Methods for Treating Myopia with Vinpocetine

Abstract

The present application relates to a method for treating myopia using vinpocetine, which can not only effectively prevent myopia and / or control the progression of myopia, but also is safe and has no obvious side effects, and is expected to be of good clinical use.

Description

[Technical field]

[0001] The present application belongs to the field of medicine and relates to a method for treating myopia with vinpocetine, in particular to the method and use for controlling the progression of myopia, and provides corresponding drugs or preparations. [Background technology]

[0002] Myopia is the most common refractive error, and refers to a refractive state in which parallel light rays are refracted by the refractive system of the eye when adjusted to a relaxed state, and the focal point is located in front of the retina. In the case of myopia, distant objects appear blurred, which causes many inconveniences in life. Although corrective measures such as frame glasses can improve the distant vision of myopic patients, such techniques or methods cannot improve the social phenomenon of a high myopia rate and an increasing degree of myopia. Therefore, the number of myopic people worldwide is increasing year by year, and the situation of severe myopic patients, especially in East Asian countries, is not optimistic. Meanwhile, there are many types of myopia and its etiology is still unknown, and currently there is still a lack of drugs that have significant therapeutic effects and are safe to treat myopia, especially to control the progression of myopia. Therefore, the clinical needs for this disease have not yet been met.

[0003] Vinpocetine has the chemical formula C 22 H 26 It is N2O2, an average molecular weight of 350.46, a white crystalline powder, soluble in chloroform or 96% ethanol, but practically insoluble in water, and derived from an indole alkaloid extracted from the plant Vinca punctata. Its structure is: [ka] (I)

[0004] It has been found that the solubility of vinpocetine in water is acidic pH-dependent, it is more soluble in the gastric environment pH (1.2) and intestinal environment pH (6.8), and it has higher biological activity than vincamine, and has less toxicity and side effects. Vinpocetine is highly lipid-soluble, and the compound can enter the blood-brain barrier, blood-retinal barrier, placenta and milk, and has high pharmacological activity on the function of the blood vessels of the heart and brain and the central nervous system.

[0005] Currently, vinpocetine is mainly used to treat cerebrovascular-related diseases and cognitive disorders, and the target population is mostly elderly people. When administered systemically, it has been reported that vinpocetine can selectively act on the cerebrovascular system to suppress phosphodiesterase activity in the brain (i.e., as a phosphodiesterase inhibitor), relax vascular smooth muscle, and increase blood supply to the brain. Such drugs have characteristics such as rapid metabolism in the body, short half-life, and low bioavailability in oral dosage forms in humans. When administered externally, vinpocetine can easily pass through physical barriers such as the cornea and crystalline lens, so vinpocetine is also an auxiliary ingredient in many ophthalmic drugs, and is mainly used as a microcirculatory promoter to promote blood circulation in the eye. Promoting blood circulation in the eye makes the eye more comfortable and improves the vision of patients with refractive errors, but this is not the same as treating myopia, and it has been reported that administration of vinpocetine may actually cause myopia (biosintez.com / en / catalog / product / 283). Summary of the Invention

[0006] The present application unexpectedly finds a new use of vinpocetine, and through repeated testing, it has been proven that vinpocetine can treat myopia and control the progression of myopia. That is, vinpocetine is used as a direct active ingredient to treat myopia, rather than as a supplement or auxiliary ingredient, for example, as a microcirculation promoter (inhibition of phosphodiesterase activity), or as an auxiliary, accompanying or assisting agent for other myopia treatment active substances in myopia treatment drugs to improve the myopia treatment effect of the active substances (for example, allowing more of the drug main ingredient to reach the target cells where it exerts its effect).

[0007] The present application also studies the mechanism of myopia treatment by vinpocetine. Until the present application, vinpocetine has been used as a phosphodiesterase inhibitor to improve blood flow, but the present application has conducted experiments and found that when vinpocetine is used to treat myopia and control the progression of myopia, it does not depend on the improvement of choroidal blood flow. In other words, vinpocetine may not treat myopia and inhibit the progression of myopia by dilating blood vessels or promoting blood circulation (i.e., the known functions of phosphodiesterase inhibitors), but may rely more on its unique but yet unknown novel pharmacological action. Therefore, the present application actually utilizes the unknown function of vinpocetine, and this discovery is also an important basis for forming the present application.

[0008] This application proves for the first time that vinpocetine alone has a significant inhibitory effect on the progression of myopia, and thus confirms that vinpocetine can effectively treat various myopia, including simple myopia or axial myopia (e.g., juvenile myopia), mild or moderate myopia, etc. Compared with the use of vinpocetine to treat elderly myopia, high myopia, high elderly myopia, or pathological myopia, the effect is significantly better when vinpocetine is used to treat myopia with a persistent decrease in refractive power (e.g., simple myopia, axial myopia, axial simple myopia, low and moderate myopia, pediatric and juvenile myopia, or progressive myopia, etc.).

[0009] Vinpocetine can also be used to prevent various types of myopia. For example, drug intervention using vinpocetine during the progression of myopia can prevent and inhibit the occurrence of elderly myopia, high myopia, elderly high myopia, and pathological myopia.

[0010] The present application further studies the concentration, ratio, and composition of vinpocetine in drugs or preparations for treating myopia, as well as administration methods such as administration frequency and concomitant treatment of related drugs, etc. Among them, local (ocular) administration is not only safe, but also has a therapeutic effect that is significantly superior to that of systemic administration.

[0011] The present application provides a use of vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances, said use comprising: (1) Preventing and / or treating myopia and its associated symptoms and / or correcting myopia; or (2) Suppressing (controlling) the progression of myopia, or (3) For use in preventing or controlling myopia or in delaying the onset or progression of myopia (eye); or (4) inhibiting or slowing the increase in axial elongation and / or the length (depth) of the vitreous chamber of the eye in individuals who are myopic or prone to developing myopia; or (5) Preventing, retarding, mitigating, or treating abnormal eye development associated with vision impairment; or (6) The individual achieves clearer distance vision without the need to wear eyeglasses (e.g., framed eyeglasses or orthokeratology lenses) or resort to vision correction procedures (e.g., refractive surgery) than was present prior to use of the substance or procedure and / or without the use of the substance or procedure; or (7) Inhibiting, postponing, or slowing the process or rate of negative refractive power in an individual who is myopic or prone to developing myopia; or (8) To be used for producing a drug, a formulation, a composition, or a device for realizing at least one of the uses (1) to (7) described above; Any one of the above or two or more of the above at the same time.

[0012] In some embodiments, the methods of administration are systemic (e.g., oral, intravenous), and / or local (eye drops, intraocular injection, intraocular implants, periocular application of skin ointment / emulsion or ophthalmic ointment), and / or parenteral (e.g., transmucosal, transdermal, microneedle), and / or non-invasive (e.g., using eye sprays) administration.

[0013] In some embodiments, the drug, formulation or composition may be an injection, tablet, lyophilized powder for injection, capsule, effervescent tablet, chewable tablet, orally disintegrating tablet, granule, ointment, syrup, oral liquid, aerosol, nasal drop, topical preparation, oral preparation, etc., and is preferably an ophthalmic dosage form, including, but not limited to, eye drops, eye ointment, spray eye drops, implant, eye gel, eye pad, ophthalmic microsphere, ophthalmic sustained release preparation, periocular injection, intraocular injection, The group may also include free solutions, oil-water mixtures, suspensions, ointments, detergents, lotions, drops, powders, sprays, plasters, patches, pastes, pills, suppositories, and emulsions prepared by containing cellulose (e.g., methylcellulose), polyhydric alcohols, cyclodextrins (e.g., hydroxypropyl-β-cyclodextrin), acidic cosolvents (e.g., citric acid), dendrimers, nanomaterials, sustained-release materials, liposomes, or combinations thereof.

[0014] In some embodiments, the myopic individuals or individuals prone to developing myopia are children and / or adolescents, preferably the 3-26 year old population, more preferably the 6-18 year old population, or minors, preferably a population where the eye is still growing and developing, or a school-age population, preferably a population of 1st to 12th graders, or a population with parents who are highly myopic, or individuals with insufficient hyperopic reserve.

[0015] In some embodiments, myopia is classified as refractive or axial myopia, congenital myopia (myopia from birth or before school age), early onset myopia (before age 14), late onset myopia (ages 16-18), late onset myopia (after adulthood), low myopia (mild myopia), moderate myopia, high myopia (high myopia), pseudomyopia, true myopia, pediatric and / or juvenile myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), minor myopia, Myopia, adult myopia, geriatric myopia, simple myopia, pathological myopia, simple axial myopia, simple axial myopia, paediatric and / or adolescent axial myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), axial myopia in school and pre-school age population, primary myopia, secondary myopia, paediatric and / or adolescent primary myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), or paediatric and / or adolescent axial myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years). The present invention relates to progressive myopia in young people (preferably in the age group of 3-26 years old, more preferably in the age group of 6-18 years old), curvature myopia, exponential myopia, astigmatic myopia, positional myopia, curvature myopia, axial myopia in which the refraction is continuously negative, myopia caused by using the eyes at close distances for a long time, myopia and pseudomyopia caused by eye strain, negative refraction caused by adverse drug reactions, myopic eyes, myopia caused by reading, myopia caused by using electronic products such as mobile phones, etc. Myopia caused by eye strain, myopia caused by incompatibility of the refractive medium (components), refractive myopia, myopia caused by developmental abnormalities in the refractive system, myopia caused by excessive growth of the eyeball, myopia caused by unhygienic eye use, myopia in which the imaging focus of distant objects is located in front of the retina due to various causes, myopia in which atropine is poorly or ineffective for treatment, myopia caused by lack of outdoor exercise, accommodative myopia, childhood myopia, infantile myopia, hereditary myopia, and myopia caused by environmental factors.

[0016] In some embodiments, myopia-related symptoms include complications resulting from myopia, such as complications of high myopia, such as floaters, glaucoma, posterior staphyloma, retinal detachment, retinal breaks, amblyopia, macular hemorrhage, choroidal neovascularization, choroidal atrophy, macular degeneration or maculopathy, visual field defects, progressive or sudden decrease in visual acuity (especially near vision), swelling and / or pain in the eye, night blindness, astigmatism, anisometropia, blindness, vitreous liquefaction, vitreous opacification, strabismus, frequent blinking, frequent eye rubbing, anisometropia, blurred vision when looking at distant objects, need to squint or partially close eyelids to see distant objects clearly, headaches due to eye strain, distractibility due to myopia, difficulty seeing when driving, especially at night (nocturnal myopia), retinal atrophy and degeneration (bleeds and breaks), subretinal neovascularization, or ocular atrophy.

[0017] In some embodiments, the drug, formulation, composition or device further comprises another drug or ophthalmic formulation, which may be a drug for treating myopia (e.g., pirenzepine, muscarinic antagonists, methocarbamol (Robaxin), indoramine, timolol maleate, adrenaline, pyrazine, perlapine, methylamine, chlorisondamine, acetylcholinesterase inhibitors, dopamine agonists, gamma-aminobutyric acid, naloxone, glucagon, tretinoin, salidroside, formononetin, etc.), M receptor blockers (e.g., blockers or antagonists or inhibitors for M2 or M3 receptors), bendazac and its various salt forms (bendazac L-lysine), atropine, bendazol, polyunsaturated fatty acids (e.g., DHA, EPA), prazosin, homatropine, raceanisodamine, tropic ... do, 7-methylxanthine, nicotinic acid, piracetam, danshen extract, safflower extract, fish oil, yutan extract, vitamins, adenosine triphosphate (ATP), smooth muscle relaxant, vasospasm prevention agent, non-selective adenosine antagonist, vasodilator, pupil dilating component, congestion relief component, eye muscle (e.g. ciliary muscle) regulating component, anti-inflammatory component, astringent component, antihistamine component, anti-allergic component, collagen decomposition inhibitor component, These include, but are not limited to, hepatoprotective components (avoiding or attenuating liver toxicity), blood-retinal barrier strengthening components (making it more difficult for a compound to penetrate the physiological barrier), amino acids, antibacterial components, antioxidant components, carbohydrates, polymers or derivatives thereof, cellulose or derivatives thereof, local anesthetic components, components for treating amblyopia, components for treating glaucoma, components for treating cataracts, phosphodiesterase I inhibitors (specific or non-specific), miRNA and modifications thereof, components for treating ophthalmic diseases, additives, and the like.

[0018] In some embodiments, vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances and one or more myopia prevention and control agents and / or myopia treatment agents are formulated or designed for sequential administration, or for simultaneous administration, or for sequential administration, or for alternating administration, or for interval administration, or for single administration.

[0019] In some embodiments, the vinpocetine-related compound or extract is a metabolite of vinpocetine (e.g., apovincaminic acid, hydroxyvinpocetine, hydroxyl-apovincaminic acid, and dihydroxy-vinpocetine-glycinate), a vinca alkaloid, apovincamine, periwinkle extract, vincamine, voacanga africana extract, apocynaceae plant extract, vincristine, tabersonine, vinblastine, vindoline, apovincaminic acid hydrochloride ... Hydrochloride, catharanthine, ethyl vincaminate, methoxyvinpocetine, and dihydrovinpocetine.

[0020] In some embodiments, the formulation is an oral product such as a health food, food, dietary supplement, nutritional food, drink, or cosmetic. The cosmetic may be one or more combinations of a free solution, an oil-water mixture, a suspension, an ointment, a detergent, a spray, a lotion, a drop, a powder, an ointment, a paste, a pill, a suppository, an emulsion, and a patch.

[0021] In some embodiments, the apparatus may be an instrument, device, consumable, system, medical device, health product or product that alters the appearance of the eye that can release a drug or has a drug delivery function or potential drug delivery capability, such as a corneal contact lens, eyeglasses, intraocular lens, suture, orthokeratology lens cleaning (maintenance) system, eye pad, eye patch for improving eye function, colored contact lens, microneedle, eye spray system, eye massager, eye fumigation device, ocular surface drug delivery device, intraocular drug delivery device, fundus drug delivery device, implantable pump, wearable device, acupoint massager, eye relaxation device, myopia treatment device or a drug and device combination for preventing and controlling myopia.

[0022] In some embodiments, vinpocetine, or an optical isomer thereof or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances is used as the sole active ingredient, or the main active ingredient, or the direct active ingredient, or the content or efficacy of vinpocetine, or an optical isomer thereof or a racemate thereof, or a solvate thereof, or a pharma-ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances, accounts for 1% or less, or 1% or more, 10% or more, 20% or more, 30% or more, 40% or more, or 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, or 100% of the total active ingredients in the use, and the percentage (%) may be a mass ratio, a molar ratio, or a potency ratio.

[0023] In some embodiments, the concentration of vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances in the drug, formulation, composition, or device is 0.001 μM to 10 mM, preferably 0.01 to 1000 μM, preferably 0.05 to 100 μM, more preferably 0.1 to 25 μM, more preferably 0.1 to 15 μM, or the concentration or proportion of the substance or combination thereof in the drug, formulation, composition, or device is less than 25%, preferably less than 5%, preferably less than 1%, more preferably less than 0.01%, more preferably less than 0.001%, and the percentage (%) may be a mass / volume concentration (g / 100 mL) or a mass percentage or a molar (number) ratio.

