IL-2 / IL-15Rβγ agonist dosing regimens for treating cancer or infectious disease

Abstract

The present invention provides pulse cyclic dosing regimes and pulse dosing regimes for interleukin-2 / interleukin-15 receptor βγ (IL-2 / IL-15Rβγ) agonists for treating or managing cancer or infectious disease in human patients. The dosing regimes include, inter alia, daily administration of an IL-2 / IL-15Rβγ agonist on two, three, and four consecutive days followed by a dosing-free day.

Description

[Technical Field]

[0001] Background of the Invention Despite recent advances in the treatment of cancer and infectious diseases, there remains an unmet medical need for more effective and well-tolerated treatments. Immunotherapies, treatments that harness the body's own immune system to help fight disease, aim to harness the power of the immune system to kill malignant or infected cells while leaving healthy tissue intact. While the immune system has an inherent ability to detect and eliminate malignant tumors, tumors and persistent infections have developed mechanisms to escape immune surveillance (Robinson and Schluns 2017). Potential reasons for immune tolerance include failed innate immune activation, the involvement of dense stroma as a physical barrier, and the possible contribution of immunosuppressive oncogene pathways (Gajewski et al. 2013). One group of immunotherapies with some clinical success is cytokine treatment, more specifically interleukin-2 (IL-2), which stimulates the innate immune response through NK cells and CD8 + IL-2 is known to activate both adaptive immune responses via T cells (Steel et al. 2012; Conlon et al. 2019), and is commercially available as aldesleukin / PROLEUKIN® (Prometheus Laboratories Inc.) and interleukin-15 (IL-15) treatments. While impressive tumor regressions have been observed with IL-2 treatment, responses have been limited to a small percentage of patients and have been associated with high levels of even life-threatening toxicity. Furthermore, IL-2 has demonstrated not only immune-enhancing but also immunosuppressive activity through the induction of activation-induced cell death of T cells and the expansion of immunosuppressive regulatory T cells (Tregs) (Robinson and Schluns 2017).

[0002] Both IL-2 and IL-15 act through heterotrimeric receptors with α, β, and γ subunits, and share a common gamma chain receptor (γ cor γ) and IL-2 / IL-15Rβ (also known as IL-2Rβ, CD122). c The heterotrimeric receptor (or γ) is also shared with IL-4, IL-7, IL-9, and IL-21. As a third subunit, the heterotrimeric receptor contains specific subunits for IL-2 or IL-15, namely, IL-2Rα (CD25) or IL-15Rα (CD215). Downstream, the IL-2 and IL-15 heterotrimeric receptors share JAK1 (Janus kinase 1), JAK3, and STAT3 / 5 (signal transducer and activator of transcription 3 and 5) molecules for intracellular signaling, leading to similar functions. However, both cytokines also have distinct roles, as reviewed in Waldmann (2015, see e.g., Table 1) and Conlon (2019). Therefore, the activation of different heterotrimeric receptors by binding of IL-2, IL-15, or their derivatives may lead to specific immune system modulation and potential side effects. Recently, novel compounds have been reported to activate NK cells and CD8 + It was designed to specifically target T cell activation.

[0003] These are intermediate affinity IL-2 / IL-15Rβγ, i.e., IL-2 / IL-15Rβ and γ c Compounds that target receptors consisting of subunits, which are expressed on NK cells, CD8 +It is expressed in T cells, NKT cells, and γδT cells. The designed compounds RLI-15, ALT-803, and hetIL-15 already contain (part of) the IL-15Rα subunit and therefore stimulate transpresentation of the α subunit by antigen-presenting cells. RLI-15 binds only to the intermediate-affinity IL-15Rβγ receptor, which is important for safe and potent immune stimulation mediated by IL-15 transpresentation because it contains a covalently attached sushi domain of IL-15Rα. On the other hand, RLI-15 does not bind to either IL-15Rα or IL-2Rα. Similarly, ALT-803 and hetIL-15 possess the IL-15Rα sushi domain or soluble IL-15Rα, respectively, and therefore bind to the intermediate-affinity IL-15Rβγ receptor. However, due to their noncovalent binding, the complexes may dissociate in vivo, thereby allowing the dissociated fraction of the applied complex to exert additional binding (see below). The likelihood of dissociation is likely to be higher for ALT-803 versus hetIL-15 because ALT-803 contains only the sushi domain of IL-15Rα, which is known to mediate only partial binding to IL-15, whereas the sushi domain is required for complete binding (Wei et al. 2001).

[0004] Another example of targeting the intermediate-affinity IL-2 / IL-15Rβ receptor is NKTR-214, whose hydrolysis to its most active 1-PEG-IL-2 state generates a compound whose position at the IL-2 / IL-2Rα interface interferes with binding to the high-affinity IL-2Rα but leaves binding to the intermediate-affinity IL-2 / IL-15Rβ unperturbed (Charych et al. 2016). Furthermore, the mutant IL-2 IL2v, which does not bind to the IL-2Rα subunit, is an example of this class of compound (Klein et al. 2013; Bacac et al. 2016). Targeting the intermediate-affinity IL-2 / IL-15Rβγ receptor avoids the tendencies associated with targeting the high-affinity IL-2 and IL-15 receptors, such as T regulatory cell activation induced by IL-2 or vascular leak syndrome (which can be induced by high concentrations of soluble IL-2 or IL-15).

[0005] This is because the IL-2Rαβγ high-affinity receptor binds to CD4 + This is due to the fact that it is additionally expressed on Tregs and vascular endothelium and activated by IL-2 cis-presentation. Therefore, compounds that also target the high-affinity IL-2Rαβγ potentially lead to Treg proliferation and vascular leak syndrome (VLS), as observed with native IL-2 or soluble IL-15 (Conlon et al. 2019). Potentially, VLS could also be caused by dePEGylated NKTR-214. DePEGylated NKT2-214, however, has a short half-life, and it remains to be seen whether this side effect plays a role at all or to what extent.

[0006] The high-affinity IL-15R receptor, activated by IL-15 cis-presentation, is constitutively expressed in T-cell leukemia and mediates the expression of inflammatory NK cells, inflammatory CD8 +It is upregulated on T cells and fibroblast-like synoviocytes (Kurowska et al. 2002, Perdreau et al. 2010), i.e., these cells also express the IL-15Rα subunit. Such activation should be avoided because cis-presentation of IL-15 on these cells is involved in the development of T cell leukemia and exacerbated immune responses, potentially inducing autoimmune diseases. Similarly, the high-affinity IL-15Rαβγ receptor is expressed on vascular endothelium, and soluble IL-15 can also induce VLS. IL-15 / IL-15Rα complexes do not bind to this high-affinity receptor because they already possess at least the sushi domain of IL-15Rα, which sterically prevents binding to the heterotrimeric IL-15Rαβγ receptor. These side effects, induced via engagement of the high-affinity IL-15Rαβγ receptor, are induced by native IL-15, but also by non-covalent IL-15 / IL-15Rα complexes, such as ALT-803 and hetIL-15 (when disruption of the complex occurs in vivo).

[0007] Finally, the high-affinity IL-15Rα is constitutively expressed on myeloid cells, macrophages, B cells, and neutrophils (Chenoweth et al. 2012) and can be activated by native IL-15 and again by non-covalent IL-15 / IL-15Rα complexes, such as ALT-803 and hetIL-15 (when disruption of the complex occurs in vivo).

[0008] In summary, IL-15 has similar immune-enhancing properties as IL-2, but it does not share immunosuppressive activities such as Treg cell activation and is thought not to cause VLS in the clinic (Robinson and Schluns 2017). On the other hand, drawbacks of IL-15 treatment are its short in vivo half-life and its dependence on transpresentation by other cell types (Robinson and Schluns 2017). This has led to the development of artificial IL-2 / IL-15Rβγ agonists, some of which have recently entered clinical development.

[0009] Although high-dose IL-2 treatment has been approved for renal cell carcinoma and metastatic melanoma (600,000 IU / kg administered by intravenous bolus over 15 minutes every 8 hours for up to 14 doses, followed by a 9-day rest period before repeating the regimen if tolerated by the patient), IL-2 is still under investigation to define lower-dose schedules (e.g., infusion over 90 days at a low dose to expand NK cells with intermediate pulses of IL-2 to provide activation of the expanded NK cell pool) that provide sufficient immune activation with a better-tolerated high safety profile, and many other low-dose intravenous or subcutaneous treatments, usually given in combination with other immunotherapies, have been evaluated, but with inconclusive results (Conlon et al. 2019). Low-dose subcutaneous regimens (1–30 million IU / m 2 / day) have been investigated because they may reduce toxicity but impair efficacy (Fyfe et al. 1995), but preferentially activate Tregs. Therefore, low-dose IL-2 is used in immunosuppressive treatment (Rosenzwajg et al. 2019).

[0010] Thus, the administration, dosing, and dosing schedule of artificial IL-2 / IL-15Rβγ agonists may be key to their clinical success, which is driven by multiple factors related to, for example, efficacy, side effects, patient compliance, and convenience (e.g., in combination with other drugs).

[0011] Recently, the pharmacokinetics and pharmacodynamics of hetIL-15 in rhesus monkeys were published (Bergamaschi et al. 2018). HetIL-15 was administered subcutaneously at fixed doses of 0.5, 5, or 50 μg / kg in dosing cycles with administration on days 1, 3, 5, 8, 10, and 12 (dosing cycle 1) and days 29, 31, 33, 36, 38, and 40 (dosing cycle 2). Additionally, monkeys were administered doses of 2, 4, 8, 16, 32, and 64 μg / kg using a doubling escalating dose regimen with injections on days 1, 3, 5, 8, 10, and 12. Intravenous administration led to peak IL-15 plasma levels 10 minutes after injection with a half-life of approximately 1.5 hours, whereas subcutaneous administration of hetIL-15 resulted in a T of approximately 12 hours. 1 This resulted in a 2-fold increase in systemic exposure and comparable trough levels. Both AUC and Cmax were shown to decrease 2-fold and 4-fold at a fixed dose of 5 μg / kg, and a further 9-fold and 8-fold at a fixed dose of 50 μg / kg, between days 1 and 40 during fixed-dose (subcutaneous) treatment. The authors concluded that "consumption of administered hetIL-15 progressively increased during the treatment cycle, reflecting an increase in the pool of cells responsive to IL-15" and that "the fixed-dose regimen provided excess IL-15 early in the 2-week cycle, but did not provide sufficient cytokine later in the treatment cycle." The authors therefore interpreted continuing with a dosing scheme consisting of six progressively doubling doses of hetIL-15 from 2 to 64 μg / kg over the course of 2 weeks as leading to a progressive increase in systemic exposure and comparable trough levels, which overall better matches the increasing IL-15 requirement due to the expanding target cell pool during treatment. CD8 + Regarding T cell proliferation, the authors used a fixed dose regimen to investigate the proliferation of Ki67 + CD8 + For T cells, a decrease was observed at day 15, whereas macaques treated with the graded dose regimen had high and comparable CD8 T cells at days 8 and 15. + demonstrated T cell proliferation.

[0012] The majority of engineered IL-2 / IL-15Rβγ agonists aim to increase their in vivo half-life by fusing IL-15, IL-2, or variants thereof to another protein, for example, soluble IL-15Rα (hetIL-15, where complex formation with the receptor is accompanied by a significant extension of the half-life), adding the Fc portion of an antibody to the complex (ALT-803) or the IL15 / IL-15Rα Fc fusion disclosed in US Pat. No. 10,206,980 (P22339), and IL15 / IL15Rα heterodimeric Fc fusion with extended half-life (Bernett et al. 2017) (WO 2014 / 145806), to a non-binding IgG (IgG-IL2v), or to an albumin-binding domain (see WO 2018 / 151868A2). Other examples of IL-2 / IL-15Rβγ agonists include PEGylated IL-2 molecules such as CT101-IL2 (Ghasemi et al. 2016, Lazear et al. 2017), NKTR-214 (Charych et al. 2016), and THOR-924 (Caffaro et al. 2019) (WO 2019 / 028419, WO 2019 / 028425), polymer-coated IL-15 NKTR-255 (Miyazaki et al. 2018), NL-201 / NEO-201 (Silva et al. 2019), RGD-targeted IL-15 / IL-15RαFc complex (US 2019 / 0092830), and Rubius. These include RTX-240 (erythroid cells expressing an IL-15 / IL-15Rα fusion protein) by Therapeutics, WO 2019 / 173798, and THOR-707 (Joseph et al. 2019). Additionally, targeted IL-2 / IL-15Rβγ agonists (where the agonist is fused to a binding molecule that targets specific cells, e.g., tumors, tumor microenvironments, or immune cells) have increased in vivo half-lives (RG7813, RG7461, immunocytokines in WO 2012 / 175222A1, modulokine and Kadmon in WO 2015 / 018528A1, KD033 in WO 2015 / 109124).

[0013] Studies have shown that ALT-803 has a serum half-life of 7.5 hours in mice (Liu et al. 2018) and 7.2–8 hours in cynomolgus monkeys (Rhode et al. 2016), compared with <40 minutes for IL-15 (Han et al. 2011). In the clinic, ALT-803 was administered intravenously or subcutaneously weekly for four consecutive weeks in a Phase I dose-escalation trial, starting at 0.3 μg / kg and increasing to 20 μg / kg for two 6-week treatment cycles, followed by a 2-week rest period for continuous monitoring. Results from the trial led to a weekly subcutaneous dose of 20 μg / kg as the optimal dose and delivery route for ALT-803 (Margolin et al. 2018). www.clinicaltrials.gov

[0014] Due to its long in vivo half-life, NKTR-214 has been described as a highly combinatorial cytokine, dosing more like an antibody than a cytokine. Its estimated dosing schedule in humans is once every 21 days. However, NKTR-214 offers a mechanism of direct immune stimulation characteristic of cytokines. PEGylation dramatically alters the pharmacokinetics of NKTR-214 compared to IL-2, providing a 500-fold increase in AUC in tumors compared to an equivalent dose of IL-2. The pharmacokinetics of NKTR-214 was determined after intravenous administration in mice. The most active species of NKTR-214 (i.e., 2-PEG-IL2, 1-PEG-IL2, and free IL2) resulted in a gradual increase, reaching Cmax 16 hours after dosing and declining with a t1 / 2 of 17.6 hours (Charych et al. 2017). Based on the increased half-life due to PEGylation, NKTR-214 was tested at a 5-dose regimen in combination with nivolumab in NCT02983045 (see www.clinicaltrials.gov). NKTR-214 0.006 mg / kg every 3 weeks (q3w) and nivolumab 240 mg every 2 weeks (q2w), -0.003 mg / kg NKTR-214 q2w and 240 mg nivolumab q2w, -0.006 mg / kg NKTR-214 q2w and 240 mg nivolumab q2w, -0.006 mg / kg NKTR-214 q3w and 360 mg nivolumab q3w, -0.009 mg / kg NKTR-214 q3w and 360 mg nivolumab q3w.

[0015] After completion of the first part of the study, nivolumab was continued at a dose of 360 mg q3w and NKTR-214 at 0.006 mg / kg q3w.

[0016] Recently, IL-2 / IL-15 mimetics were designed using computational approaches and reported to bind to the IL-2Rβγ heterodimer, but do not have a binding site for IL-2Rα (Silva et al. 2019), and therefore qualify as IL-2 / IL-15Rβγ agonists. Due to their small size of approximately 15 kDa (see Figure S13 in the Supporting Information), they are expected to have a fairly short half-life in vivo.

[0017] Another example of such an IL-2-based IL-2 / IL-15Rβγ agonist is the IL-2 variant (IL2v) by Roche, which is used in a fusion protein with an antibody. RO687428 is an example containing IL2v and is administered intravenously in the clinic. -On days 1, 15, and 29, and every 2 weeks from day 29 onwards, starting at a 5 mg dose with subsequent increases, or on a q3w schedule (NCT03063762, see www.clinicaltrials.gov), Once weekly (qw) at a starting dose of 5 mg as monotherapy -At a starting dose of 5 mg qw in combination with cetuximab -at a starting dose of 10 mg qw in combination with trastuzumab (NCT02627274, see www.clinicaltrials.gov), Alternatively, in combination with atezolizumab, qw for the first four doses and once every two weeks (q2w) for the remaining doses, starting at a dose of 10 mg for the first dose and 15 mg for the second and subsequent doses, for up to 36 months from initiation QW for the first 4 doses and q2w for the remaining doses, starting with a 10 mg dose for the first dose and a 15 mg dose for the second and subsequent doses, for up to 36 months -q3w for up to 36 months using a 10 mg dose QW for 4 weeks followed by q2w, starting at 15 mg and subsequent doses at 20 mg; or -15 mg q3w (NCT03386721, see www.clinicaltrials.gov). [Table 1]

[0018] However, exposure of cells expressing the receptor for native IL-15 to IL-15 (10 ng / ml) for less than 15 min already leads to maximal levels of Stat5 activation and subsequent pharmacodynamic effects (Castro et al. 2011).

[0019] In summary, IL-2 / IL-15Rβγ agonists are currently administered to achieve sustained availability of the molecule in patients by continuous infusion of short-lived molecules or by dramatically extending the half-life of IL-2 / IL-15Rβγ agonists by PEGylation or fusion to Fc fragments or antibodies. This is consistent with the general understanding that both NK cell tumor homing and in vivo antitumor activity depend on the sustained availability of IL-2 or IL-15, whereas NK cells rapidly die if they are not frequently stimulated by IL-15 (Larsen et al. 2014). Furthermore, such treatments significantly increase the CD8 + The focus is on maximizing T cell proliferation while simultaneously attempting to minimize Treg expansion (Charych et al. 2013 ).

[0020] On the other hand, Frutoso et al. showed that injection of two cycles of IL-15 or an IL-15 agonist resulted in little or no proliferation of NK cells in vivo in immunocompetent mice, whereas CD44+CD8 + We demonstrated that T cells remained responsive after a second cycle of stimulation with IL-15 or its agonist (Frutoso et al. 2018). Increasing the dose in the second cycle did not result in significant differences. Furthermore, NK cells extracted from mice after two cycles of stimulation had lower IFN-γ secretion compared with that after one cycle, but it was equivalent to that of untreated mice (Frutoso et al. 2018). This phenomenon can be explained by the finding that chronic stimulation of NK cells with strong activating signals alters the activation state and preferentially expands mature NK cells with reduced function (Elpek et al. 2010). Similarly, prolonged treatment with IL-15 has been described to deplete human NK cells. This effect is thought to be due to the influence of fatty acid oxidation on NK cell activity, suggesting that induction of fatty acid oxidation has the potential to significantly enhance IL-15-mediated NK cell immunotherapy (Felices et al. 2018).

[0021] Thus, despite recent advances in understanding the function of IL-2 / IL-15Rβγ agonists, it remains unclear how such IL-2 / IL-15Rβγ agonists should be optimally dosed and incorporated into treatment regimens as single agents or in combination with other treatments.

[0022] Summary of the Invention.

[0023] The present inventors have surprisingly found that pulsed cyclic dosing and pulsed dosing of interleukin-2 / interleukin-15 receptor βγ (IL-2 / IL-15Rβγ) agonists in primates enhances NK cell and CD8 + This leads to optimal activation of T cells, i.e., administration of IL-2 / IL-15Rβγ agonists, leading to increased Ki-67 + NK cells and CD8 + Significant increase in T cells and / or NK cells and CD8 + An increase in T cell numbers is produced that is repeated / maintained over multiple administrations.

[0024] Thus, the present invention provides novel pulsatile periodic and pulsed administration regimes for use in the treatment or management of cancer or infectious disease in humans using IL-2 / IL-15Rβγ agonists.

[0025] Definitions, Abbreviations, and Acronyms

[0026] An "IL-2 / IL-15Rβγ agonist" refers to a complex of IL-2 or an IL-2 derivative or IL-15 or an IL-15 derivative that targets intermediate-affinity IL-2 / IL-15Rβγ and has reduced or abolished binding to IL-2Rα or IL-15Rα. Reduced binding in this context means reduced by at least 50%, preferably at least 80%, and particularly at least 90% to the respective receptor α compared to wild-type IL-15 or IL-2, respectively. As described and exemplified below, reduced or abolished binding of IL-15 to the respective IL-15Rα can be mediated by forming a complex (covalently or non-covalently) with an IL-15Rα derivative, by mutations in IL-15 that lead to reduced or abolished binding, or by site-specific PEGylation or other post-translational modifications of IL-15 that lead to reduced or abolished binding. Similarly, reduced or abolished binding of IL-2 to the respective IL-2Rα can be mediated by mutations in IL-2 that lead to reduced or abolished binding, or by site-specific PEGylation or other post-translational modifications of IL-15 that lead to reduced or abolished binding.

[0027] "Interleukin-2," "IL-2," or "IL2" refers to the human cytokine described by NCBI Reference Sequence AAB46883.1 or UniProt ID P60568 (SEQ ID NO: 1). Its precursor protein has 153 amino acids, with a 20-aa peptide leader, resulting in a 133-aa mature protein. Its mRNA is described by NCBI GenBank Reference S82692.1.

[0028] An "IL-2 derivative" refers to a protein having at least 92%, preferably at least 96%, more preferably at least 98%, and most preferably at least 99% identity with the amino acid sequence of mature human IL-2 (SEQ ID NO: 2). Preferably, the IL-2 derivative has at least about 0.1%, preferably at least 1%, more preferably at least 10%, more preferably at least 25%, even more preferably at least 50%, and most preferably at least 80% of the activity of human IL-2 as determined by a lymphocyte proliferation bioassay. Because interleukins are extremely potent molecules, even a low activity, such as 0.1% of that of human IL-2, can still be sufficiently potent, especially when administered at high doses or if the loss of activity is compensated for by an extended half-life. The activity is expressed in international units established by the World Health Organization's First International Standard for Interleukin-2 (human) and superseded by the Second International Standard (Gearing and Thorpe 1988; Wadhwa et al. 2013). The relationship between potency and protein amount is as follows: 18 million IU of PROLEUKIN = 1.1 mg of protein. As described above, mutations (substitutions) may be introduced to extend half-life, as was done for THOR-707 (Joseph et al. al. 2019) (WO2019 / 028419A1), or to modify the binding properties of the molecule, for example by mutation of L72, F42 and / or Y45, in particular F42A, F42G, F42S, F42T, F42Q, F42E, F42N, F42D, F42R, F42K, Y45A, Y45G, Y45S, Y45T, Y45Q, Y45E, Y45N, Y45D, Y45R, Y45K, L72G, L72A, L72S, L72T, L72Q, L72E, L72N, L72D, L72R and L72K, preferably by mutations F42A, Y45A and L72G, to reduce binding to the IL-2α receptor as was done for IL2v (Klein et al. al. 2013, Bacac et al. 2016) (WO 2012 / 107417A1) PEG is specifically linked to IL-2.Various other mutations of IL-2 have been reported: R38W (US 2003 / 0124678) to reduce toxicity due to reduced vascular permeability activity (Hu et al. 2003); N88R (Shanafelt et al. 2000) to enhance selectivity for T cells over NK cells; R38A and F42K (Heaton et al. 1993) to reduce secretion of inflammatory cytokines from NK cells (US 5,229,109); D20T, N88R, and Q126D (US 2007 / 0036752) to reduce VLS; R38W and F42K to reduce interaction with CD25 and activation of Treg cells to enhance efficacy (WO 2008 / 003473); and additional mutations, such as T3A to avoid aggregation and C125A to abolish O-glycosylation, can be introduced (Klein et al. (Also see, e.g.,

[0014] ,

[0015] ,

[0016] , and

[0017] ). Other mutations or combinations of the above may be generated by genetic engineering methods, which are well known in the art. Amino acid numbers refer to the 133 amino acid mature IL-2 sequence.

