters correctly at 4 meters can be tested at 1 meter.

[0070] Two commonly used tools for testing visual acuity (VA) or BCVA include the Snellen and the Early Treatment Diabetic Retinopathy Study (ETDRS) VA charts (Early Treatment Diabetic Retinopathy Study research group. Photo- coagulation for diabetic macular edema. Early Treatment Diabetic Retinopathy Study report number 1, Arch Ophthalmol. 1985 Dec;103(12):1796‑806; Chen et al., Comparison of visual acuity estimates using three different letter charts under two ambient room illuminations. 2012;60(2):101‑104; Bailey & Lovie, New design principles for visual acuity letter charts, 1976;53(11):740‑745; Shamir et al., Comparison of Snellen andEarly Treatment Diabetic Retinopathy Study charts using a computer simulation, Int. J. Opthamology 9(1): 119‑123 (2016); Kaiser, Prospective Evaluation of Visual Acuity Assessment: AComparison of SnellenVersusETDRSCharts inClinical Practice (AnAOSThesis), TransAmOphthalmol Soc 2009;107:311‑324). A version of the Bailey-Lovie chart (Bailey & Lovie, New design principles for visual acuity letter charts. Am J Optometry Physiol Opt 1976;53:740‑745) was modified in 1982 based on the recommendations of the Committee onVision of theNational Academyof Sciences, National ResearchCouncil, andWorkingGroup 39, and byDr. RickFerris for use in theEarlyTreatmentDiabeticRetinopathyStudy (ETDRS).The "ETDRSchart" and theprotocol to test visionwith the chart is commonly used in clinical trials. TheETDRSchart is typically tested froma shorter distance (13 feet (or 4meters) rather than20 feet) thanSnellen, but doesnot allow theuseofmirrors to simulate thecorrect distance, has the same amount of letters in every row (five letters each), and has an equal spacing of both the letters and the rows on a logarithmic scale. The Snellen Chart uses a geometric scale to measure visual acuity, with normal vision at a distance 20 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 beingsetat20 / 20. Inanembodimentof the invention,VAorBCVAcanbeexpressed in termsofETDRSorSnellen.ETDRS VA values can be converted to a corresponding Snellen equivalent using methods known in the art. In an embodiment of the invention, VA or BCVA is measured with an ETDRS chart or with a Snellen chart. Precision Dose Drug Delivery

[0071] The present invention provides methods as set forth herein wherein a VEGF antagonist (e.g., aflibercept) is deliveredwithahighamount of precision,e.g., with adrugdelivery device (DDD) (e.g., with a0.5mLvolume),whether pre- filledor capableof beingfilled fromavial, anddeliveringavolumeof between70and100microliterwithanaveragevolume of about 81or 82or 81‑82microliters,e.g., with astandarddeviationof about 4or 5or 4‑5microliters (e.g., about 4.5or 4.46 microliters) or less. In an embodiment of the invention, the DDD is a syringe, e.g., with a 30 gauge, ½ inch needle.

[0072] One means for ensuring precision of a dose to be delivered with a device, such as a syringe, is by employing a syringe wherein the dose volume is device-determined. If the dose volume is device-determined, the device is designed only to deliver a single volume (e.g., 87 microliters) or a single volume with a limited amount of acceptable error (± 4‑5 microliters). Thus, if used properly, the user cannot deliver the wrong dose (e.g., cannot deliver more than the intended volume from the device).

[0073] Thepresent invention includes embodimentswherein, a precise dosageof about 8mgormore is a dose of about 9, 9.3, 9.33, 9.7, 9.8, 9.9, 9.7‑9.9mgormore± about 0.5, or±about 0.51mg is delivered to a subject’s eye. The volume in which adose is delivered canbe, for example, about 70, 81, 82, 81.7, 85, 86, 87, 85‑87microliters±about 4, 4.45, 4.5, or 5 microliters. Doses may be delivered with a dose delivery device (DDD) which is a syringe.

[0074] Highly precise doses of VEGF antagonist (e.g., aflibercept) may be delivered, for example, in a volume that is device-determined (wherein the device is a syringe), by a method that includes the steps: (a) priming the syringe (e.g., a pre-filled syringe), thereby removing air from the syringe and, thus avoiding injection of air into the eye, by advancing the plunger rod by a predetermined distance into the syringe body until advancement of the plunger rod is resisted by a stop; (b) rotating the plunger rod about a longitudinal axis; and (c) actuating the plunger rod to dispense a predetermined (device-determined) volume (e.g., about 70, 81, 82, 81.7, 85, 86, 87, 85‑87 microliters, ± about 4, 4.45, 4.5, or 5 microliters) of the formulation.

[0075] In an embodiment of the invention, the drug delivery device (DDD), comprises: • a barrel including a longitudinal axis, a proximal end region, and a distal end region, the proximal end region including an opening, wherein the barrel is configured to receive a drug therein; • a plunger rod disposed at least partially inside the barrel and protruding from the opening, wherein the plunger rod includes a rack having a plurality of teeth; and • a pinion having a plurality of teeth configured to engage with the plurality of teeth of the rack, wherein rotation of the pinion against the rack moves at least a part of the plunger rod along the longitudinal axis of the barrel; for example, which further comprises a shaft affixed to the pinion, wherein rotation of the shaft rotates the pinion against the rackwhichmay include a knobaffixed to the shaft. In an embodiment of the invention, theDDD further includes a magnifier disposed on the distal end region of the barrel. In an embodiment of the invention, the DDD further includes a stopper inside thebarrel,wherein thestopper is affixed toadistal endof theplunger rod. Inanembodiment of the invention, the DDD further includes a circular ratchet disposed coaxially with the pinion, wherein the circular ratchet has a diameter smaller than a diameter of the pinion; a spring-loaded pawl disposed on an internal circumference of the pinion, wherein the pawl is configured to engage the ratchet; and a shaft affixed to the ratchet, wherein rotation of the shaft in one direction causes rotationof thepinion,and rotationof theshaft inaseconddirectiondoesnot cause rotationof thepinion forexample wherein the ratchet is disposed inside the pinion. In an embodiment of the invention, the pinion includes a plurality of teeth having a first height, and a stopper tooth having a second height greater than the first height, for example, wherein the second height of the stopper tooth prevents the pinion from engaging the plurality of teeth of the rack, and / or wherein the second height of the stopper tooth is configured to contact one of the plunger rod and the rack to stop rotation of the pinion. In an embodiment of the invention, the plunger rod includes an inner column and an outer lumen, and wherein the rack is disposed on the inner column, e.g., wherein rotation of the pinion against the rack moves the inner column of the plunger rod independently of the outer lumen, and / or further including a shaft removably affixed to the pinion, wherein the shaft preventsmovement of the outer lumen of the plunger rod relative to the barrel, and wherein removal of the shaft allows for movement of the outer lumen of the plunger rod relative to the barrel. In an embodiment of the invention, the plunger rod further includes a body and a flange, the flange extending partially along a longitudinal length of the body and having a width greater than a width of the body; wherein the barrel further comprises a plunger lock, the plunger lock including a through hole configured to allow the flange to pass through the second plunger lock in a specific orientation.

[0076] In an embodiment of the invention, the drug delivery device (DDD), comprises: 21 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 • abarrel includinga longitudinal axis, aproximal end region, adistal end region, andan interior, theproximal end region including an opening and the interior including a threaded region; and • a plunger rod disposed at least partially inside the barrel and protruding from the opening, the plunger rod including a threaded region configured to engage the threaded region of the barrel interior, wherein rotation of the plunger rod about the longitudinal axis of the drug delivery devicemoves the plunger rod along the longitudinal axis. In an embodiment of the invention, the plunger rod further includes a tab protruding from the plunger rod inafirst directionand locatedproximally from the threaded regionof theplunger rod, andwherein the threaded region in the interior of the barrel further includes a slot sized and configured to allow for the tab to pass through the threaded region in the interior of the barrel, e.g., wherein the slot includes a first segment parallel to the longitudinal axis of the drug delivery device and a second segment perpendicular to the longitudinal axis of the drug delivery device-the slotmay include a third segment parallel to the longitudinal axis of the drug delivery device, wherein the second segment is in between the first segment and the third segment. In anembodiment of the invention, the tab is a first tab, andwherein theplunger rod further includes a second tab protruding from the plunger rod in a second direction opposite to the first direction, and wherein the threaded region in the interior of the barrel further includes a second slot sizedand configured to allow for the second tab to pass through the threaded region in the interior of the barrel.

[0077] In an embodiment of the invention, the drug delivery device, includes: • a barrel having a proximal end region, a distal end region, an opening in the proximal end region, an interior, and a threaded region in the interior; • a sleeve disposed partly inside the barrel and protruding from the opening in the proximal end region of the barrel, the sleeve including a threaded region engaged with the threaded region of the barrel interior; • a plunger rod disposed at least partially inside the sleeve; and • astopper inside thebarrel and locateddistally from thesleeve, thestopper connected toadistal endof theplunger rod, wherein rotation of the sleeve in a first direction around a longitudinal axis of the drug delivery device moves the sleeve towards the distal end region of the barrel. In an embodiment of the invention, rotation of the sleeve in the first direction moves the stopper towards the distal end region of the barrel. In an embodiment of the invention; the sleeve includes an innerpassage,and thestopperhasadiameter larger thanadiameterof the innerpassage; and / or thesleeve includesa tab disposedonanexterior of the sleeve, the tab locatedproximally from the threaded regionof the barrel interior, andwherein the tab stopsmovement of the sleeve towards the distal end region of the barrel, e.g., wherein the tab is configured to stop movement of the sleeve towards the distal end region of the barrel after the drug delivery device has been primed or wherein the tab is a first tab, andwherein the sleeve further includes a second tabdisposedonanexterior of the sleeve, the second tab located distally from the threaded region of the barrel interior, wherein the second tab stops movement of the sleeve towards the proximal end region of the barrel.

[0078] In an embodiment of the invention, the drug delivery device, comprises: • a barrel including a proximal end region and a distal end region, the proximal end region including an opening; • a plunger rod including a body and a flange, the flange extending partially along a longitudinal length of the body and having a width greater than a width of the body, the plunger rod disposed at least partially inside the barrel and protruding from the opening; • a first plunger lock disposed on the barrel, the first plunger lock configured to block the flange fromentering the barrel; and • a second plunger lock disposed in the barrel, the second plunger lock including a through hole configured to allow the flange to pass through the second plunger lock in a specific orientation. For example, in an embodiment of the invention, the first plunger lock is removable and / or frangible. In an embodiment of the invention, a distance between the first plunger lock and the second plunger lock is equivalent to the distance that the stopper must travel to prime the drug delivery device; and / or the plunger rod is rotatable around a longitudinal axis of the drug delivery device.

[0079] Substances fromsuchaDDD (e.g., a formulation includingaflibercept as describedherein), having aplunger rod and a barrel, may be dispensed as follows: • advancing theplunger rod by apredetermineddistance into the barrel until advancement of the plunger rod is resisted by a stop; • deactivating the stop; and • actuating the plunger rod (e.g., which includes a flange, wherein the stop includes a lock that prevents the flange from entering thebarrel; orwhich includesaflange,wherein thestopcomprisesa lock thatprevents theflange fromentering 22 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 the barrel) to deliver the substance. Advancing the plunger rod may include the step of rotating a pinion against a rack disposed on the plunger rod, e.g., wherein the stop comprises a shaft removably affixed to thepinion, andwherein deactivating the stop comprises removing the shaft from the pinion. Deactivating the stopmay include the step of rotating the plunger rod. In an embodiment of the invention, deactivating the stop includes the step of removing the lock and / or breaking the lock.

[0080] In an embodiment of the invention, the drug delivery device, includes: • a barrel including a longitudinal axis, a proximal end region, and a distal end region, the proximal end region including an opening and a rack disposed on the interior of the barrel, the rack having a plurality of teeth, wherein the barrel is configured to receive a drug therein; • a plunger rod disposed at least partially inside the barrel and protruding from the opening, wherein the plunger rod includes a rack having a plurality of teeth; a pinion having a plurality of teeth configured to engage with the plurality of teeth of the plunger rod rack; and • an inner plunger coupled to the pinion by a rod, wherein rotation of the pinion against the plunger rod rack results in movement of the inner plunger along the longitudinal axis of the barrel; for example, wherein the teeth of the pinion are further configured to engagewith the plurality of teeth of the rack disposed on the barrel. In an embodiment of the invention, the pinion is a first pinion, and further includes: a second pinion disposed coaxiallywith thefirst pinion, thesecondpinionhavingadiameter smaller thanadiameterof thefirst pinionandaplurality of teeth configured to engage with the plurality of the teeth of the rack disposed on the barrel, wherein rotation of the first pinion results in rotation of the second pinion against the rack disposed on the barrel and inmovement of the inner plunger along the longitudinal axis of the barrel.

[0081] See International patent application publication no. WO2019 / 118588.