[0024] The present application provides a drug, formulation, composition, or device to be administered to the eye, wherein the concentration of vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances, in the drug, formulation, composition, or device is 0.001 μM to 10 mM, preferably 0.01 to 1000 μM, and preferably 0.05 to 100 μM. and more preferably 0.1-25 μM, and more preferably 0.1-15 μM; or the concentration or proportion of said substances or combinations thereof in said drug, formulation, composition or device is less than 25%, preferably less than 5%, preferably less than 1%, more preferably less than 0.01%, and more preferably less than 0.001%, and said percentage (%) may be a mass / volume concentration (g / 100 mL) or a mass percentage or a molar (number) ratio.

[0025] The present application also provides a pharmaceutical composition or combination preparation comprising at least two active substances, including vinpocetine, or its optical isomer or its racemate, or its solvate, or its pharmaceutically acceptable salt, or its prodrug, or its metabolite, or its related compound or extract, or its crystalline compound, or a combination of these substances and another myopia treatment active substance.Preferably, the dosage, concentration and / or efficacy of vinpocetine, or its optical isomer or its racemate, or its solvate, or its pharmaceutically acceptable salt, or its prodrug, or its metabolite, or its related compound or extract, or its crystalline compound, or a combination of these substances is not less than that of any other myopia treatment active substance, said efficacy being for the treatment of myopia or the control of the progression of myopia.

[0026] The present application also provides a pharmaceutical composition or combination formulation comprising vinpocetine, or an optical isomer thereof or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances and another active substance for treating myopia, wherein said other active substance for treating myopia does not include a long-acting beta-adrenergic receptor agonist, a long-acting muscarinic antagonist and / or a muscarinic antagonist.

[0027] The present application further provides an ophthalmic formulation or medicament in which vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances is used as the direct, sole or primary active ingredient.

[0028] In some embodiments, the formulation or drug includes, but is not limited to, eye drops (eye drops), eye ointments, eye sprays, implants, eye gels, eye pads, ophthalmic microspheres, ophthalmic sustained release formulations, periocular injections, or intraocular injections.

[0029] In some embodiments, the concentration of vinpocetine, or an optical isomer thereof or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances is 0.001 μM to 10 mM, preferably 0.01 to 1000 μM, preferably 0.05 to 100 μM, more preferably 0.1 to 25 μM, more preferably 0.1 to 15 μM, or the concentration or proportion of vinpocetine is less than 25%, preferably less than 5%, preferably less than 1%, more preferably less than 0.01%, more preferably less than 0.001%, and the percentage (%) may be a mass / volume concentration (g / 100 mL) or a mass percentage or a molar (number) ratio.

[0030] In some embodiments, the phosphodiesterase I inhibitor is selected from the group consisting of PDE1-IN-2, LY1 (Sherif Khedr et al.,Selective Phosphodiesterase 1 Inhibitor LY1 Reduces Blood Pressure in Spontaneously Hypertensive and Dahl Salt Sensitive Rats,The FASEB Journal,2020 April 1,Volume34,IssueS1,Pages1-1.), Lu AF41228, Lu AF58027 (Morten Laursen et al.,Novel selective PDE type 1 inhibitors cause vasodilatation and lower blood pressure in rats,Br J Pharmacol,2017 Aug;174(15):2563-2575.), BTTQ (Asim B Dey et al.,Elective Phosphodiesterase 1 Inhibitor BTTQ Reduces Blood Pressure in Spontaneously Hypertensive and Dahl Salt Sensitive Rats:Role of Peripheral Vasodilation,Front Physiol,2020 Sep 8;11:543727.), Nimodipine, Zaprinast, Caffeine, Deprenyl, Amantadine (Alexandre E Medina,Therapeutic utility of phosphodiesterase type I inhibitors in neurological conditions,Front Neurosci,.2011 Feb 18;5:21.), KS505a, bepridil, flunarizine, amiodarone, zaprinast, 8-methoxymethyl IPMX, SCH 51866, nimodipine, IC224 (Claire Lugnier,Cyclic nucleotide phosphodiesterase (PDE) superfamily: a new target for the development of specific therapeutic agents,Pharmacol Ther,2006 Mar;109(3):366-98.), ITI-214 (Peng Li et al.,Discovery of Potent and Selective Inhibitors of Phosphodiesterase 1 for the Treatment of Cognitive Impairment Associated with Neurodegenerative and Neuropsychiatric Diseases,J Med Chem,2016 Feb 11;59(3):1149-64.), etc. Vinpocetine belongs to the class of phosphodiesterase I inhibitors (PDE1 inhibitors), and other phosphodiesterase I inhibitors (whether specific or not) known prior to the filing date may have the same unknown activity or efficacy as vinpocetine, for example, to prevent and / or treat myopia and control the progression of myopia.

[0031] In some embodiments, the miRNA and modifications thereof are MicroRNA-328 or MicroRNA-328 negative sense compositions.

[0032] In some embodiments, a combination of two or more of vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, is administered over the same period of time, e.g., simultaneously or sequentially in a single particular course of treatment, administered on the same day, administered in the same week, administered in the same month, administered in the same year, or staggered at intervals, e.g., 4 hour intervals, 12 hour intervals, alternating every other day, every other week, every other month, every other year, or Vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances and one or more other drugs are administered over the same period of time, e.g., simultaneously or sequentially in a single particular course of treatment, on the same day, in the same week, in the same month, in the same year, or in alternating intervals, e.g., alternating at 4 hour intervals, alternating at 12 hour intervals, alternating every other day, every other week, every other month, every other year, or Vinpocetine, or an optical isomer thereof or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances, is used in combination with a device (e.g., a corneal contact lens) and / or surgery (e.g., refractive surgery, myopic laser corneal surgery, lens surgery).

[0033] In some embodiments, the one or more other drugs are myopia prevention / control drugs and / or drugs for treating myopia (e.g., bendazac L-lysine, atropine, bendazole, polyunsaturated fatty acids, DHA, fish oil, prazosin, M receptor blockers, nicotinic acid, pirenzepine, muscarinic antagonists, 7-methylxanthine (7MX), methocarbamol (Robaxin), indoramine, timolol maleate, adrenaline, pyrazine, perlapine, methylamine, chlorisondamine, acetylcholine ... alcholinesterase inhibitors, dopamine agonists, gamma-aminobutyric acid, naloxone, glucagon, tretinoin, salidroside, formononetin, etc.), vasodilators, smooth muscle relaxants, vasospasm prevention drugs, collagen metabolism regulators, piracetam, antiallergic drugs, hepatoprotectants, vinpocetine, or an optical isomer or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination thereof.

[0034] In some embodiments, the apparatus is an instrument, device, consumable, medical equipment or health product having a vision protection function or a myopia treatment (correction) effect, such as various glasses that postpone the progression of myopia, orthokeratology lenses, frame glasses, eye pads, (myopia) acupressure massagers, eye relaxation devices, myopia treatment equipment, etc.

[0035] In some embodiments, the drug, one or more other drugs, myopia prevention / control drugs, myopia treatment drugs, or ophthalmic preparations may not be long-acting β-adrenoceptor agonists (LABAs), long-acting muscarinic antagonists (LAMAs) and / or muscarinic antagonists, e.g., not salmeterol and / or tiotropium bromide.

[0036] In some embodiments, in the course of achieving said uses, systemic dosage forms (e.g., oral tablets) and topical dosage forms (e.g., eye drops) are used simultaneously, in combination, alternating, spaced apart, or alone.

[0037] In some embodiments, the abnormal development of the eye is a developmental abnormality of the refractive system primarily induced by environmental factors or primarily caused by human factors (e.g., prolonged close reading, frequent use of electronic screens, lack of continuous close and far vision opportunities, improper use of corrective glasses, side effects of medications, obesity, trauma, insufficient lighting in the learning environment, lack of outdoor exercise) and is not related to genetic factors or genetic factors are secondary, concomitant or synergistic factors, such as a developmental abnormality of eye size during childhood and adolescence (e.g., ages 3-26).

[0038] In some embodiments, the abnormal growth or developmental abnormality comprises an axial length that is too long or a rate of axial elongation that is not matched to the refractive system, such that the imaging focus of parallel light rays is located in front of the retina after passing through the normal or abnormal refractive system of the eye. [Brief description of the drawings]

[0039] [Figure 1] Figure 1 shows the effect of administration of three concentrations of vinpocetine (high, medium, and low) on refraction, vitreous cavity depth, and axial length in the FDM group, where A is a graph showing the difference in refraction between the experimental eye and the contralateral eye, B is a graph showing the difference in vitreous cavity depth between the experimental eye and the contralateral eye, and C is a graph showing the difference in axial length between the experimental eye and the contralateral eye. [Diagram 2] Figure 1 shows the effect of administration of three concentrations of vinpocetine (high, medium, and low) on refraction, vitreous cavity depth, and axial length in the LIM group, where A is a graph showing the difference in refraction between the experimental eye and the contralateral eye, B is a graph showing the difference in vitreous cavity depth between the experimental eye and the contralateral eye, and C is a graph showing the difference in axial length between the experimental eye and the contralateral eye. [Diagram 3]Figure 1 shows the effect of administration of three concentrations of vinpocetine, high, medium, and low, on choroidal thickness and blood flow in the FDM group, where A is the effect of vinpocetine on the choroidal thickness ChT of the eye, and B is the effect of vinpocetine on the choroidal blood flow ChBP. [Figure 4] The effect of administration of three concentrations of vinpocetine, high, medium, and low, on choroidal thickness and blood flow in the LIM group. A is the effect of vinpocetine on the choroidal thickness ChT of the eye, and B is the effect of vinpocetine on the choroidal blood flow ChBP. Note: * represents p<0.05, ** represents p<0.01, and *** represents p<0.001. The measurement results are displayed in five bar graphs for different periods (before administration, 3 days after administration, and 7 days after administration for the LIM group, or before administration, 1 week after administration, and 2 weeks after administration for the FDM group). In Figures 1 and 3, the set of five consecutive bars is, from left to right, FDM+Vehicle, FDM+Atropine (0.1%), FDM+VPN (0.01 μM), FDM+VPN (0.1 μM), and FDM+VPN (1 μM). In Figures 2 and 4, the set of five consecutive bars is, from left to right, LIM+Vehicle, LIM+Atropine (0.1%), LIM+VPN (0.01 μM), LIM+VPN (0.1 μM), and LIM+VPN (1 μM). VPN=vinpocetine. [Diagram 5] Changes in refraction and axial parameters in myopic individuals after systemic administration of different doses of vinpocetine. Comparisons are made between the refraction (A), vitreous cavity depth (B) and axial length (C) of both eyes of the subjects before, one week after and two weeks after the experiment. VPN is vinpocetine, Vehicle is solvent, Week is week, Refraction is refraction, VCD is vitreous cavity depth, AL is axial length and N is sample size. Repeated measures analysis of variance (A-C). [Figure 6]Treatment of myopia with salmeterol and tiotropium bromide. Compare the effect on the change in the difference in refraction (A), vitreous cavity depth (B), axial length (C), anterior chamber depth (D), lens thickness (E) and corneal curvature (F) of both eyes of myopic individuals for different drug groups before and after the end of the experiment. VPN=V is vinpocetine, T is tiotropium bromide, S is salmeterol, Vehicle is vehicle, Week is week, Refraction is refraction, VCD is vitreous cavity depth, AL is axial length, ACD is anterior chamber depth, LT is lens thickness, RCC is corneal curvature, N is sample size. * is p<0.05, ** is p<0.01, *** is p<0.001. Repeated measures analysis of variance (A–F). [Figure 7] The intervention effect of vinpocetine eye drops on the refraction, vitreous cavity depth and axial length of myopic individuals. The changes in the difference in refraction (A), vitreous cavity depth (B), axial length (C), anterior chamber depth (D), lens thickness (E) and corneal curvature (F) of both eyes of the same subject individual before and after 2 weeks of administration in different administration groups are compared. VPN is vinpocetine, Vehicle is the solvent, Refraction is refraction, VCD is vitreous cavity depth, AL is axial length, ACD is anterior chamber depth, LT is lens thickness, RCC is corneal curvature, and N is sample size. * is p<0.05, ** is p<0.01, and *** is p<0.001. Repeated measures analysis of variance (A-F). [Figure 8]The intervention effect of AVA, a metabolite of vinpocetine, on the refraction, vitreous cavity depth, and axial length of a myopic individual. The differences in refraction (A), vitreous cavity depth (B), and axial length (C) of both eyes of the subject individual before and one week after the experimental administration are compared. AVA is apovincaminic acid, a metabolite of vinpocetine, Vehicle is the solvent, Week is the week, Refraction is the refraction, VCD is the vitreous cavity depth, AL is the axial length, and N is the sample size. * is p<0.05, ** is p<0.01, and *** is p<0.001. Repeated measures analysis of variance (A to C). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0040] The following are illustrative examples of the present application. Although the present application is described using these specific embodiments, it should be understood that it is not intended to limit the present application to these specific embodiments. Rather, the present application is intended to cover all alternatives, modifications, permutations, variations, and equivalents that may be included within the spirit and scope of the present application as defined by the claims.

[0041] The present application provides a method for preventing and treating myopia involving topical administration of vinpocetine or related compounds to the eye.

[0042] The present application further provides a drug for treating myopia and controlling the progression of myopia, which contains vinpocetine as the sole or main active ingredient and is administered locally to the eye. In the prior art, vinpocetine is mainly in the form of tablets and injections, and is administered systemically. When vinpocetine is used to treat myopia, systemic administration is inevitably affected by the first-pass effect of the drug, the blood-retinal barrier (BRB), etc., and therefore, unless a high dose of the drug is administered, it cannot be guaranteed that vinpocetine or its metabolites entering the eye will reach the therapeutic concentration threshold, and such a treatment method has a potential risk of systemic adverse events, especially when the subject is a young person and long-term continuous administration is required. In addition, systemic administration is more affected by individual differences, so the uncertainty of the therapeutic effect of vinpocetine in preventing and controlling myopia increases. Therefore, the present application develops a vinpocetine drug that is administered locally to the eye and has better efficacy and safety. Such a drug development approach is for the use of vinpocetine and related compounds (e.g., fluoride) in the prevention and control of pediatric and juvenile myopia, with the advantages being ease of administration to patients, high compliance, the ability to administer for long periods (e.g., one month, six months, one year, three years, five years, ten years), minimal impact on the growth and development of young individuals, and a safe, reliable ophthalmic formulation.

[0043] The present application also provides a method, which comprises administering to a suitable subject an effective dose of vinpocetine or a related compound thereof to treat myopia and / or inhibit axial elongation thereof.

[0044] The method or pharmaceutical composition of the present application can significantly suppress myopia, and in particular suppress pediatric and / or juvenile myopia (preferably in the age group of 3-26 years, more preferably in the age group of 6-18 years), or early, intermediate myopia, or mild or moderate myopia, or non-pathological myopia, or simple axial myopia, or pediatric and / or adolescent axial myopia (preferably in the age group of 3-26 years, more preferably in the age group of 6-18 years), or pediatric and / or adolescent progressive myopia (preferably in the age group of 3-26 years, more preferably in the age group of 6-18 years), or primary myopia, or non-age-related myopia, or juvenile myopia, or progressive myopia, or non-refractive myopia.