[0029] "Interleukin-15," "IL-15," or "IL15" refers to the human cytokine described by NCBI Reference Sequence NP_000576.1 or UniProt ID P40933 (SEQ ID NO: 3). Its precursor protein has 162 amino acids, with a long 48-aa peptide leader, resulting in a 114-aa mature protein (SEQ ID NO: 4). Its mRNA, complete coding sequence, is described by NCBI GenBank Reference U14407.1. The IL-15Rα sushi domain (or IL-15Rα sushi, SEQ ID NO: 6) is a domain of IL-15Rα essential for binding to IL-15.

[0030] "IL-15 derivative" or "derivative of IL-15" refers to a protein having at least 92%, preferably at least 96%, more preferably at least 98%, and most preferably at least 99% identity with the amino acid sequence of mature human IL-15 (114 aa) (SEQ ID NO: 4). Preferably, the IL-15 derivative has at least 10%, more preferably at least 25%, even more preferably at least 50%, and most preferably at least 80% of the activity of IL-15. More preferably, the IL-15 derivative has at least 0.1%, preferably 1%, more preferably at least 10%, more preferably at least 25%, even more preferably at least 50%, and most preferably at least 80% of the activity of human IL-15. With respect to IL-2, as described above, interleukins are extremely potent molecules, and even low activity, such as 0.1% of human IL-15, can still be sufficiently potent, especially when administered at higher doses or if the loss of activity is compensated for by an extended half-life. Also, for IL-15, numerous mutations have been described to achieve various defined changes in the molecule: IL-15Rβγβγ cD8N, D8A, D61A, N65D, N65A, Q108R for reducing receptor binding (WO 2008 / 143794A1); N72D as an activating mutation (ALT-803); N1D, N4D, D8N, D30N, D61N, E64Q, N65D, and Q108E for reducing proliferative activity (US 2018 / 0118805); L44D, E46K, L47D, V49D, I50D, L66D, L66E, I67D, and I67E for reducing binding to IL-15Rα (WO 2016 / 142314A1); N65K and L69R for abrogating IL-15Rb binding (WO 2014 / 207173A1); Q101D and Q108D to inhibit IL-15 function (WO 2006 / 020849A2); S7Y, S7A, K10A, K11A to reduce IL-15Rβ binding (Ring et al. 2012); L45, S51, L52 substituted with D, E, K, or R and E64, I68, L69, and N65 substituted with D, E, R, or K to increase binding to IL-15Rα (WO 2005 / 085282A1).N71 is replaced by S, A, or N, N72 by S, A, or N, N77 by Q, S, K, A, or E, and N78 by S, A, or G to reduce deamidation (WO 2009 / 135031 A1); WO 2016 / 060996 A2 defines certain regions of IL-15 as suitable for substitution (see paragraphs 0020, 0035, 00120, and 00130) and specifically provides guidance on how to identify potential substitutions to provide anchors for PEG or other modifications (see paragraph 0021); Q108D for increased affinity to CD122 and suppression of CD132 recruitment to inhibit IL-2 and IL-15 effector function, and N65K for abrogating CD122 affinity (WO 2017 / 046200 A1); N1D, N4D, D8N, D30N, D61N, E64Q, N65D, and Q108E (see Figure 51, WO 2018 / 071918A1, WO 2018 / 071919A1) to gradually decrease the activity of the respective IL-15 / IL-15Rα complex with respect to T cell activation. Additionally or alternatively, conservative amino acid substitutions can be readily made by one skilled in the art.

[0031] The activity of both IL-2 and IL-15 can be determined by inducing proliferation of kit225 cells as described by Hori et al. (1987). Preferably, proliferative activation resulting from IL-2 or IL-15 stimulation is determined using methods such as colorimetry or fluorescence, e.g., using CTLL-2 cells, as described by Soman et al. (2009). As an alternative to cell lines, e.g., kit225 cells, human peripheral blood mononuclear cells (PBMCs) or buffy coats can be used. A preferred bioassay for determining the activity of IL-2 or IL-15 is the IL-2 / IL-15 bioassay kit (Promega catalog number CS2018B03 / B07 / B05) using STAT5-RE CTLL-2 cells.

[0032] IL-15 muteins can be produced by standard genetic engineering methods and are well known in the art, e.g., from WO 2005 / 085282, US 2006 / 0057680, WO 2008 / 143794, WO 2009 / 135031, WO 2014 / 207173, WO 2016 / 142314, WO 2016 / 060996, WO 2017 / 046200, WO 2018 / 071918, WO 2018 / 071919, US 2018 / 0118805. IL-15 derivatives may be further generated by chemical modification, e.g., PEGylation or other post-translational modifications, as known in the art (see WO 2017 / 112528A2, WO 2009 / 135031).

[0033] "IL-2Rα" refers to human IL-2 receptor α or CD25.

[0034] "IL-15Rα" refers to the human IL-15 receptor alpha or CD215, as described by NCBI Reference Sequence AAI21142.1 or UniProt ID Q13261 (SEQ ID NO: 5). Its precursor protein has 267 amino acids, with a 30-aa peptide leader, resulting in a 231-aa mature protein. Its mRNA is described by NCBI GenBank Reference HQ401283.1. The IL-15Rα sushi domain (or IL-15R sushi, SEQ ID NO: 6) is the domain of IL-15Rα that is essential for binding to IL-15 (Wei et al. 2001). The sushi+ fragment (SEQ ID NO: 7), which includes the sushi domain and part of the hinge region, is defined as 14 amino acids located after the sushi domain of this IL-15Rα and is C-terminal to the sushi domain; i.e., the IL-15Rα hinge region begins with the first amino acid after the (C4) cysteine ​​residue and ends with the 14th amino acid (counting in the standard "N- to C-terminal" direction). The sushi+ fragment reconstitutes full binding activity to IL-15 (WO2007 / 046006).

[0035] "Receptor alpha" refers to IL-2Rα or IL-15Rα.

[0036] An "IL-15Rα derivative" refers to a polypeptide comprising an amino acid sequence that is at least 92%, preferably at least 96%, more preferably at least 98%, even more preferably at least 99%, and most preferably 100% identical to the amino acid sequence of the sushi domain of human IL-15Rα (SEQ ID NO: 6) and, preferably, the sushi domain of human IL-15Rα (SEQ ID NO: 7). Preferably, an IL-15Rα derivative is an N- and C-terminally truncated polypeptide, whereas the signal peptide (amino acids 1-30 of SEQ ID NO: 5) is deleted, as well as the transmembrane domain and the intracytoplasmic portion of IL-15R (amino acids 210-267 of SEQ ID NO: 5). Thus, a preferred IL-15Rα derivative comprises at least the sushi domain (aa 33-93, but does not extend beyond the extracellular portion of mature IL-15Rα, which is amino acids 31-209 of SEQ ID NO: 5). Specific preferred IL-15Rα derivatives include the sushi domain of IL-15Rα (SEQ ID NO: 6), the sushi domain of IL-15Rα (SEQ ID NO: 7), and a soluble form of IL-15Rα (amino acid 31 through any of amino acids 172, 197, 198, 199, 200, 201, 202, 203, 204, or 205 of SEQ ID NO: 5; see WO 2014 / 066527 (Giron-Michel et al. 2005)). Within the limits provided by this definition, IL-15Rα derivatives can include naturally occurring or introduced mutations. https: / / www.uniprot.org / uniprot / Q13261 Natural variants and alternative sequences are described, for example, in UniProtKB entry Q13261 (https: / / www.uniprot.org / uniprot / Q13261). Furthermore, one skilled in the art can easily identify amino acids that are less conserved among mammalian IL-15Rα homologs, or even primate IL-15Rα homologs, in order to generate derivatives that are still functional. The respective sequences of mammalian IL-15Rα homologs are described in WO2007 / 046006, pages 18 and 19. Additionally or alternatively, one skilled in the art can easily make conservative amino acid substitutions.

[0037] Preferably, the IL-15Rα derivative has at least 10%, more preferably at least 25%, even more preferably at least 50%, and most preferably at least 80% of the binding activity of the human sushi domain to human IL-15 as determined in (Wei et al. 2001).

[0038] "IL-2Rβ" refers to human IL-Rβ or CD122.

[0039] "IL-2Rγ" refers to the common cytokine receptor gamma or gamma shared by IL-4, IL-7, IL-9, IL-15, and IL-21. c Or CD132.

[0040] "R11-15" refers to the IL-15 / IL-15Rα complex, which is a receptor-linker-interleukin fusion protein of the human IL-15Rα sushi fragment and human IL-15. Suitable linkers are described in WO2007 / 046006 and WO2012 / 175222.

[0041] "RLI2" or "SO-C101" is a specific version of RLI-15 and refers to an IL-15 / IL-15Rα complex that is a receptor-linker-interleukin fusion protein of the IL-15Rα sushi+ fragment and human IL-15 (SEQ ID NO: 9) using a linker with SEQ ID NO: 8.

[0042] "ALT-803" refers to Altor BioScience Corp.'s IL-15 / IL-15Rα complex, which is a complex containing two molecules of an optimized amino acid substitution (N72D) human IL-15 "superagonist," two molecules of the human IL-15α receptor "sushi" domain fused to a dimeric human IgG1 Fc that confers stability and extends the half-life of the IL-15N72D:IL-15R sushi-Fc complex (see, e.g., US 2017 / 0088597).

[0043] "Heterodimeric IL-15:IL-Rα," "hetIL-15," or "NIZ985" refers to Novartis' IL-15 / IL-15Rα complex, which mimics IL-15, circulating with soluble IL-15Rα as a stable molecular complex; it is a recombinantly co-expressed non-covalent complex of human IL-15 and soluble human IL-15Rα (sIL-15Rα), i.e., 170 amino acids of IL-15Rα without the signal peptide and transmembrane and cytoplasmic domains (Thaysen-Andersen et al. 2016; see, e.g., Table 1).

[0044] "IL-2 / IL-15Rβγ agonists" refer to molecules or complexes that primarily target the intermediate-affinity IL-2 / IL-15R receptor, but do not bind to the IL-2Rα and / or IL-15Rα receptors, and therefore lack the ability to stimulate Tregs. An example is IL-15 conjugated to at least the sushi domain of IL-15Rα, which has the advantages of not relying on transpresentation or cell-cell interactions and a longer in vivo half-life due to the increased size of the molecule, and which has been shown to be significantly more potent than native IL-15 in vitro and in vivo (Robinson and Schluns 2017). In addition to IL-15 / IL-15Rα-based complexes, this can also be achieved with mutated or chemically modified IL-2, which binds the IL-2 / 15Rβ and γ receptors. c It has significantly reduced or timely delayed binding to the IL-2α receptor without affecting binding to the receptor.

[0045] "NKTR-214" refers to an IL-2-based IL-2 / IL-15Rβγ agonist and is a biological prodrug consisting of IL-2 conjugated by six releasable polyethylene glycol (PEG) chains (WO 2012 / 065086 A1). The presence of multiple PEG chains creates an inactive prodrug, thereby preventing rapid systemic immune activation upon administration. The use of releasable linkers allows the PEG chains to be slowly hydrolyzed, resulting in the sustained formation of active conjugated IL-2 conjugated by two PEGs or one PEG. The position of the PEG chains at the IL-2 / IL-2Rα interface interferes with binding to the high-affinity IL-2Rα, while binding to the low-affinity IL-2Rβ remains unperturbed, supporting immune activation over tumor suppression (Charych et al. 2016, Charych et al. 2017).

[0046] "IL2v" refers to Roche's IL-2-based IL-2 / IL-15Rβγ agonist, an IL-2 variant with abrogated binding to the IL-2Rα subunit, identified by SEQ ID NO: 10. IL2v is used, for example, in fusion proteins, fused to the C-terminus of an antibody. IL2v was designed to eliminate its ability to bind to IL-2Rα through amino acid substitutions F42A, Y45A, and L72G (conserved among humans, mice, and non-human primates), and to eliminate O-glycosylation through amino acid substitution T3A, thereby avoiding aggregation by the C125A mutation (numbering based on UniProt ID P60568, excluding the signal peptide) as in aldesleukin (Klein et al. 2017). IL2v is used as a fusion partner with antibodies, for example, non-targeting IgG (IgG-IL2v), to increase half-life (Bacac et al. 2017). In RG7813 (or sergutuzumab amnaleukin, RO-6895882, CEA-IL2v), IL2v is fused to an antibody targeting carcinoembryonic antigen (CEA) with a heterodimeric Fc lacking FcγR and C1q binding (Klein 2014, Bacac et al. 2016, Klein et al. 2017), and in RG7461 (or RO6874281 or FAP-IL2v), IL2v is fused to a tumor-specific antibody targeting fibroblast activation protein-alpha (FAP) (Klein 2014).

[0047] THOR-707 refers to an IL-2 / IL-15Rβγ agonist based on a site-specific, mono-PEGylated form of IL-2 that has reduced / lacks IL2Rα chain engagement while retaining binding to the intermediate affinity IL-2R signaling complex (Joseph et al. 2019) (WO 2019 / 028419A1).

[0048] NL-201 refers to an IL-2 / IL-15Rβγ agonist, which mimics IL-2 and binds to the IL-2 receptor βγ c Heterodimer (IL-2Rβγ c), but does not have binding sites for IL-2Rα or IL-15Rα (Silva et al. 2019).

[0049] NKRT-255 is an IL-2 / IL-15Rβγ agonist based on PEG-conjugated human IL-15 that retains binding affinity to IL-15Rα, exhibits reduced clearance, and provides a sustained pharmacodynamic response ( WO 2018 / 213341A1 ).

[0050] THOR-924, -908, -918 refer to IL-2 / IL-15Rβγ agonists based on PEG-conjugated IL-15 with reduced binding to IL-15Rα with unnatural amino acids used for site-specific PEGylation ( WO 2019 / 165453A1 ).

[0051] The "percentage of identity" between two amino acid sequences refers to the percentage of identical amino acids between the two sequences being compared, obtained using the best alignment of the sequences; this percentage is purely statistical, and the differences between these two sequences are randomly distributed throughout the amino acid sequence. As used herein, "best alignment" or "optimal alignment" refers to the alignment with the highest determined percentage of identity (see below). Sequence comparison between two amino acid sequences is usually achieved by comparing these sequences, which have been previously aligned according to the best alignment; this comparison is performed on a segment of comparison to identify and compare local regions of similarity. The best sequence alignment for comparison can be achieved by manual methods, or by using the global homology algorithm developed by Smith and Waterman (1981), the local homology algorithm developed by Needleman and Wunsch (1970), the similarity method developed by Pearson and Lipman (1988), computer software using such algorithms (GAP, BESTFIT, BLAST P, BLAST N, FASTA, TFASTA (in the Wisconsin Genetics software package), Genetics Computer Group, 575 Science Dr., Madison, Wisconsin, USA), the MUSCLE multiple alignment algorithm (Edgar 2004), or CLUSTAL (Goujon et al. 2010). To obtain the best local alignment, BLAST software with the BLOSUM62 matrix can be preferably used. The percentage identity between two sequences of amino acids is determined by comparing the two sequences in optimal alignment, and the amino acid sequence may include additions or deletions with respect to the reference sequence in order to obtain optimal alignment between the two sequences.The percentage of identity is calculated by determining the number of identical positions between the two sequences, dividing this number by the total number of positions compared, and multiplying the result by 100 to obtain the percentage of identity between the two sequences.

[0052] Conservative amino acid substitutions refer to the substitution of amino acids in which an aliphatic amino acid (i.e., glycine, alanine, valine, leucine, isoleucine) is replaced with another aliphatic amino acid, a hydroxyl or sulfur / selenium-containing amino acid (i.e., serine, cysteine, selenocysteine, threonine, methionine) is replaced with another hydroxyl or sulfur / selenium-containing amino acid, an aromatic amino acid (i.e., phenylalanine, tyrosine, tryptophan) is replaced with another aromatic amino acid, a basic amino acid (i.e., histidine, lysine, arginine) is replaced with another basic amino acid, or an acidic amino acid or its amide (aspartic acid, glutamic acid, asparagine, glutamine) is replaced with another acidic amino acid or its amide.

[0053] "In vivo half-life" or T 1 / 2 refers to the time required for the amount of a drug to decrease to half of its initial amount in vivo. The in vivo half-life of a particular drug can be determined in any mammal. For example, the in vivo half-life can be determined in humans, primates, or mice. The in vivo half-life determined in humans can be significantly different from the in vivo half-life in mice; i.e., the in vivo half-life in mice for a particular drug is generally shorter than the in vivo half-life determined for the same drug in humans, but such in vivo half-life determined in mice still provides an indication of the specific in vivo half-life in humans. Therefore, the in vivo half-life of a drug in humans can be estimated from the in vivo half-life determined for a particular drug in mice. This is particularly important because direct determination of the in vivo half-life of a particular drug in humans is rarely possible due to the prohibition of experiments involving humans for purely scientific purposes. Alternatively, the half-life can be determined in primates (e.g., cynomolgus monkeys), which is more similar to the half-life in humans. More specifically, the "in vivo half-life," (terminal) plasma half-life, or T 1 / 2 is the elimination half-life or terminal half-life, i.e., after administration, the in vivo half-life is the time required for the plasma / blood concentration to decrease by 50% after reaching pseudo-equilibrium of distribution (Toutain and Bousquet-Melou 2004). Determination of drugs, here polypeptides, IL-2 / IL-15βγ agonists, in blood / plasma is typically performed through polypeptide-specific ELISA. https: / / www.cancer.gov / publications / dictionaries / cancer-terms / def / immune-checkpoint-inhibitor

[0054] "Immune checkpoint inhibitors," or simply "checkpoint inhibitors," refer to a type of drug that blocks specific proteins made by certain types of immune system cells, such as T cells, and some cancer cells. These proteins can thwart the immune response and prevent T cells from killing cancer cells. When these proteins are blocked, the "brakes" on the immune system are released, allowing T cells to better kill cancer cells. Checkpoint inhibitors are therefore antagonists of immune inhibitory checkpoint molecules or antagonists of the agonist ligands of inhibitory checkpoint molecules. Examples of checkpoint proteins found in T cells or cancer cells include PD-1 / PD-L1 and CTLA-4 / B7-1 / B7-2 (see definitions from the National Cancer Institute of the National Institutes of Health, https: / / www.cancer.gov / publications / dictionaries / cancer-terms / def / immune-checkpoint-inhibitor), as reviewed, for example, by Darvin et al. (2018). Examples of such checkpoint inhibitors are anti-PD-L1 antibodies, anti-PD-1 antibodies, anti-CTLA-4 antibodies, but also antibodies against LAG-3 or TIM-3, or blockers of BTLA, which are currently being tested in the clinic (De Sousa Linhares et al. 2018). Further promising checkpoint inhibitors are anti-TIGIT antibodies (Solomon and Garrido-Laguna 2018).

[0055] "Anti-PD-L1 antibody" refers to an antibody, or antibody fragment thereof, that binds to PD-L1. Examples are avelumab, atezolizumab, durvalumab, KN035, and MGD013 (bispecific for PD-1 and LAG-3).

[0056] "Anti-PD-1 antibody" refers to an antibody or antibody fragment thereof that binds to PD-1. Examples include pembrolizumab, nivolumab, cemiplimab (REGN2810), BMS-936558, SHR1210, IBI308, PDR001, BGB-A317, BCD-100, and JS001.

[0057] "Anti-PD-L2 antibody" refers to an antibody, or antibody fragment thereof, that binds to anti-PD-L2. An example is sHIgM12.

[0058] "Anti-CTLA4 antibody" refers to an antibody, or antibody fragment thereof, that binds to CTLA-4. Examples are ipilimumab and tremelimumab (ticilimumab).

[0059] An "anti-LAG-3" antibody refers to an antibody or antibody fragment thereof that binds to LAG-3. Examples of anti-LAG-3 antibodies are leratolimab (BMS 986016), Sym022, REGN3767, TSR-033, GSK2831781, MGD013 (bispecific for PD-1 and LAG-3), and LAG525 (IMP701).

[0060] "Anti-TIM-3 antibody" refers to an antibody, or antibody fragment thereof, that binds to TIM-3. Examples are TSR-022 and Sym023.

[0061] "Anti-TIGIT antibody" refers to an antibody that binds to TIGIT, or an antibody fragment thereof. Examples include tiragolumab (MTIG7192A, RG6058) and etidilimab (WO 2018 / 102536).

[0062] A "therapeutic antibody" or "tumor-targeting antibody" refers to an antibody, or antibody fragment thereof, that has a direct therapeutic effect on tumor cells through binding of the antibody to a target expressed on the surface of the treated tumor cells. Such therapeutic activity may result from receptor binding that leads to altered signaling in the cell, antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC), or other antibody-mediated killing of tumor cells.

[0063] "Anti-CD38 antibody" refers to an antibody or antibody fragment thereof that binds to CD38, also known as cyclic ADP-ribosyl hydrolase. Examples of anti-CD38 antibodies are daratumumab, isatuximab (SAR650984), MOR-202 (MOR03087), TAK-573 or TAK-079 (Abramson 2018), or GEN1029 (HexaBody®-DR5 / DR5).

[0064] "About" when used in conjunction with a value means the value plus / minus 10%, preferably 5%, especially 1% of that value.

[0065] Where the term "comprising" is used in the present description and claims, it does not exclude other elements. For the purposes of the present invention, the term "consisting of" is considered to be a preferred embodiment of the term "consisting of." Hereinafter, when a group is defined as comprising at least a certain number of embodiments, this should also be understood to disclose a group that preferably consists only of these embodiments.

[0066] Where an indefinite or definite article is used when referring to a singular noun, e.g., "a", "an" or "the", this includes a plural of that noun unless something else is specifically stated.

[0067] The term "at least one," such as "at least one chemotherapeutic agent," can thus mean one or more chemotherapeutic agents. In the same context, the term "combination thereof" refers to a combination comprising more than one chemotherapeutic agent.

[0068] Terms are used according to their ordinary meaning. Where a specific meaning is conveyed to a particular term, the definition of the term is given below in the context in which the term is used.

[0069] "qxw", from Latin quaque / each for every x weeks, e.g., q2w for every second week. "sc" for subcutaneous. "iv" for intravenous. "ip" for intraperitoneal cavity.

[0070] Description of the invention

[0071] Pulse-periodic dosing

[0072] In a first aspect, the present invention relates to an interleukin-2 / interleukin-15 receptor (IL-2 / IL-15R) agonist for use in the treatment or management of cancer or an infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist to a human patient using a cyclical dosing regimen comprising: (a) a first period of x days, during which an IL-2 / IL-15Rβγ agonist is administered in a daily dose for y consecutive days at the beginning of the first period, followed by xy days without administration of the IL-2 / IL-15Rβγ agonist, where x is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or 21 days, preferably 7 or 14 days, and y is 2, 3, or 4 days, preferably 2 or 3 days; (b) repeating the first period at least once; and (c) a second period of z days without administration of an IL-2 / IL-15Rβγ agonist, where z is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 28, 35, 42, 49, 56, 63, or 70 days, preferably 7, 14, 21, or 56 days, and more preferably 7 or 21 days. For illustrative purposes, a graphical representation of dosing is depicted in Figure 21. In a more preferred embodiment, y is 2 days and x is 7 days.

[0073] In one embodiment, the present invention relates to an interleukin-2 / interleukin-15 receptor (IL-2 / IL-15R) agonist for use in the treatment or management of cancer or an infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist to a human patient using a cyclical dosing regimen comprising: (a) a first period of x days, during which an IL-2 / IL-15Rβγ agonist is administered in a daily dose for y consecutive days at the beginning of the first period, followed by xy days without administration of the IL-2 / IL-15Rβγ agonist, where x is 14 or 21 days, preferably 14 days, and y is 2, 3, or 4 days, preferably 2 or 3 days; (b) repeating the first period at least once; and (c) a second period of z days without administration of an IL-2 / IL-15Rβγ agonist, where z is 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 28, 35, 42, 49, 56, 63, or 70 days, preferably 7, 14, 21, or 56 days, more preferably 7 or 21 days. In a more preferred embodiment, x is 14 days, y is 2, 3, or 4 days, and z is 14 days. In particular in the case of longer pulses of 4 days, it may be required that the first period of x days be longer than 7 days, i.e., only 14 or 21 days in a weekly scheme.