[0082] In an embodiment of the invention, the drug delivery device (DDD), includes: • a body; • a plunger rod disposed partially inside the body; • a protrusion extending from the plunger rod; and • ablockingcomponent coupled toaproximal endportionof thebody,wherein theblockingcomponent is aflangepiece, wherein,when theprotrusion is inafirst position relative to theblockingcomponent, theblockingcomponent restricts distal movement of theplunger rod to afirst stoppingpoint, andwhen theprotrusion is ina secondposition relative to theblocking component, the blocking component restricts distal movement of the plunger rod to a second stopping point. In an embodiment of the invention, the DDD further includes: a stopper disposed in the body, wherein distal movement of the plunger rod distallymoves the stopper; and a drug substance disposed in the body in between the stopper and a distal end of thebody,wherein distalmovement of theplunger rod to thefirst stoppingpoint primes thedrugdeliverydevice, anddistal movement of theplunger rod to the secondstoppingpoint dispensesapredeterminedvolumeof thedrugsubstance froma distal end of the device. In an embodiment of the invention,moving the protrusion from the first position to the second position includes twisting the plunger rod relative to the blocking component. In an embodiment of the invention, the DDD further includes: a cavity in a proximal side of the blocking component, the cavity sized and configured to receive a portion of the protrusion, wherein when the protrusion is in the second position relative to the blocking component, the protrusion is positioned proximally from the cavity, such that distalmovement of the plunger rodmoves theprotrusion into the cavity;e.g., wherein the cavity is afirst cavity, and further includes:asecondcavity inaproximal sideof theblockingcomponent, thesecondcavity sizedand configured to receive a portion of the protrusion, wherein the first and second cavity are located on opposite sides of a central longitudinal axis of the drug delivery device. In an embodiment of the invention, the plunger rod passes through an opening in the blocking component. In an embodiment of the invention the DDD further includes an actuation portion at a proximal end portion of the plunger rod, wherein the protrusion extends from the actuation portion, e.g., wherein the actuation portion includes a generally cylindrical shape having a diameter greater than a width of the remainder of the plunger rod, wherein the protrusion extends from a side of the generally cylindrical shape, and wherein the actuation portion further comprises: a thumb pad on a proximal end of the actuation portion; and a ring on an exterior surface on the side of the generally cylindrical shape; e.g., further including a proximal collar on the blocking component, wherein the actuation portion partially fits inside the proximal collar; e.g., wherein the plunger rod further includes a pair of extensions protrudingdistally from theactuationportionand theblockingcomponent (e.g.,which includesoneormore indents formed alonga bottomwall of the blocking component; andwherein a portion of eachextension is configured to be received by the one ormore indents upon distal movement of the plunger rod relative to the blocking component to allow distal movement 23 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 of the plunger rod to the second stopping point; or, which includes one or more indents formed along a bottom wall of the blocking component; andwherein aportion of eachextension is configured to be received by theoneormore indents upon distal movement of the plunger rod relative to the blocking component to allow distal movement of the plunger rod to the secondstoppingpoint; or,which includesapair of internal grooves formedalongasidewall of theblockingcomponent; and wherein a portion of eachextension is configured to be received by at least one of the pair of internal grooves upon rotation of theplunger rod relative to theblockingcomponent toexpand theextensions radially-outward fromacompressedstate to a relaxed state) includes a pair of openings; andwherein a portion of each extension is configured to be received by one of the pair of openings in the first stopping point. In an embodiment of the invention, the protrusion is a first protrusion, and further includes a second protrusion extending from the plunger rod in a direction opposite to the first protrusion. In an embodiment of the invention, the blocking component is slidably coupled to the body and includes a third cavity and a pair of ribs that extend into the third cavity, wherein the body includes a top flange and the pair of ribs are configured to engage the top flange received in the third cavity; wherein the pair of internal ribs are configured to apply a distally-directed force onto the top flange. Inanembodiment of the invention, theblockingcomponent is slidably coupled to thebodyand includes a pair of movable tabs that are configured to engage the body; and the pair of movable tabs are laterally deflectable upon receiving the body in the blocking component and are configured to apply a radially-inward directed force onto the body. In an embodiment of the invention, the blocking component further includes a pair of finger flanges, and each of the finger flanges includes a textured surface having a predefined pattern that increases a grip of the blocking component.

[0083] In an embodiment of the invention, the drug delivery device (DDD), includes: • a body; • a plunger rod having a distal end contacting a stopper inside the body, and a proximal end including an actuation portion with a thumb pad; • a plurality of protrusions extending from the actuation portion; and • a blocking component disposed on the body, the blocking component including a proximal collar having a plurality of slots, wherein, when the protrusions and the slots are in a first configuration relative to one another, the blocking component restricts distalmovement of the plunger rod to a first stopping point, andwhen the protrusions and the slots are in a second configuration, the blocking component restricts distal movement of the plunger rod to a second stopping point, wherein, in the second configuration, the slots are configured to receive theprotrusionsupondistalmovement of theplunger rod. In an embodiment of the invention, the protrusions and the slots are movable from the first configuration to the second configuration by rotation of the actuation portion about a longitudinal axis in relation to the blocking component, and whereinwhen theprotrusionsand theslots are in thesecondconfiguration, theprotrusionsand theslotsarenotmovable to the first configuration; and / or a difference between the first stopping point and the second stopping point is equivalent to a distance that the stopper must travel to expel a predetermined volume of a drug product from a distal end of the body, and wherein the plunger rod is prevented from moving from the second stopping point to the first stopping point; and / or the plurality of protrusions includes two protrusions disposed symmetrically about the actuation portion; and / or the blocking component further comprises apair of finger flanges; and / or the drugdelivery device is a pre-filled syringe; and / or the drug delivery device is changeable: (a) from a pre-use state to a primed state, by longitudinally moving the plunger rod (e.g., wherein the plunger rod includes a neck disposed distally from the actuation portion, wherein the neck interfaces with an opening in theblockingcomponent toprevent proximalmovementof theplunger rod, for example,wherein theneck further interfaces with the opening in the blocking component to prevent movement of the drug delivery device from the delivery state to theprimedstate) until theplunger rod reaches thefirst stoppingpoint; (b) from theprimedstate toadelivery stateby rotating the plunger rod in relation to the blocking component until the protrusions and the blocking component are in the second configuration; and (c) fromadelivery state to a used state by longitudinallymoving theplunger rod until the plunger reaches the second stopping point, wherein the drug delivery device is not changeable from the used state to the delivery state, from the delivery state to the primed state, or from the primed state to the pre-use state. In an embodiment of the invention, when the plunger rod is at the second stopping point, the stopper does not contact a distal end of the body.

[0084] In an embodiment of the invention, a drug delivery device, includes: • a body; • a plunger rod, including: • a distal portion contacting a stopper inside the body; • a proximal end including a generally cylindrical actuation portion disposed outside of the body; and • two protrusions extending from opposite sides of the actuation portion in a symmetrical configuration; and • ablockingcomponent coupled to thebody, theblockingcomponent including:acollar configured toacceptadistal part of the actuation portion; and two cavities in the collar having proximally-facing openings, wherein each cavity is configured to accept a distal portion of one of the two protrusions; 24 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 wherein the plunger rod is longitudinally movable and rotatable about a longitudinal axis relative to the blocking component, and wherein, when the drug delivery device is in a pre-use state, the protrusions and the cavity openings are not longitudinally aligned, andwhen the drug delivery device is in a delivery state, the protrusions and the cavity openings are longitudinally aligned. In an embodiment of the invention, the blocking component further includes a finger flange, and further includes a ribbed surface on a side of the actuation portion. In an embodiment of the invention, the plunger rod further includes: two extensions protruding distally from the actuation portion; and a plurality of openings in the collar of the blocking component, wherein a portion of each extension is configured to be received by one of the plurality of openings upon distal movement of the plunger rod relative to the blocking component.

[0085] In an embodiment of the invention, a drug delivery device includes: • a body; • a stopper disposed inside the body; • a sleeve having a proximal end and a distal end, the distal end being disposed inside the body, proximally from the stopper; and • a plunger rod disposed at least partially inside the sleeve; wherein, when the stopper is in a ready position, distal advancement of one of (a) only the sleeve, (b) only the plunger rod, or (c) both the sleeve and the plunger rod together, relative to the body advances the stopper to a primed position, and wherein, when the stopper is in the primed position, distal advancement of another of (a) only the sleeve, (b) only the plunger rod, or (c) both the sleeve and the plunger rod together, relative to the body advances the stopper to a dose completion position. For example, in an embodiment of the invention, a DDD further includes a removable blocking component (e.g., wherein the blocking component is a clip removably secured around at least a portion of the sleeve) disposed between a proximal portion of the sleeve and a proximal end of the body, the blocking component obstructing distal advancement of the sleeve relative to the body, wherein distal advancement of the sleeve relative to the body after removal of the blocking component advances the stopper to the primed position. In an embodiment of the invention, the DDD further includesa removable locking component (e.g., a pin, a tab, or a bar) that couples theplunger rod to the sleeve, wherein distal advancement of both the sleeve and the plunger rod together relative to the body advances the stopper to the primed position, wherein distal advancement of only the plunger rod relative to the body after removal of the locking component advances the stopper to the dose completion position. In an embodiment of the invention, in the dose completion position, a proximal end of the plunger rod abuts against a distal end of the sleeve, such that the plunger rod is prevented from advancing distally any further relative to the body. In an embodiment of the invention, the DDD further includesaprotrusiondisposedon theplunger rod; andan inner protrusiondisposedonan interiorwall of the sleevedistally to the protrusion of the plunger rod, wherein distal advancement of only the plunger rod relative to the body advances the stopper to theprimedpositionandcauses theprotrusionof theplunger rod tocontact the innerprotrusionof thesleeve, and wherein distal advancement of both the plunger rod and the sleeve relative to the body, after the protrusion of the plunger rod has contacted the inner protrusion of the sleeve, advances the stopper to the dose completion position. In an embodiment of the invention, the sleeve includes a finger flange. In an embodiment of the invention, the DDD further includes a stop disposed at a proximal end of the body, the stop sized to block distal advancement of the sleeve or the plunger rod once the stopper is in the completion position.

[0086] In an embodiment of the invention, a drug delivery device, includes: • a body; • a plunger rod having a distal portion disposed inside the body and a proximal portion disposed outside a proximal end of the body, the proximal portion having a width greater than a width of the distal portion; and • an obstruction that, in an obstructing position relative to the plunger rod, prevents distal advancement of the plunger rod from a primed position to a dose completion position, wherein displacement of the obstruction from the obstructing position permits distal advancement of the plunger rod to the dose completion position, for example, further including a collar affixed to a proximal end portion of the body, the collar surrounding the proximal portion of the plunger rod; and a collar projection extending radially inward from the collar, wherein the proximal portion of the plunger rod includes a channel into which the collar projection protrudes, the channel including a circumferential path and an axial dose completion path, wherein the obstruction comprises the collar projection, which, when disposed in the circumferential path of the channel, prevents distal advancement of the plunger rod to the dose completion position, and wherein displacement of the obstruction from the obstructing position comprises twisting the plunger rod about a longitudinal axis to align the collar projection with the axial dose completion path. For 25 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 example, in an embodiment of the invention, the channel further includes an axial priming path offset from the axial dose completion path, and connected to the axial dose completion path by the circumferential path, and distal movement of the plunger rod such that the collar projection travels on theaxial primingpath advances theplunger rod to theprimedposition. In an embodiment of the invention, the DDD further includes a finger flange. In an embodiment of the invention, the proximal portion of the plunger rod includes a projection extending radially outward, and the drug delivery device further includes: a rotatable alignment component disposed in between the proximal portion of the plunger rod and the body, the alignment component including a channel, the channel sized and configured to accommodate the plunger rod projection, wherein theobstructioncomprisesawall of thechannel that blocksadistal axial pathof theplunger rodprojectionwhen the plunger rod is in the primed position, andwherein displacement of the obstruction from the obstructing position comprises rotating the alignment component to remove thewall of the channel from the distal axial path of the plunger rod projection, e.g., further including a finger flange coupled to a proximal end portion of the body, wherein the rotatable alignment component is disposed between the finger flange and the proximal portion of the plunger rod. In an embodiment of the invention, the DDD further includes a flange piece disposed at the proximal end of the body, wherein the obstruction includes a removable cap that, when in the obstructing position relative to the plunger rod, is disposed partially in between the proximal portion of the plunger rod and the flange piece. In an embodiment of the invention, removal of the cap allows the proximal portion of the plunger rod to advance to a dose completion position, wherein, in the dose completion position, the proximal portion of the plunger rod contacts the flange piece. In an embodiment of the invention, the removable cap covers theproximal portionof the plunger rodwhen in theobstructingposition. In anembodiment of the invention, theDDD further includes a collar disposed between the proximal end of the body and the proximal portion of the plunger rod, the collar defining an opening sized to accommodate the proximal portion of the plunger rod upon distal advancement of the plunger rod beyond a primed position; wherein the obstruction comprises a tab protruding radially outward from the proximal portion of the plunger rod, the tabpreventing the proximal portion of the plunger rod fromfitting into theopening of the collar, and wherein a depth of the collar opening coincides with a distance the plunger rod must travel to advance distally to the dose completion position, e.g., wherein displacement of the obstruction from the obstructing position comprises either removing the tab or compressing the tab into a side of the proximal portion of the plunger rod; and / or wherein the tab is a first tab, and wherein the obstruction further comprises a second tab protruding radially outward from the proximal portion of the plunger rod in a direction opposite the protruding direction of the first tab; and / or wherein the obstruction comprises a tab that, when in the obstructing position, is disposed between the body and the proximal portion of the plunger rod, and wherein the plunger rod includes a geometry disposed proximally from the tab, wherein the geometry cannot advancedistally past the tabwhen the tab is in theobstructingposition. For example, displacement of the obstruction may include removing the tab from the drug delivery device by pulling the tab. In an embodiment of the invention, the DDD further includes a flange piece, wherein a portion of the tab is disposed inside a cavity of the flange piece. In an embodiment of the invention, displacement of the obstruction comprises removing the tab from the drug delivery device by breaking the tab. In an embodiment of the invention, the obstruction includes a flange piece that, in the obstructing position, is disposed proximally from the proximal end of the body, between the proximal portion of the plunger rod and the body, and is spaced from the proximal end of the body by a removable blocking component, and wherein displacement of the obstruction from the obstructing position comprises: removing the blocking component; and shifting theflangepiecedistally towards theproximal endof thebody. Inanembodiment of the invention, theplunger rod includesa projection extending radially outward, wherein the obstruction includes a lever having an end that, in the obstructing position, is locateddistally from theprojectionandblocksdistalmovementof theprojectionand therebydistalmovementof theplunger rod, andwherein displacement of theobstruction from theobstructingposition comprisesactuating the lever to remove the end of the lever from its location distal from the projection. In an embodiment of the invention, distal advancement of the plunger rod beyond the dose completion position is prevented by contact between the proximal portion of the plunger rod and a portion of a flange piece coupled to the body.