[0045] The method or pharmaceutical composition of the present application can significantly inhibit or slow the increase in axial elongation and / or vitreous cavity length in myopic individuals (including individuals who are not yet myopic but will progress to myopia). Preferably, the population to which the method or pharmaceutical composition of the present application is applied is a population with pediatric and / or juvenile myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), or early, intermediate myopia, or mild or moderate myopia, or non-pathological myopia, or simple axial myopia, or pediatric and / or adolescent axial myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), or pediatric and / or adolescent axial myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), or pediatric and and / or adolescent progressive myopia (preferably in the age group 3-26 years, more preferably in the age group 6-18 years), or primary myopia, or non-age-related myopia, or juvenile myopia, or progressive myopia, or non-refractive myopia, in which the increase in axial elongation and / or vitreous chamber length in such myopic individuals (including individuals who are not yet myopic but will progress to myopia) is inhibited or halted by the method or pharmaceutical composition of the present application.

[0046] The present application provides a method for treating, preventing or delaying myopia and its associated symptoms in a subject, comprising administering to the subject a therapeutically effective amount of vinpocetine or a therapeutically acceptable salt thereof or a related compound thereof, preferably said vinpocetine is administered alone, preferably said vinpocetine is administered simultaneously, sequentially or at intervals alternating with other drugs, preferably said vinpocetine is administered in the form of a pharmaceutical composition, preferably said pharmaceutical composition is formulated as an ophthalmic formulation, preferably said ophthalmic formulation further comprises a pharma- ceutically acceptable carrier, preferably said carrier is an ophthalmologically acceptable carrier.

[0047] The present application also provides a pharmaceutical composition for treating, preventing or delaying myopia and its associated symptoms, said pharmaceutical composition comprising vinpocetine or a therapeutically acceptable salt thereof or a related compound thereof. Preferably, said pharmaceutical composition is formulated as an ophthalmic formulation, preferably said ophthalmic formulation further comprises a pharma- ceutically acceptable carrier, preferably said carrier is an ophthalmologically acceptable carrier.

[0048] The present application also provides the use of a compound or a therapeutically acceptable salt and derivative thereof in the manufacture of a pharmaceutical composition for treating, preventing or delaying myopia and its associated symptoms, the compound being a metabolite of vinpocetine (e.g., apovincaminic acid), vinca alkaloid, apovincamine, periwinkle extract, vincamine, voacanga africana extract, oleander extract, vincristine, tabersonine, vinblastine, vindoline, apovincaminic acid hydrochloride ... Hydrochloride, catharanthine, ethylvincaminate, etc., preferably, said compound is vinpocetine or a therapeutically acceptable salt or derivative thereof. Preferably, said pharmaceutical composition is formulated as an ophthalmic formulation, preferably, said ophthalmic formulation further comprises a pharma- ceutically acceptable carrier, preferably, said carrier is an ophthalmologically acceptable carrier.

[0049] The myopia-related symptoms include, but are not limited to, floaters, glaucoma, posterior staphyloma, retinal detachment, amblyopia, macular hemorrhage, visual field defects, progressive or sudden loss of visual acuity (especially near visual acuity), eye swelling and / or pain, and night blindness.

[0050] According to one aspect of the present application, the myopia is refractive myopia. According to another aspect of the present application, the myopia is axial myopia.

[0051] The present application also provides a myopia treatment (suppression of myopia progression) regimen in which vinpocetine or a salt form thereof is used in combination, at intervals, or alternating with other myopia prevention and control drugs (e.g., atropine) or optical prevention and control measures (e.g., orthokeratology lenses) in the course of preventing, slowing, or treating myopia.

[0052] The present application also provides a myopia treatment (reduction of myopia progression and / or eye lengthening) regimen in which vinpocetine or a salt form thereof is used in combination or alternation with systemic dosage forms (e.g., oral tablets) and topical dosage forms (e.g., eye drops) in the course of preventing, slowing, and treating myopia.

[0053] Terms and Definitions: "Myopia" refers to the convergence of parallel light rays in front of the retina after passing through the refractive system of the eyeball when accommodated to a relaxed state. Myopia generally manifests itself in the form of distance vision below normal levels but normal near vision. The clinical concept of a myopic individual is one with a static refraction of -0.25D or more. Clinically, it manifests in the form of blurred distant objects and good near vision, and in the early stages of myopia, the distance vision is constantly fluctuating, and no or little accommodation is required when viewing at close distances, so that the convergence function is correspondingly weakened, and exotropia or exotropia is common. In some paragraphs of this specification, there is no difference between the concepts represented by the words "myopia" and "myopic eye", and the two may be used interchangeably. Researchers in the field should correctly understand the meaning represented by "myopia" or "myopic eye" in this patent from the context in which it appears.

[0054] There are four common types of myopia: (1) Based on the magnitude of refraction, it is divided into mild (less than 300 degrees), moderate (300-600 degrees) and high (600 degrees or -6D or more); (2) Based on whether the refractive component is abnormal, it is divided into refractive myopia and axial myopia; (3) Based on whether pathological changes have occurred, it is divided into pathological myopia and simple myopia; (4) Based on the cause, it is divided into primary myopia and concomitant / secondary myopia.

[0055] In the case of "mild or moderate myopia", the patient has no other symptoms besides blurred distant objects, that is, mainly a gradual decrease in distant vision, blurred distant objects, and normal near vision, and generally no particular changes in the eye apart from the axial length.

[0056] In the case of "high myopia" (e.g., -6D), the patient's eye has a deep anterior chamber, a large pupil, and the eyeball appears slightly protruding because the anterior-posterior axis is too long. A white or gray-white crescent-shaped spot called myopic crescent is seen on the temporal side of the optic disc, which is caused by posterior extension of the sclera and detachment of the retinal pigment epithelium and choroid from the temporal edge of the optic disc, exposing the sclera or part of the choroid and sclera. As the posterior sclera continues to expand posteriorly, lacquer cracks and subretinal neovascularization may appear in the macula, and patchy atrophy and degeneration may appear in the nearby retina and choroid, resulting in posterior staphyloma. The macula is constantly pigmented and / or hemorrhagic, resulting in the formation of a Forster-Fuchs spot. These patients often have vitreous liquefaction and opacification, and rarely, retinal detachment and secondary cataracts. In addition, in the case of severe myopia, both distant and near vision are always reduced due to the opacity of the refractive medium and the degeneration of the retina and choroid, and sometimes a black shadow appears and moves in front of the eyes. When such lesions appear, this myopia is no longer simple myopia.

[0057] "Refractive myopia" is primarily caused by a cornea or lens with too great a curvature, resulting in refractive power that exceeds the normal range, but an axial length that is within the normal range.

[0058] "Axial myopia" is when the axial length of the eye exceeds the normal range, but the curvature of the cornea and lens are substantially within the normal range. Axial myopia is the predominant type of childhood and juvenile myopia.

[0059] "Pathological myopia", also known as degenerative myopia, is a degenerative lesion of the fundus. Patients generally have a high myopic refractive power (e.g., over 600 degrees), with obvious impairment of visual function, even worse distance vision, and many abnormalities in visual field, light perception, contrast sensitivity, etc., often accompanied by reduced nighttime vision (night blindness), floaters, floating objects, scintillating scotoma, etc. Patients' fundus shows thinning of the retinal pigment epithelium and choroid, often accompanied by symptoms such as retinal pigment epithelium atrophy, choroidal neovascularization, retinal detachment, and macular degeneration. Even after growth stops, pathological changes in the fundus continue to progress, and this type of myopia can lead to blindness in severe cases.

[0060] "Simple myopia" refers to myopia that occurs during the developmental stage of the eyeball, and when the development stops, myopia also tends to stabilize. For example, it often occurs during school age, the degree of myopia is 600 degrees or less, and there is generally no obvious pathological change in the fundus, and it is also called acquired myopia (eye). This type of myopia develops progressively, the axial length of the eye also increases progressively, vision can be normally corrected with appropriate lenses, and other visual function indicators are almost normal. The opposite is non-simple myopia, and examples of non-simple myopia include pathological myopia, high myopia, and elderly myopia.

[0061] "Primary myopia" is the main type of myopia. "Primary" refers to a group of myopia with unknown causes, whose causes and etiologies have not yet been identified using conventional diagnostic techniques. During its development and progression, pathological or physiological functional-structural changes specific to myopia, including congenital myopia and acquired simple myopia, appear.

[0062] "Concomitant / secondary myopia" refers to temporary myopia caused by ocular accommodation dysfunction caused by internal and external factors, or refractive abnormality (e.g. toxic myopia, drug-induced myopia, traumatic myopia, diabetic myopia, early stage cataract myopia), etc. This type of myopia is often characterized by a clear triggering factor and repeated fluctuations in vision. This type of myopia is common among the elderly.

[0063] "Simple axial myopia", also called simple axial myopia, belongs to the simple myopia and is characterized by simple myopia in which the image focus is located in front of the retina due to elongation of the eye axis and / or an increase in the depth of the vitreous cavity. In this type of myopia, the refractive tissues of the eye (e.g., the crystalline lens) are substantially normal and it is the most common type of myopia in children and adolescents, occurring more frequently in the 3-26 year old population, especially in the 6-18 year old population (Paul N Baird, Nat Rev Dis Primers. 2020 Dec 17; 6(1): 99, AJ Adams, Am J Optom Physiol Opt. 1987 Feb; 64(2): 150-2, Seang-Mei Saw, Ophthalmic Physiol Opt. 2005 Sep; 25(5): 381-91.).

[0064] "Curvature myopia" is myopia caused solely by an increased curvature of the cornea or lens.

[0065] "Exponential myopia" is myopia caused mainly by an increase in refractive power due to an increase in the refractive index of the aqueous humor and the crystalline lens, and belongs to refractive myopia.

[0066] "Progressive myopia" refers to myopia in which the refractive power continually decreases over time or with increasing age of an individual, and which, unless intervened, generally eventually progresses to high myopia.

[0067] "Child and juvenile myopia" is a simple myopia caused by using the eyes at close distances for a long time, and patients with this type of myopia rarely progress to pathological myopia. Children and adolescents have strong accommodative ability and high scleral extensibility because their eyes are still growing and developing. When reading, writing, or performing other close-up tasks, the eye is in a state where the focus is shifted, and over time, the anterior-posterior axis of the eye becomes longer, making it easy to develop pediatric and adolescent axial myopia. If the eye usage habits do not change or medical intervention is not performed for myopic eyes, the degree of myopia in children and adolescents will gradually increase, and the axial length will also increase accordingly. Therefore, in this type of myopia, the axial length is always dynamic and the refraction is constantly negative as the child or adolescent grows and develops, i.e., it belongs to progressive myopia, and is not almost static like myopia in adults or the elderly. Therefore, in clinical practice, the main indicators for evaluating the efficacy of such anti-myopia drugs are the control of the progression of myopia and the inhibition of axial elongation.

[0068] "Elderly myopia" is generally complex, susceptible to the aging of body organs and underlying diseases, and is often accompanied by symptoms such as blood sugar changes, vascular sclerosis, insufficient blood supply, and microcirculatory disorders of the eye, and is mostly severe myopia. One notable feature of adult or elderly myopic patients is that the degree of myopia generally does not increase with age, mainly because such individuals have substantially stopped growing and developing their eyes, and the axial length of the eye does not change with long periods of viewing objects at close range. Therefore, elderly (including adults) myopia and pediatric and adolescent (minor) myopia are two completely different diseases, and it is necessary to clearly distinguish between these two indications for the treatment of myopia. The drug or method of the present application is suitable for the treatment of various types of myopia, but simple myopia is preferred, and non-simple myopia such as elderly myopia, strong myopia, and pathological myopia is excluded. This is because the clinical intervention method for these myopic patients is not to inhibit the elongation of the eye axis, but to prevent blindness caused by serious eye lesions, such as blindness caused by retinal detachment.

[0069] "Myopia-related symptoms" includes complications resulting from myopia, such as complications of high myopia, such as floaters, glaucoma, posterior staphyloma, retinal detachment, retinal tears, amblyopia, macular hemorrhage, choroidal neovascularization, choroidal atrophy, macular degeneration or maculopathy, visual field defects, progressive or sudden decrease in visual acuity (especially near visual acuity), swelling and / or pain in the eye, decreased nighttime vision (e.g., night blindness), astigmatism, anisometropia, blindness, vitreous liquefaction, vitreous opacification, strabismus, frequent blinking, scintillating scotoma, frequent eye rubbing, anisometropia, blurred vision when looking at distant objects, need to squint or partially close eyelids to see distant objects clearly, headaches due to eye strain, and These include difficulty seeing during vision, especially at night (nocturnal myopia), retinal atrophy and degeneration (bleeding and tears), subretinal neovascularization, and ocular atrophy. In addition, fundus changes of varying degrees, myopic conus, macular hemorrhage, or subretinal hemangioma formation may occur. Irregularly shaped white patches of atrophy or circular black spots with pigmentation (Fuchs spots), lattice degeneration and cystic degeneration of the peripheral retina may occur. Vitreous liquefaction, opacification, and posterior vitreous detachment may occur even at a young age, and the risk of retinal tears and detachment is higher than in healthy people. The anteroposterior diameter of the eyeball becomes longer, causing the eyeball to protrude, and the posterior pole of the eyeball to expand, often resulting in scleral staphyloma.

[0070] "Accommodative myopia" is myopia caused by excessive strain on the eyeball for near vision, which causes excessive accommodation by the ciliary muscles and other muscles, resulting in accommodative tension or accommodative spasm.

[0071] "Astigmatic myopia" is myopia in which the cornea is compromised or has different degrees of curvature, causing external light to be scattered in all directions and unable to be focused on the retina.

[0072] In some embodiments, myopia according to the present invention may or may not include pathological myopia, high myopia, age-related myopia, and astigmatic myopia, which may be corrected by vinpocetine's blood flow improving function, and the progression of myopia may be prevented, treated, or slowed down (controlled) by vinpocetine's unknown mechanism.

[0073] Myopia interventions are divided into myopia correction and myopia treatment, the main feature and purpose of which is to inhibit (control) the progression of myopia.

[0074] "Correction of myopia" refers to correcting or reducing the degree of myopia by optical methods. Commonly used corrective measures include wearing framed glasses, phacoemulsification, intraocular lens implantation, laser corneal surgery, etc. However, such measures correct the individual's refractive power, but cannot postpone the progression of myopia or reverse the excessively long eye axis. In other words, such myopia intervention methods do not play a role in stopping or slowing the process of persistently negative refractive power, and cannot suppress the progression of myopia. Therefore, myopia correction methods such as laser corneal surgery can compensate for the patient's refractive error and restore their distance vision, and are suitable for improving the vision of pathological myopia, high myopia, or elderly myopic populations, but are not suitable for treating axial myopia or simple myopia, such as pediatric or juvenile myopia, primary myopia, or mild, moderate myopia, etc. In practice, an individual with axial myopia may temporarily regain distance vision when wearing eyeglass frames, but the correction method does not inhibit further axial elongation or control the rate of myopic progression, and in the absence of other medical treatments, the degree of myopia will eventually increase further, requiring the patient to periodically switch to eyeglass frames with a higher degree of myopia to continue correcting their vision.

[0075] "Suppression (control) of myopia progression" refers to the use of various methods or drugs to postpone (slow) the increase in myopia, reduce the rate at which the refraction becomes negative, control the progression of myopia, and suppress (control) the continued elongation of the eye axis. This is a pathological treatment, and most of the patients are minors whose eyes are still in the development stage. For the treatment of pediatric or juvenile myopia, the most important purpose of the development of a myopia treatment drug is to slow, control, or stop the refraction from becoming negative continuously, and to suppress the corresponding increase in the axial length. In other words, the treatment of myopia should have the effect of controlling or suppressing the progression of myopia for types of myopia such as pediatric or juvenile myopia, axial myopia, and simple myopia, and not simply reverse or correct such refractive error conditions.