[0074] In a second aspect, the present invention relates to an interleukin-2 / interleukin-15 receptor (IL-2 / IL-15Rβγ) agonist for use in the treatment or management of cancer or an infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist to a human patient using a cyclical dosing regimen comprising: (a) a first period of x days during which an IL-2 / IL-15Rβγ agonist is administered in a daily dose for y consecutive days at the beginning of the first period, followed by xy days without administration of the IL-2 / IL-15Rβγ agonist, where x is 5, 6, 7, 8, or 9 days and y is 2, 3, or 4 days; (b) repeating the first period at least once; and (c) a second period of z days without administration of an IL-2 / IL-15Rβγ agonist, where z is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 days. For illustrative purposes, a graphical representation of dosing is depicted in FIG.

[0075] This dosing scheme can be described as "pulse-cyclic" dosing - "pulse" because the IL-2 / IL-15R agonist is administered, for example, on days 1 and 2 of the week, to stimulate NK cell and CD8 + Both T cells are activated and expanded ("pulsed"), followed by no administration of agonist for the remainder of the week (step (a)). This on / off administration is repeated at least once, e.g., for 2 or 3 weeks (step (b)), followed by another period, e.g., another week, without administration of the IL-2 / IL-15Rβγ agonist (step (c)). Thus, examples of cycles are (a)-(a)-(c) (where (a) is repeated once) or (a)-(a)-(a)-(c) (where (a) is repeated twice). Pulse dosing occurs during a first period according to step (a) and in the repetition of the first period in step (b). Steps (a), (b), and (c) together, i.e., pulse dosing in combination with a second period without administration of the IL-2 / IL-15Rβγ agonist, are referred to as one cycle or one treatment cycle. This entire treatment cycle (first and second periods) may be repeated multiple times.

[0076] The present inventors have surprisingly found that pulse dosing of the IL-2 / IL-15Rβγ agonist RLI-15 / SO-C101 on consecutive days significantly increased NK cell and CD8 + Strong dose-dependent activation (expression of Ki67, i.e., Ki67) of T cells (both for intravenous and subcutaneous administration) +We found that the first administration of IL-2 / IL-15Rβγ agonist in primates on day 1, followed by a second administration of the same dose on day 2, induced the induction of NK cells and CD8 + Surprisingly, this led to a further increase in both T cell activation. A fourth dose on day 4 did not result in a further increase in activation, but still kept activation levels high. A rest period of several days was then sufficient to achieve a similar level of activation in the second pulse.

[0077] RLI-15 was used in primates to measure NK cell and CD8 + This is surprising given the relatively short half-life of RLI-15, which still resulted in high levels of proliferating NK cells and CD8 T cells 4 days after the first dose and 3 days after the second dose. + Leads to T cells.

[0078] Long-term sustained stimulation of the intermediate affinity IL-2 / IL-15Rβγ receptor results in increased proliferation of NK cells and CD8 cells compared to shorter stimulation with two consecutive daily doses of a relatively short-lived IL-2 / IL-15Rβγ receptor agonist, such as RLI-15. + On the other hand, too frequent dosing or sustained stimulation with agonists with significantly long half-lives may result in increased NK cell and CD8 T cell activity in primates. + T cell depletion and even anergy can occur.

[0079] The pulse-periodic and pulse-dosing methods provided herein contrast with previously described dosing regimens for IL-2 / IL-15Rβγ agonists tested in primates and humans, which apply continuous dosing of such agonists and, similar to classical drugs, seek to optimize AUC and Cmax over time, i.e., aim for constant drug levels and, therefore, sustained stimulation of effector cells.

[0080] For example, IL-2 and IL-15 are continuously dosed: IL-2 intravenous bolus over 15 minutes every 8 hours; and IL-15 subcutaneously on days 1-8 and 22-29, or intravenous continuous infusion for 5 or 10 consecutive days, or daily intravenous infusion for 12 consecutive days (see clinical trials: NCT03388632, NCT01572493, NCT01021059). The IL-2 / IL-15Rβγ agonist hetIL-15 was continuously dosed in primates on days 1, 3, 5, 8, 10, 12, and 29, 31, 33, 36, 38, and 40 (i.e., always on days 1, 3, and 5 of the week). We attempted to overcome this lack of response by increasing the dose of the IL-2 / IL-15Rβγ agonist to a much higher dose of 64 μg / kg (Bergamaschi et al. 2018), much higher than is tolerated in humans (Conlon et al. 2019). In humans, hetIL-15 (NIZ985) was administered subcutaneously at 0.25–4.0 μg / kg, 2 weeks on / 2 weeks off, again three times weekly (TIW) (Conlon et al. 2019). In comparison, ALT-803 was administered once weekly (weeks 1–5 of four 6-week cycles) in human clinical trials (Wrangle et al. 2018). NKT-214 was administered once every 3 weeks.

[0081] Our findings were further in contrast to a report by Frutoso et al., in which pulse dosing in mice (days 1 and 3, followed by treatment withdrawal) with a second stimulation with IL-15 or IL-2 / IL-15Rβγ agonists did not lead to significant activation of NK cells in vivo (Frutoso et al. 2018).

[0082] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic administration regimen, where x is 6, 7, or 8 days, preferably 7. For reasons of convenience, it is advantageous for patients to be treated on a weekly rhythm, especially when such a rhythm is repeated over many weeks, i.e., where x is preferably 7 days, however, it can be reasonably assumed that changing the rhythm to 6 or 8 days will have a significant impact on the treatment outcome, making 6 or 8 days also a preferred embodiment.

[0083] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, where y is 2 or 3 days, preferably 2 days. + Optimal activation of both T cells (Ki67 + (measured as IL-16) can be achieved by two consecutive daily administrations per week on two consecutive days, whereas four consecutive daily administrations within one week significantly increased the activation of NK cells and CD8 + It has been shown in cynomolgus monkeys that it does not provide any additional benefit with respect to T cells. In other words, NK cells and CD8 + T cell activation plateaued between the second and fourth doses. Therefore, two and three, and more preferably two, consecutive daily doses are preferred to minimize patient exposure to the drug, while still achieving high levels of effector cell activation.

[0084] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, where z is 6, 7, or 8 days. To stay on a weekly rhythm for patient convenience, period z (during which no administration of the IL-2 / IL-15Rβγ agonist occurs) is preferably 7 or 14 days, more preferably 7 days.

[0085] A dosing regimen according to the present invention may be preceded by a pretreatment period in which the IL-2 / IL-15Rβγ agonist is administered at a lower daily dose, less frequently, or an extended treatment break is applied to test the patient's response, to acclimate the patient to the treatment, or to stimulate the immune system for a subsequent higher immune cell response. For example, in a treatment period x (e.g., 7 days), there is one additional treatment cycle as pretreatment with y days (e.g., 2 or 3 days) of treatment, while z is expected to be extended compared to the following treatment cycle (e.g., 14 days instead of 7 days).

[0086] In a particularly preferred embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, where x is 7 days, y is 2 days, and z is 7 days. This particularly preferred treatment cycle involves two doses on two consecutive days, followed by 7 = 2 = 5 days without dosing, thus creating a one-week cycle, combining a minimum exposure of two doses of the IL-2 / IL-15Rβγ agonist, and promoting NK cell and CD8 + Achieve maximum activation of T cells with weekly cycling convenient for patients.

[0087] In a particularly preferred embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclic administration regimen, where x is 7 days, y is 2, 3, or 4 days, and z is 7 days. Two administrations on two consecutive days already result in increased NK cell and CD8 + Four doses on four consecutive days resulted in the greatest activation of activated NK cells and CD8 + Such activation was maintained for an additional two days without leading to a significant decrease in NK cells. Therefore, an alternative preferred treatment regimen, where x is 7 days, y is 3 days, and z is 7 days, i.e., 3 doses on 3 consecutive days, followed by 7-3=4 days with no doses, is used, which results in a significant increase in NK cell and CD8 activation. +Long-term activation of T cells can be beneficial if it translates into higher efficacy. Another alternative preferred treatment regimen is where x is 7 days, y is 4 days, and z is 7 days, i.e., 4 doses on 4 consecutive days, followed by 7-4=3 days without doses, which is beneficial for NK cell and CD8 + Long-term activation of T cells may be beneficial if it translates into higher efficacy.

[0088] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclic dosing regimen, wherein the daily dose is from 0.1 μg / kg (0.0043 μM) to 50 μg / kg (2.15 μM) of the IL-2 / IL-15Rβγ agonist.

[0089] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclic dosing regimen, wherein the daily dose is between 0.0043 μM and 2.15 μM of the IL-2 / IL-15Rβγ agonist.

[0090] The present inventors have investigated the effects of RLI-15 / SO-C101 (for which 1 μM is equivalent to 23 μg / kg) on ​​human NK cells and CD8 + In vitro NK and CD8 T cells +A good correlation between T cell proliferation and in vivo data obtained from cynomolgus monkeys could be shown, which allows predicting a predicted minimum effective dose (MABEL) of about 0.25 μg / kg, a pharmacologically effective dose (PAD) of between about 0.6 μg / kg and 10 μg / kg, together with a no observed adverse effect level (NOAEL) of about 25 μg / kg and a maximum tolerated dose (MTD) of about 32 μg / kg for RLI-15 and IL-2 / IL-15Rβγ agonists, preferably with approximately the same molecular weight. These values ​​equate to a MABEL of approximately 0.011 μM for IL-2 / IL-15Rβγ agonists, a PAD of approximately 0.026 μM to 0.43 μM for IL-2 / IL-15Rβγ agonists, a NOAEL of approximately 1.1 μM for IL-2 / IL-15Rβγ agonists, and an MTD of approximately 1.38 μM for IL-2 / IL-15Rβγ agonists.

[0091] Taking into account potential deviations from predictions, a starting dose of 0.1 μg / kg (0.0043 μM) has been determined for clinical trials, and the observed MTD in humans may be up to 50 μg / kg (2.15 μM). Preferably, this dose is between 0.25 μg / kg (0.011 μM) (MABEL) and 25 μg / kg (1.1 μM) (NOAEL), more preferably between 0.6 μg / kg (0.026 μM) and 10 μg / kg (0.43 μM) (PAD), more preferably between 1 μg / kg (0.043 μM) and 15 μg / kg (0.645 μM), and especially between 2 μg / kg (0.087 μM) and 10 μg / kg (0.43 μM).

[0092] Thus, in another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic dosing regimen, wherein the daily dose is 0.0043 μM to 2.15 μM of the IL-2 / IL-15Rβγ agonist, preferably the dose is between 0.011 μM (MABEL) and 1.1 μM (NOAEL), more preferably between 0.026 μM and 0.43 μM (PAD).

[0093] In a preferred embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic dosing regimen, wherein the daily dose selected within the dose range of 0.1 to 50 μg / kg, preferably 0.25 to 25 μg / kg, more preferably 0.6 to 10 μg / kg, especially 2 to 10 μg / kg, does not increase substantially during the dosing regimen, and preferably wherein this dose is maintained during the dosing regimen. Surprisingly, the dosing regimen according to the present invention results in an increase in the number of NK cells and CD8 + It demonstrated repeated T cell activation and did not require dose escalation over time. This was not observed, for example, in the dosing regimen used for hetIL-15, which was compensated for by progressively doubling the dose from 2 to 64 μg / kg (Bergamaschi et al. 2018). Therefore, an important advantage is that the selected daily dose, within the range of 0.1 to 50 μg / kg, does not need to be increased within the first repeated period of administration or from one cycle to the next. This allows repeated cycles of treatment without risking toxic doses or ineffective treatment over time. Furthermore, maintaining the same daily dose throughout the dosing regimen ensures higher compliance because doctors or nurses do not need to adjust the dose from one treatment to another.

[0094] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, whereby the daily dose is between 3 μg / kg (0.13 μM) and 20 μg / kg (0.87 μM), preferably between 6 μg / kg (0.26 μM) and 12 μg / kg (0.52 μM) of the IL-2 / IL-15Rβγ agonist.

[0095] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic dosing regimen, wherein the daily dose is a weight-independent fixed dose of 7 μg to 3500 μg (0.30 mol to 150 mol), preferably 17.5 μg to 1750 μg (0.76 mol to 76 mol), more preferably 42 μg to 700 μg (1.8 mol to 30 mol), especially 140 μg to 700 μg (6.1 mol to 30 mol).

[0096] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, where the daily dose is increased during the dosing regimen. Because the IL-2 / IL-15Rβγ agonist leads to proliferation of cells expressing the IL-2 / IL-15R receptor and to increased expression of the receptor on the surface, an equal dose of the agonist may lead to decreased plasma concentrations of the agonist over time because more agonist molecules are bound to the cells. To compensate for the increasing uptake of molecules by target cells, the daily dose is preferably increased during the dosing regimen.

[0097] Such an increase in daily dose can preferably occur after each period of x days. Typically, such an increase can be best managed operationally if the increase occurs after each pulse of x days. In particular, CD8 + T cells appear to lose sensitivity to stimulation by IL-2 / IL-15Rβγ agonists after x days of pulsing, so it is preferable to increase the daily dose after each x-day pulse (until the upper limit of the tolerated daily dose is reached).

[0098] In one embodiment, the next treatment cycle begins again with the initial daily dose, which is increased again after each pulse on x days (see Figure 21, option A). Alternatively, the next treatment cycle begins with a daily dose that is the same as the last daily (increased) dose of the previous pulse on x days (see Figure 21, option B).

[0099] In one embodiment, the daily dose is increased by about 20% to about 100%, preferably by about 30% to about 50%, after each period of x days to compensate for proliferation of target cells.

[0100] Such an increase may be limited by an upper limit, which cannot be exceeded, for example, due to dose-limiting toxicity. However, assuming the binding of the agonist to target cells, this upper limit is expected to depend on the number of target cells, i.e., patients with expanded target cell compartments are expected to tolerate higher doses of agonist compared to (untreated) patients with fewer target cells. Still, the upper limit of the tolerated daily dose after dose escalation is expected to be 50 μg / kg (2.15 μM), preferably 32 μg / kg (1.4 μM), particularly 20 μg / kg (0.87 μM).

[0101] In another embodiment, the daily dose is increased only once after a first period of x days, preferably by about 20% to about 100%, preferably by about 30% to about 50% after a first period of x days. Already one increase in the daily dose may reach the upper limit of the tolerated daily dose, but further increases in IL-2 / IL-15Rβγ agonist levels of NK cells and CD8 + During z days without cell administration, a return to near normal levels is expected, with one increase being sufficient.

[0102] In another embodiment, the daily dose is increased after each daily dose within pulse period y. A preferred embodiment may then further increase the next daily dose for the next treatment period x within the same cycle (see FIG. 21 , option C) or continue at the same daily dose level as the last daily dose of the previous treatment period x (see FIG. 21 , option D). During a treatment cycle, the daily dose may always be restarted at the initial dose level (see FIG. 21 , options C and B) or may continue at the increased dose level from the first treatment day of the preceding treatment period x (see FIG. 21 , option E). Again, such increases may be limited by an upper limit, which cannot be exceeded, for example, due to dose-limiting toxicity. Given agonist binding to target cells, however, this upper limit is expected to be dependent on the number of target cells; i.e., patients with an expanded target cell compartment are expected to tolerate higher doses of agonist compared to (untreated) patients with a lower number of target cells. Still, the upper limit of the acceptable daily dose after dose escalation is envisaged to be 50 μg / kg (2.15 μM), preferably 32 μg / kg (1.4 μM), in particular 20 μg / kg (0.87 μM).

[0103] In one embodiment, the IL-2 / IL-15Rβγ agonist is for use where the daily dose is administered in a single injection. A single daily injection is convenient for the patient and healthcare provider and is therefore recommended.

[0104] However, given the short half-life of the molecule and the hypothesis that immune cell activation is dependent on increased IL-2 / IL-15Rβγ agonist activity rather than sustained levels of such agonist, another preferred embodiment is for the daily dose to be divided into two or three individual doses administered within one day, where the time interval between administration of the individual doses is at least about 4 hours, preferably not more than 12 hours (high-intensity pulsed cyclic administration). The same amount of agonist (divided into several doses and administered during the day) activates NK cells and especially CD8 cells in human patients. +It is expected that the latter will be more effective in stimulating cells, and that the latter will exhibit lower sensitivity to stimulation than if administered in a single injection alone. This has surprisingly been observed in mice. Indeed, such multiple dosing could be incorporated into the routine of a hospital, physician's practice, or outpatient setting; thus, two to three equivalent doses administered during a business day, including an 8- to 12-hour shift, may still be conveniently manageable, although an 8- or 10-hour interval is preferred as the maximum time difference between the first and last dose. Thus, a preferred embodiment is one in which the daily dose is divided into three individual doses administered within one day, with the time interval between the administration of the individual doses being about 5 to about 7 hours, preferably about 6 hours. This means that patients could be dosed daily at 7:00 AM, 2:00 PM, and 7:00 PM (with a 6-hour interval), or at 7:00 AM, 1:00 PM, and 6:00 PM (with a 5-hour interval). In another preferred embodiment, the daily dose is divided into two individual doses administered within one day, wherein the time interval between the administration of the individual doses is about 6 to about 10 hours, preferably 8 hours. In the case of two doses, the patient may be dosed, for example, at 8:00 AM and 4:00 PM (with an 8-hour interval). Given the routine practice of a hospital, the interval between doses may vary within a day or from day to day.

[0105] In another preferred embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, wherein the IL-2 / IL-15Rβγ agonist is administered subcutaneously (sc) or intraperitoneally (ip), preferably subcutaneously. + It has been observed that subcutaneous administration is more potent than intravenous administration in terms of T cell activation.Intraperitoneal administration has the same pharmacodynamic effect as subcutaneous administration.Therefore, intraperitoneal administration is another preferred embodiment, particularly for cancer originating in the organs of the abdominal cavity, such as ovarian cancer, pancreatic cancer, colorectal cancer, gastric cancer, and liver cancer, and for peritoneal metastasis due to local regional spread and distant metastasis of extraperitoneal cancer.

[0106] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, wherein administration of the IL-2 / IL-15Rβγ agonist in step (a) increases Ki-67 of total NK cells compared to no administration of the IL-2 / IL-15Rβγ agonist. + and wherein the administration of the IL-2 / IL-15Rβγ agonist in step (b) results in an increase in the % of NK, and wherein the administration of the IL-2 / IL-15Rβγ agonist in step (a) + At least 70% of NK cells have Ki-67 + Ki-67 is a marker of proliferating cells, so the Ki-67 of all NK cells + The percentage of NK cells is a measure for determining the activation state of each NK cell population. Surprisingly, repeating the daily administration after xy days without administration of agonist again led to a strong activation of NK cells, which was at least 70% of the level of NK cell activation during the first period with daily administration for x days (step a). The level of NK cell activation was measured by Ki-67 of total NK cells. + Measured as % of NK cells.

[0107] Furthermore, in another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic administration regimen, wherein IL-2 / IL-15Rβγ agonist administration results in a maintenance of NK cell numbers or preferably an increase in NK cell numbers by at least 110% compared to no administration of the IL-2 / IL-15Rβγ agonist after at least one repetition of the first period, preferably after at least two repetitions of the first period. Instead of, or in addition to, measuring NK cell activation, the total number of NK cells is also important, and it has been shown that repeated daily administration after xy days without administration of the agonist leads to an increase in the total number of NK cells, on average, over one or two repetitions of the first period (a). In absolute numbers, IL-2 / IL-15Rβγ agonist administration results in an increase in the total number of NK cells of at least about 1.1 x 10 after at least one repetition of the first period, preferably after at least two repetitions of the first period. 3Resulting in NK cell counts of NK cells / µl.

[0108] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, wherein the cyclical administration is repeated for at least 3 cycles, preferably 5 cycles, more preferably at least 10 cycles, and even more preferably until disease progression. NK cell and CD8 activity were measured in a Phase 1 pharmacokinetic and pharmacodynamic study in cynomolgus monkeys after 4 consecutive daily doses followed by an 18-day treatment break. + Given our findings, after an initial strong activation of T cells, NK cells and CD8 + Although T cells can be strongly activated again, it can be reasonably concluded that two or three repetitions of daily administration on consecutive days can be repeated after treatment interruption.Therefore, for example, for infectious diseases, at least three cycles, preferably five cycles, or preferably at least ten cycles are foreseen to enhance the immune system.Since tumors often develop resistance to most treatment modalities, for tumor treatment, it is particularly foreseen to repeat cycles until disease progression.

[0109] The IL-2 / IL-15Rβγ agonists are for use in cyclic administration regimens, where the cancer is a hematological cancer or a solid cancer. The mechanism of action of these agonists is activation of the innate immune response through activation of NK cells and CD8 +Because these agonists activate adaptive immune responses through T cell activation, they are generally assumed to have great potential for treating both (advanced) solid tumors and hematological malignancies, as they have already been tested in numerous mouse cancer models and in numerous clinical trials for various tumor indications (Robinson and Schluns 2017). Thus, IL-2 / IL-15Rβγ agonists have been tested in colorectal cancer, melanoma, renal cell carcinoma, adenocarcinoma, carcinomatous tumors, leiomyosarcoma, breast cancer, ocular melanoma, osteosarcoma, thyroid cancer, bile duct cancer, salivary gland cancer, adenoid cystic carcinoma, gastric cancer, head and neck squamous cell carcinoma, ovarian cancer, and urothelial carcinoma (Conlon et al. 2019). ALT-803, as an example of hematological malignancies, has been tested in AML and MDS (Romee et al. 2018). Patients with particularly advanced tumor diseases, such as metastatic tumors, may benefit from such treatment. In this regard, ALT-803 has therefore been tested in metastatic non-small cell lung cancer (Wrangle et al. 2018). A planned Phase 1 / 1b clinical trial (see Example 9) with SO-C101 is open to patients with renal cell carcinoma, non-small cell lung cancer, small cell lung cancer, bladder cancer, melanoma, Merkel cell carcinoma, cutaneous squamous cell carcinoma, microsatellite-high solid tumors, triple-negative breast cancer, mesothelioma, thyroid cancer, thymic cancer, cervical cancer, biliary tract cancer, hepatocellular carcinoma, ovarian cancer, gastric cancer, head and neck squamous cell carcinoma, and anal cancer. Examples of hematological cancers are leukemias such as acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), and acute monocytic leukemia (AMoL), lymphomas such as Hodgkin's lymphoma, non-Hodgkin's lymphoma, and myeloma.

[0110] Thus, renal cell carcinoma, non-small cell lung cancer, small cell lung cancer, bladder cancer, melanoma, Merkel cell carcinoma, cutaneous squamous cell carcinoma, microsatellite unstable high solid tumors, triple negative breast cancer, mesothelioma, thyroid cancer, thymic cancer, cervical cancer, biliary tract cancer, hepatocellular carcinoma, ovarian cancer, gastric cancer, squamous cell carcinoma of the head and neck, and anal cancer, as well as ALL, AML, CLL, CML, AMoL, Hodgkin's lymphoma, non-Hodgkin's lymphoma, and myeloma are preferred cancer indications.

[0111] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic dosing regimen, wherein the IL-2 / IL-15Rβγ agonist has an in vivo half-life of 30 minutes to 24 hours, preferably 1 hour to 12 hours, and more preferably 2 hours to 6 hours. Preferably, the in vivo half-life is 30 minutes to 12 hours, more preferably 1 hour to 6 hours, as determined in mice. In another preferred embodiment, the in vivo half-life is 1 hour to 24 hours, more preferably 2 hours to 12 hours, as determined in cynomolgus monkeys or macaques. In another embodiment, the in vivo half-life is 30 minutes to 12 hours, more preferably 30 minutes to 6 hours, as determined in cynomolgus monkeys.