[0087] In an embodiment of the invention, the drug delivery device, includes: • a body; • a sleeve affixed to the body, the sleeve including a proximal end, a distal end, and an opening disposed in a circumferential wall of the sleeve; • aplunger rodpassing through the sleeve, theplunger rod includingadistal endportiondisposed inside thebody, anda radially-extending protrusion; wherein the plunger rodmay be distally advanced into the body from a ready position to a primed position, wherein, in the primed position, the protrusion of the plunger rod is disposed inside the opening, and further distal advancement of the plunger rod is resisted by contact between the protrusion and awall of the opening, andwherein pressuremay be exerted on the protrusion to overcome the resistance to further distal advancement of the plunger rod. In an embodiment of the invention, the opening in the sleeve is a second opening, and the sleeve further includes a first opening disposed in the circumferential wall of the sleeve proximally from the second opening, and a third opening disposed in the circumferential 26 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 wall of the sleeve distally from the second opening, wherein, in the ready position, the protrusion of the plunger rod is disposed in the first opening, and further distal advancement of the plunger rod is resisted by contact between the protrusion and a wall of the first opening, and wherein, after further distal advancement of the plunger rod past the primed position, theprotrusionof theplunger rod isdisposed in the thirdopening, and furtherdistal advancementof theplunger rod is prevented. In an embodiment of the invention, the radially-extending protrusion is a first protrusion, and wherein the plunger rod further includes a second radially-extending protrusion opposite the first protrusion, and wherein squeezing the first and secondprotrusions towards oneanotherwhile applyingaxial pressure in thedistal direction on the plunger rod overcomes the resistance to further distal advancement of the plunger rod. In an embodiment of the invention, the protrusion includes a distally-tapering profile to aid in distal advancement of the plunger rod.

[0088] In an embodiment of the invention, a drug delivery device, includes: • a body; • a plunger rod including a distal end portion disposed inside the body and a rotatable element; and • a sleeve affixed to the body, the sleeve including a proximal opening into which the plunger rod may be advanced, wherein rotating the rotatable element causes distal advancement of the plunger rod to a primed position, and wherein once the plunger rod is in the primed position, further rotation of the rotatable element is resisted. In an embodiment of the invention, the DDD further includes a collar disposed at a proximal end of the body, an interior of the collar including a proximal threaded portion forming a proximal helical path, wherein the rotatable element comprises a proximal portion of the plunger rod including a protrusion, wherein the proximal portion of the plunger rodmay be rotated about a longitudinal axis to cause the protrusion to travel distally along the proximal helical path, and wherein once the protrusion reaches the end of the proximal threaded portion of the collar, the plunger rod is in the primed position, e.g., wherein once the plunger rod is in the primed position, the plunger rodmay bedepressedaxially into the body to distally advance the plunger rod to a dose completion position; and / or wherein the interior of the collar further includes a distal threaded portion, wherein threads of the distal threaded portion form a distal helical path offset from, and opposite to, the proximal helical path, wherein alignment of the protrusion with the distal helical path places the plunger rod in the primed position, and wherein rotation of the proximal portion of the plunger rod to cause the protrusion to travel distally along the distal helical path causes distal advancement of the plunger rod to a dose completion position.

[0089] A substance may be dispensed using such a DDD having a plunger rod and a body, may be done by a method including: (a) advancing the plunger rod by a predetermined distance into the body until advancement of the plunger rod is resisted by a stop; (b) rotating the plunger rod about a longitudinal axis; and (c) actuating the plunger rod to dispense a predetermined volume of the substance, wherein none of steps (a), (b), and (c) are reversible. In an embodiment of the invention, theDDD further includes a flange piece having a collar, and advancing the plunger rod and actuating the plunger rod comprise pressing an actuation portion of the plunger rod into the collar of the flange piece; for example, wherein the plunger rod comprises a protrusion, and wherein thecollar of the flangepieceabuts against theprotrusion to resist advancementof theplunger rod. For example, in anembodiment of the invention,wherein rotating theplunger rodcomprises twistinganactuationportionof theplunger rod relative to the flange piece, until a protrusion on the plunger rod becomes longitudinally alignedwith a cavity in the collar of the flangepiece,whichmay further includeadvancing theprotrusion into the cavity until theprotrusionabuts adistal sideof thecavity,wherein thepredeterminedvolumeof thesubstance isdispensedwhen theprotrusionabuts thedistal sideof the cavity.

[0090] See International patent application publication no. WO2020 / 247686. EXAMPLES Example 1: A Randomized, Single-Masked, Active-Controlled Phase 2 Study of the Safety, Tolerability, and Ef- ficacy of Repeated Doses of High-Dose Aflibercept in Patients with Neovascular Age-Related Macular Degen- eration (CANDELA trial).

[0091] This phase 2, multi-center, randomized, single-masked study in patients with nAMD investigated the efficacy, safety, and tolerability of HD (8 mg doses) versus IAI (2mg doses). The Study dosing regimen is summarized in Figure 1. The Study consisted of a screening / baseline period, a treatment period, and an end of study (EOS) visit at week 44. Patientswere seenmonthly throughweek44.Onehundredandsixeligible patientswere randomized into2groups ina1:1 ratio. One group received IAI and the other receivedHD. The investigational product was administered intravitreally (IVT) 27 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 monthly for 3 initial injections (baseline, week 4, and week 8), followed by additional doses at weeks 20 and 32. At weeks 24, 28, 36and40,patientswereevaluatedandgivenadose (at their randomizeddose level) if eitherof the followingcriteria are met (PRN criteria): • Loss of ≥5 letters from week 20 BCVA due to disease progression; or • Anatomical findings that are considered vision threatening, such as worsening or persistent retinal fluid, new or worsening PED (pigment epithelial detachment), new or persistent hemorrhage, etc.

[0092] The following are the portions of the protocol by which the CANDELA human clinical trial was conducted.

[0093] The study also includes a pharmacokinetic (PK) sub-study, with dense blood sampling (dense PK sub-study) for systemic drug concentrations and PK assessments for approximately 15 patients from each group from selected sites. Additional patients (up to approximately 50%more in each treatment group)may be enrolled in the densePK sub-study to ensure adequate data is are captured. Dosing schedule

[0094] The dosing schedule for the IAI and HD groups are set forth below in Table 1‑1. Table 1‑1. Dosing schedule of IAI and HD groups in CANDELA study. Wk 4 Safety Analysis Wk 16 Efficacy Analysis Wk 44 Analysis ECS Screen 1 & 2 Day 1 (BL) Wk 4 Wk 8 Wk 8 Wk 12 Wk 16’ Wk 20 Wk 24 Wk 28 Wk 32 Wk 38 Wk 40 Wk 44 IAI - 2 mg 50 µl X X X BP / PK X PRN PRN X PRN PRN HD- 8 mg 70 µl X x X BP / PK X PRN PRN X PRN PRN

[0095] Additional visits for Dense PK Substudy: • Days 2, 3, 5, 8, 15 and 22 • Blood pressure & pharmacokinetic draws at all visits • Urinalysis (UA) at days 8 & 15

[0096] Week 16: Additional treatment allowed after discussion with sponsor

[0097] SeealsoTable 1‑2herein.Asdiscussed in thisExample, IAI dosing regimenscall for 2mgdosesgivenasdefined in Table 1‑1; and HD dosing regimens call for 8 mg doses given as defined in Table 1‑1. Primary Endpoints

[0098] The co-primary endpoints are: • Safety, which will be evaluated by assessment of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) through week 4; and • The proportion of patients without retinal fluid in the center subfield at week 16. 28 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 Secondary Endpoints

[0099] There are no secondary endpoints in this study. Exploratory Endpoints

[0100] The exploratory endpoints are: • The proportion of patients without retinal fluid in the center subfield at week 44; • The proportion of patients without retinal fluid in the center subfield at week 16; • Change in central retinal thickness (CRT) from baseline through week 16 and week 44; • The proportion of patients without intraretinal fluid (IRF) at week 16 and week 44; • The proportion of patients without subretinal fluid (SRF) at week 16 and week 44; • The proportion of patients without sub-retinal pigment epithelium (RPE) fluid at week 16 and week 44; • The proportion of patients able to maintain dry retina (total fluid, IRF, and / or SRF) through week 44; • The proportion of patients able to maintain a 12-week dosing interval from week 8 through week 44; • Change in CRT between dosing visits from week 8 through week 44; • Change in Best Corrected Visual Acuity (BCVA) from baseline, and proportions of patients gaining and losing vision, through week 16 and week 44; • Change in lesion size and choroidal neovascularization (CNV) size from baseline through week 20 and week 44; • Other safety outcomes (e.g., TEAEs,SAEs, vital signs, clinical laboratory values; and intraocular pressure [IOP]) from baseline through week 16 and week 44; and • Systemic PK of free and bound aflibercept assessed from baseline through week 44. Efficacy Variables

[0101] The efficacy variable relevant to the primary efficacy endpoint is the assessment of retinal fluid. The efficacy variables relevant to the exploratory endpoints are: • Assessmentof retinal fluid levels (total fluid, IRF, andSRF)and retinal thicknessonspectral domainoptical coherence tomography (SD-OCT, or just OCT) • Dosing interval; • Visual acuity; • Lesion size. Safety Variables

[0102] The safety variable relevant to the primary safety endpoint is the proportion of patients with TEAEs and SAEs.

[0103] The safety variables relevant to the exploratory endpoints are: • Ocular exams • Vital signs • Clinical laboratory values • IOP Pharmacokinetic Variables

[0104] The PK variables are the concentrations of free and bound aflibercept in plasma at each time point using both sparse sampling and dense sampling. Number of Patients Planned

[0105] The study will enroll approximately 100 patients to be randomized in a 1:1 ratio. Study Population

[0106] The study population consists of treatment-naïve patients with nAMD. 29 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 Inclusion Criteria

[0107] A patient must meet the following criteria at both the screening and / or the randomization visits to be eligible for inclusion in the study: 1. Men or women ≥50 years of age with active subfoveal CNV secondary to nAMD, including juxtafoveal lesions that affect the fovea in the study eye as assessed by an independent reading center. 2. Best Corrected Visual Acuity (BCVA) Early Treatment Diabetic Retinopathy Study (ETDRS) letter score of 78 to 24 (Snellen equivalent of 20 / 32 to 20 / 320) in the study eye. 3. Willing and able to comply with clinic visits and study-related procedures. 4. Provide informed consent signed by study patient or legally acceptable representative. Exclusion Criteria

[0108] A patient who meets any of the following criteria at either the screening or randomization visits will be excluded from the study: 1. Evidence of CNV due to any cause other than nAMD in either eye. 2. Subretinal hemorrhage in the study eye that is ≥50% of the total lesion area. 3. Evidence of DMEor diabetic retinopathy (defined asmore than 1microaneurysm) in either eye in diabetic patients. 4. Prior use of IVTanti-VEGF agents (aflibercept, ranibizumab, bevacizumab, brolucizumab, pegaptanib sodium) in the study eye. 5. Prior IVT investigational agents in either eye (e.g., anti-ang‑2 / anti-VEGF bispecific monoclonal antibodies, gene therapy). 6.Previoususeof intraocular orperiocular corticosteroidswithin120daysof screeningor treatmentwithan IVTsteroid implant at any time in the study eye. 7. Treatment with ocriplasmin in the study eye at any time. 8. Yttrium-aluminium-garnet capsulotomy in the study eye within 14 days of the screening Visits. 9. History of vitreoretinal surgery (including scleral buckling) in the study eye. 10. Intraocular pressure ≥25 mm Hg in the study eye. 11. Evidence of infectious blepharitis, keratitis, scleritis, or conjunctivitis in either eye. 12. Any intraocular inflammation / infection in either eye within 90 days of the screening visit. 13. Any history of macular hole of stage 2 and above in the study eye. 14. Current iris neovascularization, vitreous hemorrhage, or tractional retinal detachment visible at the screening assessments in the study eye. 15.Only 1 functional eye, even if that eyewas otherwise eligible for the study (e.g., BCVAof counting fingers or less in the eye with worse vision). 16. Ocular conditions with poorer prognosis in the fellow eye. 17. Inability to obtain fundusphotographs, fluorescein angiography (FA), orOCT (e.g., due tomedia opacity, allergy to fluorescein dye or lack of venous access) in the study eye. 18. Any prior systemic anti-VEGF administration. 19. Uncontrolled diabetes mellitus in the opinion of the investigator. 20. Uncontrolled BP (defined as systolic >140 mm Hg or diastolic >90 mm Hg). Patients may be treated with up to 3 agents known to have anti-hypertensive effects for arterial hypertension to achieve adequate BP control. This limit applies to drugs that could be used to treat hypertension even if their primary indication in the patient was not for BP control. Any recent changes inmedications known toaffectBPneed tobestable for 90daysprior to the screeningvisit. 21.Variationbymore than10% in the3pre-randomizationBPmeasures recordedat the screening1, screening2, and randomization visits. 22. History of cerebrovascular accident / transient ischemic attack ormyocardial infarction / acute coronary syndrome within 180 days of screening visit. 23. Renal failure, dialysis, or history of renal transplant. 24. Known sensitivity to any of the compounds of the study formulation. 25. Members of the clinical site study team and / or his / her immediate family, unless prior approval granted by the sponsor. 26. Pregnant or breastfeeding women 27. Women of childbearing potential* who are unwilling to practice highly effective contraception prior to the initial dose / start of the first treatment, during the study, and for at least 90 days after the last dose. Highly effective contraceptive measures include: 30 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 a. stable use of combined (estrogen and progestogen containing) hormonal contraception (oral, intravaginal, transdermal) or progestogen-only hormonal contraception (oral, injectable, implantable) associated with inhibi- tion of ovulation initiated 2 or more menstrual cycles prior to screening. b. intrauterine device (IUD); intrauterine hormone-releasing system (IUS) c. bilateral tubal ligation d. vasectomized partner e. and or sexual abstinence†, ‡ *Postmenopausal women must be amenorrhoeic for at least 12 months in order not to be considered of childbearing potential. Pregnancy testing and contraception are not required for women with documented hysterectomy or tubal ligation. †Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. ‡Periodic abstinence (calendar, symptothermal, post-ovulation methods), withdrawal (coitus interruptus), sper- micides only, and lactational amenorrhea method (LAM) are not acceptable methods of contraception. Female condom and male condom should not be used together. 28. Participation in an investigational studywithin 30 days prior to screening visit that involved treatmentwith any drug (excluding vitamins and minerals) or device. 29. Any other intraocular surgery within 12 weeks (84 days) before the screening visit (see Exclusion Criterion #9). 30. History of corneal transplant or corneal dystrophy in study eye. 31. Any concurrent ocular condition in the study eyewhich, in the opinion of the investigator, could either increase the risk to the patient beyond what is to be expected from standard procedures of IVT injections, or which otherwise may interfere with the injection procedure or with evaluation of efficacy or safety. 32. History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that might affect interpretation of the results of the study or render the patient at high risk for treatment complications.