[0076] Unless otherwise specified, in this application, "treatment (of myopia)" refers to inhibiting (controlling) the progression of myopia, not correcting myopia. As used herein, the terms "treat," "slow," "postpone," "inhibit," "control," or "prevention / control" refer to therapeutic treatment measures and prophylactic or preventative measures aimed at preventing or slowing (alleviating) or halting the target disease or disorder. For example, after receiving a therapeutic amount of a vinpocetine compound or a pharmaceutical composition containing the same according to the methods described herein, the subject is successfully treated with an ophthalmic disease if one or more symptoms and signs of the ophthalmic disease are observably and / or measurably inhibited, postponed, reduced or eliminated, or the progression of the disease condition is slowed or postponed. It should also be understood that "significant" with respect to the various patterns of treating or preventing a medical condition described herein includes complete treatment or prevention and less than complete treatment or prevention, where a specific biologically relevant or medically relevant result is obtained. In some embodiments, "treatment" does not necessarily mean 100% elimination of myopia or myopia-related symptoms. In some embodiments, "treatment" of myopia or myopia-related symptoms according to the methods of the present application prevents, reduces, inhibits, or stops the progression of myopia, for example, by at least about 5%, at least about 10%, or at least about 20%, compared to levels observed in the absence of the compositions or methods of the present application (e.g., without exposure to a biologically compatible control subject or specimen of the compounds of the compositions or methods of the present application). In some embodiments, the myopia or myopia-related symptoms are treated by at least about 30%, at least about 40%, at least about 50%, or at least about 60%, at least about 70%, at least about 80%, at least about 90%, or more (about 100%), compared to the myopia or myopia-related symptoms in the absence of the compounds of the methods of the present application. Therefore, as will be understood by those skilled in the art, "treat," "delay," "postpone," "suppress," "control," or "prevention or control" does not refer to measures that aid in the treatment of myopia in an indirect manner, such as by providing an ocular health benefit or a complementary therapeutic effect, such as improving blood circulation in the eye or providing increased comfort when administered to the eye.

[0077] The evaluation of the effectiveness of myopia treatment depends on various factors, such as whether the sample population is scientifically selected, whether an objective control is set, whether an effective dose is administered, etc. Specifically, if the sample population is mostly elderly (the development of the eye has stopped and there is a possibility of underlying diseases such as arteriosclerosis), it is difficult to prove that vinpocetine has a therapeutic effect on myopia, and if the efficacy is evaluated only by visual acuity tests and no parallel control (e.g., placebo group) is designed, it cannot be proven that vinpocetine has a therapeutic effect on myopia. In this application, the efficacy of compounds in preventing and controlling myopia, in particular in preventing and controlling pediatric and juvenile myopia and / or simple myopia, is evaluated using two classic myopia disease models, namely form deprivation and minus lens induction in guinea pigs whose eyes are still in the growth and development stage, which are commonly used in the preclinical development stage of actual myopia drugs, and the standards of scientific tests in the field (DA Goss, Am J Optom Physiol Opt. 1981 Oct; 58(10): 859-69., Hao Wu, Proc Natl Acad Sci USA. 2018 Jul 24; 115(30): E7091-E7100., Sen Zhang, Invest Ophthalmol Vis Sci. 2019 Jul 1; 60(8): 3074-3083.).

[0078] "Distance visual acuity", also known as distance visual acuity without a lens, is medically defined as the visual acuity measured at a horizontal distance of 5 meters facing an eye chart, with the eyes normally open and looking straight ahead, without wearing glasses or any assistive device that enhances vision (e.g. framed glasses, contact lenses, colored contacts, pinhole glasses, etc.).

[0079] "Local administration" refers to administration directly to the affected area of ​​the body or to a mode of administration that satisfies a localized effect, including, but not limited to, epidermal administration, inhalation administration, enema administration, ocular administration, and intranasal administration.

[0080] "Systemic administration" is also called systemic administration and includes administration methods such as intravenous administration, oral administration, intramuscular injection, and subcutaneous injection, in which the drug is distributed throughout the body via blood transport.

[0081] "Improved systemic administration" refers to a systemic administration method that can effectively reduce drug toxicity of systemic administration by utilizing specific drug targeting techniques, while at the same time making the bioaccumulation of vinpocetine drug in the eye safe, efficient, and convenient.

[0082] A "directly active ingredient", also called an "active pharmaceutical ingredient", refers to a substance that has a direct therapeutic effect on a disease (e.g., myopia), which is a sufficient condition for treating the disease, or whose parameters such as the administration dose and administration method directly affect the therapeutic effect on the disease, and there is a causal relationship between the administration of the ingredient and the achievement of the therapeutic effect on the disease.

[0083] "Sole active ingredient" refers to a single ingredient in the final product (eg, drug) that exerts a medicinal effect and directly exerts an inhibitory, preventive and / or therapeutic effect on myopia.

[0084] The term "main active ingredient" refers to an active ingredient whose amount, ratio, concentration, or medicinal effect is not less than that of other active ingredients (e.g., myopia treatment effect) in a final product (e.g., a drug).

[0085] "These substances" refers to vinpocetine, or an optical isomer thereof, or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof.

[0086] In this specification and claims, unless the context clearly dictates otherwise, the singular forms "a," "an," and "the" specifically cover plural referents of the terms designated by them. Also, as used herein, unless otherwise specified, the term "or" is used in the inclusive sense of "and / or" rather than the exclusive sense of "or / or."

[0087] As used herein, reference to a numerical range for a variable is intended to convey that the present application may be practiced with the variable equal to any value within that range. Thus, for a variable that is inherently discrete, the variable may be equal to any integer value within the numerical range, including the end points of the range. Similarly, for a variable that is inherently continuous, the variable may be equal to any real value within the numerical range, including the end points of the range. For example, when a variable is described as having a numerical value between 0 and 2, the value may be 0, 1, or 2 for an essentially discrete variable, and 0.0, 0.1, 0.01, 0.001, or any other real value for an essentially continuous variable.

[0088] Those of skill in the art will understand that "about," as used herein, is somewhat dependent on the context in which it is used. If the use of the term is unclear to one of skill in the art, then "about" will refer to a numerical value within plus or minus 10% of the stated value, in the context in which the term is used.

[0089] As used herein, "administering" a compound, formulation, or drug to a subject includes any route for introducing or delivering a compound to a subject to perform its expected function. "Administration" may be performed by any suitable route, including oral, intraocular, ocular surface, intranasal, parenteral (intravenous, intramuscular, intraperitoneal, or subcutaneous), or topical administration (e.g., topical administration at a site on the skin, such as the periocular area). "Administration" includes self-administration and administration by another person. In the case of ocular or periocular administration, administration may be to the affected eye, the unaffected eye, or both of the subject.

[0090] The term "effective amount" as used herein refers to an amount sufficient to obtain a desired therapeutic and / or prophylactic effect, for example, an amount that leads to the prevention or alleviation of symptoms associated with an ophthalmological disease. The amount of the composition administered to a subject is determined by the type and severity of the disease and the individual's characteristics, such as general health status, age, sex, weight, and tolerance to drugs. The amount is also determined by the extent, severity, and type of the disease. Those skilled in the art can determine the appropriate dose based on these and other factors. The composition may also be administered in combination with one or more other therapeutic compounds. In the methods described herein, a vinpocetine compound or a pharmaceutical composition containing the same may be administered to a subject with one or more symptoms or symptoms of an ophthalmological disease. For example, a "therapeutically effective amount" of vinpocetine refers to the average level of pharmacological action that results in minimal relief of an ophthalmological disease.

[0091] The terms "formulation" and "composition" may be used interchangeably herein and refer to a mixture of two or more compounds, elements, or molecules. In some embodiments, the terms "formulation" and "composition" may refer to a mixture of one or more active agents and a carrier or other excipient. A composition may be in almost any physical state, including a solid, liquid (e.g., solution), or gas.

[0092] The term "dosage form" may also include one or more formulations or compositions provided in a form suitable for administration to a subject. For example, an injectable dosage form may be a formulation or composition that is manufactured in a form suitable for administration by injection.

[0093] As used herein, the term "pharmaceutical acceptable" means, for example, a drug carrier, a drug concentration, or a form in which a drug is present, that is approved for use in animals, preferably humans, by a regulatory authority, for example, CFDA (China), EMEA (Europe) and / or FDA (USA) and / or a regulatory authority of any other country.

[0094] As used herein, the term "concurrent" therapeutic use refers to the administration of at least two active ingredients (compounds) by the same route and at the same or substantially the same time.

[0095] As used herein, the term "single" therapeutic use refers to the administration of at least two active ingredients (compounds) by different routes at the same or substantially the same time.

[0096] The term "sequential" treatment as used herein refers to administering at least two active ingredients at different times, and the administration route is the same or different.More specifically, sequential use refers to administering one of the active ingredients completely before starting administration of the other active ingredient.Therefore, one active ingredient may be administered minutes, hours or days before administration of the other active ingredient.In this situation, simultaneous treatment is not performed.

[0097] As used herein, the term "prevention" of a disorder or disease refers to a compound reducing the occurrence of the disorder or disease in a treated sample relative to an untreated control sample, or delaying the occurrence of one or more symptoms of the disorder or disease or reducing the severity of one or more symptoms of the disorder or disease in a statistical sample relative to an untreated control sample.

[0098] As used herein, the term "related compounds" includes, but is not limited to, derivatives or structural analogs of vinpocetine.

[0099] The term "derivative" or "analog" of a compound as used herein includes any molecule related to the function and / or structure of said compound, such as an acid, amide, ester, ether, acetylated variant, hydroxylated variant or alkylated variant of said compound. The term "derivative" further includes compounds related to said structure that lack one or more of the above-mentioned substituents. Preferred derivatives of a compound are molecules that have significant similarity to said compound, for example, as determined by known methods. Similar compounds and their similarity index with their parent molecules can be found in a large number of databases, such as PubChem (http: / / pubchem.ncbi.nlm.nih.gov / search / ) or DrugBank (http: / / www.drugbank.ca / ). In a more preferred embodiment, the derivative should have a Tanimoto coefficient with respect to the parent drug of more than 0.4, preferably more than 0.5, more preferably more than 0.6, and even more preferably more than 0.7. The Tanimoto coefficient is widely used to measure the degree of structural similarity of two molecules. The Tanimoto coefficient may be calculated by software available online, for example, Small Molecule Subgraph Detector (http: / / www.ebi.ac.uk / thornton-srv / software / SMSD / ). Preferred derivatives should be both structurally and functionally related to the parent compound, i.e., they should retain at least some activity of the parent drug. The term "derivative" also includes metabolic products of a drug, which are generated, for example, from (biochemical) modification or processing of the drug after administration of the molecule to an organism, typically by a specific catalytic system, and which exhibit or retain the biological activity of the drug. The term "derivative" also includes halogenated (e.g., fluorinated), hydrogenated, deuterated, tritiated compounds or compositions thereof in the form of vinpocetine or a salt thereof.

[0100] In certain embodiments, as used herein, "metabolite" refers to a modified or processed drug that retains at least some activity of the parent drug and preferably has an inhibitory effect on phosphodiesterase activity or an effect on treating, preventing or slowing myopia and related conditions.

[0101] "Extract" or "Plant Extracts" refers to a substance extracted or processed from a plant (whole plant or part thereof) using appropriate chemical or physical methods, such as solvent extraction or pressing, and the substance may be pure, contain small amounts of impurities, or be a mixture.

[0102] An "ophthalmic composition" or "ophthalmic preparation" or "ophthalmic preparation" refers to an ophthalmic composition, or an ophthalmic pharmaceutical composition, or an ophthalmic drug product, or a drug, preparation, cosmetic, health food, drug-device combination, or device for preventing and / or treating an ophthalmic disease, protecting, maintaining, improving vision, or avoiding, slowing, or reversing vision loss, or may be an eye drop, eye ointment, eye spray, implant, eye gel, eye pad, ophthalmic microsphere, ophthalmic sustained release preparation, periocular injection, intraocular injection, and the like.

[0103] "Fish oil" refers to lipids derived from higher animals, particularly fish (e.g., cod, salmon), squid, and seal, and in particular the polyunsaturated fatty acids therein, including, but not limited to, omega-3 unsaturated fatty acids, DHA, EPA, DPA, ALA, nisinic acid, stearidonic acid, eicosatetraenoic acid, or combinations thereof.

[0104] In the present application, a compound, namely vinpocetine, is identified for treating, preventing or retarding myopia and its associated symptoms in order to improve the efficacy of alleviating or retarding myopia while avoiding or minimizing adverse side effects, such as those observed with atropine therapy.

[0105] The present application relates to pharmaceutical compositions and methods for treating, preventing, or slowing myopia and its associated symptoms in an individual, such as a toddler, school-age child, adolescent, or young adult. In some instances, treating, preventing, or slowing myopia and its associated symptoms may include administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition or dosage form.

[0106] The pharmaceutical composition includes a therapeutically effective amount of a vinpocetine compound or a salt thereof or a related compound thereof.

[0107] In another aspect, the present application provides an ophthalmic device containing a pharmaceutical composition, wherein the pharmaceutical composition comprises vinpocetine or a therapeutically acceptable salt or derivative thereof, preferably, the ophthalmic device delivers the pharmaceutical composition in a sustained release manner, preferably, the ophthalmic device delivers the pharmaceutical composition in a pulsatile manner.

[0108] Through our experiments, we have unexpectedly found that the use of vinpocetine alone can significantly slow down the process of negative refractive power in a form deprivation or lens-induced guinea pig myopia model, completely inhibit (stop) the process of negative refractive power in some individuals, and significantly inhibit axial elongation, thereby demonstrating that the vinpocetine compound has the effect of preventing or treating, preventing or controlling the progression of myopia in animals, particularly humans, for example, infants, school-age children, children and adolescents, minors, the 3-26 year old group, or young adults.

[0109] In some embodiments, the subject of the technical solution of the present application is a child or adolescent, with an age range of 3 to 26 years old, preferably 6 to 18 years old or 12 to 18 years old. In some embodiments, the subject of the technical solution of the present application is an adult, for example, with an age range of 16 to 65 years old, preferably 16 to 26 years old.

[0110] In topical administration experiments, no discomfort or abnormal ocular phenomena were observed in any of the administered animals, and no toxic reactions such as weight loss or decreased food intake were observed. Based on the previous clinical use of vinpocetine, those skilled in the art can predict that it will have good drug safety during clinical treatment when used to treat, prevent or improve myopia and its associated symptoms.

[0111] The pharmaceutical composition of the present application has a significantly superior technical effect to atropine in treating, preventing or delaying myopia and its associated symptoms, and no adverse events such as eye irritation, pupil dilation, inflammation or allergy were observed in experiments.

[0112] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the patient is treated for a period of about 1 month to 20 years, e.g., at least 6 months, at least 1 year, at least 2 years, at least 3 years, at least 5 years, at least 7 years, or at least 9 years.

[0113] In one embodiment, in the pharmaceutical composition, ophthalmic device or method of treatment of the present application, the pharmaceutical composition comprises vinpocetine and a therapeutically acceptable salt or derivative thereof, preferably with a pharma- ceutically acceptable carrier.

[0114] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is an aqueous composition.

[0115] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any of the above embodiments and any other embodiments herein, the pharmaceutical composition is an ophthalmic formulation.

[0116] In another embodiment, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is an aqueous ophthalmic formulation.

[0117] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is an eye drop formulation.