[0112] The pharmacokinetic and pharmacodynamic properties of the IL-2 / IL-15Rβγ agonists of the present invention depend on their in vivo half-life. Due to various engineering techniques, in vivo half-life has been increased by fusion to the Fc portion of antibodies (e.g., ALT-803, RO687428) or antibodies (RG7813, RG7461, immunocytokines in WO 2012 / 175222A1, WO 2015 / 018528A1, WO 2015 / 109124), creating larger proteins, or by PEGylation (NKT-214). However, too long a half-life can actually stimulate NK cells for too long, leading to preferential expansion of mature NK cells with altered activation and diminished functional capacity (Elpek et al. 2010, Felices et al. 2018). Thus, preferred IL-2 / IL-15Rβγ agonists have an in vivo half-life of 30 minutes to 24 hours, preferably 1 hour to 12 hours, more preferably 2 hours to 6 hours, or preferably 30 minutes to 12 hours, more preferably 30 minutes to 6 hours. Preferably, this in vivo half-life refers to the half-life in humans. However, because determining the in vivo half-life in humans can be unethical if not published, it is also preferred to use the in vivo half-life in mice or primates, such as cynomolgus monkeys or macaques. Given the generally short half-life in mice, the in vivo half-life determined in mice is preferably 30 minutes to 12 hours, more preferably 1 hour to 6 hours or 30 minutes to 6 hours, and the in vivo half-life determined in cynomolgus monkeys or macaques is preferably 1 hour to 24 hours, more preferably 2 hours to 12 hours or 30 minutes to 6 hours.

[0113] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, wherein the IL-2 / IL-15Rβγ agonist is at least 70% monomeric, preferably at least 80% monomeric. Aggregates of such agonists can also have an effect on the pharmacokinetic and pharmacodynamic properties of the agonist and therefore should be avoided for reproducible results.

[0114] In another preferred embodiment, the IL-2 / IL-15Rβγ agonist is for use in a periodic dosing regimen, wherein the IL-2 / IL-15Rβγ agonist is an interleukin-15 (IL-15) / interleukin-15 receptor alpha (IL-15Rα) complex, an IL-15 / IL-15Rα complex, i.e., a complex comprising IL-15 or a derivative thereof and at least the sushi domain of IL-15Rα or a derivative thereof (covalently or non-covalently bound). They are intermediate affinity IL-2 / IL-15R, i.e., IL-2 / IL-15Rβ and γ. c It targets receptors consisting of subunits, which are expressed on NK cells, CD8 + It is expressed on T cells, NKT cells, and T cells. While these complexes are well known in the art and their binding capabilities are well understood, other attempts by modifying IL-2 to reduce / avoid IL-2Rα binding or synthetic approaches may face unpredictable risks. Preferably, the complex comprises human IL-15 or a derivative thereof and the sushi domain of IL-15Rα (SEQ ID NO: 6), the sushi domain of IL-15Rα (SEQ ID NO: 7), or a soluble form of IL-15Rα (amino acid 31 to any of amino acids 172, 197, 198, 199, 200, 201, 202, 203, 204, or 205 of SEQ ID NO: 5; see WO 2014 / 066527 (Giron-Michel et al. 2005)).

[0115] In a more preferred embodiment, the IL-15 / IL-15Rα complex is a fusion protein comprising the human IL-15Rα sushi domain or a derivative thereof, a flexible linker, and human IL-15 or a derivative thereof, preferably wherein the human IL-15Rα sushi domain comprises the sequence of SEQ ID NO: 6, more preferably the sushi fragment (SEQ ID NO: 7), and wherein the human IL-15 comprises the sequence of SEQ ID NO: 4. Such a fusion protein is preferably ordered (from N-terminus to C-terminus) as IL-15Rα-linker-IL-15 (RLI-15). A particularly preferred IL-2 / IL-15Rβγ agonist is the fusion protein designated RLI2 (SO-C101), which has the sequence of SEQ ID NO: 9.

[0116] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, in which an additional therapeutic agent is administered in combination with the IL-2 / IL-15Rβγ agonist. Over the past few years, cancer treatments have typically been combined with existing or new therapeutic agents to address tumors through multiple modes of action. At the same time, replacing established treatments with new ones is difficult or unethical, so new treatments are typically combined with standard treatments to achieve additional benefits for patients. Therefore, the provided dosing regimens must also be combined with other therapeutic drug regimens. The additional therapeutic agent and the IL-2 / IL-15Rβγ agonist may be administered on the same day and / or on different days. Same-day administration is typically more convenient for patients because it minimizes visits to the hospital or doctor. On the other hand, scheduling administration over different days can be important for certain combinations, where there may be undesired interactions between the agonist of the present invention and another drug.

[0117] When referring to "administered in combination," this typically does not mean that the two agents are co-formulated and co-administered, but rather that one agent has a label that specifies its use in combination with the other. So, for example, an IL-2 / IL-15Rβγ agonist is for use in the treatment or management of cancer or an infectious disease, involving simultaneous, separate, or sequential administration of an IL-2 / IL-15Rβγ agonist and an additional therapeutic agent, or vice versa. However, nothing in this application precludes the two combination agents from being provided as a bundle or kit, or even from being co-formulated and administered when the dosing schedules are consistent.

[0118] Because the typical clinical development strategy is in combination with standard therapy, administration of the concomitant agent is maintained and therefore independent of the administration regimen of the IL-2 / IL-15Rβγ agonist.

[0119] In another embodiment, the IL-2 / IL-15Rβγ agonist is for use in a cyclical dosing regimen, wherein the additional therapeutic agent is an immune checkpoint inhibitor (or, briefly, a checkpoint inhibitor) or a therapeutic antibody.

[0120] Preferably, the checkpoint inhibitor or therapeutic antibody is administered at the beginning of each period (a) of each cycle. To ensure high compliance with the timely administration of therapeutic agents and minimize procedures, the treatment cycles of the agonist and the checkpoint inhibitor or therapeutic antibody are ideally started together, for example, in the same week. Depending on the potential interaction between the agonist and the concomitant antibody, this can be on the same day or on different days in the same week. For example, before adding the checkpoint inhibitor or therapeutic antibody, NK cells and CD8 + Expanding the T cells for 1, 2, 3, or 4 days may result in improved efficacy of the treatment.

[0121] In one embodiment, an IL-2 / IL-15Rβγ agonist is for use, where x days and z days are matched and an integer multiple of x days + z days (n×x+z, with n∈{2, 3, 4, 5, ...}) equals the number of days in one treatment cycle of the checkpoint inhibitor or therapeutic antibody, or, if the treatment cycles of the checkpoint inhibitor or therapeutic antibody vary over time, equals each individual treatment cycle of the checkpoint inhibitor or therapeutic antibody.

[0122] For example, a checkpoint inhibitor or therapeutic antibody is typically administered every three or four weeks. For example, a treatment schedule for an IL-2 / IL-15Rβγ agonist of the present invention is consistent with a treatment schedule for a checkpoint inhibitor, where both the IL-2 / IL-15Rβγ agonist and the checkpoint inhibitor are administered at the beginning of first period (a) (treatment period x), preferably on day 1 of first period (a), and the checkpoint inhibitor or therapeutic antibody is not further administered for the remainder of the treatment cycle. For all subsequent treatment cycles, the checkpoint inhibitor or therapeutic antibody is then administered again at the beginning of period (a), preferably on day 1. Thus, if x is 7 (i.e., 1 week), (a) is repeated once (so that the integer multiple n is 2), and z is 7, the checkpoint inhibitor or therapeutic antibody can be administered every 3 weeks (2 x 7 + 7 = 3 weeks); alternatively, if x is 7, (a) is repeated twice (so that the integer multiple n is 3), and z is 7, the checkpoint inhibitor or therapeutic antibody can be administered every 4 weeks (3 x 7 + 7 = 4 weeks). In the case of a 6-week schedule for a checkpoint inhibitor or therapeutic antibody, the agonist may be scheduled in either a 3-week cycle (2 x 7 + 7) or one 6-week cycle (5 x 7 + 7 or 4 x 7 + 14). When the treatment regimen of a checkpoint inhibitor or therapeutic antibody changes over time, the scheduled rhythm is typically adapted by extending the period z (e.g., extending z = 7 to z = 14) to synchronize the rhythm.

[0123] In a preferred embodiment, the checkpoint inhibitor may be an anti-PD-1 antibody, anti-PD-L1 antibody, anti-PD-L2 antibody, anti-LAG3, anti-TIM-3, anti-CTLA4 antibody or anti-TIGIT antibody, preferably an anti-PD-L1 antibody or an anti-PD-1 antibody. These antibodies block / antagonize cellular interactions that block or downregulate immune cells, particularly T cells, from killing cancer cells, and therefore all of these antibodies have in common that they are antagonistic antibodies. Examples of anti-PD-1 antibodies are pembrolizumab, nivolumab, cemiplimab (REGN2810), BMS-936558, SHR1210, IBI308, PDR001, BGB-A317, BCD-100, and JS001; examples of anti-PD-L1 antibodies are avelumab, atezolizumab, durvalumab, KN035, and MGD013 (bispecific for PD-1 and LAG-3); an example of a PD-L2 antibody is sHIgM12; an example of an anti-LAG-3 antibody is leratolimab (BMS 986016), Sym022, REGN3767, TSR-033, GSK2831781, MGD013 (bispecific for PD-1 and LAG-3), and LAG525 (IMP701); examples of anti-TIM-3 antibodies are TSR-022 and Sym023; examples of anti-CTLA-4 antibodies are ipilimumab and tremelimumab (ticilimumab); examples of anti-TIGIT antibodies are tiragolumab (MTIG7192A, RG6058) and etigilimab.

[0124] Particularly preferred is the combination of an IL-2 / IL-15Rβγ agonist, particularly SO-C101, for use in a cyclic administration regimen with pembrolizumab. Currently, pembrolizumab is administered every 3 weeks. Therefore, in a preferred embodiment, the agonist is also administered in a 3-week cycle, i.e., x is 7 days and repeated twice, y is 2, 3, or 4 days, and z is 7 days. In one embodiment, pembrolizumab is administered to increase NK cell and CD8 activity before the addition of a checkpoint inhibitor. +To allow for T cell proliferation / activation, the agonist is administered on day 1 of each treatment cycle or any other day within such a treatment cycle, preferably on day 3, 4, or 5 of such a treatment cycle. Our in vitro experiments have shown that both simultaneous and sequential treatments result in a significant increase in IFNγ production from PBMCs. Recently, the labeling of pembrolizumab has been broadened to allow for administration every 6 weeks. Compared to the schedules described in this section above, the agonist schedule can be adapted by preferably having two 3-week cycles (e.g., x=7 repeated once, z=7) or by having a 6-week cycle (e.g., x=7 repeated four times with z=7, or x=7 repeated three times with z=14).

[0125] In a preferred embodiment, the therapeutic or tumor-targeting antibody may be selected from anti-CD38, anti-CD19, anti-CD20, anti-CD30, anti-CD33, anti-CD52, anti-CD79B, anti-EGFR, anti-HER2, anti-VEGFR2, anti-GD2, anti-Nectin-4, and anti-Trop-2 antibodies, with anti-CD38 antibodies being preferred. Such therapeutic or tumor-targeting antibodies may be linked to a toxin, i.e., an antibody-drug conjugate. Therapeutic antibodies exert a direct cytotoxic effect on tumor target cells through binding to targets expressed on the surface of tumor cells. Therapeutic activity may result from receptor binding, leading to altered signal transduction in the cell, antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC), or other antibody-mediated tumor cell killing. For example, the inventors have shown that the IL-2 / IL-15Rβγ agonist RLI-15 / SO-C101 synergizes with an anti-CD38 antibody (daratumumab) in tumor cell killing of Daudi cells in vitro, both in sequential and simultaneous settings, which was confirmed in an in vivo multiple myeloma model. Therefore, anti-CD38 antibodies are particularly preferred. Examples of anti-CD38 antibodies are daratumumab, isatuximab (SAR650984), MOR-202 (MOR03087), TAK-573, TAK-079, or GEN1029 (HexaBody®-DR5 / DR5), while daratumumab is most preferred. Preferably, daratumumab is administered according to its label, particularly preferably via intravenous infusion and / or according to the dose recommended by its label, preferably at a dose of 16 mg / kg.

[0126] In a preferred embodiment, an IL-2 / IL-15Rβγ agonist is for use, wherein an anti-CD38 antibody, preferably daratumumab, is administered in combination with the IL-2 / IL-15Rβγ agonist, wherein (i) the anti-CD38 antibody is administered once weekly for a first 8-week phase, followed by (ii) a second phase consisting of four 4-week sections (16 weeks), wherein during each 4-week section, the anti-CD38 antibody is administered once weekly for the first 2 weeks of the section, followed by two weeks without treatment, and (iii) a third phase with administration of the anti-CD38 antibody once every 4 weeks until disease progression. Thus, it is preferred that the anti-CD38 antibody is administered once weekly for an initial 8-week period, followed by 16 weeks of two treatments once per week and a 2-week treatment break, and then once every 4 weeks until disease progression. Starting from the day of the first treatment with the agonist, and adjusted for the IL-2 / IL-15Rβγ agonist treatment schedule, in the week with anti-CD38 antibody administration, the anti-CD38 antibody is administered on day 1 (concurrent treatment) or day 3 (concurrent treatment) of that week. A treatment schedule with one repetition of x=7 and z=14 corresponds to the first phase of an 8-week anti-CD38 treatment (see Figure 13A or B), followed by a second phase with one repetition of x=7 and z=14 (see Figure 14A or B), and a third phase with one repetition of x=7 and z=14 (see Figure 15A or B). Alternatively, the agonist schedule can be two repetitions of x=7 and z=7 to correspond to the 4-week rhythm of the anti-CD38 antibody.

[0127] An example of an anti-CD19 antibody is blinatumomab (bispecific for CD19 and CD3), for anti-CD20 antibodies are ofatumumab and obinutuzumab, for anti-CD30 antibody is brentuximab, for anti-CD33 antibody is gemtuzumab, for anti-CD52 antibody is alemtuzumab, for anti-CD79B antibody is polatuzumab, for anti-EGFR antibody is cetuximab, for anti-HER2 antibody is trastuzumab, for anti-VEGFR2 antibody is ramucirumab, for anti-GD2 antibody is dinutuximab, for anti-Nectin4 antibody is enfortumab, and for anti-Trop-2 antibody is sacituzumab.

[0128] An example of an adjusted dosing schedule is the combination of SO-C101 and ramucirumab, which are infused every 2-3 weeks depending on the indication. For a 3-week cycle of ramucirumab, SO-C101 may be administered with one repeat of x=7 and z=7. For two 2-week cycles of ramucirumab, SO-C101 may be administered with two repeats of x=7 and z=7.

[0129] Pulse dosing

[0130] Another embodiment relates to an IL-2 / IL-15Rβγ agonist for use in the treatment or management of cancer or infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist according to the following dosing regimen, comprising: (i) administering to a human patient a daily dose of an IL-2 / IL-15Rβγ agonist on a first number of consecutive days; and (ii) no administration of IL-2 / IL-15Rβγ agonists for a number of days; Here, the first number is 2, 3, or 4 days, the second number is 3, 4, or 5 days, and the first and second numbers add up to 7 days.

[0131] This administration scheme can be described as "pulse" dosing - "pulsed" because the IL-2 / IL-15Rβγ agonist is administered, for example, on days 1 and 2 of the week, to stimulate NK cell and CD8+ Both T cells are activated and expanded ("pulsed"), and no agonist is administered for the remainder of the week. This pulsed dosing regimen is repeated at least once, preferably at least twice, more preferably at least four times, and most preferably until disease progression. Preferably, the first and second days total 7 days (2 + 5 days, 3 + 4 days, or 4 + 3 days), and such first and second days are a cycle for the pulsed periodic regime.

[0132] The embodiments described above for pulse periodic dosing also apply to pulse dosing, to the extent that they do not relate to periodic dosing, particularly to embodiments relating to the dose of IL-2 / IL-15Rβγ agonist administered, the method of administration (e.g., sc or ip), the effect on NK cell activation and NK cell numbers, the condition being treated, the half-life of the IL-2 / IL-15Rβγ agonist, and co-administration of the IL-2 / IL-15Rβγ agonist and a checkpoint inhibitor.

[0133] Preferably, the IL-2 / IL-15Rβγ agonist is for use in a pulse dosing regimen, wherein the daily dose is from 0.1 μg / kg (0.0043 μM) to 50 μg / kg (2.15 μM), preferably from 0.25 μg / kg (0.011 μM) to 25 μg / kg (1.1 μM), more preferably from 0.6 μg / kg (0.026 μM) to 10 μg / kg (0.43 μM), especially from 2 μg / kg (0.087 μM) to 10 μg / kg (0.43 μM), preferably wherein the daily dose selected within the dose range of 0.1 μg / kg (0.0043 μM) to 50 μg / kg (2.15 μM) is not substantially increased during the dosing regimen, preferably wherein the dose is maintained during the dosing regimen. The daily dose is preferably 3 μg / kg (0.13 μM) to 20 μg / kg (0.87 μM), more preferably 6 μg / kg (0.26 μM) to 12 μg / kg (0.52 μM).

[0134] In another embodiment, pulse dosing applies to a daily dose, wherein the daily dose is a weight-independent fixed dose of 7 μg to 3500 μg, preferably 17.5 μg to 1750 μg, more preferably 42 μg to 700 μg, and especially 140 μg to 700 μg.

[0135] In another embodiment, pulse dosing is applied to a daily dose, where the daily dose is increased during the administration regimen. Preferably, the daily dose is increased after each period of x days. In a further embodiment, the daily dose is increased by 20% to 100%, preferably by 30% to 50%, after each period of x days.

[0136] In another embodiment, the daily dose is increased once after the first cycle. Preferably, the daily dose is increased by 20% to 100%, preferably by 30% to 50%, after the first cycle.

[0137] In one embodiment of pulse dosing, the daily dose is administered in a single injection.

[0138] In alternative pulse dosing embodiments, the daily dose is divided into two or three individual doses administered within one day, wherein the time interval between administration of the individual doses is at least about 4 hours, and preferably not more than 14 hours. Preferably, the daily dose is divided into three individual doses administered within one day, wherein the time interval between administration of the individual doses is about 5 to about 7 hours, preferably about 6 hours. Or, also preferably, the daily dose is divided into two individual doses administered within one day, wherein the time interval between administration of the individual doses is about 6 to about 10 hours, preferably about 8 hours.

[0139] In another embodiment of pulse dosing, the IL-2 / IL-15Rβγ agonist is administered subcutaneously (sc) or intraperitoneally (ip), preferably subcutaneously.

[0140] Preferably, as further described above, administration of an IL-2 / IL-15Rβγ agonist in step (a) results in: (1) an increase in Ki-67 of total NK cells compared to administration of no IL-2 / IL-15Rβγ agonist; + and wherein the administration of the IL-2 / IL-15Rβγ agonist in step (b) results in an increase in the % of Ki-67 in step (a). + At least 70% of NK cells have Ki-67 + or (2) after at least one repetition of the first period, preferably after at least two repetitions of the first period, a maintenance of the number of NK cells, or preferably an increase in the number of NK cells to at least 110% compared to administration of no IL-2 / IL-15Rβγ agonist; and / or (3) after at least one repetition of the first period, preferably after at least two repetitions of the first period, a maintenance of the number of NK cells to at least 110% compared to administration of no IL-2 / IL-15Rβγ agonist. 3 Result in NK cell counts in NK cells / µl.

[0141] For pulse dosing, it is further preferred that the periodic administration be repeated for at least 5 cycles, preferably 8 cycles, more preferably at least 15 cycles, and even more preferably until disease progression.

[0142] In another embodiment of the pulse dosing regimen, the IL-2 / IL-15Rβγ agonist has an in vivo half-life of 30 minutes to 24 hours, preferably 1 hour to 12 hours, and more preferably 2 hours to 6 hours. In another embodiment, the in vivo half-life is 30 minutes to 12 hours, and more preferably 30 minutes to 6 hours, preferably as determined in cynomolgus monkeys.

[0143] In another embodiment for the pulse dosing regimen, the IL-2 / IL-15Rβγ agonist is a fusion protein comprising an interleukin-15 (IL-15) / interleukin-15 receptor alpha (IL-15Rα) complex, preferably a human IL-15Rα sushi domain or a derivative thereof, a flexible linker, and human IL-15 or a derivative thereof, preferably wherein the human IL-15Rα sushi domain comprises the sequence of SEQ ID NO: 6, and wherein the human IL-15 comprises the sequence of SEQ ID NO: 4, more preferably wherein the IL-15 / IL-15Rα complex is SEQ ID NO: 9.

[0144] Additionally, IL-2 / IL-15Rβγ agonists for use in pulse dosing may be administered in combination with an additional therapeutic agent. Preferably, the additional therapeutic agent and the IL-2 / IL-15Rβγ agonist are administered on the same day and / or on different days. Furthermore, it is preferred that the administration of the additional therapeutic agent occurs according to a dosing regimen that is independent of the dosing regimen of the IL-2 / IL-15Rβγ agonist.

[0145] In one embodiment of the pulse dosing regimen, the additional therapeutic agent is selected from a checkpoint inhibitor or a therapeutic antibody.

[0146] Preferably, the checkpoint inhibitor is selected from an anti-PD-1 antibody, an anti-PD-L1 antibody, an anti-PD-L2 antibody, an anti-LAG-3 antibody, an anti-TIM-3 antibody, an anti-CTLA4 antibody, or an anti-TIGIT antibody, preferably an anti-PD-L1 antibody or an anti-PD-1 antibody.

[0147] And preferably, the therapeutic antibody is selected from an anti-CD38 antibody, an anti-CD19 antibody, an anti-CD20 antibody, an anti-CD30 antibody, an anti-CD33 antibody, an anti-CD52 antibody, an anti-CD79B antibody, an anti-EGFR antibody, an anti-HER2 antibody, an anti-VEGFR2 antibody, an anti-GD2 antibody, an anti-Nectin-4 antibody, and an anti-Trop-2 antibody, preferably an anti-CD38 antibody.

[0148] Preferably, an IL-2 / IL-15Rβγ agonist is for use, wherein an anti-CD38 antibody is administered once weekly for an initial 8 weeks, followed by 16 weeks of two treatments, once per week and a 2-week treatment break, and then once every 4 weeks until disease progression. For example, the first number is 2 days and the second number is 5 days, and the anti-CD38 antibody is administered once per week on each 3rd day of the week or on each 1st day of the week; and wherein treatment is continued for 8 weeks. Alternatively, the first number is 2 days and the second number is 5 days, and the anti-CD38 antibody is administered once per week for 16 weeks on day 3 of each of the first and second weeks of each four week cycle, or on day 1 of each of the first and second weeks of each four week cycle, followed by administration of the anti-CD38 antibody once per week on day 3 of each of the first week of each four week cycle, or on day 1 of each of the first week of each four week cycle, until disease progression.

[0149] The anti-CD38 antibody is preferably daratumumab, MOR202, isatuximab, GEN1029, TAK-573, or TAK-079, and more preferably, the anti-CD38 antibody is daratumumab. Preferably, daratumumab is administered via intravenous infusion at the dose recommended according to its label, preferably using a dose of 16 mg / kg.

[0150] High-Density Pulse Dosing

[0151] In another aspect of the invention, the interleukin-2 / interleukin-15 receptor (IL-2 / IL-15R) agonist is for use in the treatment or management of cancer or infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist to a human patient using a high-density pulse dosing regimen, wherein the high-density dosing regimen comprises the following ("high-density pulse"): (a) a first period of x days, during which an IL-2 / IL-15Rβγ agonist is administered in a daily dose for y consecutive days at the beginning of the first period, followed by xy days without administration of the IL-2 / IL-15Rβγ agonist, where x is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or 21 days, preferably 7 or 14 days, and y is 2, 3, or 4 days, preferably 2 or 3 days; (b) repeating the first period at least once; and wherein the daily dose is divided into 2 or 3 individual doses administered within one day, wherein the time interval between administration of the individual doses is at least about 4 hours, preferably not more than 12 hours.