[0109] Additional Exclusion Criteria for the Dense PK Sub-study 1. Prior IAI in the fellow eye 2. Patients on more than 2 anti-hypertensive medications 3. Patients with known cardiac arrhythmia 4. Patients who, in the opinion of the investigator, are unlikely to have stable BP over the course of the study (e.g., due to known non-compliance with medication) Investigational and Reference Treatments

[0110] The HD will be provided as a liquid formulation in a vial. The target concentration of aflibercept is 114.3 mg / mL. The dose will be delivered in an injection volume of 70 microliters. The IAI will be provided as a liquid formulation in a vial. The target concentration of aflibercept is 40 mg / mL. The dose will be delivered in an injection volume of 50 microliters. Additional Treatment

[0111] Deviation from the treatment schedule defined in the protocol is discouraged. Efforts should be made to ensure adherence to the protocol-specified dosing intervals. If, however, in the investigator’s judgement, a patient cannot adhere to the protocol-specified dosing interval due to persistent or worsening disease and requires an interim injection, the patient may receive additional treatment at week 16. The investigator must make reasonable efforts to consult with the study director or sponsor designee prior to additional treatment being allowed.

[0112] Patients will receive their randomized dose of aflibercept if it is determined that additional treatment will be administered. Patientswho receive additional treatment will continue to receive their randomized treatment at future visits and will remain masked to treatment assignment. Data from patients receiving additional treatment will be censored from the time additional treatment is administered. Dose Modification

[0113] Dose modification for an individual patient is not allowed. 31 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 Concomitant Medications

[0114] Any treatment administered from the time of informed consent to the final study visit will be considered concomitant medication. This includes medications that were started before the study and are ongoing during the study.

[0115] If a pretreatment concomitant medication is administered in the study eye before injection (e.g., antibiotic or anesthetic), it must be administered for fellow eye treatment as well. Prohibited Medications

[0116] Patients are not allowed to receive any standard or investigational treatment for nAMD in the studyeyeother than their assigned study treatment with HD or IAI, as specified in the protocol. This includesmedications administered locally (e.g., IVT, topical, juxtascleral, or periorbital routes), as well as those administered systemically, with the intent of treating nAMD in the study eye or fellow eye.

[0117] If the fellow eye has nAMD, or any other approved indication, IAI (2 mg) will be allowed and supplied through the IWRS (Interactiveweb response system). Patients are not allowed to receive any other anti-VEGFagent in the fellow eye. Patients enrolled in the dense PK sub-study cannot receive IAI (2 mg) in the fellow eye before week 12.

[0118] Non-ocular (systemic) standard or investigational treatments for nAMD of the study or fellow eye are not permitted. Systemic anti-angiogenic agents and anti-Ang2 inhibitors are not permitted during the study. Permitted Medications

[0119] Any other medications that are considered necessary for the patient’s welfare, and that are not expected to interfere with the evaluation of the study drug, are allowed. 32 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55

[0120] BCVA=Best Corrected Visual Acuity, ECG=electrocardiogram, EOS=end of study, ETDRS=Early Treatment Diabetic Retinopathy Study, FA=fluorescein angiography, FBR=future biomedical research, FP=fundus photography, IOP=Intraocular pressure, PK=pharmacokinetics, PRN=pro re nata (as needed), SDOCT= spectral domain optical coherence tomography, UPCR=urine protein:creatinine ratio.

[0121] Footnotes: 1. For patients in the dense PK sub-study, the visit window is ± 0 days. 2. For patients in the dense PK sub-study, the visit window is ± 2 days. 3. Signed only by patients participating in the dense PK sub-study and in addition to the study ICF. 4. The optional genomic and FBR sub-study ICF (informed consent form) should be presented to patients at the screening visit andmay be signed at any subsequent visit at which the patient chooses to participate after screening. The genomic DNA sample should be collected on day 1 / baseline (pre-dose) or at any study visit from patients who have signed the sub-study ICF. 5. Refer to pharmacy manual for study drug injection guidelines. Following study drug injection, patients will be 33 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 observed for approximately 30 minutes. 6. Patients will be dosed as needed per criteria herein. 7. Patients enrolled at sites participating in the optional visual function sub-study may undergo additional visual function tests. See study procedure manual for details. 8. Intraocular pressure will be measured bilaterally at all study visits. On days when study drug is administered, IOP should also be measured approximately 30 minutes after administration of study drug, in the study eye only. Intraocular pressure will be measured using Goldman applanation tonometry or Tono-pen™ and the same method of measurement must be used in each patient throughout the study. 9. Indirect ophthalmoscopy should be performed bilaterally at all visits. On days when study drug is administered, it should also be performed immediately after administration of study drug (study eye only). 10. The same SD-OCT / FA / FP imaging system used at screening and day 1 must be used at all subsequent visits in each patient. Images will be taken in both eyes before dosing at each required visit. 11. Vital signs (temperature, BP, heart rate) should bemeasured pre-injection, per the procedure outlined in the study proceduremanual. Bloodpressure assessmentswill be takenusing automatedofficebloodpressure (AOBP)with the OmronModel HEM907XL (or comparable). Measures will be taken in triplicate and ameanmeasure as displayed by the device will be recorded in the EDC. Detailed instructions can be found in the study procedure manual. 12. Timing of BP assessment at all visits must be within 2 hours of planned time of dosing on day 1 for patients in the dense PK sub-study. For all other patients, this window should be adhered to as closely as possible. 13. For patients participating in the densePK sub-study, HRandBPalsowill be collected according to the schedule in Table 1‑2. 14. Only BP and heart rate will be measured at these visits. No temperature measures are required. 15. All samples collected for laboratory assessments should be obtained prior to administration of fluorescein and prior to administration of study drug. 16. For women of childbearing potential, a negative serum pregnancy test at screening is required for eligibility. A negative urine pregnancy test is required before treatment is administered at subsequent visits. 17. For patients participating in the dense PK sub-study, urinalysis / UPCR will also be collected according to the schedule in Table 1‑2. 18. Week 4 collection of urinalysis / UPCR only for patients in the dense PK sub-study. 19. Dense PK sampling will be performed in approximately 30 patients (15 in each group) drawn according to the schedule in Table 1‑2. On dosing days, BP (blood pressure) and PK samples must be collected prior to study drug administration. Additional patients (up to approximately 50% more in each treatment group) may be enrolled in the dense PK sub-study to ensure adequate data is are captured. 20. Sparse PK sampling will be performed in all patients not enrolled in the dense PK sub-study according to the schedule defined in Table 1‑2. On dosing days, PK samples should be collected prior to study drug administration. 21. Exploratory research serum sample should be drawn prior to the administration of study drug at baseline (visit 3, day 1) and week 44. Table 1‑3. Dense PK Study Schedule of Events Visit Dose Assessment Day and Time (h) Dense PK Sample Collection Heart Rate and Blood Pressure1,2 Urinalysis / UPCR Visit 3 (Baseline) X 1 Time of first dose X (pre-dose) X 4h post-dose (±30 mm)3 X 8h post-dose (±2 h)4 X 2 ±2h5 X X 3 ±2h5 X X 5 ±2h5 X X 8 ±2h5 X X X6 15 ±2h5 X X X6 22 ±2h5 X X

[0122] Footnotes: 34 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 1.Timingof all BPassessmentsmust bewithin±2hoursof the timeof dosingonday1.Thismaybedoneat the clinical study site or by the site personnel or another healthcare professional at a remote location (e.g., the patient’s home or other appropriate location).Regardless ofwhereBPmeasurements are taken, the procedures described hereinmust be followed. 2. Blood pressure assessments will be taken using automated office blood pressure (AOBP) with the Omron Model HEM907XL (or comparable). Measures will be taken in triplicate and ameanmeasure as displayed by the device will be recorded in the EDC. Detailed instructions can be found in the study procedure manual. 3. Intraocular pressure will be measured at approximately 4 hours post-dose only if the IOP measurement from approximately 30 minutes to 60 minutes post-dose remains clinically significantly higher than the pre-injection reading. 4. Intraocular pressure will be measured at approximately 8 hours post-dose only if the IOP measurements from approximately 30 minutes to 60 minutes and approximately 4 hours post-dose remain clinically significantly higher than the pre-injection reading. 5. PK draw for all assessment days are to be performed within ±2 hours of the time of dosing on day 1. 6. This may be done at the clinical study site or by the site personnel or another healthcare professional at a remote location (e.g., the patient’s home or other appropriate location). Ocular Procedures

[0123] Intraocular Pressure. Intraocular pressure will be measured in both eyes at every visit using Goldmann applanation tonometry or Tono pen™, as specified in Table 1‑2. The same method of IOP measurement must be used throughout the study for each individual patient. On dosing visits, IOP will also be measured approximately 30 minutes post-dose (study eye).

[0124] For patients in the dense PK sub-study, IOP will also be measured 4 hours post-dose if the reading from approximately 30 minutes to 60 minutes post-dose remains clinically significantly higher than the pre-dose reading, and again at approximately 8 hours post-dose if the reading from approximately 4 hours post-dose remains clinically significantly higher than the pre-dose reading.

[0125] Slit Lamp Examination. Patients’ anterior eye structure and ocular adnexa will be examined bilaterally pre-dose at each study visit using a slit lamp (see study procedure manual) by the investigator, as specified herein

[0126] Indirect Ophthalmoscopy. Patients’ posterior pole and peripheral retina will be examined by indirect ophthalmo- scopy at each study visit pre-dose (bilateral) and post-dose (study eye) by the investigator, as specified herein. Post-dose evaluation must be performed immediately after injection.

[0127] FundusPhotography / Fluorescein Angiography. The anatomical state of the retinal vasculaturewill be evaluated byFPandFAas specified herein. Fundus photographyandFAwill be captured and transmitted to an independent reading center for both eyes. For FA, the study eye will be the transit eye.

[0128] Fundus and angiographic images will be sent to an independent reading center where images will be read by masked readers. All FPs and FAswill be archived at the site as part of the source documentation. Photographersmust be certified by the reading center to ensure consistency and quality in image acquisition. A detailed protocol for image acquisition and transmission can be found in the study proceduremanual. Imaging technicians should remain masked to treatment assignment.

[0129] Spectral Domain Optical Coherence Tomography. Retinal characteristics will be evaluated at every visit using SD-OCT. Images will be captured and transmitted for both eyes. Images will be sent to an independent reading center where they will be read by masked readers. All OCTs will be electronically archived at the study site as part of the source documentation. Optical coherence tomography techniciansmust be certified by the reading center to ensure consistency and quality in image acquisition. A detailed protocol for acceptable OCTmachines and OCT image acquisition / transmis- sion can be found in the study procedure manual. Imaging technicians should remain masked to treatment assignment.

[0130] Best Corrected Visual Acuity. Visual function of the study eye and the fellow eye will be assessed using the ETDRS protocol (Early Treatment Diabetic Retinopathy Study Research Group, 1985) at 4 meters at each study visit, as specified in Table 1‑2. Visual acuity examiners must be certified to ensure consistent measurement of BCVA, and must remain masked to treatment assignment, treatment schedule and study eye. Best corrected visual acuity should be done before any other ocular procedures are performed. Patients enrolled at sites participating in the optional visual function sub-study may undergo additional visual function tests. Definitions

[0131] Adverse Event. An AE is any untoward medical occurrence in a patient administered a study drug which may or may not have a causal relationship with the study drug. Therefore, an AE is any unfavorable an unintended sign (including abnormal laboratory finding), symptom, or diseasewhich is temporally associatedwith the use of a study drug, whether or 35 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 not considered related to thestudydrug (ICHE2AGuideline.ClinicalSafetyDataManagement:DefinitionsandStandards for Expedited Reporting, Oct 1994).

[0132] Serious Adverse Event. An SAE is any untoward medical occurrence that at any dose: • Results in death - includes all deaths, even those that appear to be completely unrelated to study drug (e.g., a car accident in which a patient is a passenger). Is life-threatening - in the view of the investigator, the patient is at immediate risk of death at the timeof the event. This does not includeanAE that had it occurred in amore severe form, might have caused death. • Requires in-patient hospitalization or prolongation of existing hospitalization. Inpatient hospitalization is defined as a hospital admission (any duration) or an emergency room visit for longer than 24 hours. Prolongation of existing hospitalization is defined as a hospital stay that is longer than was originally anticipated for the event or is prolonged due to the development of a new AE as determined by the investigator or treating physician • Results in persistent or significant disability / incapacity (substantial disruption of one’s ability to conduct normal life functions). • Is a congenital anomaly / birth defect • Is an important medical event - Important medical eventsmay not be immediately life-threatening or result in death or hospitalization, but may jeopardize the patient or may require intervention to prevent one of the other serious outcomes listed above (e.g., intensive treatment in an emergency room or at home for allergic bronchospasm; blood dyscrasias or convulsions that do not result in hospitalization; or development of drug dependency or drug abuse).

[0133] Ocular important medical event. An ocular important medical event may include the following: • An AE that requires either surgical or medical intervention to prevent permanent loss of vision; • Substantial, unexplained vision loss or an AE that causes substantial vision loss Criteria for reporting SAEs must be followed for these events.

[0134] Severity. The severity of AEs will be graded according to the following scale: • Mild: Does not interfere in a significant manner with the patient normal functioning level. It may be an annoyance. Prescription drugs are not ordinarily needed for relief of symptoms, but may be given because of personality of the patient. • Moderate: Produces some impairment of functioning but is not hazardous to health. It is uncomfortable or an embarrassment. Treatment for symptom may be needed. • Severe: Produces significant impairment of functioning or incapacitation and is a definite hazard to the patient’s health. Treatment for symptommay be given and / or patient hospitalized. If a laboratory value is considered anAE, its severity should be based on the degree of physiological impairment the value indicates.