[0118] In another embodiment, the pharmaceutical composition, ophthalmic device or method of treatment according to any one or more of the above embodiments and any other embodiments herein, is an ophthalmic spray formulation.In another embodiment, the pharmaceutical composition, ophthalmic device or method of treatment according to any one or more of the above embodiments and any other embodiments herein, is an ophthalmic pharmaceutical composition contained within a blister pack of contact lenses.

[0119] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any of the above embodiments and any other embodiments herein, the pharmaceutical composition is a topical formulation.

[0120] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is an ophthalmic composition.

[0121] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any of the above embodiments and any other embodiments herein, the pharmaceutical composition is a topical ophthalmic composition.

[0122] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is an ophthalmic gel formulation.

[0123] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is an ophthalmic emulsion.

[0124] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is an ophthalmic liposome.

[0125] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is a nanodisc.

[0126] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is a nanoparticle suspension.

[0127] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is an ointment or an ointment or an oily ointment.

[0128] In other embodiments, the drug, composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, is an ophthalmic ointment (e.g., eye ointment).

[0129] In other embodiments, the drug, formulation, composition, device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, is wherein the drug, formulation, composition is an oral formulation, such as a tablet or capsule or powder or syrup.

[0130] In other embodiments, according to any one or more of the drugs, formulations, compositions, devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the drug, formulation, composition further comprises one or more other ophthalmically acceptable excipients and additives, including carriers, stabilizers, osmolality adjusting agents, preservatives, antioxidants, buffers, tonicity adjusting agents, viscosity enhancing agents, or other excipients.

[0131] In another embodiment, according to any one or more of the drugs, formulations, compositions, devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the drug, formulation, composition, device, or method of treatment comprises a polyhydric alcohol and / or an acidic co-solvent, and optionally comprises hydroxypropyl-β-cyclodextrin and citric acid or tartaric acid.

[0132] In another embodiment, according to any one or more of the drugs, formulations, compositions, devices, or methods of treatment according to any one of the above embodiments and any other embodiments herein, the carrier is selected from, but is not limited to, water, a mixture of water and a water-miscible solvent, vegetable or mineral oil containing 0.01-5% by weight of hydroxyethylcellulose, ethyl oleate, carmellose, carboxymethylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, ethyl acrylate, polyacrylamide, pectin, alginate, starch derivatives, polyvinyl alcohol, polyvinylpyrrolidone, poly(vinyl methyl ether), polyethylene oxide, cross-linked polyacrylic acid, carbopol, lecithin, polyethylene glycol stearate, polyhydric alcohols, acidic cosolvents, heptadecanoethyleneoxycetyl alcohol oxide, or polyoxyethylene sorbitan monooleate.

[0133] In another embodiment, the drug, formulation, composition, device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, the osmolality adjusting agent is sodium chloride.

[0134] In another embodiment, according to any one or more of the drugs, formulations, compositions, devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the preservative is selected from benzalkonium chloride, cetrimonium, sodium perborate, stable oxychlorine complex, sofia, polyquaternium-1, chlorobutanol, disodium ethylenediaminetetraacetate, polyhexamethylene biguanide, or combinations thereof.

[0135] In another embodiment, according to any one or more of the drugs, formulations, compositions, devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the buffer is selected from borate, a borate-polyol complex, a phosphate buffer, a citrate buffer, an acetate buffer, a carbonate buffer, an organic buffer, an amino acid buffer, or a combination thereof.

[0136] In another embodiment, according to any one or more of the drugs, formulations, compositions, devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the tonicity adjusting agent is selected from sodium chloride, sodium nitrate, sodium sulfate, sodium hydrogen sulfate, potassium chloride, calcium chloride, magnesium chloride, zinc chloride, potassium acetate, sodium acetate, sodium bicarbonate, sodium carbonate, sodium thiosulfate, magnesium sulfate, disodium hydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate, glucose, mannitol, sorbitol, glucose, sucrose, urea, propylene glycol, glycerin, or combinations thereof.

[0137] In another embodiment, for the purposes of this application, the preventive or control (treatment) effect of vinpocetine, or an optical isomer thereof or a racemate thereof, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof, or a related compound or extract thereof, or a crystalline compound thereof, or a combination of these substances on myopia or inhibition of axial length is independent of the sex, age, type of myopia, rate of progression of myopia, and severity of myopia of the subject to which it is administered.

[0138] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is a sustained release formulation or a subconjunctival depot.

[0139] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any of the above embodiments and any other embodiments herein, the pharmaceutical composition is a sustained release formulation.

[0140] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is a sustained release formulation contained in an ophthalmic device.

[0141] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and other embodiments herein, the pharmaceutical composition is contained within an ophthalmic device, for example, an eye pad, a suture, or a corneal contact lens.

[0142] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is an ophthalmic composition, and the ophthalmic composition is included in an ophthalmic device.

[0143] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a contact lens, an ophthalmic insert, a corneal covering, a corneal inlay, a nanodisc, a liposome, a nanoparticle, a punctal plug, or a hydrogel base with a microfluidic reservoir.

[0144] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a contact lens.

[0145] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is an ophthalmic insert.

[0146] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a corneal covering.

[0147] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a corneal inlay.

[0148] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a nanodisc.

[0149] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a liposome.

[0150] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a nanoparticle.

[0151] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a punctal plug.

[0152] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment according to any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device is a hydrogel base having a microfluidic reservoir.

[0153] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, wherein the ophthalmic device delivers the pharmaceutical composition in a sustained release manner.

[0154] In another embodiment, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is manufactured as an ophthalmic composition for treating an ophthalmic disease or condition.

[0155] In another embodiment, according to any one or more of the pharmaceutical compositions, ophthalmic devices or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is manufactured as an ophthalmic composition for treating pre-myopia, myopia, true myopia, pseudomyopia or progression of myopia.

[0156] In another embodiment, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the pharmaceutical composition is manufactured as an ophthalmic composition for treating high myopia, moderate myopia, or low myopia.

[0157] In another embodiment, according to any one or more of the pharmaceutical compositions, ophthalmic devices or methods of treatment described in any of the above embodiments and any other embodiments herein, the pharmaceutical composition is manufactured as an ophthalmic composition for treating a patient diagnosed with a pre-stage of myopia (or at risk of developing myopia).

[0158] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is substantially uniformly distributed throughout the ophthalmic device.

[0159] In other embodiments, according to any one or more of the pharmaceutical compositions, ophthalmic devices, or methods of treatment described in any one of the above embodiments and any other embodiments herein, the ophthalmic device is contained in a blister package of contact lenses.

[0160] In other embodiments, the pharmaceutical composition, ophthalmic device, or method of treatment described in any one or more of the above embodiments and any other embodiments herein, wherein the pharmaceutical composition is immersed in the ophthalmic device within a blister package of a contact lens.

[0161] The form of drug formulation, administration pattern and dosage may be any method known to those skilled in the art to contact cells, organs or tissues with the vinpocetine compound. Suitable methods include in vitro, ex vivo or in vivo methods. In vivo methods generally involve administering the vinpocetine compound of the present application or a pharmaceutical composition containing it to a mammal, preferably a human. When used internally for treatment, the vinpocetine compound or a pharmaceutical composition containing it may be administered to a subject in an effective amount (i.e., an amount that produces the desired therapeutic effect). The dosage and administration schedule are determined from the extent of the ophthalmological condition in the subject, the subject and the subject's medical history.

[0162] The compounds disclosed herein may exist as prodrugs. Prodrugs of the compounds described herein are susceptible to chemical changes under physiological conditions to yield modified forms of vinpocetine or related compounds. Prodrugs can also be converted to the compounds by chemical or biochemical methods in an ex vivo environment. For example, when placed in a transdermal patch reservoir with appropriate enzymes or chemical reagents, the prodrugs can be slowly converted to the compounds. Prodrugs are generally useful because, in some cases, they are easier to administer than the compounds or parent drugs. For example, they are bioavailable when administered orally, whereas the parent drugs are not. Prodrugs have a higher solubility in pharmaceutical compositions than the parent drugs. Many prodrug derivatives are known in the art, for example, those that rely on hydrolytic cleavage or oxidative activation of the prodrug. One non-limiting example of a prodrug is a compound that is administered as an ester ("prodrug") but is subsequently metabolically hydrolyzed to a carboxylic acid (the active agent).

[0163] The compounds disclosed herein may exist as therapeutically acceptable salts. The present application includes salt forms of the above compounds, including acid addition salts. Suitable salts include salts formed with organic and inorganic acids. Such acid addition salts are generally pharmaceutically acceptable. On the other hand, pharmaceutically unacceptable salts can be used to prepare and purify compounds in question. Base addition salts may also be formed, which are pharmaceutically acceptable.

[0164] As used herein, the term "therapeutically acceptable salts" refers to salts or zwitterionic forms of the compounds disclosed herein that are water- or oil-soluble or therapeutically acceptable dispersible, as defined herein. The salts may be prepared during the final isolation and purification of the compounds, or may be prepared separately by reacting a suitable free base form of the compound with a suitable acid. Representative acid addition salts include acetate, adipate, alginate, L-ascorbate, aspartate, benzoate, benzenesulfonate (besylate), hydrogen sulfate, butyrate, (±)-10-camphorsulfonate, dl-camphorsulfonate, citrate, saccharate, formate, fumarate, gentisate, glutarate, glycerophosphate, glycolate, hemisulfate, enanthate, hexanoate, hippurate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate (isethionate), lactate, maleate, malonate, etc. Salts include, for example, salts of L-glutamate, DL-mandelate, mesitylenesulfonate, methanesulfonate, naphthalenesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphonate, citrate, picrate, pivalate, propionate, L-pyroglutamate, succinate, sulfonate, tartrate, L-tartrate, trifluoroacetate, phosphate, DL-glutamate, bicarbonate, para-toluenesulfonate, p-tosylate and undecanoate. Additionally, basic groups in the compounds disclosed herein may be quaternized with the following materials: chlorides, bromides and iodides of methyl, ethyl, propyl and butyl groups; the dimethyl, diethyl, dibutyl and dipentyl esters of sulfuric acid; chlorides, bromides and iodides of decyl, lauryl, myristyl and steryl groups; and bromides of benzyl and phenethyl groups.Examples of acids that can be used to form therapeutically acceptable addition salts include inorganic acids (e.g., hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid) and organic acids (e.g., oxalic acid, maleic acid, succinic acid, citric acid). Salts may also be formed by coordination of the compounds with alkali metal or alkaline earth metal ions. Thus, the present application includes sodium, potassium, magnesium, calcium salts, etc. of the compounds disclosed herein.

[0165] Crystalline forms of vinpocetine include all known types, for example, crystal forms described in the literature by Samuel Golob (Samuel Golob, Improving Biopharmaceutical Properties of Vinpocetine Through Cocrystallization, J Pharm Sci. 2016 Dec;105(12):3626-3633.).

[0166] During the final isolation and purification of the compounds, the carboxyl group may be reacted with a suitable base (e.g., hydroxide, carbonate, or bicarbonate of a metal cation) or ammonia or an organic primary, secondary, or tertiary amine to prepare a base addition salt. Therapeutically acceptable salt cations include lithium, sodium, potassium, calcium, magnesium, aluminum, and non-toxic quaternary ammonium cations such as ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, trimethylamine, diethylamine, ethylamine, tributylamine, pyridine, N,N-dimethylaniline, N-methylpiperidine, N-methylmorpholine, dicyclohexylamine, procaine, dibenzylamine, N,N-dibenzylphenylethylamine, 1-diphenylhydroxymethanamine, N,N'-dibenzylethylenediamine. Other representative organic amines suitable for the formation of base addition salts include ethylenediamine, ethanolamine, diethanolamine, piperidine, and piperazine.

[0167] The compounds of the present application may be administered in the form of crude chemicals, but they may also be provided as pharmaceutical formulations. Thus, the present specification provides pharmaceutical formulations that include one or more of the compounds disclosed herein, or one or more pharma-ceutically acceptable salts, esters, prodrugs, amides, or solvates thereof, one or more pharma-ceutically acceptable carriers thereof, and optionally one or more other therapeutic ingredients. By "acceptable" it is meant that the carrier is compatible with the other ingredients of the formulation and is not harmful to the subject. The appropriate formulation is determined from the chosen route of administration. Any known techniques, carriers, and excipients that are suitable and understood in the art may be used, see, for example, Remington's Pharmaceutical Sciences. The pharmaceutical compositions disclosed herein may be produced in any manner known in the art, for example, by using conventional mixing, dissolving, granulating, sugar-coating, grinding, emulsifying, encapsulating, embedding, or compressing processes, and may be manufactured as a combination of drug and device.

[0168] The formulations include those suitable for oral administration, parenteral (including subcutaneous, intradermal, intramuscular, intravenous, intraarticular and intramedullary), intraperitoneal, transmucosal, transdermal, rectal and topical (including cutaneous, buccal, sublingual, ocular, intranasal and intraocular) administration, the optimal route may be determined, for example, from the condition and symptoms of the subject. The formulations may conveniently be presented in unit dosage form and may be prepared by any method known in the art of pharmacy. In general, these methods include the step of bringing into association the compound of the present application or a pharma-ceutically acceptable salt, ester, amide, prodrug or solvate thereof ("active ingredient") with the carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers, or both, and then, if necessary, shaping the product into the desired formulation.

[0169] Formulations of the compounds disclosed herein suitable for oral administration may be presented as discrete units, such as capsules, cachets or tablets, each containing a predetermined amount of the active ingredient, as a powder or granules, as a solution or suspension in an aqueous liquid or a non-aqueous liquid, or as an oil-in-water or water-in-oil emulsion. The active ingredient may also be presented as a bolus, lozenge, or paste.

[0170] Pharmaceutical formulations available for oral administration include tablets, push-fit capsules made of gelatin, and sealed soft capsules made of gelatin and a plasticizer (e.g., glycerin or sorbitol). Tablets may be produced by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be produced by compressing the active ingredient in a free-flowing form (e.g., powder or granules) optionally mixed with a binder, inert diluent or lubricant, surfactant or dispersant in a suitable machine. Molded tablets may be produced by molding a mixture of powdered compound moistened with an inert liquid diluent in a suitable machine. Tablets may be optionally coated or scored, and may be formulated to provide a slow or controlled release of the active ingredient. The dosage of any formulation for oral administration should be suitable for the purpose of preventing or treating myopia to be achieved by such administration. Push-fit capsules may contain the active ingredients mixed with fillers (e.g., lactose), binders (e.g., starches) and / or lubricants (e.g., talc or magnesium stearate) and, optionally, stabilizers. In soft capsules, the active compound may be dissolved or suspended in a suitable liquid (e.g., fatty oils, liquid paraffin or liquid polyethylene glycol). Stabilizers may also be added. Dragee cores are provided with suitable coatings. For this purpose, concentrated sugar solutions, optionally containing gum arabic, talc, polyvinylpyrrolidone, carbopol gel, polyethylene glycol and / or titanium dioxide, lacquer solutions and suitable organic solvents or solvent mixtures may be used. Dyestuffs or pigments may be added to the tablets or dragee coatings to identify or indicate different combinations of active compound doses.

[0171] Examples of fillers or diluents used in oral drug formulations (e.g., capsules, tablets) include, but are not limited to, lactose, mannitol, xylitol, D-glucose, sucrose, sorbitol, compressed sugar, microcrystalline cellulose (MCC), powdered cellulose, corn starch, gelatinized starch, dextrates, dextran, dextrin, D-glucose, maltodextrin, calcium carbonate, calcium hydrogen phosphate, calcium phosphate, calcium sulfate, magnesium carbonate, magnesium oxide, poloxamer (e.g., polyethylene oxide), methylcellulose, hydroxypropylmethylcellulose. The filler may comprise a complex solvent molecule, such as when the lactose used is lactose monohydrate.