[0152] Preferably, the administration regimen further comprises (c) a second period of z days without administration of an IL-2 / IL-15Rβγ agonist ("high-intensity pulsed cycle"), where z is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 28, 35, 42, 49, 56, 63, or 70 days, preferably 7, 14, 21, or 56 days, more preferably 7 or 21 days.

[0153] The same amount of agonist (divided into several doses and administered over the course of the day) stimulates NK cells and especially CD8 + It is more effective in stimulating cells, the latter being less sensitive to stimulation than when administered in a single injection alone.

[0154] Such multiple dosing could be incorporated into the routine of a hospital, physician's practice, or outpatient setting, and thus, while 2-3 equivalent doses administered during a business day, including shifts of between 8 and 12 hours, may still be conveniently manageable, an 8- or 10-hour interval is preferred as the maximum time difference between the first and last dose. Thus, a preferred embodiment is one in which the daily dose is divided into three individual doses administered within one day, with the time interval between the administration of the individual doses being about 5 to about 7 hours, preferably about 6 hours. This means that a patient could be dosed at 7:00 AM, 2:00 PM, and 7:00 PM (with a 6-hour interval) or at 7:00 AM, 1:00 PM, and 6:00 PM (with a 5-hour interval). In another preferred embodiment, the daily dose is divided into two individual doses administered within one day, with the time interval between the administration of the individual doses being about 6 to about 10 hours, preferably 8 hours. In the case of two doses, patients could be dosed, for example, at 8 AM and 4 PM (with an 8-hour interval). Given the routine of a hospital, the interval between doses could vary within a day or from day to day. Surprisingly, in mice, the same amount (approximately 40 μg / kg) of SO-C101 divided into three doses (13 μg / kg) administered over the course of a day significantly increased the proliferation of CD8 + As a measure of T cells, CD8 + T cell count and Ki67 + Even at doses divided into 3 x 7 μg / kg, the CD8 T cells were still significantly increased. + showed much higher proliferation and activation of T cells (see Figure 19).

[0155] Thus, in a preferred embodiment, the daily dose is divided into three individual doses administered within one day, with the time interval between the administration of the individual doses being about 5 to about 7 hours, preferably about 6 hours. This means that the patient can be dosed, for example, at 7:00 AM, 2:00 PM, and 7:00 PM (with a 6-hour interval) or at 7:00 AM, 1:00 PM, and 6:00 PM (with a 5-hour interval) every day. In another preferred embodiment, the daily dose is divided into two individual doses administered within one day, with the time interval between the administration of the individual doses being about 6 to about 10 hours, preferably 8 hours. In the case of two doses, the patient can be dosed, for example, at 8:00 AM and 4:00 PM (with an 8-hour interval). Given the routine practice of a hospital, the interval between doses can vary within one day or from day to day.

[0156] The embodiments herein above regarding pulse-periodic dosing apply to high-intensity pulses (and high-intensity pulse-periodic dosing as a subform of high-intensity pulse dosing), particularly to embodiments relating to the dose of IL-2 / IL-15Rβγ agonist administered, the method of administration (e.g., subcutaneous or intraperitoneal), the effect on NK cell activation and numbers, the condition being treated, the half-life of the IL-2 / IL-15Rβγ agonist, and co-administration of the IL-2 / IL-15Rβγ agonist and a checkpoint inhibitor.

[0157] Preferably, the IL-2 / IL-15Rβγ agonist is for use in a high-intensity pulse or high-intensity pulse periodic dosing regimen, wherein the daily dose is from 0.1 μg / kg (0.0043 μM) to 50 μg / kg (2.15 μM), preferably from 0.25 μg / kg (0.011 μM) to 25 μg / kg (1.1 μM), more preferably from 0.6 μg / kg (0.026 μM) to 10 μg / kg (0.43 μM), especially from 2 μg / kg (0.087 μM) to 10 μg / kg (0.43 μM), preferably wherein the selected daily dose within the dose range of 0.1 μg / kg (0.0043 μM) to 50 μg / kg (2.15 μM) does not increase substantially during the dosing regimen, preferably wherein the dose is maintained during the dosing regimen. It is further preferred that the daily dose is between 3 μg / kg (0.13 μM) and 20 μg / kg (0.87 μM), preferably between 6 μg / kg (0.26 μM) and 12 μg / kg (0.52 μM).

[0158] In another embodiment, high-density pulse dosing is applied in a daily dose, wherein the daily dose is a weight-independent fixed dose of 7 μg to 3500 μg, preferably 17.5 μg to 1750 μg, more preferably 42 μg to 700 μg, especially 140 μg to 700 μg.

[0159] In another embodiment, high-density pulse dosing is applied to a daily dose, wherein the daily dose is increased during the administration regimen. Preferably, the daily dose is increased after each period of x days. In a further embodiment, the daily dose is increased by 20% to 100%, preferably by 30% to 50%, after each period of x days.

[0160] In another embodiment, the daily dose is increased once after the first cycle. Preferably, the daily dose is increased by 20% to 100%, preferably by 30% to 50%, after the first cycle.

[0161] In another embodiment of high-density pulse dosing, the IL-2 / IL-15Rβγ agonist is administered subcutaneously (sc) or intraperitoneally (ip), preferably subcutaneously.

[0162] Preferably, as further described above, administration of an IL-2 / IL-15Rβγ agonist in step (a) results in: (1) an increase in Ki-67 of total NK cells compared to administration of no IL-2 / IL-15Rβγ agonist; + an increase in the percentage of NK, wherein the administration of the IL-2 / IL-15Rβγ agonist in step (b) increases the Ki-67 + At least 70% of NK cells have Ki-67 + or (2) after at least one repetition of the first period, preferably after at least two repetitions of the first period, a maintenance of NK cell numbers, or preferably an increase in NK cell numbers of at least 110% compared to administration of no IL-2 / IL-15Rβγ; and / or (3) after at least one repetition of the first period, preferably after at least two repetitions of the first period, a maintenance of NK cell numbers, or preferably an increase in NK cell numbers of at least 1.1×10 3 yields NK cell counts in NK cells / µl.

[0163] For high-intensity pulse cyclic dosing, it is further preferred that the cyclic administration is repeated for at least 5 cycles, preferably 8 cycles, more preferably at least 15 cycles, and even more preferably until disease progression.

[0164] In another embodiment for a high-density pulse dosing regimen, the IL-2 / IL-15Rβγ agonist has an in vivo half-life of 30 minutes to 24 hours, preferably 1 hour to 12 hours, more preferably 2 hours to 6 hours.

[0165] In another embodiment for the high-density pulse dosing regimen, the IL-2 / IL-15Rβγ agonist is an interleukin-15 (IL-15) / interleukin-15 receptor alpha (IL-15Rα) complex, preferably a fusion protein comprising a human IL-15Rα sushi domain or a derivative thereof, a flexible linker, and human IL-15 or a derivative thereof, preferably wherein the human IL-15Rα sushi domain comprises the sequence of SEQ ID NO: 6, and wherein the human IL-15 comprises the sequence of SEQ ID NO: 4, more preferably wherein the IL-15 / IL-15Rα complex is SEQ ID NO: 9.

[0166] Additionally, IL-2 / IL-15Rβγ agonists for use in high-density pulse dosing can be administered in combination with an additional therapeutic agent. Preferably, the additional therapeutic agent and the IL-2 / IL-15Rβγ agonist are administered on the same day and / or on different days. Furthermore, it is preferred that the administration of the additional therapeutic agent occurs according to a dosing regimen that is independent of the dosing regimen of the IL-2 / IL-15Rβγ agonist.

[0167] In one embodiment of the high-density pulse dosing regimen, the additional therapeutic agent is selected from a checkpoint inhibitor or a therapeutic antibody.

[0168] Preferably, the checkpoint inhibitor is selected from an anti-PD-1 antibody, an anti-PD-L1 antibody, an anti-PD-L2 antibody, an anti-LAG-3 antibody, an anti-TIM-3 antibody, an anti-CTLA4 antibody, or an anti-TIGIT antibody, preferably an anti-PD-L1 antibody or an anti-PD-1 antibody.

[0169] And preferably, the therapeutic antibody is selected from an anti-CD38 antibody, an anti-CD19 antibody, an anti-CD20 antibody, an anti-CD30 antibody, an anti-CD33 antibody, an anti-CD52 antibody, an anti-CD79B antibody, an anti-EGFR antibody, an anti-HER2 antibody, an anti-VEGFR2 antibody, an anti-GD2 antibody, an anti-Nectin-4 antibody and an anti-Trop-2 antibody, preferably an anti-CD38 antibody.

[0170] Another embodiment of the present invention is a kit of parts comprising several doses of an IL-2 / IL-15Rβγ agonist of the present invention, instructions for administration of such IL-2 / IL-15Rβγ agonist in a cyclical dosing regimen according to any of the above embodiments, and, optionally, an administration device for the IL-2 / IL-15Rβγ agonist.

[0171] Another embodiment of the present invention is a kit of parts comprising several doses of an IL-2 / IL-15Rβγ agonist of the present invention, instructions for administering such IL-2 / IL-15Rβγ agonist in a pulsed dosing regimen according to any of the above embodiments, and, optionally, an administration device for the IL-2 / IL-15Rβγ agonist.

[0172] Another embodiment of the present invention is a kit of parts comprising several doses of an IL-2 / IL-15Rβγ agonist of the present invention, instructions for administering such IL-2 / IL-15Rβγ agonist in a high-density pulse administration regimen according to any of the above embodiments, and optionally an administration device for the IL-2 / IL-15Rβγ agonist.

[0173] Another embodiment is the use of an IL-2 / IL-15Rβγ agonist in the manufacture of a kit of parts for the treatment of cancer or an infectious disease, wherein the kit of parts comprises: several doses of an IL-2 / IL-15Rβγ agonist of the present invention, instructions for administering such IL-2 / IL-15Rβγ agonist in a cyclical dosing regimen according to any of the above embodiments, and optionally an administration device for the IL-2 / IL-15Rβγ agonist.

[0174] Another embodiment is the use of an IL-2 / IL-15Rβγ agonist in the manufacture of a kit of parts for the treatment of cancer or an infectious disease, wherein the kit of parts comprises: several doses of an IL-2 / IL-15Rβγ agonist of the present invention, instructions for administering such IL-2 / IL-15Rβγ agonist in a pulsed dosing regimen according to any of the above embodiments, and optionally an administration device for the IL-2 / IL-15Rβγ agonist.

[0175] Another embodiment is the use of an IL-2 / IL-15Rβγ agonist in the manufacture of a kit of parts for the treatment of cancer or an infectious disease, wherein the kit of parts comprises: several doses of an IL-2 / IL-15Rβγ agonist of the present invention, instructions for administration of such IL-2 / IL-15Rβγ agonist in a high-density pulse administration regimen according to any of the above embodiments, and optionally an administration device for the IL-2 / IL-15Rβγ agonist.

[0176] In a preferred embodiment, the kit further comprises a checkpoint inhibitor and instructions for use of the checkpoint inhibitor or therapeutic antibody.

[0177] The present invention also relates to methods of treating cancer and infectious diseases comprising the pulse-periodic, pulse- and high-density pulse-dosing regimens described above, and methods of treating NK cell and / or CD8 + A method for stimulating T cells is included.

[0178] High-Density Dosing

[0179] In another aspect of the invention, an interleukin-2 / interleukin-15 receptor βγ (IL-2 / IL-15Rβγ) agonist is for use in the treatment or management of cancer or an infectious disease, and comprises administering the IL-2 / IL-15Rβγ agonist to a human patient using a high-density dosing regimen, wherein the high-density dosing regimen comprises administering a daily dose to the patient, wherein the daily dose is divided into two or three individual doses administered within one day, and wherein the time interval between administration of the individual doses is at least about 4 hours, and preferably not more than 12 hours.

[0180] The time intervals between administration of the individual doses may be as described for the above embodiments. The amount of IL-2 / IL-15Rβγ agonist may also be as described for the above embodiments. [Brief explanation of the drawings]

[0181] [Figure 1]Pharmacodynamic study in cynomolgus monkeys: In phase 1, RLI-15 / SO-C101 was administered daily at the indicated doses on days 1-4 in cynomolgus monkeys (groups depicted in Table 2, 2 animals / group) by 60-minute intravenous or subcutaneous injection (see dosing schedule (A), left side, for details). Proliferating Ki67+ NK cells (B) and proliferating Ki67+ CD8+ T cells (C) were determined by immunofluorescence analysis on day 5. In phase 2, after a 2-week washout period, cynomolgus monkeys were dosed by 60-minute intravenous or subcutaneous injection in groups on study days D22 (1 dose), D22, D23 (2 doses), or D22-D25 (4 doses) as depicted in (A) and Table 3. (D) Flow cytometry analysis was performed 5 days after the first dose on D26. The fraction of Ki67-positive cells was determined in the CD3-CD8+CD45+ (NK cells) and CD3+CD8+CD45+ (CD8+ T cells) cell fractions. Data were collected from Group 1 (1 dose), Groups 4, 5, 7 (pooled, 2 doses), and Group 6 (4 doses). (E) Increase in total lymphocyte, CD8+ T cell, and NK cell counts in cynomolgus monkeys after subcutaneous administration for 2 doses (Group 5) during Phase 1 (10 μg / kg RLI subcutaneously, 4 times daily on D1, D2, D3, and D4) and Phase 2 (2 consecutive doses over 3 consecutive weeks, D22, D23, D29, D30, D36, and D37, indicated by arrows, 15 μg / kg subcutaneously) (with a 2-week rest period between Phases 1 and 2). Lymphocyte analysis was performed on day 5 of each dosing week. Lymphocyte counts were determined during hematological evaluation, and CD8+ T cells and NK cells were determined by flow cytometry and multiplication of their relative percentages among CD45+ cells with total leukocyte counts. (F)-(I) Cell activation is shown by recalculation of NK and CD8+ T cell activation obtained by flow cytometry analysis of each flow cytometry data (Ki67+ NK cells and Ki67+ CD8+ T cells) as a percentage of total NK cells or CD8+ T cells, respectively (F, H, left panels) and cell counts of animals 69 and 70 (group 5) by hematological evaluation (G, I, right panels).(J)-(Q) Comparison of two doses (L, M, P, Q) with four doses (J, K, N, O) in each of weeks 1 and 3 of Phase 2 (Groups 3 and 4) for NK cells (J, K, L, M) and CD8+ T cells (N, O, P, Q). [Figure 2] RLI-15 / SO-C101 was administered subcutaneously at a dose of 100 μg / kg on four consecutive days per week (D1-D4, D8-D11, D15-D18, and D22-D25) in cynomolgus monkeys (two animals). Cell proliferation measured by flow cytometry as cell counts (103 / μl) of NK cells (triangles), CD8+ T cells (circles, dotted line), and total lymphocytes (circles, solid line) is depicted over time (days). [Figure 3] Dose relationships of RLI-15 / SO-C101-mediated NK and CD8+ T cell activation from humans / in vitro to cynomolgus monkeys / in vivo (including pharmacodynamics and pharmacokinetics) and observed Cmax in vivo. In vivo doses are shown according to the achieved Cmax. Data obtained from flow cytometry on NK and CD8+ T cell proliferation (CFSE-stained proliferating cells) induced by RLI-15 in vitro stimulation of human PBMCs (7 days) and in vivo cynomolgus monkey treatment with RLI-15 (subcutaneous for 4 consecutive days, FACS, day 5) were correlated. Similarly, the concentrations used in vitro and obtained from PK studies in cynomolgus monkeys are incorporated into the x-axis. Human equivalent doses were calculated by allometric scaling using 3.1 as a factor. MABEL: estimated lowest pharmacologically effective dose; PAD: pharmacologically effective dose; NOAEL: no observed adverse effect level; MTD: maximum tolerated dose. [Figure 4]Concentration-dependent RLI-15-induced proliferation of NK cells, memory CD8+ T cells, and T regulatory cells. The pharmacodynamics of RLI-15 / SO-C101 in vivo in mice was tested using various RLI-15 concentrations (10, 20, 35, and 50 μg / dose) injected subcutaneously or intraperitoneally once daily for 4 consecutive days (2 animals per group). The relative proliferation of (A) NK cells (CD3-, CD49b / DX5+), (B) memory CD8+ T cells (CD8+CD44+CD122+ T cells), and (C) T regulatory cells (CD4+CD25+FoxP3+ T cells) was determined by flow cytometry from splenocytes on day 5 (control—untreated mice). Lung wet weight was determined as a measure of vascular leak syndrome (VLS), assessed on day 5 (D). [Figure 5] Evaluation of RLI-15-induced anti-metastatic effects in the RENCA mouse tumor model after intraperitoneal administration. (A) Experimental scheme. RLI-15 / SO-C101 was administered intraperitoneally once daily according to the provided schedule after Renca tumor cells were intravenously injected on day 0. Spleens for immune cell FACS analysis were collected on days 5 and 12 for pharmacodynamics. Animal weight and survival were monitored until day 16. Mice were sacrificed on day 16, and lungs were collected for analysis of metastatic burden. (B) Lung weight (as a surrogate for metastatic burden) (g) was assessed on day 16 for a given treatment group. (C) Assessment of mouse weight during the course of RLI-15 treatment in the RENCA tumor model at selected days. Data were normalized to 100% of the mean body weight in each group on day 0. Solid black line with lowest endpoint: tumor; dotted black line with second lowest endpoint: D1+D8; gray line with third lowest endpoint - runs just above the solid black line most of the time: D1-D2+D8-D9. Five and 12 days after the start of RLI-15 treatment, splenocytes were analyzed for relative proliferation of NK cells and Ki-67+ NK cells (dividing NK cells) (D) and CD3+ CD8+ T cells and Ki-67+ CD8+ T cells (dividing CD8+ T cells) (E) in CD3+ cells; control = naive - non-tumor-bearing, untreated; tumor = tumor-bearing mice, untreated; other groups: tumor-bearing mice treated with a single daily dose of RLI-15 on the days indicated. [Figure 6] Evaluation of RLI-15-induced anti-metastatic effects in the RENCA mouse tumor model after subcutaneous administration compared with IL15N72D:IL15Rα sushi-Fc. 10 μg or 20 μg of RLI-15 / SO-C101 or 5 μg of IL15N72D:IL15Rα sushi-Fc was administered subcutaneously once daily according to the provided schedule after Renca tumor cells were intravenously injected on day 0. Animal weight and survival were monitored until day 16. Mice were sacrificed on day 16, and lungs were harvested for further analysis. (A) Lung weight (as a surrogate for metastatic burden) (g) was assessed on day 16 for a given treatment group. (B) Assessment of mouse weight over the course of treatment in the RENCA tumor model at selected days. Data were normalized to 100% of the mean body weight in each group on day 0. Black line with lowest endpoint: tumor; red line with second lowest endpoint and second lowest starting point: RLI-15 20 μg at D1-D3; blue line with second highest endpoint: RLI-15 10 μg at D1-D4; green line with second lowest endpoint and second lowest midpoint: RLI-15 20 μg at D1-D4; orange line with highest endpoint: IL15N72D:IL15Rαsushi-Fc 5 μg at D1. [Figure 7] Dosing schedule for the first-in-human clinical trial. *± 1 day; DLT dose-limiting toxicity; (A) Part A: SO-C101 dosing schedule (B) Part B: SO-C101 in combination with pembrolizumab dosing schedule. [Figure 8]In vitro tumor cell killing by simultaneous combination of RLI-15 and daratumumab. Human PBMCs from five healthy donors were co-cultured with Daudi tumor cells for 20 hours at 37°C in the absence (-) or presence (+) of RLI-15 / SO-C101 (RLI 1 nM) and / or increasing concentrations of daratumumab (0, 0.1 nM, 1 nM, or 10 nM DAR). The percentage of dead Daudi tumor cells is shown as determined by DAPI+ staining by flow cytometry. Results were considered statistically significant if p<0.05 (*) or p<0.01 (**). [Figure 9] In vitro tumor cell killing by sequential combination of RLI-15 and daratumumab. Human PBMCs from six healthy donors were incubated in vitro for 48 hours at 37°C in either heat-inactivated (HI) or activated serum, with or without RLI-15 / SO-C101 (1 nM). Stimulated hPBMCs were then co-cultured with Daudi tumor cells for 4 hours at 37°C in the absence (-) or presence (+) of increasing amounts of daratumumab (0, 0.1 nM, 1 nM, or 10 nM DAR). The percentage of dead Daudi tumor cells is shown as determined by DAPI+ staining by flow cytometry. Results were considered statistically significant if p<0.05 (*) or p<0.01 (**). [Figure 10]In vivo antitumor efficacy demonstrated by the simultaneous combination of RLI-15 and daratumumab. CB17 SCID mice were inoculated subcutaneously with 1 x 10 RPMI8226 myeloma cells. Treatment was initiated with either saline (10 μl / g subcutaneously on days 0, 1, 2, and 3), RLI-15 / SO-C101 (1 mg / kg subcutaneously on days 0, 1, 2, and 3), daratumumab (20 mg / kg intraperitoneally on day 4), or RLI-15 / SO-C101 and daratumumab at the concentrations and days indicated above. (A) Tumor volume (mm3) dependent on time (day), starting from day 0, when subcutaneous treatment with saline or RLI-15 was initiated (day 0 = day of randomization to groups with tumor volume ∼100 mm3). Saline control group (black circles on solid line), RLI-15 / SO-C101-treated group (black circles on dotted line), daratumumab-treated group (gray circles on dotted line), and RLI-15 + daratumumab combination group (gray circles on solid line). (B) Percentage of mice with rejected tumors depending on the time (days) starting from day 0 when subcutaneous administration of saline or RLI-15 was initiated. Saline control group (black solid line - not visible on the x-axis), RLI-15-treated group (black dotted line), daratumumab-treated group (gray dotted line - not visible on the x-axis), and RLI-15 + daratumumab combination group (gray solid line). [Figure 11]In vivo antitumor efficacy demonstrated by sequential combination of RLI-15 and daratumumab. CB17 SCID mice were inoculated subcutaneously with 1 x 10 RPMI8226 myeloma cells. Treatment was initiated with either saline (10 μl / g subcutaneously on days 0, 1, 2, and 3), RLI-15 / SO-C101 (1 mg / kg subcutaneously on days 7, 8, 9, and 10), daratumumab (20 mg / kg intraperitoneally on day 0), or RLI-15 / SO-C101 and daratumumab at the concentrations and days indicated above. (A) Tumor volume (mm3) dependent on time (day) starting from day 0 when subcutaneous saline or intraperitoneal daratumumab administration was initiated (day 0 = day of randomization to groups with tumor volume ∼100 mm3). Saline control group (black circles on solid line), RLI-15 treatment group (black circles on dotted line), daratumumab treatment group (gray open circles on dotted line), and RLI-15 + daratumumab combination group (gray circles on solid line). (B) Percentage of mice with rejected tumors depending on the time (days) starting from day 0 when subcutaneous administration of saline or daratumumab was initiated. Saline control group (black solid line - not visible on x-axis), RLI-15 treatment group (black dotted line - not visible on x-axis), daratumumab treatment group (gray dotted line), and RLI-15 + daratumumab combination group (gray solid line). [Figure 12] Dosing schedules for clinical trials of RLI-15 / SO-C101 in combination with daratumumab; RLI-15—subcutaneous at the dose determined in the first-in-human clinical trial (solid arrow for days of administration); daratumumab—16 mg / kg intravenous infusion once weekly for 8 weeks (8 doses total, dotted arrow for days of administration): (A) Combination schedule with RLI-15 administered on D1+D2 and D8+D9 of a 3-week cycle and daratumumab administered on D3, D10, and D17. (B) Combination schedule with RLI-15 administered on D1+D2 and D8+D9 of a 3-week cycle and daratumumab administered on D1, D8, and D15. [Figure 13]Dosing schedules for clinical trials of RLI-15 / SO-C101 in combination with daratumumab. RLI-15—subcutaneous at the dose determined in the first-in-human clinical trial (solid arrow for days of administration); daratumumab—16 mg / kg intravenous infusion once weekly for 8 weeks (8 doses total, dotted arrow for days of administration): (A) Combination schedule with RLI-15 administered on D1+D2 and D8+D9 of a 4-week cycle and daratumumab administered on D3, D10, D17, and D24. (B) Combination schedule with RLI-15 administered on D1+D2 and D8+D9 of a 4-week cycle and daratumumab administered on D1, D8, D15, and D22. [Figure 14] Dosing schedule of the clinical trial for RLI-15 / SO-C101 in combination with daratumumab over weeks 9–24; RLI-15—subcutaneous at the dose determined in the first-in-human clinical trial (solid arrows for days of administration); daratumumab—two 16 mg / kg intravenous infusions over 4 weeks (8 doses total, starting at week 9 of overall treatment, dotted arrows for days of administration): (A) Combination schedule with RLI-15 administered on days D1+D2 and D8+D9 of a 4-week cycle and daratumumab administered on days D3 and D10. (B) Combination schedule with RLI-15 administered on days D1+D2 and D8+D9 of a 4-week cycle and daratumumab administered on days D1 and D8. [Figure 15] Clinical trial dosing schedule for RLI-15 / SO-C101 in combination with daratumumab from week 25 onward until disease progression. RLI-15—subcutaneous at the dose determined in the first-in-human clinical trial (solid arrow for day of administration); daratumumab—a single 16 mg / kg intravenous infusion every 4 weeks (starting at week 25 of overall treatment, dotted arrow for day of administration): (A) Combination schedule with RLI-15 administered on days D1+D2 and D8+D9 of a 4-week cycle and daratumumab administered on day D3. (B) Combination schedule with RLI-15 administered on days D1+D2 and D8+D9 of a 4-week cycle and daratumumab administered on day D1. [Figure 16] Pharmacodynamic study of RLI-15 / SO-C101 in cynomolgus monkeys: Dosing schedule for groups G1-G8 administered during study weeks W1-W10. Each point represents a single daily dose of 40-80 μg / kg of RLI-15 / SO-C101, as indicated. [Figure 17] a) and b) Time course (days) of NK cell counts and CD8+ T cell counts in cells / μl for males (closed circles) and females (closed squares) for treatment groups 1, 8, 3, 2, and 6 provided; days of dosing are underlined. c) and d) Time course of Ki67+ NK cells and Ki67+ CD8+ T cells (percent) for males (closed circles) and females (closed squares) for treatment groups 1, 8, 3, 2, and 6 provided; days of dosing are underlined. [Figure 18] Pharmacodynamic testing of RLI-15 / SO-C101 in cynomolgus monkeys for a sustained exposure study through three doses per day: Dosing schedule for Groups 1, 2, and 3 administered on study days D1-D14. Each dot represents a single administration of RLI-15 / SO-C101 at a dose of 7-40 μg / kg, as indicated. [Figure 19] Time course (days) of NK cell and CD8 T cell counts in 10 cells / L (left panel), Ki67 NK cells and CD8 T cells (middle panel), CD8 expression by CD8 T cells as mean fluorescence intensity (top right panel), and percentage of CD122 cells among CD8 cells (bottom right panel) for treatment Group 1 (circles, 1 × 40 μg / kg), Group 2 (triangles, 3 × 7 μg / kg), and Group 3 (squares, 3 × 13 μg / kg). Black circles / triangles / squares indicate male animals, and open circles / triangles / squares indicate female animals. [Figure 20]Pharmacodynamic study of RLI-15 / SO-C101 in cynomolgus monkeys: Dosing schedule for groups G1-G6 administered during study weeks W1-W10 for G3-G6 and W12 for G1 and G2. Each dot represents a daily dose of 13-30 μg / kg divided into two or three doses (filled circles: two doses 8 hours apart; open circles: three doses 6 hours apart) as indicated. For G1-G6, there was no daily dose escalation over the study period. For G6, the initial daily dose was 20 μg / kg administered on days 1 and 2 of weeks 1 and 2, and this daily dose increased to 30 μg / kg on days 1 and 2 of weeks 4, 5, 7, and 8 (enlarged filled circles). [Figure 21] Graphical representation of a pulsatile cyclic dosing regimen. A-E depict various scenarios of daily dose escalation: A - after the first treatment period x of each treatment cycle, where each treatment cycle is restarted at the initial dose; B - after each treatment period x of each treatment cycle, where the daily dose is not increased after discontinuation z; C - after each day of treatment within each treatment period x, where each treatment cycle is restarted at the initial dose; D - after each day of treatment within each treatment period x, where the daily dose is not increased from one treatment period x to the next within the cycle, and where each treatment cycle is restarted at the initial dose; E - after each day of treatment within each treatment period x, where the daily dose is not increased from one treatment period x to the next within the cycle, and where the daily dose of the first treatment period x of the new cycle begins with the daily dose of day 1 of the previous treatment period x.