[0135] Causality.The investigatormust provide causality assessment aswhether or not there is a reasonable possibility that thedrugcaused theadverseevent, basedonevidenceor facts, his / her clinical judgment, and the followingdefinitions. The causality assessment must be made based on the available information and can be updated as new information becomes available.

[0136] The following factors should be considered when assessing causality: • Temporal relationship: time to onset vs time drug was administered; • Nature of the reactions: immediate vs. long term; • Clinical and pathological features of the events; • Existing information about the drug & same class of drugs; • Concomitant medications; • Underlying and concurrent illnesses; • Response to de-challenge (drug discontinuation) or dose reduction; • Response to re-challenge (re-introduction of the drug) or dose increase, when applicable; • Patient’s medical and social history.

[0137] Causality to the Study Drug. • Related: The AE follows a reasonable temporal sequence from study drug administration, and cannot be reasonably explained by the nature of the reaction, patient’s clinical (e.g., disease under study, concurrent diseases, concomitant 36 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 medications), or other external factors; or the AE follows a reasonable temporal sequence from study drug administration, and is a known reaction to the drug under study or its class of drugs, or is predicted by known pharmacology. • Not Related: The AE does not follow a reasonable sequence from study drug administration, or can be reasonably explained by the nature of the reaction, patient’s clinical state (e.g., disease under study, concurrent diseases, and concomitant medications) or other external factors.

[0138] Causality to the Injection Procedure. The relationship of AEs to the injection procedure is assessed by the investigator, and is a clinical decision based on all available information. The following question is addressed: Is there a reasonable possibility that the AE may have been caused by the injection procedure? The possible answers are: • Not Related: There is a reasonable possibility that the event may have been caused by the injection procedure • Related: There is a reasonable possibility that the event may have been caused by the injection procedure Causality to the Study Conduct (Protocol-Specified Procedure). • Related: The AE follows a reasonable temporal sequence from a protocol-specified procedure, and cannot be reasonably explained by the nature of the reaction, patient’s clinical (e.g., disease under study, concurrent diseases, concomitant medications), or other external factors. • Not Related: The AE does not follow a reasonable sequence from a protocol-specified procedure, or can be reasonably explained by the nature of the reaction, patient’s clinical state (e.g., disease under study, concurrent diseases, and concomitant medications) or other external factors Analysis of Drug Concentration Data-Main Study

[0139] The concentrations of free and bound aflibercept over time will be summarized by descriptive statistics for each treatment group. No formal statistical hypothesis testing will be performed. Dense PK Sub-study

[0140] The PK parameters to be determined after the first dose for free and bound aflibercept may include, but are not limited to: • Cmax; • Cmax / Dose; • tmax; • tlast; • Clast; • AUCinf; • AUCinf / Dose; • t1 / 2; • Ctrough;

[0141] After repeat dosing in the dense PK sub-study, PK parameters to be determinedmay include, but are not limited to, Ctrough, time to reach steady-state, and accumulation ratio. The concentrations of free and bound aflibercept over time and selected PK parameters will be summarized by descriptive statistics by treatment group. This descriptive statistical assessment will include the geometric means and ratios of the geometric means for selected PK parameters, as deemed appropriate. No formal statistical hypothesis testing will be performed. Results at week 16 (n=55)‑values as reported at the time for patients reaching week 16.

[0142] The baseline demographics, eye characteristics, and blood pressure of "All patients" at this point in this trial are set forth in Figures 2‑4.

[0143] After 16 weeks of study duration, patients receiving the 8 mg doses of aflibercept (HD dosing regimen) maintained (on average) greater vision improvements and anatomical improvements than that of patients receiving the 2 mg dose (IAI dosing regimen) (relative to baseline).

[0144] Patients (Completers) receiving the HD dosing regimen maintained a greater mean change in best corrected visual acuity (7.4) than the IAI patients (5.2) at week 16 (Figure 6).

[0145] Anatomical improvements were also remarkable at week 16. The central retinal thickness (CRT) of patients receiving the HD dosing regimen remained below that of patients (Completers) receiving the IAI dosing regimen-a mean 37 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 change of ‑142 micrometers in HD patients vs ‑133 micrometers in IAI patients at week 16 (Figure 5).

[0146] Measuresof retinal drynesswerealso strikingly better inpatients receiving theHDdosing regimen.Overall,more patients (Completers) receiving the HD regimen had complete resolution of intraretinal / subretinal fluid at week 16. The proportion of HD patients with dry retinas at week 16 was 44%whereas the proportion of IAI patients with dry retinas was just 9% (Figure 7). A dry retina was regarded as a retina exhibiting no intraretinal fluid (IRF) and subretinal fluid (SRF). Conversely, a greater proportion of patients receiving the IAI dosing regimen had "not-dry" retinas at week 16 than that of HDpatients (86%vs56%, respectively) (Figure8).FewerHDpatientsexhibited IRF (IRFonlyorboth IRFandSRF)orSRF (SRF only or both IRF and SRF) at week 16 than IAI patients (Figures 9‑10, respectively). Similar trends were apparent when the retinal fluid status (Dry, IRFonly, SRFonly or both IRFandSRF) of IAI andHDpatients at baseline, week4,week 8,week12andweek16wasobserved (Figures11‑12, respectively). Thenumberof treatments in theHDand IAI treatment groups ("All patients") was comparable (Figure 13).

[0147] The HD and IAI dosing regimens were generally well tolerated. The ocular treatment-emergent adverse events (TEAEs) (Figure 14‑15), intraocular pressure (IOP) (Figure 16), non-ocular TEAEs (Figures 17‑18), non-ocular SAEs (Figure 19), hypertension AEs (Figure 20), mean systolic blood pressure (Figure 21), mean diastolic blood pressure (Figure 22), mean IOP (Figure 23), mean change of IOP (Figure 24) were comparable in each treatment group. Results‑ additional patients reaching week 16 (n=106) -values as reported at the time for a larger set of patients reaching week 16

[0148] Atweek16, a higher proportion of thesepatients in theHDaflibercept 8mggrouphadno retinal or subretinal fluid (50.9%, n=27 / 53) in the center (1 mm) subfield on optical coherence tomography compared to patients treated with IAI EYLEA 2 mg (34.0%, n=18 / 53) (p=0.08). During the initial 16 weeks of the trial, treatment emergent adverse events (TEAEs) in the study eye occurred in 17.0% (9 of 53) of aflibercept 8 mg patients and 22.6% (12 of 53) of EYLEA 2 mg patients. AEs that occurredmore frequently in the aflibercept 8mg groupwere conjunctival hemorrhage (5.7%aflibercept 8mg,3.8%EYLEA2mg)andvitreousdetachment (3.8%aflibercept 8mg,1.9%EYLEA2mg).SeriousocularAEs (SAEs) occurred in two patients overall, one in the aflibercept 8 mg group (retinal tear) and one in the EYLEA 2 mg group (visual acuity reduced). No intraocular inflammation, occlusive vasculitis, arterial thromboembolic events (adjudicated according to the AntiPlatelet Trialists’ Collaboration definitions) or death in either patient group were identified through week 16.

[0149] The disposition and exposure, baseline demographics, baseline characteristics, and baseline blood pressure and medical history of patients in this analysis are set forth in Figures 26, 27, 28 and 29.

[0150] The proportion of HD patients achieving a dry retina (no IRF and no SRF in the central subfield on SD-OCT (spectral domain optical coherence tomography)) was 51% whereas the proportion of IAI patients was 34% (Figure 30) (last observation carried forward (LOCF) values). HD patients without IRF (dry or with SRF only) was 70% (IAI patients: 68%) and without SRF (dry or with IRF only) was 70% (IAI patients: 51%) (Figure 31) (LOCF). At week 16, there was a greatermedian (Figure32) andmean (Figure33)decrease in central retinal thickness frombaseline inHDpatients (‑161.0 micrometers, - 156.2 micrometers, respectively) relative to IAI patients (‑96.0 micrometers, ‑143.5 micrometers, respec- tively) (LOCF). Themean change frombaseline toweek 12 in choroidal neovascularization and total lesion size is set forth in Figure 34 showing greater reductions in the HD group relative to the IAI group. Regarding best corrected visual acuity (BCVA), HD patients achieved a mean change, from baseline through week 16, of 8.4 (ETDRS letters) whereas IAI patients achieved 6.5 (Figure 35) (LOCF). A smaller proportion of HD patients lost letters than IAI patients, and a greater proportion of HD patients gained letters than IAI patients at week 16 (Figure 36).

[0151] The proportion of HD patients receiving additional treatment at week 16 (19%) was smaller than that of IAI patients (27%).Also, theoccurrenceof ocular TEAEs throughweek16was17%amongHDpatients and22.6%among IAI patients (Figure 38(A)). The occurrence of ocular serious treatment emergent adverse events and intraocular inflamma- tion TEAEs amongHDand IAI patients, throughweek 16, was comparable (Figure 38(B), Figure 38(C)).Mean intraocular pressure change from baseline, occurrence of intraocular pressure events, occurrence of APTC events or deaths, hypertension adverse events among HD and IAI patients was comparable at week 16 (Figure 39, Figure 40, Figure 41, Figure 42). Mean changes in blood pressure (systolic or diastolic) through week 16 among all HD and IAI patients or patients in a dense PK sub-study was comparable (Figure 43 (A-B), Figure 44(A-B)). Results‑ patients reaching week 44 (n=100) -values as reported at the time for patients reaching week 44

[0152] The study ended at week 44with 100 patients.With an identical dosing regimen and slightly fewer rescue and / or PRN doses, a higher proportion of eyes receiving 8mg aflibercept (HD) were dry in the center subfield relative to the eyes receiving 2 mg aflibercept (IAI). In addition, a change from baseline in central subfield thickness (CST) suggested better anatomic outcomes in the 8mgHDgroup relative to the 2mg IAI group.Changes in visual acuity frombaseline favored the 8 mg dosing regimen (HD) over the 2 mg regimen (IAI) (+7.9 letters vs. +5.1 letters).

[0153] Nonewsafety signalswere seen and the safety profile for theHDgroupwas comparable to that of IAI. Therewas 38 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 one case of mild iritis in the HD group that resolved with topical therapy. Changes from baseline blood pressure and intraocular pressure were similar between the groups.

[0154] Out of the 106 patients that started in the study, 100 reached the 44-week point‑49 in the IAI group and 51 in the HDgroup (Figure45).Thebaselinedemographicsof thepatients in thestudyweremajoritywhiteandhavingmore females than males with an average age of about 77 years as set forth in Figure 46. In addition, the baseline characteristics of the study eye in patients are set forth in Figure 47. The IAI and HD groups received the samemean number of injections (5.8) through week 44 (see Figure 48) with slightly more HD patients than IAI patients not receiving additional or PRN treatments.

[0155] Patients in theHDgroupachievednumerically superior anatomical improvements in theeye.Retinal drying (lack of fluid in the center subfield-no intraretinal fluid (IRF) and no subretinal fluid (SRF)) at weeks 16 to 44was higher in theHD group relative to that of the IAI group (Figure 49, Figure 51). Moreover, at weeks 16 and 44, therewas a greater proportion of eyes, in the HD group than in the IAI group, without fluid in the macula (no IRF and no SRF in the macula by SD-OCT) (Figure 50). The proportion of patients in each groupwithout IRF (dry or SRF only) at weeks 16 and 44 is set forth in Figure 52. At weeks 16 and 44, 70%of patients in the HDgroup exhibited no subretinal fluid (SRF) (dry or with IRF only) whereas 51% of the IAI group patients exhibited no SRF (Figure 53). Through much of the 44-week trial, the HD group achieved greater mean and median reductions in central retinal thickness (CRT) from baseline (Figure 54, Figure 55).

[0156] Patients in the HD group also achieved greater gains in vision. By week 44, the mean change, from baseline, in best corrected visual acuity (BCVA) was 7.9 in the HD group and 5.1 in the IAI group (Figure 56). Fewer patients in the HD group than in the IAI group lost vision (≥ 5, ≥10 or ≥15 letters lost) by week 44. Moreover, more patients in the HD group gained vision ( ≥10 or ≥15 letters gained) (Figure 57) by week 44.

[0157] Ocular TEAEs and ocular serious TEAEs, intraocular inflammation TEAEs, intraocular pressure events, non- ocular TEAEs and non-ocular serious TEAEs were comparable between treatment groups (Figure 58, Figure 59 and Figure 60, Figure 61, Figure 63, Figure 64). Intraocular pressure (IOP) observed between treatment groups were also comparable (Figure 62).Moreover, the administration of the 8mgdose in theHDgroupwasnot observed to havean effect on the occurrence of hypertension TEAEs (Figure 65). One patient died during the trial due to glioblastoma (Figure 66). Example 2: Characterization of Dose Accuracy

[0158] This Example documents the procedure and execution results of deliverable volume characterization testing conducted to compare different presentations of a formulation including aflibercept (REGN3) at a concentration of 114.3 mg / ml.

[0159] The following devices will be compared: • REGN3-PFS‑0.5mL (see International Design Registration. DM / 212509 and International Patent Application Publication No. WO2020 / 247686) and • 1mL BD (Becton Dickinson) Luer Lok syringe.(a plastic disposable syringe that is currently used as part of the commercially available EYLEA Vial Kit presentation). PFS=pre-filled syringe Testing Procedures

[0160] Testing was conducted separately for each presentation. All samples were filled with 114.3 mg / mL aflibercept formulated drug substance.