[0172] Examples of disintegrants used in orally administered drug formulations (e.g., capsules, tablets) include, but are not limited to, sodium starch glycolate, sodium carboxymethylcellulose, calcium carboxymethylcellulose, croscarmellose sodium, polyviton, crospolyviton (polyvinylpolypyrrolidone), methylcellulose, microcrystalline cellulose, powdered cellulose, low-substituted hydroxypropylcellulose, starch, pregelatinized starch, and sodium alginate.

[0173] Glidants and lubricants may also be used in oral drug formulations to ensure that excipients are uniformly blended during mixing. Examples of lubricants include, but are not limited to, calcium stearate, glyceryl monostearate, distearoyl palmitoyl glycerol, hydrogenated vegetable oil, light mineral oil, magnesium stearate, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, sodium stearoyl fumarate, stearic acid, talc, and zinc stearate. Examples of glidants include, but are not limited to, silica (SiO2), talc corn starch, and poloxamer. Poloxamer (or may be provided by BASF Corporation) is an ABA block copolymer, in which the A block is a hydrophilic polyethylene glycol homopolymer and the B block is a hydrophobic polypropylene glycol homopolymer.

[0174] Examples of tablet binders include, but are not limited to, gum arabic, alginic acid, carbomer, sodium carboxymethylcellulose, dextrin, ethylcellulose, gelatin, guar gum, hydrogenated vegetable oils, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, copolyvidone, methylcellulose, liquid glucose, maltodextrin, polymethacrylate, polyvitone, gelatinized starch, sodium alginate, starch, sucrose, gum tragacanth, and zein.

[0175] The compounds may be formulated for parenteral administration by injection, for example, by bolus injection or continuous infusion. The formulations for injection may be provided in unit dosage form, for example in ampoules or multi-dose containers to which a preservative has been added. The compositions may be in the form of suspensions, solutions or emulsions in oily or aqueous media and may contain formulating agents such as suspending, stabilizing and / or dispersing agents. The formulations may be provided in unit-dose or multi-dose containers, for example in sealed ampoules, vials, and may be stored in powder form or in a lyophilized state, requiring only the addition of a sterile liquid carrier, for example physiological saline or sterile pyrogen-free water, immediately prior to use. Ready-to-use injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the above-mentioned types. In a preferred embodiment, the pharmaceutical composition of the present application is in the form of an injection, particularly a syringe. The pharmaceutical composition is preferably administered by intraocular injection, more preferably by intravitreal injection into the vitreous body.

[0176] Formulations for parenteral administration include, but are not limited to, aqueous and non-aqueous (oily) sterile injection solutions of the active compound, which may contain antioxidants, buffers, bacteriostatic agents, and solutes that render the formulation isotonic with the subject's blood, and aqueous and non-aqueous sterile suspensions, which may contain suspending agents and thickening agents. Suitable lipophilic solvents or vehicles include fatty oils (e.g., sesame oil) or synthetic fatty acid esters (e.g., ethyl oleate or triglycerides) or liposomes. Aqueous injection suspensions may contain substances that increase the viscosity of the suspension, such as methylcellulose, sodium carboxymethylcellulose, sorbitol, or dextran. Optionally, such as ethyl oleate or triglycerides, or liposomes. Aqueous injection suspensions may contain substances that increase the viscosity of the suspension, such as sodium carboxymethylcellulose, sorbitol, or dextran. Optionally, the suspension may further contain suitable stabilizers or agents that increase the solubility of the compounds to allow for the preparation of highly concentrated solutions.

[0177] In addition to the formulations described above, the compounds mentioned in this patent, such as vinpocetine, may be formulated as a storage preparation. Such long-acting formulations may be administered by implantation (e.g., subcutaneous or intramuscular) or intramuscular injection. Thus, for example, the compounds may be formulated with suitable polymeric or hydrophobic materials (e.g., as an emulsion in an acceptable oil) or ion exchange resins, or may be formulated as sparingly soluble derivatives, e.g., as a sparingly soluble salt.

[0178] For buccal or sublingual administration, the compositions may be in the form of tablets, troches, pills, or gels formulated in the usual manner. Such compositions may contain the active ingredient, e.g., a compound such as vinpocetine mentioned in this patent, in a flavored base (e.g., sucrose, gum arabic, or gum tragacanth).

[0179] The compounds may also be formulated in rectal compositions (e.g., suppositories or retention enemas, e.g., those containing conventional suppository bases such as cocoa butter, polyethylene glycol, or other fatty acid esters of glycerin).

[0180] In addition to the formulations described above, the compounds referred to in this patent, such as vinpocetine, may be formulated as disposable preparations for topical administration, devices, products that alter the appearance of the eye, or medical consumables, such as single-use eye drops (each package containing only one therapeutically effective dose), individually packaged eye pads, colored contact lenses, and daily disposable contact lenses.

[0181] The compounds mentioned herein, such as vinpocetine, may be administered locally, i.e. non-systemically. This includes applying the compounds disclosed herein to the eye, epidermis or externally to the oral cavity, and instilling such compounds into the ear, eye and nose, so that the compounds do not obviously enter the bloodstream. In contrast, systemic administration refers to oral administration, intravenous administration, intraperitoneal administration and intramuscular administration.

[0182] Formulations suitable for topical administration include liquid or semi-liquid formulations suitable for penetrating the skin to reach the site of effect (e.g., gels, ointments, washes, lotions, plasters or pastes) and formulations suitable for administration to the eye, ear or nose, e.g., drops, sprays. The active ingredient for treating myopia may comprise, for example, 0.0000001-99% w / w (by weight) of the total content of the formulation. In some embodiments, the active ingredient may comprise up to 50% w / w or more. In other embodiments, it may comprise less than 1% w / w. In some embodiments, the active ingredient may comprise 0.01-1% w / w. In other embodiments, it may comprise 0.00001-0.001% w / w of the formulation, or the active ingredient for topical administration may comprise, for example, 0.0000001-100% w / v (mass to volume basis) of the formulation, or in some embodiments, the active ingredient may comprise up to 50% w / v or more. In other embodiments, it may comprise less than 1% w / v. In some embodiments, the active ingredient may comprise 0.01-1% w / v. In other embodiments, it may comprise 0.00001-0.001% w / v of the formulation.

[0183] The gel formulation includes a formulation formed by binding a hydrogel to vinpocetine or a prodrug thereof or a related compound thereof, and preferably, the hydrogel of vinpocetine or a prodrug thereof to which the hydrogel is bound is a biodegradable hydrogel.

[0184] The hydrogel comprises, and preferably consists of, at least one polymer, which may be selected from the group consisting of poly(acrylic acid), poly(acrylate), poly(acrylamide), poly(alkoxy)polymers, poly(amides), poly(amidoamines), poly(amino acids), poly(anhydrides), poly(asparagine), poly(butyric acid), poly(caprolactone), poly(carbonates), poly(cyanoacrylates), poly(dimethylacrylamide), poly(esters), poly(ethylene), poly(ethylene glycol), poly(ethylene oxide), poly(ethyl oxazoline), poly(glycolic acid), poly(hydroxyethyl acrylate), poly(hydroxyethyl oxazoline), poly(hydroxypropyl methacrylamide), poly(hydroxypropyl acrylate ... methacrylate), poly(hydroxypropyloxazoline), poly(iminocarbonate), poly(N-isopropylacrylamide), poly(lactic acid), poly(lactic-co-glycolic acid)acid), poly(methacrylamide), poly(methacrylate), poly(methyloxazoline), poly(propylene glycol fumarate), poly(phosphazene), poly(orthoester), poly(oxazoline), poly(propylene glycol), poly(siloxane), poly(urethane), poly(vinyl alcohol), poly(vinylamine), poly(vinyl methyl ether), poly(vinylpyrrolidone), siloxane, ribonucleic acid, deoxyribonucleic acid, albumin, antibodies and their fragments Preferably, the polysaccharide is selected from the group consisting of cellulose, plasma proteins, collagen, elastin, fascin, fibrin, keratin, polyaspartic acid, polyglutamic acid, prolamin, transferrin, cytochromes, flavoproteins, glycoproteins, hemoglobin, lipoproteins, metalloproteins, phytochromes, phosphoproteins, opsins, agar, agarose, alginates, arabin, arabinogalactan, carrageenan, cellulose, carboxymethyl cellulose, hydroxypropyl methylcellulose and other carbohydrate-based polymers, chitosan, dextran, dextrin, gelatin, hyaluronic acid and its derivatives, mannan, pectin, rhamnogalacturonan, starch, hydroxyalkyl starch, xylan, and copolymers and functionalized derivatives thereof.

[0185] Preferably, the hydrogel is a biodegradable polyethylene glycol (PEG)-based hydrogel.

[0186] Preferably, the polyethylene glycol (PEG) is of a single molecular weight or a group of different molecular weights mixed in a predetermined ratio.

[0187] The hydrogel is a molded article, preferably in the form of microparticles. More preferably, the hydrogel is in the form of microbeads. More preferably, the microbeads have a diameter of 1 to 1000 μm, more preferably 5 to 500 μm, more preferably 10 to 100 μm, and even more preferably 20 to 80 μm. The diameter of the beads is measured by suspending the microbeads in an isotonic aqueous buffer. In a preferred embodiment, the vinpocetine or prodrug thereof to which the hydrogel is bound is in the form of microbeads. More preferably, the vinpocetine or prodrug thereof to which the hydrogel is bound is in the form of beads. More preferably, the microbeads have a diameter of 1 to 1000 μm, more preferably 5 to 500 μm, more preferably 10 to 100 μm, and even more preferably 20 to 80 μm. The diameter of the beads is measured by suspending the microbeads in an isotonic aqueous buffer. Such hydrogels may be polymerized in various ways, for example, by free radical polymerization, ionic polymerization, or complexation reaction.

[0188] When the hydrogel is processed by free radical or ionic polymerization, the at least two raw materials are a crosslinking macromer or crosslinking monomer (called a crosslinking reagent) and a multifunctional macromer (called a backbone reagent). The crosslinking reagent has at least two functional groups capable of bonding with each other, and the backbone reagent has at least one functional group capable of bonding with each other and at least one chemical functional group that is not used to participate in the polymerization step. Other diluent monomers may or may not be present. Useful functional groups capable of bonding with each other include, but are not limited to, groups capable of free radical polymerization, such as vinyl groups, vinylbenzene, acrylates, acrylamides, methacrylates, methacrylamides, and groups capable of ionically polymerizing, such as oxetanes, azetidines, and ethylene oxides. In an alternative optional manufacturing method, the hydrogel is produced by a chemical complexation reaction. In such a reaction, the raw materials are at least one polymeric raw material with complementary functionality to undergo a reaction, such as a condensation or addition reaction. In one embodiment, only one polymeric starting material is used, which is a heteromultifunctional backbone reagent that contains a large amount of polymerizable functional groups that may be the same or different.

[0189] In addition to the active ingredient, such as vinpocetine, the topical ophthalmic, otic and nasal formulations of the present application may further comprise excipients. Excipients commonly used in such formulations include, but are not limited to, isotonicity agents, preservatives, chelating agents, buffers, surfactants. Other excipients include solubilizers, stabilizers, comfort enhancers, polymers, emollients, pH adjusters and / or lubricants. Any of a variety of excipients may be used in the formulations of the present application, including water, mixtures of water and water-miscible solvents (e.g., C1-C7 alkanols), vegetable or mineral oils containing 0.5-5% of non-toxic water-soluble polymers, natural products (e.g., alginates, pectins, tragacanth gum, karaya gum, guar gum, xanthan gum, carrageenan, agar, gum arabic), starch derivatives (e.g., starch acetate, hydroxypropyl starch) and other synthetic products (e.g., polyvinyl alcohol, polyvinylpyrrolidone, polyvinyl methyl ether, polyethylene oxide, preferably cross-linked polyacrylic acid and mixtures of these products). The concentration of the excipient is generally 1-100,000 times the concentration of the active ingredient. In a preferred embodiment, the excipients included in the formulation are generally selected for their inertness towards the active ingredient composition of the formulation.

[0190] For ophthalmic, otic and nasal formulations, suitable isotonicity adjusting agents include, but are not limited to, mannitol, D-glucose, sodium chloride, glycerin, sorbitol, etc. Suitable buffering agents include, but are not limited to, phosphates, citrates, borates, acetates, etc. Suitable surfactants include, but are not limited to, ionic and non-ionic surfactants (with non-ionic surfactants being preferred, such as polysorbate 80, RLM100, POE20 cetyl stearyl ether (e.g., CS20) and poloxamers (e.g., F68)). The formulation may contain a substance that increases the viscosity of the solution or suspension, such as sodium carboxymethylcellulose, hypromellose, microcrystalline cellulose, sorbitol or dextran. Optionally, the formulation may further contain a suitable stabilizer or agent that increases the solubility of the compound, such as, but not limited to, ethanol, benzyl alcohol, polyethylene glycol, phenethyl alcohol, glycerin, so that highly concentrated solutions can be prepared.

[0191] The formulations described herein may include one or more preservatives. Examples of such preservatives include benzalkonium chloride, paraoxybenzoic acid esters, sodium perborate, sodium chlorite, alcohols (e.g., chlorobutanol, benzyl alcohol, or phenethyl alcohol), guanidine derivatives (e.g., polyhexamethylene biguanide), sodium perborate, polyquaternium-1, aminoalcohols (e.g., AMP-95), or sorbic acid. In some embodiments, the formulation itself may be preservative, and thus preservatives are not required. In some embodiments, the formulation itself is not preservative, but preservatives are not required because packaging materials or packaging designs can be used to avoid drug degradation (e.g., changes in physical and chemical properties and / or changes in biological effects).

[0192] For administration to the eye, ear or nose, the formulation may be a solution, suspension or gel. In a preferred embodiment, the formulation for topical administration to the eye or ear in an aqueous solution or suspension is in the form of drops. The formulation for topical administration to the nose in an aqueous solution or suspension is in the form of drops, spray or aerosol. The term "aqueous" generally refers to an aqueous formulation in which the water content of the formulation is greater than 20%, greater than 50%, more preferably greater than 75% and especially greater than 90%, by weight. These drops may be delivered by a single-dose eye dropper, which is preferably sterile, thus obviating the need for a bacteriostatic component of the formulation. Alternatively, the drops may be delivered by a multi-dose eye dropper, which preferably includes a device that removes any preservatives therefrom as the formulation is delivered, such devices being known in the art. Solution and suspension formulations may be administered intranasally using a nebulizer. Intranasal delivery of solutions, suspensions or dry powders may be facilitated by propellant-based aerosol systems, including but not limited to hydrofluoroalkane-based propellants, or may deliver the active drug ingredient in dry powder form.

[0193] For ocular conditions, the ingredients of the present application may be delivered to the eye as a concentrated gel or similar vehicle or as a soluble insert placed under the eyelid.

[0194] In certain embodiments, the formulations of the present application are administered once daily. However, the formulations may be formulated to be administered at any administration frequency, including once a week, once every 5 days, once every 3 days, once every 2 days, twice a day, three times a day, four times a day, five times a day, six times a day, eight times a day, hourly administration, or more. Depending on the treatment regimen, such administration frequency is maintained for a duration of different lengths. In certain treatment regimens, the duration may extend from a single administration to a regimen spanning several months or years, etc. The formulations are administered in different doses, but a typical dose is one or two drops at a time, or a substantial amount of gel or other formulation (e.g., tablets, eye ointments). Those skilled in the art will be familiar with determining the treatment regimen for a specific indication.