[0182] array SEQ ID NO:1 - Human IL-2 [ka] SEQ ID NO:2 - mature human IL-2 [ka] SEQ ID NO:3 - Human IL-15 [ka] SEQ ID NO:4 - Mature human IL-15 [ka] SEQ ID NO:5 - Human IL-15Rα [ka] SEQ ID NO: 6—IL-15Rα sushi domain [ka] SEQ ID NO:7 - sushi+ fragment of IL-15Rα [ka] SEQ ID NO:8 - Linker [ka] SEQ ID NO:9-RLI2 [ka] SEQ ID NO: 10-IL2v [ka] SEQ ID NO: 11-(IL-15N72D)2: Leader peptide of IL-15R sushi-Fc: [ka] SEQ ID NO: 12-IL-15R sushi (65aa)-Fc (IgG1 CH2-CH3) [ka] SEQ ID NO: 13-IL-15N72D [ka] [Example]

[0183] 1. Flow Cytometry Antibodies for mouse experiments

[0184] [Table 2]

[0185] [Table 3]

[0186] [Table 4]

[0187] [Table 5]

[0188] Monkey blood processing for PBMCs Ten μl of blood was directly measured by flow cytometry with DAPI for viability detection (2 μl DAPI / well + 190 μl PBS + EDTA). 300 μl of fresh blood was incubated with 6 ml of red blood cell lysis buffer (BioLegend®, 10× buffer diluted to 1× in dH2O) for 15 minutes (to obtain PBMCs), protected from light, centrifuged, and washed twice with 10 ml of FACS buffer (PBS, Lonza® + 2% fetal bovine serum (US), heat-inactivated, Sigma Aldrich®). Centrifugation was performed at 300 g for 5 minutes at 4°C. The cell suspension was resuspended in 0.5 ml of FACS buffer, and 10 μl of the cell suspension was measured by flow cytometry with DAPI to detect viability after red blood cell lysis (+ 90 μl FACS buffer, + 1.2 μl DAPI). The cell suspension was seeded into a 96V well plate with two wells per sample, and the cells were centrifuged in the 96V plate (2200 rpm, 2 min, 4° C.) and stained by flow cytometry.

[0189] Flow cytometry (FACS) staining for cynomolgus monkey testing Extracellular antigens (CD antigens) were analyzed using the flow cytometry panel above ( 1 / 2Teff panel, 1 Cells were stained using a 1:9 mixture of appropriate extracellular antibodies and fixable viability dyes in FACS buffer (prepared at 50 μl per sample) for 30 minutes at 4°C, preventing exposure to light. Samples were washed twice with FACS buffer and centrifuged at 2200 rpm and 4°C for 2 minutes. Cells were fixed with 100 μl / well of fixation buffer (1 fixation concentration: 3 fixation dilutions) for 20 minutes at 4°C. After the fixation procedure, cells were permeabilized in Perm. buffer-dH2O 1:9 at room temperature for 5 minutes and centrifuged at 2200 rpm and 4°C for 2 minutes.

[0190] Intracellular antigens (Ki67 and FoxP3) were analyzed using the flow cytometry panel above ( 1 / 2Teff panel, 1 Cells were stained using a 96V / 2 Treg panel with a mixture of appropriate intracellular antibodies plus 3 μl of rat serum per well in permeabilization buffer (prepared at 50 μl per sample) for 30 min at 4°C, protected from light exposure. Samples were washed twice with FACS buffer and centrifuged at 2200 rpm and 4°C for 2 min. Cells were resuspended in 200 μl of staining buffer, and 120 μl of cell suspension was measured in a 96V plate immediately after staining.

[0191] Preparation of mouse splenocytes Spleens were obtained from mice and transferred into gentleMACS C tubes containing 5 ml of FACS buffer (PBS, 2 mmol EDTA + 2% FBS) and kept on ice until further processing. Each spleen was processed in a separate tube. The C tubes were sealed and placed upside down on the sleeve of a gentleMACS Dissociator. The GentleMACS program: m_spleen- was used for 60 seconds. The spleens were completely dissociated to obtain a spleen cell suspension. The cell suspension was passed through a 70 μM white strainer into a 50 ml Falcon tube. The cells were centrifuged at 1200 rpm for 10 minutes at 4°C. The pellet was resuspended in 1 ml of ACK lysis buffer (Gibco) by pipetting the cells up and down using a 1 ml tip, and another 2 ml of ACK lysis buffer was added. Red blood cells were lysed for 10 minutes to obtain splenocytes. After 10 minutes, 27 ml of FACS buffer was added. The splenocytes were centrifuged again at 1200 rpm for 10 minutes at 4°C, and the cell pellet was resuspended in 1 ml of FACS buffer. The cell suspension was passed through a 30 μM strainer (green) into a 14 ml Falcon tube.

[0192] Flow cytometry (FACS) staining for mouse studies. The splenocyte suspension was divided into 96V-well plates at 100 μl / well for duplicate staining. The plates were centrifuged at 2000 rpm for 3 minutes at 4° C. The cells were blocked with Fc receptor block (anti-mouse CD16 / CD32 - Fc block, eBioscience™, 1 μl / well) and 10% mouse serum (2 μl / well) in 17 μl of FACS buffer for 30 minutes at 4° C. The wells were washed twice with FACS buffer by centrifugation at 2000 rpm for 5 minutes at 4° C.

[0193] For extracellular staining, cells were stained with a mixture of appropriate extracellular antibodies (for T effector cells against antigen: CD3, CD4, CD8, CD44, CD122 CD62L; for Treg / NK cells against antigen: CD3, CD4, CD8, CD49b, CD25) and fixed with Fixable Viability DyeeFluor™ 780 (dilution 1:200, eBioscience™) in FACS buffer (prepared at 10 μl / sample) for 30 minutes at 4° C. (protect from light exposure). Cells were washed twice with FACS buffer (200 μl, centrifuged at 2000 rpm for 3 minutes at 4° C.).

[0194] For fixation, cells from above were fixed with 100 μl / well of fixation buffer (1:3 - Concentrate:Diluent; Fixation / Permeabilization Concentrate, eBioscience™; Fixation / Permeabilization Diluent, eBioscience™) for 30 min at 4° C. After the fixation procedure, cells were permeabilized in Perm buffer (1:9 in dH2O, 5 min at RT) and centrifuged (2200 rpm, 2 min, 4° C.).

[0195] For intracellular staining, cells from above were washed twice with 100 μl / well wash / perm buffer (eBioscience™ - 1:9 - buffer:dH2O) and centrifuged at 2000 rpm for 3 minutes at 4°C. The buffer was discarded, and a mixture of the appropriate intracellular antibodies (for T effector cells against antigen: Ki67; for Treg / NK cells against antigen: Ki67 and FoxP3) was added in permeabilization buffer (eBioscience™) at 50 μl / sample. Cells were incubated for 30 minutes at 4°C, protected from light exposure. Cells were washed twice with wash / perm buffer and centrifuged at 2000 rpm for 3 minutes at 4°C. Cells were resuspended in 100 μl of FACS buffer and transferred into FACS tubes or a 96V plate for FACS analysis.

[0196] Flow cytometry was performed using a BD LSRFortessa™ flow cytometer (Becton Dickinson) according to the manufacturer's instructions. Cytometry data were collected using BD DiVA™ (BD BioSciences) software and analyzed using FlowJo® software (Tree Star).

[0197] Wet lung weight determination The lungs were gently removed from the mice and placed in a 1.5 ml microcentrifuge tube. The weight of the wet lungs in the microcentrifuge tube was determined. The lungs were then gently dried for 10 hours, and the dry lungs were weighed in an Eppendorf tube. The wet and dry weights were recorded for VLS calculation and were equal to the wet lung weight minus the dry lung weight.

[0198] 2. Pharmacokinetic and pharmacodynamic study of RLI-15 by intravenous and subcutaneous routes in cynomolgus monkeys - Pharmacodynamic part The pharmacodynamics of RLI-15 / SO-C101 was tested by assessing immune cell profiles after repeated intravenous or subcutaneous administration in cynomolgus monkeys in two phases.

[0199] Phase 1 - Comparison, Intravenous vs Subcutaneous In Phase 1, cynomolgus monkeys (2 males per group) were treated with RLI-15 at doses of 4, 10, and 25 μg / kg per intravenous (over 60 minutes) or subcutaneous administration for 4 consecutive days according to the design depicted in Table 2 and Figure 1 A. On the fifth day (D5) after daily dosing, blood samples (0.5 ml) were collected in K2-EDTA tubes, processed, stained, and analyzed by flow cytometry as described above, and compared with blood samples taken before dosing on Day 5 (D-5). [Table 6]

[0200] After four consecutive days of RLI-15 administration, proliferating Ki67 + NK cells and CD8 + T cells were determined by immunofluorescence analysis on day 5. Both subcutaneous and intravenous administration increased the proliferation of Ki67 in a dose-dependent manner. + NK cells (see Figure 1B) and CD8 + This led to increased numbers of T cells (see Figure 1C) (compared to pre-dose values ​​on day -5). Importantly, subcutaneous administration was more potent than intravenous administration, although the latter increased Ki67 + Whereas a plateau was reached for NK cells at a dose of 10 μg / kg RLI, only a slight further increase was seen between 10 and 25 μg / kg for intravenous administration; therefore, 15 μg / kg was selected as the subcutaneous dose for Phase 2. The difference between subcutaneous and intravenous administration was likely caused by differences in the pharmacokinetics of RLI-15 following different routes of administration. Subcutaneous administration resulted in longer circulating biologically active serum concentrations compared with intravenous administration, which may explain the stronger NK cell and CD8 activation with subcutaneous administration. + This is interpreted as resulting in T cell activation.

[0201] Phase 2 - comparative, 2 vs. 4 doses In Phase 2, after a two-week washout period, animals were treated for three weeks (starting on D22) according to the experimental groups as depicted in Table 3 and Figure 1A. Cynomolgus monkeys were subcutaneously administered 15 μg / kg / dose on study day 22 (D22), D29, and D36 (administered once per week in weeks 1, 2, and 3, Group 1), D22, D23, D36, and D37 (administered twice in weeks 1 and 3, Group 4), D22, D23, D29, D30, D36, and D37 (administered twice in weeks 1, 2, and 3, Groups 5 and 7), and D22-D25 and D36-D39 (administered four times in weeks 1 and 3, Group 6). Two groups continued intravenously on D22, D23, D36, and D37 (two doses at 1 and 3 weeks, Group 2) and on D22-D25 and D36-D39 (four doses at 1 and 3 weeks, Group 3) at 40 μg / kg / dose.

[0202] Immunofluorescence analysis was performed and further samples were collected according to the schedule in Figure 1A. + The cell fraction was divided into CD3 - CD8 + CD45 + (NK cells) and CD3 + CD8 + CD45 + (CD8 + T cell fractions. Data were collected from Group 1 (one dose per week), Groups 4, 5, 7 (pooled, two doses in weeks 1 and 3), and Group 6 (four doses).

[0203] Lymphocyte counts were determined during hematological evaluation, and CD8 + T cells and NK cells were analyzed by immunofluorescence and CD45 + The lymphocyte count was determined during hematological evaluation, as well as CD8 counts, by multiplying their relative proportions within the cells by the total white blood cell count. + T cells and NK cells were multiplied by the total white blood cell count and CD45 + were determined according to their relative ratios within the cells.

[0204] [Table 7]

[0205] Ki67 in total NK cells + (Activated) NK cells and total CD8 + Ki67 in T cells + (activation)CD8 + The percentages of T cells are shown in Figure 1D. NK cells and CD8 + Optimal activation of both T cells (Ki67 + (measured as activated NK cells and CD8+) can be achieved by subcutaneous administration twice daily for two consecutive days per week, whereas four consecutive daily administrations within one week resulted in a significant increase in activated NK cells and CD8+ measured on the fifth day after administration. + It does not provide any additional benefit with respect to T cells, which is surprising given the short in vivo half-life of RLI-15 of only a few hours.

[0206] Phase 2 - Repeated weekly dosing Looking at the total lymphocyte counts from animals from Group 5 (two animals, lymphocyte analysis performed on the fifth day of each dosing week, i.e., D5, D26, D39, and D46), twice daily subcutaneous administration for three weeks in Phase 2 significantly increased the total lymphocyte counts, CD8 + The increase in T cells and NK cells was promoted, whereas the increase in NK cells and CD8 + T cell levels were maintained but did not increase further (see Figure 1E). Therefore, repeated treatment of monkeys, i.e., with two daily doses, one or two times on two consecutive days over two or three weeks, was considered optimal, as a plateau was reached by the third week and no additional benefit was expected with further repetitions.

[0207] Phase 1 and Phase 2 - Repeating monthly cycle After treatment interruption between phase 1 and phase 2, NK cells and CD8 +Given the finding that T cells can be reactivated 18 days after the last treatment (day 22 to day 4), it is envisioned that two or three repetitions of two daily doses on consecutive days could be repeated again after a break in treatment of approximately 5 to 20 days.

[0208] Phase 2 - Comparison, Cell Activation vs. Cell Proliferation Figure 1F-I shows Ki-67 + NK cells (F) and CD8 + Ki-67 + Cellular activation of T cells (H), total NK cells or CD8 + T cells) or NK cells (G) and CD8 + The pulse dosing of two consecutive daily doses in Phase 2 showed either cell proliferation of T cells (I) (as cell counts), NK cells, and CD8 + In both the second and third cycles, the two doses led to a strong activation of both NK cells and CD8 T cells, which declined again sharply during the 5-day treatment break. + There was a distinct activation of T cells, with a trend towards weaker activation of NK cells over later cycles. + Looking at T cell proliferation, the first two cycles of two consecutive daily doses led to a steady increase in cell numbers, whereas the third cycle did not lead to a further increase, and for animal 70, NK cell numbers were declining even after the third dosing cycle of phase 2.

[0209] 3. Pharmacokinetic and Pharmacodynamic Study of RLI-15 by Intravenous and Subcutaneous Routes in Cynomolgus Monkeys - High-Density Dosing In another experiment, we tested whether four daily doses of RLI-15 / SO-C101 on four consecutive days in a four-week cycle would lead to improved pharmacodynamic effects. RLI-15 at a dose of 100 μg / kg was subcutaneously injected in one female and one male cynomolgus monkey on four consecutive days (D1-4; D8-11, D15-18, D22-25). Pharmacodynamic activity was evaluated on days 5, 12, 19, and 26. The absolute and relative numbers of lymphocyte subsets in the peripheral blood of all animals were determined by flow cytometry. Absolute lymphocyte subset counts were determined using BD TruCount™ tubes, and included NK cells (CD16+)-CD3-CD16+, total T lymphocytes (CD3 + )-CD3 + , helper T lymphocytes (CD4)-CD3 + CD4 + CD8-, cytotoxic T lymphocytes (CD8 + )-CD3 + CD4-CD8 + , and B lymphocytes (CD20+)-CD3-CD20+, each reported as cells per μl of whole blood (Figure 2).

[0210] NK cells and CD8 + Looking at T cell counts (Figure 2), the first cycle of four daily doses on four consecutive days significantly increased NK cell and CD8 + This leads to a strong proliferation of lymphocytes with an increased number of T cells. However, already after the second cycle, lymphocytes, NK cells, and CD8 + T cell numbers also declined, which continued over cycles 3 and 4. Comparing these results to the less intensive dosing schedule shown in Figure 1E, where increasing / high cell numbers were observed in treated monkeys over 3 cycles, the benefit was greater in NK and CD8 + It becomes clear that T cell expansion was not observed with a very high density continuous schedule involving four consecutive doses per week.

[0211] 4. Human / in vitro and cynomolgus monkey / in vivo correlation In vitro expansion of immune cell populations in peripheral blood obtained from humans and cynomolgus monkeys after RLI-15 / SO-C101 exposure was measured using human and cynomolgus monkey NK cells and CD8 + To calculate the half maximal effective concentration (EC50) and 10% and 90% effective concentrations (EC10, EC90) of RLI-15 for T cell proliferation, they were determined by flow cytometry.

[0212] As shown in Figure 3, NK cells and CD8 + There was a strong correlation between T cell activation. The in vitro concentration-response relationship was measured by measuring Cmax and NK and CD8 T cell activity after subcutaneous administration in cynomolgus monkeys. + The relationship between T cell activation levels correlated well. For example, RLI-15 at 4 μg / kg and a corresponding Cmax of 1.2 ng / ml (approximately 48 pM) resulted in 71% of activated NK cells and 18% of activated CD8 + Similar activation levels were observed in human NK cells (64%) and CD8 T cells. + Using T cells (17%), a dose of 0.93 ng / ml (approximately 37 pM) was achieved in vitro (Figure 3). This dose and concentration response was used to determine the estimated minimum effective dose (MABEL), pharmacologically effective dose (PAD), and, together with the no observed adverse effect level (NOAEL) and maximum tolerated dose (MTD), to select the starting dose and dose escalation step for clinical trial SC103 (Figure 3).

[0213] Minimal activation of NK cells and CD8 +T cell activation was observed in vitro at an RLI-15 concentration of 0.1 ng / ml (approximately 4 pM) (Figure 3). This concentration is considered the MABEL. A dose of 0.7 μg / kg was estimated to achieve this Cmax of 0.1 ng / ml based on the observed relationship between SC dose and Cmax. The calculated receptor occupancy (RO) for this dose is between 0.5% and 2%, considering KDs of 200 pM and 800 pM, respectively. Pharmacological doses ranged from 1.5 μg / kg to 25 μg / kg, corresponding to Cmax of 0.3 ng / ml (approximately 12 pM) to 14 ng / ml (approximately 560 pM) and ROs of 1.5% to 6%, 40%, and 65%, respectively. NK cell and CD8 activation at the upper limit were observed. + At the lower end of this dose range, approximately 50% of NK cells, but no CD8 + T cell activation was observed. A NOAEL of 80 μg / kg and an MTD of 100 μg / kg after SC administration were calculated, promoting an 80%-95% ROI. The cynomolgus monkey doses listed above were converted to the corresponding human doses by allometric scaling using a factor of 3.1 (CDER 2005).

[0214] NK cells and CD8 + Because T cell activation is a more sensitive parameter than receptor occupancy, the pharmacological activity of RLI-15 determined in vitro and in cynomolgus monkeys was used to determine the starting dose and titration steps planned for clinical trial SC103. Therefore, a starting dose of 0.25 μg / kg was selected (Figure 3). This dose, representing MABEL, stimulated CD8 + It is expected to stimulate approximately 20% NK cell activation without affecting T cells. Subsequent dose levels shown in Figure 3 were selected to gradually increase NK cell activation and stimulate CD8 + The activation of T cells was enhanced to 60% and <10% at dose level 2 and 80% and 25% at dose level 3, respectively, and 100% NK cells and CD8 +T cell activation was reached. Subsequent dose levels will be increased by 66%, 60%, and 50%. Dose level 7 may still be below the NOAEL human equivalent (26 μg / kg). Dose escalation in Study SC103 may be made dependent on the safety observed at each dose level. Additionally, PK parameters as well as NK cell and CD8 activity were analyzed in patients at each dose cohort. + T cell activation is taken into account in determining dose escalation.