[0161] REGN3-PFS‑0.5mL testing: - Sample Size: n = 60 - PFS filled with 187 microliters and primed (air volume expelled) by hand - A volume of 85‑87 microliters was targeted to be delivered from the PFS - Delivered sample volume was determined by weighing (discussed below) - PFS was fitted with BD Hypoint 30G ½" needles

[0162] 1mL BD Luer Lok Syringe testing: - Sample Size: n = 310 - Syringe fitted with BD PrecisionGlide 30G ½" needles - Sample was drawn up into the syringe samples from a beaker and manually primed - A volume of 70 microliters was targeted to be delivered from the syringe 39 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 - Delivered sample volume was determined by weighing (discussed below) Results of Deliverable Volume Testing

[0163] Deliverable volume was calculated by collecting the dose delivered through manual injection after the syringe wasmanually primedandweighing the collecteddoseonabalance. Thecollectedmasswas thendividedby thedensity of the FDS (1.059 g / ml) to calculate the volume delivered. where V is the delivered volume (µL),mdose is the dose mass (g), and ρ is the solution density (g / mL). Preconditioning of samples at 5°C was conducted for the testing in order to maintain drug product integrity.

[0164] REGN3-PFS‑0.5mL: - Mean delivered dose volume: 81.670 microliters - Std Dev: 4.458 - Min: 64.684 microliters - Max: 89.481 microliters

[0165] 1mL BD (Becton Dickinson) Luer Lok syringe: - Mean delivered dose volume: 75.740 microliters - Std Dev: 8.665 - Min: 44.287 microliters - Max: 97.828 microliters

[0166] The testingofREGN3-PFS‑0.5mLdemonstrated that 59out of 60 sampleswereable to administer a volumewith high precision with 1 sample delivering volume of 64.684 microliters. See the histogram of delivered doses of REGN3- PFS‑0.5mL in Figure 25 (A).

[0167] Threehundredsix (306) samplesdeliveredwith the1mLBD(BectonDickinson)LuerLoksyringewereutilized for data analysis. Samples 21, 74, 117 and 125were removed from analysis due to operator error in dose preparation prior to collection. Testing showed that 252out of 306 sampleswere70microliters ‑100microliters. See thehistogramof delivered doses in Figure 25(B).

[0168] The deliverable volume data of both devices showed the difference in variability and accuracy. The 1mL BD (Becton Dickinson) Luer Lok syringe has a lower average delivered volume at 74.7 microliters than the 0.5mL PFS with 81.6 microliters. However, it has a larger spread of volumes delivered with a range of 53.5 microliters compared to 24.8 microliters for the 0.5mLPFS. The increased variability depicted in the 1mLBD (Becton Dickinson) Luer Lok syringemay be attributed to user variability in setting the dose to 70 microliters as well as the variability in graduation printing on the syringe. Individual delivered volumes for each device are set forth in Figure 25 (C).

[0169] Both devices were able to provide a dose within a 70 microliters ‑100 microliters range; however, the REGN3- PFS‑0.5mLwas able to delivermore consistent doseswithin a limited deliverable volume rangewith increased precision. Numbered further embodiments:

[0170] 1. A method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, comprising administering to an eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed byoneormoresecondary dosesof about 8mgormoreof theVEGFantagonist, followedbyoneormore tertiary doses of about 8mgormore of theVEGFantagonist; wherein each secondary dose is administered about 2 to 4weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. 2. The method of embodiment 1 wherein, while receiving said treatment: (i) with respect to visual acuity or best corrected visual acuity (BCVA), the subject achieves: 40 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 ∘ no loss in visual acuity or BCVA; ∘ a gain in visual acuity or BCVA; ∘ maintenance of visual acuity or BCVA ∘ no loss of visual acuity or BCVAby about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; o no loss of visual acuity or BCVA of about 5 or more, about 10 or more, or about 15 or more letters by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; o a gain in visual acuity or BCVA, of about 5 ormore, about 6 ormore, about 7 ormore, about 8 ormore, about 9 ormore, about 10 ormore or about 15 ormore letters, by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose, wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; and / or oagain invisual acuityorBCVAofabout6or7or8 lettersbyaboutweek8andmaintainingagainofabout6or 7 or 8 letters until at least about week 44wherein visual acuity or BCVA is according to ETDRSor the Snellen equivalent; (ii) with respect to central retinal thickness (CRT), the subject achieves: o a decrease in central retinal thickness; o no increase in central retinal thickness; o maintenance in central retinal thickness; ∘ a decrease in central retinal thickness by at least about 123, 125, 131, 142, 147, 149, 150, 151, 156, 157, 158, 159, 161, 162, 166, 167, 168, 172, 173, 175, 177, 178 or 183micrometers by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose; o a decrease in central retinal thickness of about 47 micrometers from about week 12 to about week 20 following the initial dose; o a decrease in central retinal thickness of about 17 micrometers from about week 24 to about week 32 following the initial dose; o a decrease in central retinal thickness of about 18 micrometers from about week 36 to about week 44 following the initial dose; and / or ∘ a decrease in central retinal thickness of about 149, about 150, about 160 or about 149‑160micrometers by about week 4 following the initial dose and achieving said decrease (±1, 2, 3, 4, 5, 10, 12, 13, 14 or 15 micrometers) by about week 44 following the initial dose; o a decrease ranging from about 131‑178 or about 123‑175 micrometers from about weeks 4 to 44; ∘ a reduction in central retinal thickness of about 160 or 161 or 162 micrometers by about week 12 and maintaining said reduction (±1, 2, 3, 4 or 5 micrometers) by about week 44; o a reduction in central retinal thickness of about 156 micrometers by about week 16 and maintaining said reduction ( ±1, 2, 3, 4 or 5 micrometers) by about week 44 (iii) with respect to retinal fluid, the subject achieves: o a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield or macula as measured by spectral domain optical coherence tomography; o a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield asmeasured by spectral domain optical coherence tomographybyaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose; ∘ no SRF and IRF in the macula as measured by SD-OCT by week 16 or week 44 following the initial dose; o no sub-retinal pigment epithelium (RPE) fluid until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or o maintenance of a dry retina once achieved until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or and / or (iv) the subject achieves: o a reduction in total choroidal neovascularization (CNV) lesion size by at least about 3.2 or 3.3micrometers by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose; ∘no significant increase in intraocular pressure frombaseline byaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 41 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 40 or 44 or later following the initial dose; and / or onosignificant increase insystolic (S) and / ordiastolic (D)bloodpressure frombaselinebyaboutweek4,8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later following the initial dose. 3. The method of embodiment 2, wherein a dry retina lacks intraretinal fluid and / or subretinal fluid. 4. Themethodof embodiment 2or 3,wherein, at or before said initial dose, the subject hasoneormoreof the following characteristics: • best corrected visual acuity of about 57, 58 or 57‑58 ETDRS letters; • central retinal thickness, as measured by SD-OCT, of about 488, 516, 502 or 488‑516 micrometers; • intraocular pressure of about 14, 15 or 14‑15 mmHg; • neovascular age-related macular degeneration lesion size of about 7, 8 or 7‑8 mm2; • choroidal neovascularization lesion size of about 7, 8 or 7‑8 mm2; • has occult choroidal neovascularization as measured by fluorescein angiography; • has minimal classic choroidal neovascularization as measured by fluorescein angiography; and / or • has predominantly classic choroidal neovascularization as measured by fluorescein angiography. 5. A method for improving best corrected visual acuity, decreasing central retinal thickness and / or achieving a dry retina, in aneyeof a subject in need thereof suffering fromanangiogenic eyedisorder, comprisingadministering to the eyeof the subject, a single initial doseof about 8mgormoreof aVEGFantagonist, followedbyoneormore secondary doses of about 8mg ormore of the VEGF antagonist, followed by one ormore tertiary doses of about 8mg ormore of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. 6. A method for promoting retinal drying, in an eye of a subject with an angiogenic eye disorder, comprising administering to the eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed byoneormoresecondary dosesof about 8mgormoreof theVEGFantagonist, followedbyoneormore tertiary doses of about 8mgormore of theVEGFantagonist; wherein each secondary dose is administered about 2 to 4weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. 7. The method of any one of embodiments 1‑6 wherein 4, 8 or 12 weeks is 12 weeks. 8. The method of any one of embodiments 1‑7, wherein about 2 to 4 weeks is 2, 3, 4 or 5 weeks. 9. The method of any one of embodiments 1‑8 wherein 2 to 4 weeks is 4 weeks. 10. The method of any one of embodiments 1‑9 wherein: • the single initial dose is followed by only 2 secondary doses, • each secondary dose is administered about 4 weeks after the immediately preceding dose, • the first tertiary dose is administered about 8 weeks after the immediately preceding dose, • the first tertiary dose is administered about 12 weeks after the immediately preceding dose, • each tertiary dose is administered about 12 weeks after the immediately preceding dose. 11. Themethod of any one of embodiments 1‑10 further comprising administering one or more additional pro re nata doses. 12. The method of any one of embodiments 1‑11 wherein the angiogenic eye disorder is: • neovascular age-related macular degeneration, • macular edema (ME), • macular edema following retinal vein occlusion (ME-RVO), • retinal vein occlusion (RVO), • central retinal vein occlusion (CRVO), • branch retinal vein occlusion (BRVO), 42 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 • diabetic macular edema (DME), • choroidal neovascularization (CNV), • iris neovascularization, • neovascular glaucoma, • post-surgical fibrosis in glaucoma, • proliferative vitreoretinopathy (PVR), • optic disc neovascularization, • corneal neovascularization, • retinal neovascularization, • vitreal neovascularization, • pannus, • pterygium, • vascular retinopathy, • diabetic retinopathy (DR), • non-proliferative diabetic retinopathy, • diabetic retinopathy characterized by a Diabetic Retinopathy Severity Scale (DRSS) level of about 47 or 53, • proliferative diabetic retinopathy, • proliferative diabetic retinopathy in a subject that does not suffer from DME, and / or • diabetic retinopathy in a patient who has diabetic macular edema (DME). 13. The method of any one of embodiments 1‑12 wherein - the method comprises administering the secondary doses to a subject who has received the initial dose, - themethodcomprisesadministering the remainingsecondarydoses toasubjectwhohasalready receivedoneor more secondary doses, - the method comprises administering one or more tertiary doses to a subject who has already received the secondary doses, or - the method comprises administering one or more tertiary doses to a subject who has already received one or more tertiary doses. 14. Themethodof embodiment 6,wherein retinal drying is characterizedbyno intraretinal fluid (IRF)andnosubretinal fluid (SRF) in the eye of the subject, after the subject has received three monthly doses of the VEGF antagonist. 15. The method of any one of embodiments 1‑14, wherein the VEGF antagonist is a VEGF receptor fusion protein. 16. The method of any one of embodiments 1‑15, wherein the VEGF antagonist is: (i) a VEGF receptor fusion protein comprising two polypeptides that comprise (1) a VEGFR1 component comprising amino acids 27 to 129 of SEQ ID NO: 2; (2) a VEGFR2 component comprising amino acids 130‑231 of SEQ ID NO: 2; and (3) a multimerization component comprising amino acids 232‑457 of SEQ ID NO: 2; (ii) aVEGF receptor fusionprotein comprising twopolypeptides that comprisean immunoglobin-like (Ig) domain2 of VEGFR1, an Ig domain 3 of a VEGFR2, and a multimerizing component; (iii) a VEGF receptor fusion protein comprising two polypeptides that comprise an immunoglobin-like (Ig) domain 2 of VEGFR1, an Ig domain 3 of VEGFR2, an Ig domain 4 of VEGFR2 and a multimerizing component; (iv) a VEGF receptor fusion protein comprising two VEGFR1R2-FcΔC1(a) polypeptides encoded by the nucleic acid sequence of SEQ ID NO: 1; or (v) selected from the group consisting of: aflibercept, conbercept, an anti-VEGF antibody or antigen-binding fragment thereof or biopolymer conjugate thereof, bevacizumab, ranibizumab, pegaptanib, brolucizumab, faricimab, abicipar pegol, an anti-VEGF DARPin and a bispecific anti-VEGF / ANG2 antibody. 17. The method of any one of embodiments 1‑16, wherein the VEGF antagonist is aflibercept or conbercept. 18. The method of any one of embodiments 1‑17 wherein VEGF antagonist is in a pharmaceutical formulation comprising: at least about 100 mg / ml of a VEGF receptor fusion protein, L-arginine, and 43 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 a histidine-based buffer. 19. The method of any one of embodiments 1‑18, wherein the VEGF antagonist is in a pharmaceutical formulation selected from the group consisting of A-KKKK. 20. The method of any one of embodiments 1‑19, wherein the VEGF antagonist is in a pre-filled syringe. 21. The method of embodiment 20, wherein the pre-filled syringe is glass or plastic, and / or sterile. 22.Themethodof anyoneof embodiments1‑21wherein saidabout 8mgormore isadoseof about7.2mg,8mg,8.01 mg, 8.8 mg, 7.2‑8.8 mg, 9.3 mg, 9.33 mg, 9.7 mg, 9.8 mg, 9.9 mg, or 9.7‑9.9 mg, or more. 23. Themethod of any one of embodiments 1‑22wherein said dose is± about 10%,± about 0.5, or± about 0.51mg. 24. Themethod of any one of embodiments 1‑23 wherein said VEGF antagonist is delivered in a volume of about 70, 81, 82, 81.7, 85, 86, 87, 85‑87 microliters. 25. Themethod of any one of embodiments 1‑24wherein VEGF antagonist is delivered in a volume that is± about 4, 4.45, 4.5, or 5 microliters. 26. Themethodof any oneof embodiments 1‑25wherein saidVEGFantagonist is deliveredby intravitreal dosewith a dose delivery device which is a syringe. 27. Themethodof anyoneof embodiments 1‑26wherein theVEGFantagonist is administeredby intravitreal injection of a volume that is device-determined. 28.Themethodofanyoneofembodiments1‑27wherein theVEGFantagonist isadministeredby intravitreal injection, of a formulation comprising the VEGF antagonist, with a pre-filled syringe wherein said method comprises the steps: (a) priming thesyringebyadvancing theplunger rodbyapredetermineddistance into thebodyuntil advancement of the plunger rod is resisted by a stop; (b) rotating the plunger rod about a longitudinal axis; and (c) actuating the plunger rod to dispense a predetermined volume of the formulation. Claims 1. A VEGF antagonist for use in a method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, wherein the method comprises administering, to an eye of the subject, a single initial dose of about 8 mg or more of the VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. 2. The VEGF antagonist for use according to claim 1 wherein, while receiving said treatment: (i) with respect to visual acuity or best corrected visual acuity (BCVA), the subject achieves: ∘ no loss in visual acuity or BCVA; ∘ a gain in visual acuity or BCVA; ∘ maintenance of visual acuity or BCVA ∘ no loss of visual acuity or BCVAby about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according to Early Treatment Diabetic Retinopathy Study (ETDRS) or the Snellen equivalent; ∘ no loss of visual acuity or BCVA of about 5 or more, about 10 or more, or about 15 or more letters by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; ∘again in visual acuity orBCVA,of about 5ormore, about6ormore, about 7ormore, about8ormore, about 9 44 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 ormore, about 10ormoreor about 15ormore letters, by aboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40or 44 following the initial dose, wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; and / or oagain invisual acuityorBCVAofabout6or7or8 lettersbyaboutweek8andmaintainingagainofabout6or 7 or 8 letters until at least about week 44wherein visual acuity or BCVA is according to ETDRSor the Snellen equivalent; (ii) with respect to central retinal thickness (CRT), the subject achieves: ∘ a decrease in central retinal thickness; ∘ no increase in central retinal thickness; ∘ maintenance in central retinal thickness; ∘ a decrease in central retinal thickness by at least about 123, 125, 131, 142, 147, 149, 150, 151, 156, 157, 158, 159, 161, 162, 166, 167, 168, 172, 173, 175, 177, 178 or 183micrometers by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose; ∘ a decrease in central retinal thickness of about 47 micrometers from about week 12 to about week 20 following the initial dose; ∘ a decrease in central retinal thickness of about 17 micrometers from about week 24 to about week 32 following the initial dose; ∘ a decrease in central retinal thickness of about 18 micrometers from about week 36 to about week 44 following the initial dose; ∘ a decrease in central retinal thickness of about 149, about 150, about 160 or about 149‑160micrometers by about week 4 following the initial dose and achieving said decrease (±1, 2, 3, 4, 5, 10, 12, 13, 14 or 15 micrometers) by about week 44 following the initial dose; ∘ a decrease ranging from about 131‑178 or about 123‑175 micrometers from about weeks 4 to 44; o∘ a reduction in central retinal thickness of about 160 or 161 or 162 micrometers by about week 12 and maintaining said reduction (±1, 2, 3, 4 or 5 micrometers) by about week 44; and / or ∘ a reduction in central retinal thickness of about 156 micrometers by about week 16 and maintaining said reduction (±1, 2, 3, 4 or 5 micrometers) by about week 44 (iii) with respect to retinal fluid, the subject achieves: ∘ a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield or macula as measured by spectral domain optical coherence tomography (SD-OCT); ∘ a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield asmeasured by spectral domain optical coherence tomographybyaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose; ∘ no SRF and IRF in the macula as measured by SD-OCT by week 16 or week 44 following the initial dose; ∘ no sub-retinal pigment epithelium (RPE) fluid until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or ∘maintenanceof adry retinaonceachieveduntil at least aboutweek44 following the initial doseasmeasured by spectral domain optical coherence tomography; and / or (iv) the subject achieves: ∘ a reduction in total choroidal neovascularization (CNV) lesion size by at least about 3.2 or 3.3 micrometers by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose; ∘no significant increase in intraocular pressure frombaseline byaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later following the initial dose; and / or ∘no significant increase in systolic (S) and / or diastolic (D) bloodpressure frombaselinebyaboutweek4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later following the initial dose. 3. The VEGF antagonist for use according to claim 2, wherein a dry retina lacks intraretinal fluid and / or subretinal fluid. 4. The VEGF antagonist for use according to claim 2 or 3, wherein, at or before said initial dose, the subject has one or more of the following characteristics: 45 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 • best corrected visual acuity of about 57, 58 or 57‑58 ETDRS letters; • central retinal thickness, as measured by SD-OCT, of about 488, 516, 502 or 488‑516 micrometers; • intraocular pressure of about 14, 15 or 14‑15 mmHg; • neovascular age-related macular degeneration lesion size of about 7, 8 or 7‑8 mm2; • choroidal neovascularization lesion size of about 7, 8 or 7‑8 mm2; • has occult choroidal neovascularization as measured by fluorescein angiography; • has minimal classic choroidal neovascularization as measured by fluorescein angiography; and / or • has predominantly classic choroidal neovascularization as measured by fluorescein angiography. 5. AVEGFantagonist for use in amethod for improving best corrected visual acuity, decreasing central retinal thickness and / or achieving a dry retina, in an eye of a subject in need thereof suffering froman angiogenic eye disorder, wherein the method comprises administering to the eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one ormore secondary doses of about 8mg ormore of the VEGFantagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4weeks after the immediately preceding dose; andwherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. 6. A VEGF antagonist for use in a method for promoting retinal drying, in an eye of a subject with an angiogenic eye disorder, wherein the method comprises administering to the eye of the subject, a single initial dose of about 8 mg or more of a VEGFantagonist, followed by one ormore secondary doses of about 8mgormore of theVEGFantagonist, followedbyoneormore tertiary dosesof about 8mgormoreof theVEGFantagonist; wherein each secondary dose is administeredabout 2 to4weeksafter the immediatelyprecedingdose;andwherein each tertiary dose isadministered about 4, 8 or 12 weeks after the immediately preceding dose. 7. The method of any one of the preceding claims wherein: (a) 4, 8 or 12 weeks is 12 weeks; and / or (b) about 2 to 4 weeks is: (i) 2, 3, 4 or 5 weeks; or (ii) 4 weeks. 8. The VEGF antagonist for use according to any one of the preceding claims wherein: • the single initial dose is followed by only 2 secondary doses, • each secondary dose is administered about 4 weeks after the immediately preceding dose, • the first tertiary dose is administered about 8 weeks after the immediately preceding dose, • the first tertiary dose is administered about 12 weeks after the immediately preceding dose, • each tertiary dose is administered about 12 weeks after the immediately preceding dose. 9. The VEGF antagonist for use according to any one of the preceding claims, wherein the method further comprises administering one or more additional pro re nata doses. 10. The VEGF antagonist for use according to any one of the preceding claims, wherein the angiogenic eye disorder is: • neovascular age-related macular degeneration, • macular edema (ME), • macular edema following retinal vein occlusion (ME-RVO), • retinal vein occlusion (RVO), • central retinal vein occlusion (CRVO), • branch retinal vein occlusion (BRVO), • diabetic macular edema (DME), • choroidal neovascularization (CNV), • iris neovascularization, • neovascular glaucoma, • post-surgical fibrosis in glaucoma, • proliferative vitreoretinopathy (PVR), • optic disc neovascularization, • corneal neovascularization, • retinal neovascularization, • vitreal neovascularization, 46 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 • pannus, • pterygium, • vascular retinopathy, • diabetic retinopathy (DR), • non-proliferative diabetic retinopathy, • diabetic retinopathy characterized by a Diabetic Retinopathy Severity Scale (DRSS) level of about 47 or 53, • proliferative diabetic retinopathy, • proliferative diabetic retinopathy in a subject that does not suffer from DME, and / or • diabetic retinopathy in a patient who has diabetic macular edema (DME). 11. The VEGF antagonist for use according to any one of the preceding claims wherein: - the method comprises administering the secondary doses to a subject who has received the initial dose; - themethod comprises administering the remaining secondary doses to a subject who has already received one or more secondary doses; - the method comprises administering one or more tertiary doses to a subject who has already received the secondary doses; or - the method comprises administering one or more tertiary doses to a subject who has already received one or more tertiary doses. 12. The VEGF antagonist for use according to claim 11, wherein retinal drying is characterized by no intraretinal fluid (IRF) and no subretinal fluid (SRF) in the eye of the subject, after the subject has received threemonthly doses of the VEGF antagonist. 13. The VEGF antagonist for use according to any one of the preceding claims, wherein the VEGF antagonist is a VEGF receptor fusion protein, optionally, wherein the VEGF antagonist is: (i) a VEGF receptor fusion protein comprising two polypeptides that comprise (1) a VEGFR1 component comprising amino acids 27 to 129 of SEQ ID NO: 2; (2) a VEGFR2 component comprising amino acids 130‑231 of SEQ ID NO: 2; and (3) a multimerization component comprising amino acids 232‑457 of SEQ ID NO: 2; (ii) aVEGF receptor fusionprotein comprising twopolypeptides that comprisean immunoglobin-like (Ig) domain2 of VEGFR1, an Ig domain 3 of a VEGFR2, and a multimerizing component; (iii) a VEGF receptor fusion protein comprising two polypeptides that comprise an immunoglobin-like (Ig) domain 2 of VEGFR1, an Ig domain 3 of VEGFR2, an Ig domain 4 of VEGFR2 and a multimerizing component; (iv) a VEGF receptor fusion protein comprising two VEGFR1R2-FcΔC1(a) polypeptides encoded by the nucleic acid sequence of SEQ ID NO: 1; or (v) selected from the group consisting of: aflibercept, conbercept, an anti-VEGF antibody or antigen-binding fragment thereof or biopolymer conjugate thereof, bevacizumab, ranibizumab, pegaptanib, brolucizumab, faricimab, abicipar pegol, an anti-VEGF DARPin and a bispecific anti-VEGF / ANG2 antibody. 14. The VEGF antagonist for use according to any one of the preceding claims, wherein the VEGF antagonist is aflibercept or conbercept. 15. The VEGF antagonist for use according to any one of the preceding claims wherein VEGF antagonist is in a pharmaceutical formulation comprising: at least about 100 mg / ml of a VEGF receptor fusion protein, L-arginine, and a histidine-based buffer. 16. The VEGF antagonist for use according to any one of the preceding claims, wherein: (a) the VEGF antagonist is in a pharmaceutical formulation selected from the group consisting of A-KKKK; (b) in a pre-filled syringe; (c) in a pre-filled syringe, wherein the pre-filled syringe is glass or plastic, and / or sterile; (d) said about 8mgormore is adoseof about 7.2mg, 8mg, 8.01mg, 8.8mg, 7.2‑8.8mg, 9.3mg, 9.33mg, 9.7mg, 47 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 9.8 mg, 9.9 mg, or 9.7‑9.9 mg, or more; and / or (e) said dose is ± about 10%, ± about 0.5, or ± about 0.51 mg; (f) the VEGF antagonist is delivered in a volume of about 70, 81, 82, 81.7, 85, 86, 87, 85‑87 microliters; and / or (g) the VEGF antagonist is delivered in a volume that is ± about 4, 4.45, 4.5, or 5 microliters. 17. The VEGF antagonist for use according to any one of the preceding claims wherein said VEGF antagonist is: (a) delivered by intravitreal dose with a dose delivery device which is a syringe; and / or (b) administered by intravitreal injection of a volume that is device-determined. 18. The VEGF antagonist for use according to any one of the preceding claims wherein the VEGF antagonist is administered by intravitreal injection, of a formulation comprising the VEGF antagonist, with a pre-filled syringe wherein said method comprises the steps: (a) priming thesyringebyadvancing theplunger rodbyapredetermineddistance into thebodyuntil advancement of the plunger rod is resisted by a stop; (b) rotating the plunger rod about a longitudinal axis; and (c) actuating the plunger rod to dispense a predetermined volume of the formulation. 48 EP 4 647 125 A2 5 10 15 20 25 30 35 40 45 50 55 49 EP 4 647 125 A2 50 EP 4 647 125 A2 51 EP 4 647 125 A2 52 EP 4 647 125 A2 53 EP 4 647 125 A2 54 EP 4 647 125 A2 55 EP 4 647 125 A2 56 EP 4 647 125 A2 57 EP 4 647 125 A2 58 EP 4 647 125 A2 59 EP 4 647 125 A2 60 EP 4 647 125 A2 61 EP 4 647 125 A2 62 EP 4 647 125 A2 63 EP 4 647 125 A2 64 EP 4 647 125 A2 65 EP 4 647 125 A2 66 EP 4 647 125 A2 67 EP 4 647 125 A2 68 EP 4 647 125 A2 69 EP 4 647 125 A2 70 EP 4 647 125 A2 71 EP 4 647 125 A2 72 EP 4 647 125 A2 73 EP 4 647 125 A2 74 EP 4 647 125 A2 75 EP 4 647 125 A2 76 EP 4 647 125 A2 77 EP 4 647 125 A2 78 EP 4 647 125 A2 79 EP 4 647 125 A2 80 EP 4 647 125 A2 81 EP 4 647 125 A2 82 EP 4 647 125 A2 83 EP 4 647 125 A2 84 EP 4 647 125 A2 85 EP 4 647 125 A2 86 EP 4 647 125 A2 87 EP 4 647 125 A2 88 EP 4 647 125 A2 89 EP 4 647 125 A2 90 EP 4 647 125 A2 91 EP 4 647 125 A2 92 EP 4 647 125 A2 93 EP 4 647 125 A2 94 EP 4 647 125 A2 95 EP 4 647 125 A2 96 EP 4 647 125 A2 97 EP 4 647 125 A2 98 EP 4 647 125 A2 99 EP 4 647 125 A2 100 EP 4 647 125 A2 101 EP 4 647 125 A2 102 EP 4 647 125 A2 103 EP 4 647 125 A2 104 EP 4 647 125 A2 105 EP 4 647 125 A2 106 EP 4 647 125 A2 107 EP 4 647 125 A2 108 EP 4 647 125 A2 109 EP 4 647 125 A2 110 EP 4 647 125 A2 111 EP 4 647 125 A2 REFERENCES CITED IN THE DESCRIPTION This list of references cited by the applicant is for the reader’s convenience only. 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[0070] (19) *EP004647125A3* (11) EP 4 647 125 A3 (12) EUROPEAN PATENT APPLICATION (88) Date of publication A3: 28.01.2026 Bulletin 2026 / 05 (43) Date of publication A2: 12.11.2025 Bulletin 2025 / 46 (21) Application number: 25189523.1 (22) Date of filing: 16.05.2022 (51) International Patent Classification (IPC): A61K 38 / 17 (2006.01) A61P 27 / 02 (2006.01) (52) Cooperative Patent Classification (CPC): A61K 38 / 179; A61P 27 / 02 (84) Designated Contracting States: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR Designated Extension States: BA ME Designated Validation States: KH MA MD TN (30) Priority: 17.05.2021 US 202163189541 P 20.08.2021 US 202163235398 P 07.01.2022 US 202263297420 P 03.02.2022 US 202263306315 P (62) Document number(s) of the earlier application(s) in accordance with Art. 76 EPC: 22728724.0 / 4 185 318 (71) Applicants: • Regeneron Pharmaceuticals, Inc. Tarrytown, NY 10591 (US) • Bayer Healthcare LLC Whippany, NJ 07981 (US) (72) Inventors: • VITTI, Robert L. Tarrytown, 10591 (US) • BERLINER, Alyson J. Tarrytown, 10591 (US) • CHU, Karen Tarrytown, 10591 (US) • ASMUS, Friedrich 14129 Berlin (DE) • DA SILVA LEAL, Sergio Casimiro 4153 Reinach (CH) • EISSING, Thomas 40764 Langenfeld (DE) • RITTENHOUSE, Kay D. Randolph, NJ 07869 (US) (74) Representative: J A Kemp LLP 80 Turnmill Street London EC1M 5QU (GB) (54) EXTENDED, HIGH DOSE VEGF ANTAGONIST REGIMENS FOR TREATMENT OF ANGIOGENIC EYE DISORDERS (57) The present invention relates to a method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, comprising administering to an eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. EP 4 64 7 12 5 A 3 Processed by Luminess, 75001 PARIS (FR) 2 EP 4 647 125 A3 5 10 15 20 25 30 35 40 45 50 55 3 EP 4 647 125 A3 5 10 15 20 25 30 35 40 45 50 55 4 EP 4 647 125 A3 5 10 15 20 25 30 35 40 45 50 55 5 EP 4 647 125 A3 5 10 15 20 25 30 35 40 45 50 55 6 EP 4 647 125 A3 5 10 15 20 25 30 35 40 45 50 55 7 EP 4 647 125 A3 5 10 15 20 25 30 35 40 45 50 55 摘要 The present invention relates to a method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, comprising administering to an eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose. 本发明涉及一种治疗或预防血管生成性眼病的方法，适用于有需要的受试者，该方法 包括：向受试者的眼睛施用单次初始剂量约 8 mg 或更多的 VEGF 拮抗剂，随后施用一 次或多次次级剂量约 8 mg 或更多的 VEGF 拮抗剂，随后施用一次或多次三级剂量约 8 mg 或更多的 VEGF 拮抗剂；其中，每次次级剂量在紧接前一次给药后约 2 至 4 周施用； 并且其中，每次三级剂量在紧接前一次给药后约 4、8 或 12 周施用。