[0195] Gels for topical or transdermal administration may generally comprise a mixture of a volatile solvent, a non-volatile solvent and water. In some embodiments, the volatile solvent component of the buffered solvent system may comprise lower (C1-C6) alkyl alcohols, lower alkyl glycols and lower glycol polymers. In further embodiments, the volatile solvent is ethanol. It is believed that the volatile solvent component acts as a penetration enhancer while at the same time providing a cooling effect to the skin as it evaporates. The non-volatile solvent portion of the buffered solvent system is selected from lower alkylene glycols and lower glycol polymers. In some embodiments, propylene glycol is used. The non-volatile solvent postpones the evaporation of the volatile solvent and reduces the vapor pressure of the buffered solvent system. The amount of this non-volatile solvent component, like the volatile solvent, is determined by the drug compound or drug used. If there is too little non-volatile solvent in the system, the drug compound may crystallize due to the evaporation of the volatile solvent, and if there is too much, the drug may be difficult to release from the solvent mixture and may lack bioavailability. The buffer component of the buffered solvent system may be selected from any buffer commonly used in the art, and in some embodiments, water is used. Typically, the ratio of ingredients is about 20% non-volatile solvent, about 40% volatile solvent, and about 40% water. Several optional ingredients may be added to the topical composition. These include, but are not limited to, chelating agents, gelling agents. Suitable gelling agents may include, but are not limited to, semi-synthetic cellulose derivatives (e.g., hydroxypropylmethylcellulose) and synthetic polymers, galactomannan polymers (e.g., guar gum and its derivatives), and cosmetic agents.

[0196] Cleansers include those suitable for application to the skin or eye. Eye cleansers may include sterile aqueous solutions, optionally containing germicides, and may be manufactured in a similar manner to the drops. Cleansers or ointments applied to the skin may further include agents for accelerating the drying or cooling of the skin (e.g., alcohol or acetone) and / or moisturizers (e.g., glycerin) or oils (e.g., castor oil or peanut oil).

[0197] The pharmaceutical compositions of the present application may be lotions, salves (e.g., 3% oily ointment, ointment) or pastes, which are semi-solid preparations used as external active ingredients. They may be manufactured by mixing the active ingredient in pulverulent or powder form, alone or in a solution or suspension in an aqueous or non-aqueous fluid, with an oleaginous or non-oleaginous base using a suitable machine. The base may include hydrocarbons, such as petrolatum, hard paraffin, soft paraffin or liquid paraffin, glycerin, beeswax, metal soaps, mucilages, oils of natural origin, such as fish oil, almond oil, corn oil, peanut oil, castor oil or olive oil, lanolin or its derivatives, or fatty acids (e.g., stearic acid or oleic acid) and alcohols (e.g., propylene glycol), or macrogels, or lanosterol or dihydrolanosterol. Any suitable surfactant, such as an anionic, cationic or non-ionic surfactant, such as an anhydrous sorbitol ester or its polyoxyethylene derivatives, may be incorporated into the formulation. Suspending agents such as natural gums, cellulose derivatives, or inorganic materials such as siliceous, and other ingredients such as lanolin, lanosterol, may further be included.

[0198] Drops or sprays may comprise a sterile aqueous or oily solution or suspension, or may be prepared by dissolving the active ingredient in an aqueous solution containing a suitable bactericide and / or antifungal agent and / or any other suitable preservative, and in some embodiments, a surfactant. The resulting solution may then be clarified by filtration and transferred to a suitable container, which may then be sealed and sterilized by autoclaving or by holding at 98-100°C for 30 minutes. Alternatively, the solution may be sterilized by filtration and transferred to a container by aseptic techniques. Examples of bactericides and antifungals suitable for inclusion in drops include azole compounds (e.g., econazole), phenylmercuric nitrate or acetate (0.002%), benzalkonium chloride (0.01%) and chlorhexidine acetate (0.01%). Suitable solvents for preparing oily solutions include glycerin, dilute alcohol, and propylene glycol.

[0199] Formulations for topical administration in the mouth (e.g., buccal or sublingual) include lozenges which comprise the active ingredient in a flavored base such as sucrose, acacia, or tragacanth, and tablets which comprise the active ingredient in a base such as gelatin, glycerin, or sucrose, acacia, or the like.

[0200] For administration by inhalation, the compounds such as vinpocetine mentioned in this patent may be conveniently delivered in a pressurized pack in an insufflator, nebulizer, or other convenient device for delivering an aerosol spray. The pressurized pack may contain a suitable propellant, for example, hydrofluoroalkane, dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas. If the aerosol is pressurized, the dosage unit may be determined by using a valve to deliver a metered amount. Alternatively, for administration by inhalation or insufflation, the compounds of the present application may be in the form of a dry powder composition, for example a powder mix of the compound and a suitable powder base (for example lactose or starch). The powder composition may be presented in unit dosage form in, for example, capsules, cartridges, gelatin or blister packs from which the powder may be administered using an inhaler or insufflator.

[0201] Preferred unit dosage formulations are those containing an effective dose, as herein described, or an appropriate amount thereof, of the active ingredient.

[0202] It should be noted that in addition to the ingredients specifically mentioned above, the formulations may further include other agents common in the art for the type of formulation in question, such as formulations suitable for microneedle, oral or intranasal administration (which may include flavoring agents).

[0203] The compound may be administered orally or by injection at a dose of 0.001-300 mg / kg daily. The dose range for adults and the elderly is generally 5-100 mg / day, and should be reduced or maintained unchanged for children or adolescents. Tablets or other forms provided as separate units may conveniently contain a predetermined amount of one or more compounds, which is effective for such a dose or multiples of such doses, for example, 0.1-1000 mg, generally about 1-10 mg units, preferably 5 mg.

[0204] Compounds such as vinpocetine mentioned in this patent may be administered in a variety of ways, for example, orally, topically or by injection, or simultaneously or alternately systemically and topically. The exact amount of compound administered to a patient is determined by the attending physician. The specific dose level for a particular patient is determined by a variety of factors, including the activity of the particular compound used, age, weight, general health, sex, diet, time of administration, route of administration, excretion rate, drug combination, the particular disease being treated, and the severity of the indication or condition being treated. The route of administration may also vary depending on the disease condition and its severity.

[0205] In some cases, it may be appropriate to administer a combination of at least one compound described herein (or a pharma- ceutically acceptable salt, ester, or prodrug thereof) with another therapeutic agent. As an example, if one of the side effects experienced by a patient receiving one of the compounds described herein is hypotension, it may be appropriate to administer an antihypotensive agent in combination with the first therapeutic agent. Or as an example, the therapeutic effect of one of the compounds described herein may be enhanced by administering an antiallergic agent (i.e., the antiallergic agent itself may have minimal therapeutic efficacy, but when combined with a therapeutic agent referred to herein, the overall therapeutic efficacy for the patient is improved). Or as an example, the efficacy in the patient may be improved by administering one of the compounds described herein with another therapeutic agent (including further treatment regimens) that has therapeutic efficacy. As an example, in a myopia treatment involving the administration of one of the compounds described herein, the efficacy of the treatment may also be improved by providing the patient with another myopia treatment. In either case, the overall efficacy in the patient may be a simple addition of the two therapeutic agents, or may be a synergistic effect in the patient, regardless of the disease, condition, or condition being treated.

[0206] The pharmaceutical compositions in dry or liquid form may be provided in the form of single-dose or multi-dose pharmaceutical compositions.

[0207] In one embodiment of the present application, the liquid or dried pharmaceutical composition is provided in a single dose, meaning that the container in which it is provided contains one drug dose.Or, the liquid or dried pharmaceutical composition is a multi-dose pharmaceutical composition, meaning that the container in which it is provided contains one or more therapeutic doses, i.e., a multi-dose composition contains at least two doses.Such a multi-dose composition can be used for different patients who need it, or can be used for one patient, but after using the first dose, the remaining doses are stored until needed.

[0208] In another aspect of the present application, the pharmaceutical composition is in a container. Containers for liquid or dried pharmaceutical compositions include, for example, eye droppers, syringes, vials, vials with stoppers and closures, ampoules, and cartridges. In particular, the liquid or dried pharmaceutical composition is provided in a syringe. When the pharmaceutical composition is a dried pharmaceutical composition, the container is preferably a dual-chamber syringe. In this embodiment, the dried pharmaceutical composition is provided in a first chamber of the dual-chamber syringe, and the reconstitution solution is provided in a second chamber of the dual-chamber syringe.

[0209] Before the dry composition is used by a patient in need thereof, the dry composition is reconstituted. Reconstitution may be performed in a container that provides the dry composition, such as an eye dropper, a syringe, a dual-chamber syringe, an ampoule, a cartridge. The dry composition is reconstituted by adding a predetermined amount of a reconstitution solution. The reconstitution solution is a sterile liquid, such as water or a buffer, and may contain other additives, such as preservatives and / or antimicrobial agents, such as benzyl alcohol, cresol. Preferably, the reconstitution solution is sterile water. When the dry composition is reconstituted, it is called a "reconstituted drug composition" or a "reconstituted pharmaceutical composition" or a "reconstituted composition".

[0210] With respect to ophthalmic formulations, the pharmaceutical compositions of the present application may be administered in the form of an ophthalmic formulation, which comprises an ophthalmologically acceptable carrier.

[0211] The amount of active ingredient which can be combined with a carrier material to produce a single dosage form may vary and will depend upon the subject of treatment and the particular mode of administration.

[0212] As used herein, an "ophthalmologically acceptable carrier" is an ophthalmologically acceptable solvent, suspension, or vehicle for applying a pharmaceutical composition to the eye of a subject. The carrier may be a solid or liquid. The carrier is "ophthalmologically acceptable" in some sense, i.e., the carrier is suitable for administration to the eye without causing any significant side effects.

[0213] Typically, the ophthalmologically acceptable carrier is or includes water. Typically, the ophthalmic formulation is in the form of eye drops or gels that are applied to the eye. Typically, the majority of the formulation is water. Typically, the formulation contains more than 50% by weight (e.g., more than 60% by weight, more than 65% by weight, more than 70% by weight, more than 75% by weight, more than 80% by weight, more than 85% by weight, or more than 90% by weight), more typically more than 95% by weight (e.g., more than 96% by weight, more than 97% by weight, more than 98% by weight, or more than 99% by weight).

[0214] In some embodiments, the ophthalmologically acceptable carrier is an oil-in-water emulsion or an oil. In such embodiments, the ophthalmic formulation may be in the form of a cream applied to the eye. In such embodiments, the formulation may contain more than 10% by weight, more typically more than 20% by weight, of an oily component.

[0215] In another embodiment, the carrier may be a biodegradable polymer, for example a biodegradable polymeric intraocular implant for sustained release of the compound of the present application and optionally other compounds. For example, a biodegradable biocompatible polymer matrix. In one embodiment, the compound may be embedded in the polymer matrix while maintaining structural integrity. The polymer may be natural, for example a polypeptide, protein or polysaccharide, or synthetic, for example a poly(alpha hydroxy acid). Examples include carriers made from the following materials: collagen, fibronectin, elastin, cellulose acetate, nitrocellulose, methylcellulose, polysaccharides, fibrin, gelatin, and combinations thereof. In one embodiment, the polymer is polylactic acid (PLA) or polylactic-co-glycolic acid (PGLA). The polymer matrix may be manufactured and separated in various formats and sizes, including microspheres and nanospheres.

[0216] In some embodiments, the therapeutic compound is formulated with a carrier that protects the therapeutic compound from rapid excretion from the body, such as a controlled release agent, including implants and microencapsulated delivery systems. Biodegradable biocompatible polymers, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, polylactic acid, may be used. Such formulations may be manufactured using known techniques.

[0217] With regard to excipients, excipients suitable for the ophthalmic formulations of the present application include, for example, emollients, softeners, tonicity enhancers, preservatives, buffers, or pH adjusters. Examples of suitable excipients include: A. Emollients: synthetic high molecular weight cross-linked acrylic polymers (e.g., Carbomer 974, Carbomer 980), cellulose derivatives (e.g., hydroxypropyl methylcellulose ("HPMC" or "hypromellose"), hydroxyethyl cellulose, methylcellulose, carboxymethylcellulose (carmellose) or sodium carboxymethylcellulose (carmellose sodium)), glucans (e.g., glucan 70), gelatin, polyols (e.g., glycerin, polyethylene glycol 300, polyethylene glycol 400, polysorbate 80, propylene glycol), polyvinyl alcohol, Polyvitone (polyvinylpyrrolidone), poloxamers, hyaluronic acid (a disaccharide polymer) or its sodium or potassium salts.

[0218] B. Emollients: lanolin (eg, anhydrous lanolin), oily ingredients (eg, light mineral oil, mineral oil, paraffin, petrolatum, liquid paraffin, white ointment, white petrolatum, white wax, yellow wax), fish oil, castor oil.

[0219] C. Preservatives: Benzalkonium chloride, sodium perborate, Oxyd (sodium chlorite 0.05%, hydrogen peroxide 0.01%), Polyquaternium-1 (polymer of 2,2',2"-nitrilotriethanol, 1,4-dichloro-2-butene, and N,N,N',N'-tetramethyl-2-butene-1,4-diamine), sodium chloride, hexamethylene biguanide, oxyborate, (sodium chlorite 0.005% m / v).

[0220] D. Ophthalmic tonicity enhancers: Sodium chloride.

[0221] E. The present ophthalmic formulations may further contain a preservative to inhibit microbial growth and extend the shelf life of the formulation. Preservatives that may be used in the present ophthalmic formulations include, for example, benzalkonium chloride, sodium perborate, Oxyd (0.05% sodium chlorite, 0.01% hydrogen peroxide), polyquaternium-1 (polymer of 2,2',2"-nitrilotriethanol, 1,4-dichloro-2-butene, and N,N,N',N'-tetramethyl-2-butene-1,4-diamine), sodium chloride, hexamethylene biguanide, and oxyborates. Sodium chlorite (0.005% m / v) has broad spectrum antimicrobial activity. It is a germicide with low toxicity to mammalian cells and protects the formulation during storage, but eventually dissociates into water, sodium ions, chloride ions, and oxygen upon exposure. Since they are also found in natural tears, the risk of preservative-induced eye irritation and corneal damage is minimized. In the long term, the use of sodium chlorite is safe and effective. Such preservatives have no side effects on epithelial cells in vitro or in vivo, and are less damaging to cell integrity than many other preservatives in use.

[0222] The present ophthalmic formulations may be manufactured by any suitable method for manufacturing ophthalmic formulations. Ophthalmic formulations are generally sterile, and therefore the method may include a step of sterilizing the ophthalmic formulation. Preferably, the ophthalmic formulations are transparent and have a reflectance similar to that of tears, and an appropriate pH (typically buffered to about pH 7.5) to avoid serious corneal irritation and to prevent microorganisms. The present formulations suitable for topical administration to the eye are preferably isotonic or slightly hypotonic to counteract the hypertonicity of tears caused by evaporation and / or disease. This requires an isotonicity agent to bring the osmolality of the formulation to or near a level of 210-320 milliosmoles per kilogram (mOsm / kg). The present formulations generally have an osmolality in the range of 220-320 mOsm / kg, and preferably have an osmolality in the range of 235-300 mOsm / kg. Surface tension values ​​close to or below observed tear film surface tension values ​​are generally preferred.Ophthalmic formulations are generally formulated as sterile aqueous solutions.