[0215] 5. Summary of a follow-up pharmacokinetic and pharmacodynamic study of RLI-15 administered subcutaneously in cynomolgus monkeys In a setting similar to that described in Example 2, additional dosing schedules are planned to be tested for subcutaneous administration of RLI-15 / SO-C101: [Table 8]

[0216] Dx indicates administration of RLI-15 on day x of each week, for example, D3 in week 6 indicates administration of RLI-15 on day 3 of week 6.

[0217] 6. Pharmacodynamics in mice at different doses NK cells and memory CD8 + The dose of RLI-15 that showed maximal activity against T cells was investigated. Mice were injected intraperitoneally or subcutaneously with RLI-15 (SO-C101, RLI2) at increasing concentrations of 10, 20, 35, and 50 μg / dose once daily for four consecutive days. On day 5, lungs were harvested, and splenocytes were isolated and analyzed for NK cells, memory CD8 + T cells and T regulatory cells (CD4 + CD25 + FoxP3 + The relative proliferation of T cells was determined by flow cytometry on day 5 (Figure 4).

[0218] All tested concentrations of RLI-15 inhibited NK cell and memory CD8+ High proliferation of T cells was induced (see Figures 4A and B). The highest proliferation of NK cells was observed when mice were injected with 20 μg / dose, whereas memory CD8 + Maximum proliferation of T cells was achieved when mice were injected with 35 μg / dose. There was no proliferation of T regulatory cells under any dose of RLI-15 tested (see Figure 4C). Interestingly, NK cells and memory CD8 cells in mice injected with 50 μg / dose of RLI-15 were significantly increased. + T cell proliferation showed a tendency to decrease when compared with the lower RLI-15 concentration of 35 μg / dose. NK cell and memory CD8 proliferation were significantly increased by RLI-15 administered via the intraperitoneal or subcutaneous route at any dose tested. + There was no significant difference in the relative proliferation of T cells. Finally, there was no significant increase in lung weight as a measure of vascular leak syndrome (VLS) at day 5 (see Figure 4D).

[0219] Phase 2 - 4 doses of intravenous versus subcutaneous treatment for 2 biweekly cycles. Figure 1J-M shows Ki-67 + NK cell percentage and Ki-67 + NK cell counts are compared for two biweekly cycles of four intravenous doses of 40 μg / kg RLI-15 each (Group 3 with animals 65 and 66) and two subcutaneous doses of 15 μg / kg RLI-15 each (Group 4 with animals 67 and 68). The same groups were compared for Ki-67 + CD8 + T cell percentage and Ki-67 + CD8 + The numbers of T cells are shown (Figure 1N-Q).

[0220] Ki-67 in all NK cells +NK cell activation, measured as a percentage of CD8, was at least equivalent for two daily doses on two consecutive days with 15 μg / kg RLI-15 subcutaneously (60 μg / kg total) compared with four daily doses on consecutive days with 40 μg / kg RLI-15 intravenously (320 μg / kg total), with intravenous activation decreasing for the second cycle, whereas subcutaneous activation tended to be equal for the first and second cycles (Figure 1 J and L). + T cell activation was stronger with two subcutaneous doses of RLI-15, with over 20% activated CD8 + The 4th intravenous dose appeared to reach 20% or less of the activated CD8 T cells. + On the other hand, four intravenous doses led to CD8 + A more consistent increase in T cell numbers appears to have been induced (Fig. 10 and Q).

[0221] In summary, two subcutaneous doses of RLI-15 on two consecutive days are at least equivalent to four intravenous doses on four consecutive days.

[0222] 7. Efficacy of Intraperitoneal Administration of RLI-15 on Varying Schedules in a Metastatic Renca Tumor Model The anti-metastatic activity of RLI-15 at a dose of 20 μg was investigated in a renal cell carcinoma (RENCA, BALB / c, female) mouse model (14 or 16 mice / group, 8 mice for tumor progression, 6 or 8 mice for pharmacodynamics). RLI-15 (SO-C101, RLI2) in 200 μl saline / daily dose was administered at 10 5 RENCA tumor cells (in 300 μl saline) were injected via intravenous injection into the tail vein on day 0, followed by administration on different schedules starting via the intraperitoneal route on day 1 (D1). Metastasis-containing lungs were weighed on day 16 (see Figure 5A). The following groups / schedules were tested: 0) Naive: No treatment 1) Renca 5×10 5 only 2) Renca 5×10 5+20μg RLI2 intraperitoneal D1-4+D8-11 3) Renca 5×10 5 +20μg RLI2 intraperitoneal D1-4 4) Renca 5×10 5 +20μg RLI2 intraperitoneal D1-2+D8-9 5) Renca 5×10 5 +20μg RLI2 intraperitoneal D1+D8

[0223] FACS analysis was performed on days 5 and 12. Mouse weight and survival were monitored 2-3 times per week, and on day 16, mice were sacrificed and lungs were collected, with only brief contact with filter paper to remove excess fluid on the surface, and assessed for their weight. [Table 9]

[0224] RLI-15 administered intraperitoneally at a daily dose of 20 μg reduced lung metastases by approximately 70% compared to control tumor-bearing mice (see Table 4 and Figure 5B), whereas a schedule involving repeated dosing on D1-D4 was superior to dosing on D1-D2 + D8-D9 and D1 + D8. Two four-day dosings (D1-D4 + D8-D11) were not significantly better than one four-day dosing (D1-D4). Four daily doses on four consecutive days (D1-D4) appeared to be better than (D1-D4 + D8-D11) over two weeks.

[0225] NK cells and memory CD8 +T cell proliferation was assessed on days 5 and 12 from two mice per group by analysis of splenocytes, which were analyzed for relative proliferation of immune cells (see Figures 5D and E). RLI-15 treatment induced high proliferation in both immune cell types, which persisted 12 days after the start of treatment. D1-D4 dosing (D1-D4 and D1-D4 + D8-D11 schedules, identical until day 5) showed high proliferation of NK cells and CD8 cells on day 5, significantly higher than schedules with fewer doses (D1-D2 and D1) until day 5. The D1-D4 weekly treatment schedule significantly increased proliferation of NK cells and CD8 cells detected on day 12. + It showed the highest pharmacodynamic (PD) activity on T cell proliferation, which was superior to the 2-week treatment schedule (no additional benefit on PD was observed with a second RLI-15 administration). Treatment on D1+D8 or D1-D2+D8-D9 resulted in a lower PD effect. A similar effect was observed on the activated subset of these cells (Ki-67 + ) was observed.

[0226] VLS was not induced by RLI-15 treatment on day 5. RLI-15 treatment at all schedules prevented weight loss in mice induced by tumor burden (control) (data not shown).

[0227] Interestingly, NK cells and CD8 + Both T cell proliferation (best for the D1-D4 and D1-D4+D8-D11 schedules) closely resembled treatment efficacy for the treatment of lung metastases and are therefore suitable surrogate markers for efficacy.

[0228] 8. Efficacy of Subcutaneous Administration of RLI-15 at Varying Doses in a Metastatic Renca Tumor Model The anti-metastatic activity of RLI-15 (SO-C101, RLI2) at a dose of 10 μg or 20 μg was evaluated using a (IL-15Rαsushi)2Fc fusion protein (same sequence as disclosed for ALT-803 in US 2017 / 0088597) non-covalently linked to two IL-15N72D muteins (hereafter referred to as IL15). N72D :IL15Rα sushi The efficacy of RLI-15 (RLI2) at 10 μg or 20 μg or 5 μg of IL15 in 200 μl saline / daily dose was investigated in a mouse model of renal cell carcinoma (RENCA, BALB / c, female) in comparison with RLI-15 (RLI2) or more precisely (IL15N72D)2:IL15Rα sushi-Fc. N72D :IL15Rα sushi -Fc, 10 5 RENCA tumor cells (in 300 μl saline) were injected via intravenous injection into the tail vein on day 0 and then administered via the subcutaneous route on different schedules starting on day 1 (D1). 0) Naive: No treatment 1) Renca5×10 5 only 2) Renca5×10 5 +20μg RLI2 subcutaneous D1-4 3) Renca5×10 5 +10μg RLI2 subcutaneous D1-4 4) Renca5×10 5 +20μg RLI2 subcutaneous D1-3 5) Renca5×10 5 +5 μg IL15 N72D :IL15Rα sushi -Fc subcutaneous D1 IL15 N72D :IL15Rα sushi -Fc was dosed less frequently at lower doses due to its higher expected half-life.

[0229] Mice were monitored for weight and survival until they were sacrificed on day 16 (see Figure 6B). Lungs were harvested on day 16, excess fluid on the surface was removed by brief contact with filter paper, and lung weight was determined as a measure of lung metastasis (see Table 5 and Figure 6A). [Table 10]

[0230] All subcutaneous RLI-15 treatment doses and schedules demonstrated significant anti-metastatic efficacy by significantly reducing lung weights on day 16. The 20 μg dose on either D1-D4 or D1-D3 was superior to the 10 μg D1-D4 schedule, and 5 μg IL15 administered once on D1 N72D :IL15Rα sushi Furthermore, the efficacy of all treatment modalities was significantly higher in mice with no (IL15) compared to untreated mice. N72D :IL15Rα sushi -Fc) or relatively mild (RLI-15-treated mice) weight loss was observed.

[0231] 9. Clinical trials of RLI-15 / SO-C101 A first-in-human, multicenter, open-label Phase 1 / 1b study to evaluate the safety and preliminary efficacy of SO-C101 as monotherapy and in combination with pembrolizumab in patients with selected advanced / metastatic solid tumors has been approved and will begin shortly (EurdraCT No. 2018-004334-15). RLI-15 will be administered subcutaneously at a starting dose of 0.25 μg / kg and up to 48 μg / kg. In the combination portion of the clinical trial, RLI-15 will be combined with Keytruda® 25 mg / ml / pembrolizumab, which will be administered intravenously at a dose of 200 mg.

[0232] This study evaluates the safety and tolerability of SO-C101 administered as monotherapy (Part A) and in combination with an anti-PD-1 antibody (pembrolizumab) (Part B) in patients with select relapsed / refractory advanced / metastatic solid tumors (renal cell carcinoma, non-small cell lung cancer, small cell lung cancer, bladder cancer, melanoma, Merkel cell carcinoma, cutaneous squamous cell carcinoma, microsatellite-high solid tumors, triple-negative breast cancer, mesothelioma, thyroid cancer, thymic carcinoma, cervical cancer, biliary tract cancer, hepatocellular carcinoma, ovarian cancer, gastric cancer, squamous cell carcinoma of the head and neck, and anal cancer) who are refractory to or intolerant of existing therapies known to provide clinical benefit for their condition.

[0233] Part A will begin with escalating doses of SO-C101 monotherapy, ranging from 0.25 μg / kg to 48 μg / kg SO-C101 administered subcutaneously, and will continue until the maximum tolerated dose (MTD) and / or recommended phase 2 dose (RP2D) of SO-C101 monotherapy are established. Patients will be treated with SO-C101 on days 1 (±1 day; Wednesday), 2 (Thursday), 8 (Wednesday), and 9 (Thursday) of a 21-day cycle (Figure 7A). The start of treatment (Day 1) will be scheduled on a Wednesday whenever possible to allow for biomarker sampling (transport of fresh peripheral blood mononuclear cells [PBMCs] to the central laboratory) on a weekday. However, there is a ±1-day flexibility for Day 1 dosing to occur on Tuesdays or Thursdays, as long as two doses per week are given on the day of outcome (Days 1 and 2) and the Week 2 dosing (Days 8 and 9) occurs 7 days after Day 1. Monotherapy dose escalation will continue until the MTD and / or RP2D are reached according to the dose escalation schema. If the MTD is not reached at the end of the planned dose escalation cohort, recruitment will stop and the RP2D will be assessed. Patients recruited in Part A will continue treatment at their assigned dose level. Patients will be discontinued from study treatment due to any of the following events: (i) radiographic disease progression; (ii) clinical disease progression (investigator assessment); (iii) AE (intercurrent illness or study treatment-related toxicity (including dose-limiting toxicity) that, in the investigator's judgment, may affect the assessment of clinical status to a significant extent or require discontinuation of study treatment).

[0234] The starting dose in Part B is planned to be 1.5 μg / kg SO-C101 administered as in Part A, in combination with a fixed dose of pembrolizumab (200 mg intravenously every 3 weeks). Patients will be treated with escalating doses of SO-C101 on Days 1 (± 1 day) (Wednesday), 2 (Thursday), 8 (Wednesday), and 9 (Thursday) along with a fixed dose of pembrolizumab (200 mg intravenously every 3 weeks) given at the time of the Day 1 administration of SO-C101 (Figure 7B). Pembrolizumab will be administered within 30 minutes after the initial dose of SO-C101 as outlined in the package insert. The start of treatment (Day 1) will be scheduled on a Wednesday whenever possible to allow for biomarker sampling (transport of fresh PBMCs to the central laboratory) on a weekday. However, there is a flexibility of ±1 day, as long as two doses of SO-C101 per week are given on the day of outcome (Days 1 and 2) and the Week 2 SO-C101 dosing (Days 8 and 9) occurs 7 days after Day 1. Patients will continue SO-C101 and pembrolizumab treatment at the assigned dose level of SO-C101. If SO-C101 needs to be discontinued for reasons other than disease progression, pembrolizumab treatment may be continued for up to 1 year, as assessed by DEC, if the patient does not progress and can tolerate treatment. If pembrolizumab needs to be discontinued, SO-C101 treatment may be continued until disease progression or unacceptable toxicity. Patients will be discontinued from study treatment due to any of the following events: (i) radiographic disease progression; (ii) clinical disease progression (investigator assessment); (iii) AE (intercurrent illness or study treatment-related toxicity (including dose-limiting toxicity) that, in the investigator's judgment, may affect the assessment of clinical status to a significant extent or require discontinuation of study treatment).

[0235] 10. In vitro tumor cell killing by simultaneous combination of RLI-15 and daratumumab Human PBMCs were isolated from the buffy coats of five healthy blood donors by Ficoll separation. The isolated human PBMCs (1 × 10 6Daudi tumor cells (40,000 cells / well) were incubated with RLI-15 (SO-C101) at a concentration of 1 nM, daratumumab at concentrations of 0.1, 1, and 10 nM, and DiD-labeled (Vybrant® DiD-labeled, ThermoFisher, according to the manufacturer's instructions) Daudi tumor cells (40,000 cells / well) for 20 hours at 37°C (E:T ratio 25:1) using heat-inactivated serum (20 min, 56°C-HI serum). Cells were then stained with a mixture of fluorescently labeled antibodies and DAPI (LAMP-1 was omitted due to the slow analysis time for this degranulation marker) as shown in Table 6. The percentage of dead (DAPI-positive) DiD+ Daudi cells was detected by flow cytometry. hPBMCs were distinguished from Daudi tumor cells using immune cell markers. DiD-labeling of Daudi cells was performed before coculture with human PBMCs. 5 μl / 1×10 6 DiD from 100 cells was added to Daudi tumor cells in serum-free RPMI and incubated for 30 minutes at 37° C. Cells were washed twice (5 minutes, 1500 rpm) with RPMI medium containing FCS. [Table 11]

[0236] The presence of RLI-15 or 0.1 nM daratumumab only non-significantly increased the number of dead tumor cells (from about 15% to about 18% or 20%, respectively), whereas the combination of RLI-15 and 0.1 nM daratumumab led to a more significant increase in dead tumor cells (about 26%). While comparatively more dead cells were observed with increasing concentrations of daratumumab at 1 nM, apparent saturation was achieved at this value, since no further increase was observed with 10 nM daratumumab. Furthermore, the presence of RLI-15 consistently increased the number of dead tumor cells compared to the respective groups without RLI-15 (see Figure 8).

[0237] In conclusion, RLI-15, when added simultaneously, synergized with daratumumab in tumor cell killing of Daudi cells in vitro.

[0238] 11. In vitro tumor cell killing by sequential combination of RLI-15 and daratumumab Human PBMCs were isolated from the buffy coats of six healthy blood donors by Ficoll separation. Isolated human PBMCs (1 × 10 6 PBMCs (cells) were incubated with 0.1 nM RLI-15 (SO-C101) for 48 hours at 37°C. Stimulated PBMCs were then incubated with either activated serum or heat-inactivated serum (20 min, 56°C) in the absence or with increasing concentrations of daratumumab (0.1, 1, or 10 nM) and DiD-labeled Daudi tumor cells (40,000 / well) for 4 hours at 37°C (E:T ratio 1:1). Cells were then stained with a mixture of fluorescently labeled antibodies and DAPI, as shown in Table 6. The percentage of dead (DAPI-positive) DiD+ Daudi cells was detected by flow cytometry. Immune cell markers were used to distinguish hPBMCs from Daudi tumor cells. DiD labeling of Daudi cells was performed before coculture with human PBMCs. 5 μl / 1 × 10 6 Single cells of DiD were added to Daudi tumor cells in serum-free RPMI and incubated for 30 min at 37° C. Cells were washed twice (5 min, 1500 rpm) with RPMI medium containing FCS.

[0239] Similar to the simultaneous setting in Example 10, the addition of daratumumab led to a synergistic increase in tumor cell death, whereas in heat-inactivated (HI) serum, there was little additional increase from 0.1 nM to 1 nM, and no increase in daratumumab from 1 nM to 10 nM. However, in contrast, the percentage of dead tumor cells further increased to >60% after incubation in activated serum, indicating a further synergistic effect with activated complement (complement-dependent cytotoxicity - CDC). Thus, RLI-15 and daratumumab synergistically killed Daudi cells in an in vitro sequential setting (see Figure 9).

[0240] 12. Antitumor efficacy of the simultaneous combination of RLI-15 and daratumumab in multiple myeloma in vivo CB17SCID mice, 1 x 10 7 Mice were inoculated subcutaneously with RPMI8226 myeloma cells (an established model for multiple myeloma). Treatment began on day 0 (the day of randomization, when tumor volumes were ∼100 mm). 3 ) RLI-15 was administered subcutaneously at 1 mg / kg on days 0, 1, 2, and 3, and daratumumab was administered intraperitoneally at 20 mg / kg on day 4. One group each had RLI-15 (SO-C101) or daratumumab alone, and one group had the combination. As a control, saline was administered subcutaneously at 10 μl / g on days 0, 1, 2, and 3. Ten animals were used per group.

[0241] While control animals treated with saline showed a steady increase in mean tumor volume (solid black line in Figure 10A), both monotherapy treatment groups with RLI-15 and daratumumab showed reduced tumor growth (gray dotted line for daratumumab and black dotted line for RLI-15, Figure 10A), with combination treatment with RLI-15 and daratumumab even leading to a synergistic reduction in tumor volume (solid gray line in Figure 10A). Looking at individual animals, combination treatment with RLI-15 and daratumumab led to tumor rejection in all test animals, compared with only 25% of RLI-15 monotherapy. For both the control and daratumumab groups, none of the test animals rejected tumors (see Figure 10B, solid gray line for the combination group, dotted black line for RLI-15; both the saline control group and the daratumumab group are run on the x-axis).

[0242] Thus, the synergistic interaction between RLI-15 and daratumumab observed in vitro was confirmed in the RPMI8226 multiple myeloma in vivo model in a parallel setting.

[0243] 13. Antitumor efficacy of sequential combination of RLI-15 and daratumumab in multiple myeloma in vivo As in Example 12, CB17 SCID mice were injected with 1 x 10 7 Treatment was initiated on day 0 (randomization day, tumor volume ∼100 mm). 3 ) were started. Daratumumab was administered intraperitoneally at 20 mg / kg on day 0, whereas in this sequential setting, RLI-15 (SO-C101) was administered subcutaneously at 1 mg / kg on days 7, 8, 9, and 10. As a control, saline was administered subcutaneously at 10 μl / g on days 0, 1, 2, and 3. Ten animals were used per group.

[0244] Again, the saline-treated control group showed a sustained increase in tumor volume (black circles on a solid black line, FIG. 11A). In this setting with a late start of treatment on day 7, the RLI-15 monotherapy treatment group showed only a slight decrease in tumor growth (black circles on a dotted black line), whereas both the daratumumab monotherapy (here starting on day 0, open circles on a dotted gray line) and the daratumumab and RLI-15 combination group (gray circles on a solid gray line, run together with the dotted gray line) showed a decrease in tumor volume (see FIG. 11A). No differences were observed in this sequential setting for the treatment groups, daratumumab + RLI-15 vs. daratumumab alone, and both the combination and daratumumab alone led to complete tumor rejection in all test animals around day 28, whereas approximately 25% of mice treated with daratumumab developed tumors again after day 28 (gray dotted line for daratumumab-only treatment vs. gray solid line for combination treatment, see Figure 11B).

[0245] Thus, the reduction in tumor volume induced by the combination of RLI-15 and daratumumab was similar to daratumumab monotherapy alone (A), but the combination treatment led to rapid and durable tumor regression in all treated animals, in contrast to single daratumumab treatment (in which some animals subsequently developed tumors again). Thus, sequential treatment with daratumumab first and RLI-15 starting one week later also led to a significant therapeutic improvement.

[0246] 14. Clinical trial of RLI-15 / SO-C101 in combination with daratumumab Clinical trials are being planned to evaluate the safety and preliminary efficacy of RLI-15 / SO-C101 in combination with daratumumab.

[0247] The initial 8 weeks of treatment. Following the 3-week cycle of SO-C101, SO-C101 is administered subcutaneously on days 1 and 2 (week 1) and days 8 and 9 (week 2) at the established dose from Example 9, followed by one week without treatment with SO-C101. Daratumumab is administered intravenously via infusion at a dose of 16 mg / kg once weekly. Infusions are administered either on day 3 of each week (i.e., days 3, 10, and 17) or on day 1 of each week (i.e., days 1, 8, and 15). Treatment according to this schedule is continued for 8 weeks (i.e., 8 doses of daratumumab), as depicted in Figures 12A (with daratumumab administered on each day 3 of each week) and B (with daratumumab administered on each day 1 of each week).

[0248] Alternatively, following an established 4-week cycle of daratumumab, SO-C101 is administered subcutaneously on days 1 and 2 (week 1) and days 8 and 9 (week 2) at the established dose from Example 9, followed by two weeks without treatment with SO-C101. Daratumumab is administered intravenously via infusion at a dose of 16 mg / kg once weekly. Infusions are administered either on day 3 of each week (i.e., days 3, 10, 17, and 24) or on day 1 of each week (i.e., days 1, 8, 15, and 22). Treatment according to this schedule is continued for 8 weeks (i.e., 8 doses of daratumumab), as depicted in Figure 13A (with daratumumab administered on each day 3 of each week) or B (with daratumumab administered on each day 1 of each week).

[0249] Weeks 9–24 of the procedure. For the following weeks of treatment, SO-C101 will be administered subcutaneously on days 1 and 2 (week 1) and days 8 and 9 (week 2) at the established dose from Example 9, followed by two weeks without treatment with SO-C101. Daratumumab will be administered intravenously via infusion at a dose of 16 mg / kg once a week for two weeks, followed by two weeks without treatment with daratumumab in a four-week cycle. Again, daratumumab will be administered on either day 3 of such week (i.e., days 3 and 10) or day 1 of such week (i.e., days 1 and 8), and this treatment will continue for 16 weeks, i.e., until the end of week 24 of total treatment. This schedule is depicted in Figures 14A (with daratumumab administered on each day 3 of each daratumumab treatment week) and B (with daratumumab administered on each day 1 of each daratumumab treatment week).

[0250] Time to disease progression at 25 weeks Beginning at week 25 of total treatment, daratumumab is only administered intravenously via infusion at a dose of 16 mg / kg once every four weeks on day 3 of such four-week cycle or on day 1 of each four-week cycle, while SO-C101 is additionally administered subcutaneously at the established dose from Example 9 on days 1 and 2 (week 1) and days 8 and 9 (week 2), followed by two weeks of no treatment with SO-C101. This schedule is depicted in Figures 15A (with daratumumab administered on day 3 of each of each daratumumab treatment week) and B (with daratumumab administered on day 1 of each of each daratumumab treatment week).