Claims

1. A VEGF antagonist for use in a method for treating or preventing an angiogenic eye disorder, in a subject in need thereof, wherein the method comprises administering, to an eye of the subject, a single initial dose of about 8 mg or more of the VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose.

2. The VEGF antagonist for use according to claim 1 wherein, while receiving said treatment: (i) with respect to visual acuity or best corrected visual acuity (BCVA), the subject achieves: ∘ no loss in visual acuity or BCVA; ∘ a gain in visual acuity or BCVA; ∘ maintenance of visual acuity or BCVA ∘ no loss of visual acuity or BCVA by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according to Early Treatment Diabetic Retinopathy Study (ETDRS) or the Snellen equivalent; ∘ no loss of visual acuity or BCVA of about 5 or more, about 10 or more, or about 15 or more letters by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; ∘ a gain in visual acuity or BCVA, of about 5 or more, about 6 or more, about 7 or more, about 8 or more, about 9 or more, about 10 or more or about 15 or more letters, by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose, wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; and / or o a gain in visual acuity or BCVA of about 6 or 7 or 8 letters by about week 8 and maintaining a gain of about 6 or 7 or 8 letters until at least about week 44 wherein visual acuity or BCVA is according to ETDRS or the Snellen equivalent; (ii) with respect to central retinal thickness (CRT), the subject achieves: ∘ a decrease in central retinal thickness; ∘ no increase in central retinal thickness; ∘ maintenance in central retinal thickness; ∘ a decrease in central retinal thickness by at least about 123, 125, 131, 142, 147, 149, 150, 151, 156, 157, 158, 159, 161, 162, 166, 167, 168, 172, 173, 175, 177, 178 or 183 micrometers by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose; ∘ a decrease in central retinal thickness of about 47 micrometers from about week 12 to about week 20 following the initial dose; ∘ a decrease in central retinal thickness of about 17 micrometers from about week 24 to about week 32 following the initial dose; ∘ a decrease in central retinal thickness of about 18 micrometers from about week 36 to about week 44 following the initial dose; ∘ a decrease in central retinal thickness of about 149, about 150, about 160 or about 149-160 micrometers by about week 4 following the initial dose and achieving said decrease (±1, 2, 3, 4, 5, 10, 12, 13, 14 or 15 micrometers) by about week 44 following the initial dose; ∘ a decrease ranging from about 131-178 or about 123-175 micrometers from about weeks 4 to 44; o∘ a reduction in central retinal thickness of about 160 or 161 or 162 micrometers by about week 12 and maintaining said reduction (±1, 2, 3, 4 or 5 micrometers) by about week 44; and / or ∘ a reduction in central retinal thickness of about 156 micrometers by about week 16 and maintaining said reduction (±1, 2, 3, 4 or 5 micrometers) by about week 44 (iii) with respect to retinal fluid, the subject achieves: ∘ a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield or macula as measured by spectral domain optical coherence tomography (SD-OCT); ∘ a dry retina having no intraretinal fluid and no subretinal fluid; or no intraretinal fluid; or no subretinal fluid; in the center subfield as measured by spectral domain optical coherence tomography by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44, following the initial dose; ∘ no SRF and IRF in the macula as measured by SD-OCT by week 16 or week 44 following the initial dose; ∘ no sub-retinal pigment epithelium (RPE) fluid until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or ∘ maintenance of a dry retina once achieved until at least about week 44 following the initial dose as measured by spectral domain optical coherence tomography; and / or (iv) the subject achieves: ∘ a reduction in total choroidal neovascularization (CNV) lesion size by at least about 3.2 or 3.3 micrometers by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 following the initial dose; ∘ no significant increase in intraocular pressure from baseline by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later following the initial dose; and / or ∘ no significant increase in systolic (S) and / or diastolic (D) blood pressure from baseline by about week 4, 8, 9, 12, 16, 20, 24, 28, 32, 36, 40 or 44 or later following the initial dose.

3. The VEGF antagonist for use according to claim 2, wherein a dry retina lacks intraretinal fluid and / or subretinal fluid.

4. The VEGF antagonist for use according to claim 2 or 3, wherein, at or before said initial dose, the subject has one or more of the following characteristics: • best corrected visual acuity of about 57, 58 or 57-58 ETDRS letters; • central retinal thickness, as measured by SD-OCT, of about 488, 516, 502 or 488-516 micrometers; • intraocular pressure of about 14, 15 or 14-15 mmHg; • neovascular age-related macular degeneration lesion size of about 7, 8 or 7-8 mm2; • choroidal neovascularization lesion size of about 7, 8 or 7-8 mm2; • has occult choroidal neovascularization as measured by fluorescein angiography; • has minimal classic choroidal neovascularization as measured by fluorescein angiography; and / or • has predominantly classic choroidal neovascularization as measured by fluorescein angiography.

5. A VEGF antagonist for use in a method for improving best corrected visual acuity, decreasing central retinal thickness and / or achieving a dry retina, in an eye of a subject in need thereof suffering from an angiogenic eye disorder, wherein the method comprises administering to the eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose.

6. A VEGF antagonist for use in a method for promoting retinal drying, in an eye of a subject with an angiogenic eye disorder, wherein the method comprises administering to the eye of the subject, a single initial dose of about 8 mg or more of a VEGF antagonist, followed by one or more secondary doses of about 8 mg or more of the VEGF antagonist, followed by one or more tertiary doses of about 8 mg or more of the VEGF antagonist; wherein each secondary dose is administered about 2 to 4 weeks after the immediately preceding dose; and wherein each tertiary dose is administered about 4, 8 or 12 weeks after the immediately preceding dose.

7. The method of any one of the preceding claims wherein: (a) 4, 8 or 12 weeks is 12 weeks; and / or (b) about 2 to 4 weeks is: (i) 2, 3, 4 or 5 weeks; or (ii) 4 weeks.

8. The VEGF antagonist for use according to any one of the preceding claims wherein: • the single initial dose is followed by only 2 secondary doses, • each secondary dose is administered about 4 weeks after the immediately preceding dose, • the first tertiary dose is administered about 8 weeks after the immediately preceding dose, • the first tertiary dose is administered about 12 weeks after the immediately preceding dose, • each tertiary dose is administered about 12 weeks after the immediately preceding dose.

9. The VEGF antagonist for use according to any one of the preceding claims, wherein the method further comprises administering one or more additional pro re nata doses.

10. The VEGF antagonist for use according to any one of the preceding claims, wherein the angiogenic eye disorder is: • neovascular age-related macular degeneration, • macular edema (ME), • macular edema following retinal vein occlusion (ME-RVO), • retinal vein occlusion (RVO), • central retinal vein occlusion (CRVO), • branch retinal vein occlusion (BRVO), • diabetic macular edema (DME), • choroidal neovascularization (CNV), • iris neovascularization, • neovascular glaucoma, • post-surgical fibrosis in glaucoma, • proliferative vitreoretinopathy (PVR), • optic disc neovascularization, • corneal neovascularization, • retinal neovascularization, • vitreal neovascularization, • pannus, • pterygium, • vascular retinopathy, • diabetic retinopathy (DR), • non-proliferative diabetic retinopathy, • diabetic retinopathy characterized by a Diabetic Retinopathy Severity Scale (DRSS) level of about 47 or 53, • proliferative diabetic retinopathy, • proliferative diabetic retinopathy in a subject that does not suffer from DME, and / or • diabetic retinopathy in a patient who has diabetic macular edema (DME).

11. The VEGF antagonist for use according to any one of the preceding claims wherein: - the method comprises administering the secondary doses to a subject who has received the initial dose; - the method comprises administering the remaining secondary doses to a subject who has already received one or more secondary doses; - the method comprises administering one or more tertiary doses to a subject who has already received the secondary doses; or - the method comprises administering one or more tertiary doses to a subject who has already received one or more tertiary doses.

12. The VEGF antagonist for use according to claim 11, wherein retinal drying is characterized by no intraretinal fluid (IRF) and no subretinal fluid (SRF) in the eye of the subject, after the subject has received three monthly doses of the VEGF antagonist.

13. The VEGF antagonist for use according to any one of the preceding claims, wherein the VEGF antagonist is a VEGF receptor fusion protein, optionally, wherein the VEGF antagonist is: (i) a VEGF receptor fusion protein comprising two polypeptides that comprise (1) a VEGFR1 component comprising amino acids 27 to 129 of SEQ ID NO: 2; (2) a VEGFR2 component comprising amino acids 130-231 of SEQ ID NO: 2; and (3) a multimerization component comprising amino acids 232-457 of SEQ ID NO: 2; (ii) a VEGF receptor fusion protein comprising two polypeptides that comprise an immunoglobin-like (Ig) domain 2 of VEGFR1, an Ig domain 3 of a VEGFR2, and a multimerizing component; (iii) a VEGF receptor fusion protein comprising two polypeptides that comprise an immunoglobin-like (Ig) domain 2 of VEGFR1, an Ig domain 3 of VEGFR2, an Ig domain 4 of VEGFR2 and a multimerizing component; (iv) a VEGF receptor fusion protein comprising two VEGFR1R2-FcΔC1(a) polypeptides encoded by the nucleic acid sequence of SEQ ID NO: 1; or (v) selected from the group consisting of: aflibercept, conbercept, an anti-VEGF antibody or antigen-binding fragment thereof or biopolymer conjugate thereof, bevacizumab, ranibizumab, pegaptanib, brolucizumab, faricimab, abicipar pegol, an anti-VEGF DARPin and a bispecific anti-VEGF / ANG2 antibody.

14. The VEGF antagonist for use according to any one of the preceding claims, wherein the VEGF antagonist is aflibercept or conbercept.

15. The VEGF antagonist for use according to any one of the preceding claims wherein VEGF antagonist is in a pharmaceutical formulation comprising: at least about 100 mg / ml of a VEGF receptor fusion protein, L-arginine, and a histidine-based buffer.

16. The VEGF antagonist for use according to any one of the preceding claims, wherein: (a) the VEGF antagonist is in a pharmaceutical formulation selected from the group consisting of A-KKKK; (b) in a pre-filled syringe; (c) in a pre-filled syringe, wherein the pre-filled syringe is glass or plastic, and / or sterile; (d) said about 8 mg or more is a dose of about 7.2 mg, 8 mg, 8.01 mg, 8.8 mg, 7.2-8.8 mg, 9.3 mg, 9.33 mg, 9.7 mg, 9.8 mg, 9.9 mg, or 9.7-9.9 mg, or more; and / or (e) said dose is ± about 10%, ± about 0.5, or ± about 0.51 mg; (f) the VEGF antagonist is delivered in a volume of about 70, 81, 82, 81.7, 85, 86, 87, 85-87 microliters; and / or (g) the VEGF antagonist is delivered in a volume that is ± about 4, 4.45, 4.5, or 5 microliters.

17. The VEGF antagonist for use according to any one of the preceding claims wherein said VEGF antagonist is: (a) delivered by intravitreal dose with a dose delivery device which is a syringe; and / or (b) administered by intravitreal injection of a volume that is device-determined.

18. The VEGF antagonist for use according to any one of the preceding claims wherein the VEGF antagonist is administered by intravitreal injection, of a formulation comprising the VEGF antagonist, with a pre-filled syringe wherein said method comprises the steps: (a) priming the syringe by advancing the plunger rod by a predetermined distance into the body until advancement of the plunger rod is resisted by a stop; (b) rotating the plunger rod about a longitudinal axis; and (c) actuating the plunger rod to dispense a predetermined volume of the formulation.

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