[0251] According to this example across the three treatment periods above (initial 8 weeks, weeks 9-24, and week 25 until disease progression), the schedule for daratumumab compared to administration of SO-C101 does not change from one period to the other; across all periods, daratumumab is always administered on day 3 of each week, if administered, or on day 1 of each week, if administered.

[0252] 15. A follow-up pharmacokinetic and pharmacodynamic study of RLI-15 administered by subcutaneous route in cynomolgus monkeys The pharmacodynamics of RLI-15 was tested by assessing immune cell profiles following subcutaneous administration in a 10-week follow-up study in cynomolgus monkeys. RLI-15 (SO-C101) was administered at 40 or 80 μg / kg once daily for 1, 1, and 2, and 1, 2, 3, and 4 consecutive days weekly (G3, G7, and G8) or for 2 weeks with a 1-week rest (G1, G2, and G5) or a 2-week rest (G4 and G6), for a total of 10 weeks (FIG. 16). One male and one female mouse was used per group. NK cells and CD8 + Pharmacodynamic activity on T cells was evaluated in all groups on days -4, 5, 12, 19, 26, 33, 40, 47, 54, 61, and 68. Absolute and relative numbers of lymphocyte subsets in the peripheral blood of all animals were determined by flow cytometry. Absolute numbers of lymphocyte subsets were determined using the percentages of cell populations obtained by flow cytometry, which were recalculated relative to hematological leukocyte counts expressed in cells per μl (FIG. 17a, b). Proliferating Ki67 + NK cells and CD8 + The percentage of T cells was assessed by flow cytometry (Fig. 17c, d).

[0253] NK cells and CD8 + Looking at the numbers of T cells (Fig. 17a, b), all treatment schedules led to increased numbers of NK cells. The doses selected were + We chose to observe possible differences between schedules focusing on the levels of T cells. NK cells were CD8 + Similar increases in NK cell numbers in all schedules were therefore expected, as CD8 are approximately one order of magnitude more sensitive to RLI-15 stimulation than T cells. + For T cells, a schedule exploring weekly continuous stimulation (G7 and G8) resulted in minimal CD8 T cell proliferation under continuous treatment. +For example, an equal total dose of RLI-15 (80 μg / kg) per treatment week, dosed over two days for two weeks with a one-week break (G1), either split between two days (G3) or once weekly (G8) for eight weeks, demonstrated T cell proliferation. For both continuous dosing schedules, + While the number of T cells already begins to decline during treatment, the dosing schedule with a one-week treatment break (i.e., also administered less RLI-15 in total) significantly reduced the number of CD8 T cells. + This effect was confirmed by the Ki-67 + CD8 + This becomes even clearer when looking at the % of T cells (Fig. 17c), where G1 clearly outperforms G8 and G3 despite the lower total dose of RLI-15. + Both treatments led to similar high activation of T cells, whereas both treatments also led to activation of CD8 + The percentage of T cells still begins to decrease during the treatment period (G8 and G3).

[0254] In conclusion, treatment interruption is beneficial and the pulse-periodic regimen significantly reduces CD8 + This leads to periodic and high proliferation and activation of T cells. Furthermore, when comparing G8 and G3, which were administered the same amount of RLI-15, the Ki67 + CD8 + The percentage of T cells was significantly higher when the same total dose was divided and administered over two consecutive days (G3) compared to when it was administered all at once on a single day (G1). Thus, the pulse dosing regimen G3 offers a clear advantage over the continuous dosing schedule G8. As noted above, the amount of RLI-15 administered increased the CD8 + Although we chose to focus on T cells and cap to see differences in NK cell responses, we can still observe that NK cell proliferation decreased with sustained treatment with RLI-15 (compare G1 with G8 and G3 in Figures 17a and c).

[0255] Comparing G2 and G6, in which the same total dose of RLI-15 was administered on two consecutive days (80 μg / kg on days 1 and 2, respectively) or split over four consecutive days (40 μg / kg on days 1, 2, 3, and 4, respectively), extending treatment from 2 to 4 days (even at a lower daily dose) significantly increased CD8 + This leads to a stronger picture of T cell numbers, while at the same time lower NK cell numbers become evident (Fig. 17b, compare G2 and G6). However, activated CD8 + T cells (Ki-67 + ), the 2-day treatment schedule appears superior (Figure 17d, G2 and G6).

[0256] 16. Pharmacokinetic and pharmacodynamic study of RLI-15 by subcutaneous route in cynomolgus monkeys with high-intensity dosing The pharmacodynamics of RLI-15 under higher dosing intensities was tested to understand the limits of stimulation by assessing immune cell profiles after subcutaneous administration in cynomolgus monkeys. RLI-15 (SO-C101) was administered at 3 x 7 μg / kg / day (G2) or 3 x 13 μg / kg / day (G3) and compared to 40 μg / kg administered 1 x / day for four consecutive days (G1) (Figure 18). One male and one female mouse was used per group. NK cells and CD8 + Pharmacodynamic activity on T cells was evaluated in all groups on days -4, 3, 5, 9, and 16. The absolute and relative numbers of lymphocyte subsets in the peripheral blood of all animals were determined by flow cytometry and the mean fluorescence intensity (MFI) of selected markers. Absolute numbers of lymphocyte subsets were determined using the percentages of the cell population obtained by flow cytometry and recalculated into hematological leukocyte counts expressed as cells per μl (FIG. 19). Proliferating Ki67 + NK and CD8 + The percentage of T cells was assessed by flow cytometry (Figure 19).

[0257] IL-2Rβ (CD122) expression levels were determined because IL-2 and IL-15 have been reported to induce exhaustion and terminal differentiation under chronic viral exposure (Beltra et al. 2016). Therefore, high CD122 expression levels can be seen as a marker of exhaustion and terminal differentiation. Additionally, CD8 expression levels were determined because low CD8 levels correlate with low sensitivity to antigens and low CD8 expression correlates with a type 2 T cell phenotype, which reduces T cell activity and responsiveness to antigens (Harland et al. 2014).

[0258] The tested high-intensity / high-density dosing schedule, with daily doses split over three doses, resulted in significantly higher NK cell counts and CD8 + Ki67 leads to T cell numbers (Figure 19, left panel). + Looking at the cells, from day 5, NK cells were CD8 + Between days 5 and 9, it becomes apparent that the number of proliferating cells begins to decline for T cells despite further stimulation (FIG. 19, center panel). There is a delay between measurable proliferation and dosing, which is more pronounced for CD8 T cells than for NK cells. + Because stimulation for more than four consecutive days is longer for CD8 T cells, no expansion is observed. + A significant increase in the expression of the exhaustion marker CD122 on T cells was again observed, suggesting that too strong and / or too long exposure to IL-2 / IL-15Rβγ agonists leads to the depletion of immune effector cells, which do not further contribute to the treatment.

[0259] On the other hand, this study demonstrated that short, high-density (i.e., daily dose divided into multiple injections within 1 day, here 3 doses per day) pulses (on several consecutive days, likely up to 4 days) with high doses of RLI-15 / SO-C101 significantly increased the number of NK cells and CD8 + Both T cells and Ki67 + NK cells and CD8 +While it resulted in very high T cell counts, exhaustion markers were not yet increased. High-density pulse-periodic dosing is therefore considered a promising alternative schedule, even in combination with longer treatment breaks / rest periods of several weeks.

[0260] 17. Pharmacokinetic and pharmacodynamic study of RLI-15 by subcutaneous route in cynomolgus monkeys using a high-density pulse cyclic dosing schedule We plan to translate the high-intensity / high-density pulsed cyclic dosing schedule into the clinic and test for single-agent activity because IL-2 / IL-15R agonists with relatively short half-lives, such as RLI-15 / SO-C101, are well suited for a high-density pulsed schedule, even at high doses, to allow for cessation of exposure in the event of safety issues. As previous experiments have shown, the high-intensity / high-density pulsed cyclic dosing schedule results in stronger NK cell and CD8 activation than the pulsed cyclic dosing schedule. + T cell expansion is expected, however, such regimens should have pulse periods with 2, 3, or 4 consecutive days to again avoid immune cell depletion.

[0261] Therefore, further pharmacokinetic and pharmacodynamic studies of RLI-15 by subcutaneous route in cynomolgus monkeys testing high-intensity / high-density pulse cyclic dosing are currently being prepared in a manner similar to Example 16 (see Figure 20) using the following dosing groups G1-G6:

[0262] G1 and G2 are groups that last for 12 weeks (study weeks 1 to 12, W1 to W12). G3 to G6 are groups that last for 10 weeks (W1 to W10).

[0263] As outlined in Figure 20, G1 and G2 were administered for three consecutive days, repeated once, followed by a three-week break, without further treatment for the remaining 14 days, while the daily dose of approximately 40 μg / kg RLI-15 was divided into three doses of 13 μg / kg in G1 and two doses of 20 μg / kg in G2.

[0264] G3 begins with pretreatment of 3 consecutive days of administration with no further treatment for the remainder of the week, followed by 2 weeks of treatment rest, followed by 3 consecutive days of administration with no further treatment for the remainder of the week, repeated once, followed by 1 week of treatment rest; the 40 μg / kg daily dose is split into two doses of 20 μg / kg.

[0265] G4, G5, and G6 are administered for two consecutive days without treatment for the remainder of the week, repeated once, followed by a one-week break; for G4, a daily dose of approximately 40 μg / kg of RLI-15 is divided into three doses of 13 μg / kg, and for G5, 40 μg / kg of RLI-15 is divided into two doses of 20 μg / kg; both G4 and G5 are scheduled to have treatment on days 1 and 2, without treatment for the remainder of the week, repeated once, followed by a one-week break from treatment. G6 is identical to G5, with the only difference being that the initial daily dose of 40 μg / kg RLI-15 (again, divided into two doses of 20 μg / kg) is increased by 50% after the first cycle (two doses administered on consecutive days per week, repeated once, with a one-week treatment break) to a daily dose of 60 μg / kg RLI-15 (divided into two doses of 30 μg / kg) administered on two consecutive days per week, repeated once, with a one-week treatment break.

[0266] Preferably high doses of IL-2 / IL-15Rβγ agonists (e.g., RLI-15 / SO-C101) over 2, 3, or 4 consecutive day pulses, followed by rest periods continuing such cycles for several weeks, result in significant CD8 (in addition to the more responsive effector cells, NK cells) expression. +It is envisioned that this could translate into T cell proliferation and activation, which may even translate into the strong single-agent activity of such agonists, as has been observed with IL-2 but not with long-acting IL-2 variants due to the avoidance of overstimulation and depletion of effector cells. Additionally, where safety issues are more likely with high doses of IL-2 / IL-15Rβ agonists, such complications may be more easily managed given the short half-life of the agonists of the present invention, since treatment can be discontinued with only a short delay before withdrawal of the drug becomes effective.

[0267] literature [Table 12] TIFF0007762570000026.tif238161 TIFF0007762570000027.tif242161 TIFF0007762570000028.tif245161 TIFF0007762570000029.tif149161

[0268] Embodiments of the present invention 1. An interleukin-2 / interleukin-15 receptor beta gamma (IL-2 / IL-15Rβγ) agonist for use in the treatment or management of cancer or an infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist to a human patient using a cyclic dosing regimen, wherein the cyclic dosing regimen comprises: (a) a first period of x days during which an IL-2 / IL-15Rβγ agonist is administered in a daily dose for y consecutive days at the beginning of the first period, followed by xy days without administration of the IL-2 / IL-15Rβγ agonist; where x is 5, 6, 7, 8, or 9 days and y is 2, 3, or 4 days; (b) repeating the first period at least once; and (c) a second period of z days without administration of an IL-2 / IL-15Rβγ agonist, where z is 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 days. 2. The IL-2 / IL-15Rβγ agonist for use according to embodiment 1, wherein x is 6, 7, or 8 days, preferably 7 days. 3. The IL-2 / IL-15Rβγ agonist for use according to embodiment 1 or 2, wherein y is 2 or 3 days, preferably 2 days. 4. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 3, wherein z is 7 days. 5. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 4, wherein x is 7 days, y is 2 days, and z is 7 days. 6. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 5, wherein the daily dose is 0.1 to 50 μg / kg, preferably 0.25 to 25 μg / kg, more preferably 0.6 to 10 μg / kg and in particular 2 to 10 μg / kg. 7. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 6, wherein the IL-2 / IL-15Rβγ agonist is administered subcutaneously (sc) or intraperitoneally (ip), preferably subcutaneously. 8. The administration of an IL-2 / IL-15Rβγ agonist in step (a) significantly reduces Ki-67 in total NK cells compared to the administration of no IL-2 / IL-15Rβγ agonist. + and the administration of the IL-2 / IL-15Rβγ agonist in step (b) increases the percentage of Ki-67 in step (a). + At least 70% of NK cells have Ki-67 + 8. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 7, which results in NK cell levels. 9. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 8, wherein administration of the IL-2 / IL-15Rβγ agonist results in the maintenance of NK cell numbers or preferably an increase in NK cell numbers to at least 110% compared to no administration of the IL-2 / IL-15Rβγ agonist after at least one repetition of the first period, preferably after at least two repetitions of the first period. 10. The IL-2 / IL-15Rβγ agonist administration is at least 1.1 × 10 after at least one repetition of the first period, preferably at least two repetitions of the first period. 3 10. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 9, resulting in an NK cell count of NK cells / μl. 11. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 10, wherein the periodic administration is repeated for at least 3 cycles, preferably 5 cycles, more preferably at least 10 cycles, and even more preferably until disease progression. 12. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 11, wherein the daily dose selected within the dose range of 0.1 to 50 μg / kg does not increase substantially during the dosing regimen, preferably the dose is maintained during the dosing regimen. 13. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 12, wherein the cancer is a blood cancer or a solid cancer. 14. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 13, wherein the IL-2 / IL-15Rβγ agonist has an in vivo half-life of 30 minutes to 24 hours, preferably 1 hour to 12 hours, more preferably 2 hours to 6 hours. 15. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 14, wherein the IL-2 / IL-15Rβγ agonist is at least 70% monomeric, preferably at least 80% monomeric. 16. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 15, wherein the IL-2 / IL-15Rβγ agonist is an interleukin-15 (IL-15) / interleukin-15 receptor alpha (IL-15Rα) complex. 17. The IL-2 / IL-15Rβγ agonist for use according to embodiment 16, wherein the IL-15 / IL-15Rα complex is a fusion protein comprising a human IL-15Rα sushi domain or a derivative thereof, a flexible linker and human IL-15 or a derivative thereof, preferably wherein the human IL-15Rα sushi domain comprises the sequence of SEQ ID NO: 6 and the human IL-15 comprises the sequence of SEQ ID NO: 4. 18. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 17, wherein the IL-15 / IL-15Rα complex is SEQ ID NO: 9. 19. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 1 to 18, wherein the checkpoint inhibitor is administered at the start of the first period (a) of each cycle. 20. The IL-2 / IL-15Rβγ agonist for use according to embodiment 19, wherein the checkpoint inhibitor is an anti-PD-1 antibody, anti-PD-L1 antibody, anti-PD-L2 antibody, anti-LAG-3 antibody, anti-TIM-3 antibody, or anti-CTLA4 antibody, preferably an anti-PD-L1 antibody or an anti-PD-1 antibody. 21. An IL-2 / IL-15Rβγ agonist for use in the treatment or management of cancer or an infectious disease, comprising administering the IL-2 / IL-15Rβγ agonist according to the following administration regime: (i) administering to a human patient a daily dose of an IL-2 / IL-15Rβγ agonist on a first number of consecutive days; and (ii) no administration of IL-2 / IL-15Rβγ agonists for a number of days; where the first number is 2, 3, or 4 days and the second number is 3, 4, or 5 days. 22. The IL-2 / IL-15Rβγ agonist for use according to embodiment 21, wherein the administration regime is repeated at least once, preferably at least twice, more preferably at least four times, and most preferably until disease progression. 23. The IL-2 / IL-15Rβγ agonist for use according to embodiment 21, wherein the first period of time is 2 days and the second period of time is 5 days. 24. The IL-2 / IL-15Rβγ agonist for use according to embodiment 21 or 23, wherein the daily dose is 0.1 to 50 μg / kg. 25. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 24, wherein the dose of 0.1 to 50 μg / kg is not substantially increased during the dosing regimen, and preferably the dose is maintained during the dosing regimen. 26. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 25, wherein the dose is 1 to 30 μg / kg, preferably 2 to 20 μg / kg, most preferably 2 to 10 μg / kg of the IL-2 / IL-15Rβγ agonist. 27. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 26, wherein the IL-2 / IL-15Rβγ agonist is preferably administered subcutaneously (sc) or intraperitoneally (ip). 28. The administration of an IL-2 / IL-15Rβγ agonist in step (i) reduces Ki-67 in total NK cells compared to when an IL-2 / IL-15Rβγ agonist is not administered. + and administration of the IL-2 / IL-15Rβγ agonist after the first repetition results in an increase in the % of NK, Ki-67 of step (i). + At least 70% of NK cells have Ki-67 + 28. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 22 to 27, which results in NK cell levels. 29. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 22 to 28, wherein administration of the IL-2 / IL-15Rβγ agonist results in the maintenance of NK cell numbers, or preferably an increase in NK cell numbers to at least 110%, compared to no administration of the IL-2 / IL-15Rβγ agonist, after at least one repetition of period (i), preferably after at least two repetitions of period (i). 30. The administration of the IL-2 / IL-15Rβγ agonist is at least 1.1 × 10 after at least one repetition of period (i), preferably at least two repetitions of the first period. 3 30. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 22 to 29, resulting in an NK cell count of NK cells / μl. 31. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 30, wherein the cancer is a blood cancer or a solid cancer. 32. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 31, wherein the IL-2 / IL-15Rβγ agonist has an in vivo half-life of 30 minutes to 24 hours, preferably 1 hour to 12 hours, more preferably 2 hours to 6 hours. 33. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 32, wherein the IL-2 / IL-15Rβγ agonist is at least 70% monomeric. 34. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 33, wherein the IL-2 / IL-15Rβγ agonist is the IL-15 / interleukin-15 receptor alpha (IL-15Rα) complex. 35. An IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 34, wherein the IL-15 / IL-15Rα complex is an induced protein comprising the human IL-15Rα sushi domain or a derivative thereof, a flexible linker and a derivative thereof, preferably wherein the human IL-15Rα sushi domain comprises the sequence of SEQ ID NO: 6 and the human IL-15 comprises the sequence of SEQ ID NO: 4. 36. The IL-2 / IL-15Rβγ agonist for use according to any of embodiments 21 to 35, wherein the IL-15 / IL-15Rα complex is SEQ ID NO: 9. 37. A kit comprising an IL-2 / IL-15Rβγ agonist according to any one of embodiments 1 to 36, instructions for use of the IL-2 / IL-15Rβγ agonist in a cyclical dosing regime according to any one of embodiments 1 to 20 or in a dosing regime according to any one of embodiments 21 to 36, and optionally a dosing device for the IL-2 / IL-15Rβγ agonist. 38. The kit of embodiment 37, further comprising a checkpoint inhibitor and instructions for use of the checkpoint inhibitor.

Claims

1. 1. A pharmaceutical composition for use in the treatment or management of cancer or an infectious disease comprising an interleukin-15 receptor beta gamma (IL-15Rβγ) agonist, wherein the IL-15Rβγ agonist is administered to a human patient using a cyclical dosing regimen comprising: (a) a first period of x days, during which an IL-15Rβγ agonist is administered in a daily dose for y consecutive days at the start of the first period, followed by x-y days without administration of the IL-15Rβγ agonist; where x is 7 or 14 days and y is 2 or 3 days; (b) repeating the first period of time at least once; and (c) a second period of z days without administration of an IL-15Rβγ agonist, where z is 7 or 14 days; Including, Here, the IL-15Rβγ agonist is one of the following: A human IL-15Rα sushi domain having the amino acid sequence shown in SEQ ID NO: 6 or the amino acid sequence shown in SEQ ID NO: 7, and Human IL-15 having the amino acid sequence set forth in SEQ ID NO: 4, or having at least 96% identity to the amino acid sequence set forth in SEQ ID NO: 4, and L45, S51 and L52 substituted by D, E, K or R; E64, I68, L69 and N65 substituted by D, E, R or K, N71 substituted by S or A N72 substituted by S or A N77 substituted by Q, S, K, A or E N78 substituted by S, A or G, and Q108E and derivatives thereof, comprising an amino acid sequence containing one or more mutations selected from the group consisting of:

1. A pharmaceutical composition comprising an interleukin-15 (IL-15) / interleukin-15 receptor alpha (IL-15Rα) complex.

2. 10. The pharmaceutical composition of claim 1, wherein the periodic administration is repeated for at least three cycles.

3. The daily dose is (i) 0.1 μg / kg to 50 μg / kg; or (ii) a body weight-independent fixed dose of 7 μg to 3500 μg; The pharmaceutical composition according to claim 1 or 2.

4. The daily dose is (i) during a dosing regimen; or (ii) Once after the first period on x days Increased The pharmaceutical composition according to any one of claims 1 to 3.

5. The daily dose is (i) administered in a single injection; (ii) divided into two or three individual doses administered within a day, with the time interval between administration of the individual doses being at least four hours; (iii) divided into three individual doses administered within a day, with the time interval between administration of the individual doses being 5 to 7 hours; or (iv) divided into two individual doses administered within one day, the time interval between administration of the individual doses being 6 to 10 hours; The pharmaceutical composition according to any one of claims 1 to 4.

6. The pharmaceutical composition of any one of claims 1 to 5, wherein the IL-15Rβγ agonist has an in vivo half-life of 30 minutes to 24 hours.

7. The administration of the IL-15Rβγ agonist in step (a) (1) Ki-67 in total NK cells compared with no administration of IL-15Rβγ agonist ＋ and the administration of the IL-15Rβγ agonist in step (b) results in an increase in the percentage of NK cells in the patient treated with the IL-15Rβγ agonist. ＋ Ki-67 in at least 70% of NK cells ＋ Elevating NK cell levels (2) after at least one repetition of the first period, results in the maintenance of NK cell numbers compared to administration of the IL-15Rβγ agonist without administration; and / or (3) at least 1.1 x 10 after at least one repetition of the first period ３ resulting in an NK cell count of NK cells / μl, The pharmaceutical composition according to any one of claims 1 to 6.

8. an additional therapeutic agent is administered in combination with the IL-15Rβγ agonist; The pharmaceutical composition according to any one of claims 1 to 7.

9. the additional therapeutic agent is (i) a checkpoint inhibitor; or (ii) therapeutic antibodies; Selected from: The pharmaceutical composition according to claim 8.

10. x days + z days is an integer multiple equal to the number of days in one treatment cycle of a checkpoint inhibitor or therapeutic antibody, or If the treatment cycles of checkpoint inhibitors or therapeutic antibodies vary over time, the treatment cycles are equal to each individual treatment cycle of checkpoint inhibitors or therapeutic antibodies. The pharmaceutical composition according to claim 9, wherein day x and day z are adapted so that

11. The pharmaceutical composition according to claim 9 or 10, wherein the checkpoint inhibitor is selected from an anti-PD-1 antibody, an anti-PD-L1 antibody, an anti-PD-L2 antibody, an anti-LAG-3 antibody, an anti-TIM-3 antibody, an anti-CTLA4 antibody, or an anti-TIGIT antibody.

12. The pharmaceutical composition according to claim 9 or 10, wherein the therapeutic antibody is selected from an anti-CD38 antibody, an anti-CD19 antibody, an anti-CD20 antibody, an anti-CD30 antibody, an anti-CD33 antibody, an anti-CD52 antibody, an anti-CD79B antibody, an anti-EGFR antibody, an anti-HER2 antibody, an anti-VEGFR2 antibody, an anti-GD2 antibody, an anti-Nectin-4 antibody, and an anti-Trop-2 antibody.

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