[0223] In some ophthalmic embodiments, the compositions of the present application are formulated with one or more tear substitutes. Various tear substitutes are known in the art, including, but not limited to, monomeric polyols such as glycerin, propylene glycol, ethylene glycol, polymeric polyols such as polyethylene glycol, cellulose esters such as hydroxypropylmethylcellulose, sodium carboxymethylcellulose, hydroxypropylcellulose, dextran such as dextran 70, vinyl polymers such as polyvinyl alcohol, and carbomers such as carbomer 934P, carbomer 941, carbomer 940, and carbomer 974P. The formulations or pharmaceutical compositions of the present application may be used with contact lenses, corneal contact lenses, or other ophthalmic products (e.g., eyeglass frames, myopia treatment devices).

[0224] Preferred formulations are prepared using a buffer system that maintains the pH of the formulation at about 4.5 to about 8. The most preferred formulation has a pH of 5.5 to 7.5. The optional buffer is a physiologically acceptable buffer that maintains the pH in the desired range, such as sodium phosphate, bicarbonate, succinate, histidine, citrate, and acetate, sulfate, nitrate, chloride, pyruvate. Antacids, such as Mg(OH)2 or ZnCO3, may be used. The amount of buffer may be adjusted to suit the conditions most sensitive to pH stability.

[0225] The ophthalmic preparation of the present application may further contain a cooling agent such as menthol, camphor, borneol, geraniol, cineol, linalool, etc. When the cooling agent is mixed, the concentration of the cooling agent is preferably 0.0001 to 0.1 w / v %.

[0226] The ophthalmic formulations of the present application may contain other commonly used ophthalmic therapeutic ingredients such as bendazac and its salt forms (e.g., bendazac L-lysine), decongestant ingredients (e.g., adrenaline, DL-adrenaline hydrochloride, ephedrine hydrochloride, tetrahydrozoline hydrochloride, naphazoline hydrochloride, naphazoline nitrate, phenylephrine hydrochloride, dl-methylephedrine hydrochloride, and the like), anti-inflammatory / astringent agents (e.g., neostigmine methylsulfate, ε-aminocaproic acid, allantoin, berberine hydrochloride hydrate, berberine sulfate hydrate, sodium guaiazulene sulfonate, dipotassium glycyrrhizinate, zinc sulfate, zinc lactate, lysozyme hydrochloride, and the like), antihistamines (e.g., diphenhydramine hydrochloride, chlorpheniramine maleate, and the like), water soluble vitamins (flavin adenine dinucleotide hydrochloride, glycyrrhizinate, glycerol ... disodium oleate, cyanocobalamin, pyridoxine hydrochloride, panthenol, calcium pantothenate, sodium pantothenate, etc.), amino acids (e.g., potassium L-aspartate, magnesium L-aspartate, potassium and magnesium L-aspartate (mixture of equal parts), aminoethylsulfonic acid, etc.), ingredients for relieving eye fatigue and / or dry eyes (e.g., taurine, vitamin A, hypromellose, vitamin E), polyunsaturated fatty acids (e.g., fish oil, omega-3 unsaturated fatty acids, DHA, EPA), piracetam, sulfanilamide drugs, nicotinic acid, tretinoin and lutein, salidroside, formononetin, atropine, bendazole, M receptor blockers (e.g., blockers or antagonists or inhibitors for M3 receptors), etc.

[0227] Regarding the content of the active substance in the pharmaceutical composition of the present application, when mixing drugs, the concentration of the therapeutically active compound may be selected as an effective appropriate amount of each substance. Considering the aspects of eye irritation, stability of the formulation, etc., the therapeutically active compound (e.g., vinpocetine) may be present in the pharmaceutical composition at a high concentration, a medium concentration, or a low concentration, for example, about 0.0000001 to 100%, about 0.00001 to 10%, about 0.001 to 20%, about 0.1 to 30% of the total amount of the pharmaceutical composition. , about 1 to 40%, about 10 to 50%, about 20 to 60%, about 30 to 70%, about 40 to 80%, about 50 to 90% (w / v), for example, about 1 μM, about 0.1 μM, about 0.01 μM, about 5 μM, about 10 μM, about 15 μM, about 25 μM, about 50 μM, or about 0.0000001%, about 0.000001%, about 0.0001%, about 0.001%, about 0.01%, about 0.1%, about 1%, or about 10% (w / v) of the total amount of the pharmaceutical composition.

[0228] With regard to delivery of the ophthalmic formulations, the ophthalmic formulations of the present application may be delivered to the patient in the form of eye drops (in the form of single or multi-dose droppers), ointments, gels, creams, or biodegradable polymeric intraocular implants (designed for sustained release) or via ocular moisturizers (e.g., multi-dose sprays).

[0229] Packaging of ophthalmic formulations should be related to the retentive or non-retentive nature of the solution. Packaging methods such as blow molding, form-fill-packaging technology that combines aseptic filling and sealing in one process can be used, particularly for packaging preservative-free formulations in unit dose containers. Typically, these single dose containers are made of low density polyethylene or polypropylene and include twist-off caps.

[0230] The formulations and methods of the present application are already used in any subject that can benefit from the formulations and methods of the present application. The subject is generally a mammal, more generally a human. However, the present application is not limited to human treatment and is also suitable for veterinary use. Thus, according to the present application, the term "subject", "patient" or "subject in need" includes humans and non-human animals, including, for example, farm animals, such as sheep, pigs, cows, horses, pets, such as dogs, cats, and laboratory animals, such as mice, rats, rabbits. In a preferred embodiment, the mammal is a human.

[0231] In another aspect, the present application provides an ophthalmic device containing a pharmaceutical composition, the pharmaceutical composition comprising vinpocetine or a therapeutically acceptable salt or derivative thereof or a combination thereof, preferably, the ophthalmic device delivers the pharmaceutical composition in a sustained release manner.

[0232] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical composition is a sustained release formulation or a subconjunctival depot.

[0233] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical composition is a sustained release formulation contained in an ophthalmic device.

[0234] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the ophthalmic device is a contact lens, a corneal contact lens, an ophthalmic insert, a corneal covering, a corneal inlay, a nanodisc, a liposome, a nanoparticle, a punctal plug, or a hydrogel base with a microfluidic reservoir.

[0235] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the ophthalmic device delivers the pharmaceutical composition in a sustained release manner.

[0236] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are formulated as ophthalmic compositions, e.g., formulated as ophthalmic compositions for treating an ophthalmic disease or condition.

[0237] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are formulated as ophthalmic compositions for treating pre-myopia, myopia, or the progression of myopia.

[0238] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are formulated as ophthalmic compositions for treating high myopia, moderate myopia, or low myopia.

[0239] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are formulated as ophthalmic compositions for treating patients diagnosed with pre-stages of myopia (or at risk of developing myopia).

[0240] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical composition is substantially uniformly distributed throughout the ophthalmic device.

[0241] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the ophthalmic device comprises a blister pack of contact lenses or corneal contact lenses.

[0242] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical composition is immersed within a blister package of a contact lens or a corneal contact lens.

[0243] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical composition is administered to the eye of the patient.

[0244] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are administered topically.

[0245] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are administered to the eye in the form of an eye drop formulation, an eye spray formulation, or an eye gel formulation.

[0246] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are administered to the eye in the form of an ophthalmic emulsion, ophthalmic liposome, nanodisc, nanoparticle suspension, or ophthalmic ointment.

[0247] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are ophthalmically administered to the patient's eye by an ophthalmic device.

[0248] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions are administered once, twice, three times, four times, or five times daily.

[0249] In some embodiments, the pharmaceutical composition disclosed herein may be an ophthalmic aqueous formulation, for example in the form of eye drops. For example, the ophthalmic aqueous formulation described herein may be packaged in an eye dropper and administered as drops. In some embodiments, the ophthalmic aqueous formulation may be administered as a single administration (i.e., a single dose), and may include 1, 2, 3 or more drops to be instilled in the patient's eye. In some embodiments, one dose of the ophthalmic aqueous formulation described herein is provided from one drop of the aqueous composition in the eye dropper.

[0250] In some embodiments, the pharmaceutical composition disclosed herein may be an ophthalmic gel formulation. For example, the ophthalmic gel formulation may be packaged in an eye dropper and administered as drops. In some embodiments, the ophthalmic gel formulation may be administered as a single administration (i.e., a single dose) and may include 1, 2, 3 or more drops to be instilled in the patient's eye. In some embodiments, one dose of the ophthalmic gel described herein is provided from one drop of gel composition in the eye dropper.

[0251] In some embodiments, the pharmaceutical composition disclosed herein may be an ophthalmic ointment formulation. For example, the ophthalmic ointment formulation may be packaged in a tube or other crushable container, and the tube or other crushable container has a distribution port for delivering a strip of ointment. In some embodiments, the ophthalmic ointment formulation may be administered as a single administration (i.e., a single dose), and may include one strip or multiple strips that enter the patient's eye. In some embodiments, one dose of ophthalmic ointment is one strip of ointment composition distributed by the port of a distribution tube.

[0252] Treatment of a subject with a therapeutically effective amount of a therapeutic composition or formulation described herein can include a single treatment or a series of treatments.

[0253] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods prevent the progression of myopia in a treated patient.

[0254] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods control the progression of myopia in a treated patient.

[0255] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods reduce the progression of myopia in a treated patient.

[0256] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods slow or reduce the progression of myopia in the treated patient.

[0257] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods control, slow, reduce, retard and / or mitigate the progression of myopia in a treated patient to the following ranges compared to an untreated case: between about 5-95%, between about 5-90%, between about 5-80%, between about 5-70%, between about 5-60%, between about 5-50%, between about 5-40%, between about 5-30%, between about 5-20%, between about 10-100%, between about 20-90%, between about 30-90%, between about 40-90%, between about 50-90%, or between about 75-90%.

[0258] In some embodiments of the pharmaceutical composition, formulation, ophthalmic device, or method of treatment disclosed herein, the magnitude by which the refractive index of the recipient's eye becomes negative upon use of the pharmaceutical composition, formulation, ophthalmic device, or method of treatment is limited to about 1.0 to 6.0D, about 1.0 to 5.0D, about 1.0 to 4.0D, about 1.0 to 3.0D, about 1.0 to 2.0D, less than about 6.0D, less than about 5.0D, less than about 4.0D, less than about 3.0D, less than about 2.0D, or less than about 1.0D.

[0259] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods reverse the progression of myopia in a treated patient.

[0260] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the patient has high myopia, moderate myopia, or low myopia.

[0261] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the patient is at a pre-myopic stage (or at risk of progressing to myopia).

[0262] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods prevent, control, slow, reduce, alleviate, retard and / or reverse axial (or longitudinal) growth of the eye of a treated patient, i.e., axial elongation and / or increase in the length of the vitreous cavity.

[0263] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions, ophthalmic devices, or methods of treatment control, slow, mitigate, reduce, delay, and / or reverse the increase in axial elongation and / or vitreous chamber length in a treated patient (e.g., mild myopia, pediatric or juvenile myopia) to the following ranges compared to an untreated patient: between about 5-95%, between about 5-90%, between about 5-80%, between about 5-70%, between about 5-60%, between about 5-50%, between about 5-40%, between about 5-30%, between about 5-20%, between about 10-100%, between about 20-90%, between about 30-90%, between about 40-90%, between about 50-90%, or between about 75-90%.

[0264] In some embodiments of the drugs, formulations, compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods control, halt, slow, reduce, retard, delay, and / or reduce the onset or progression of myopia in a patient diagnosed with or at risk of progressing to myopia, by increasing the choroidal thickness of the patient's eye (e.g., a myopic eye, a pre-myopic eye, or an eye at risk of becoming myopic) and / or reducing the axial (or longitudinal) growth rate of the patient's eye (e.g., a myopic eye, a pre-myopic eye, or an eye at risk of becoming myopic), i.e., the increase in axial elongation and / or vitreous chamber length is inhibited.

[0265] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the methods control, retard, reduce, delay and / or reduce the axial (or longitudinal) growth of the treated patient's eye by between about 5-95%, between about 5-90%, between about 5-80%, between about 5-70%, between about 5-60%, between about 5-50%, between about 5-40%, between about 5-30%, between about 5-20%, between about 10-100%, between about 20-90%, between about 30-90%, between about 40-90%, between about 50-90%, or between about 75-90% compared to an untreated eye.

[0266] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions, ophthalmic devices, or methods of treatment prevent, control, retard, reduce, alleviate, alter, delay, and / or reverse the refractive degree of myopia in the eye of a treated patient.

[0267] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions, ophthalmic devices, or methods of treatment cause less severe adverse events compared to atropine monotherapy.

[0268] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions, ophthalmic devices, or methods of treatment result in a smaller increase in pupil size or no effect on pupil size compared to atropine monotherapy.

[0269] In some embodiments of the pharmaceutical compositions, ophthalmic devices, or methods of treatment disclosed herein, the pharmaceutical compositions, ophthalmic devices, or methods of treatment reduce the progression of axial or refractive myopia in normal eyes compared to atropine therapy alone.

[0270] Example 1: Myopia animal model and treatment experiments The form deprivation and lens induced guinea pig myopia model is a classic and commonly accepted myopia animal model in the field, which can be used to evaluate the therapeutic effect and safety of myopia treatment drugs, and its construction method is familiar to those skilled in the art. The construction and administration method of the animal model of the present application refer to the scientific literature previously published by the research group (Sen Zhang, Invest Ophthalmol Vis Sci. 2019 Jul 1; 60(8): 3074-3083., Miaozhen Pan, Exp Eye Res. 2021 Jan; 202: 108332.), specifically, the construction method of the exemplary form deprivation and lens induced guinea pig myopia model used in the present application is as follows: Three-week-old tricolor guinea pigs (both males and females were used to simulate humans aged 3 to 26 years) were used and were raised in the experimental animal room of Wenzhou Medical University, in an environment of 12 hours of light (400 to 500 lux) / 12 hours of darkness, with free access to water and food. The myopia model was created using one-eyed form deprivation (FD) and lens induction (LI) modeling methods. In form deprivation, a special eye mask with a light transmittance of 1% and which does not fall off by itself was used to completely cover the right eye of the animal, and the other eye (left eye) acquired normal vision. In the lens induction group, a -4D lens was fixed in front of the right eye of the animal, and the left eye acquired normal vision. The animals washed the lens twice daily to prevent lens blurring. The experimental group animals were administered every day from 9:00 to 9:30 a.m. During administration, the animals in the negative, positive control and experimental groups were each given an eye mask or lens removed under red light, and 0.1 mL of the solvent control, test drug (different concentrations of vinpocetine), or positive control (0.1% atropine) was injected around the eyeball into the right eye. Once it was confirmed that the administration to the animals was successful and there was no trauma after the injection, the eye mask or lens was immediately replaced. The administration process for each animal was limited to about 10 seconds. Administration began on the day of model creation, and the form-blocking group was given two consecutive weeks of administration, while the lens induction group was given one consecutive week of administration. This experiment was reviewed by the Wenzhou Medical University Experimental Animal Ethics Committee.

[0271] The vinpocetine eye drops used in the experimental groups were prepared as follows. Since the solubility of vinpocetine (VPN) in water at room temperature is reported to be 2.4 μg / mL, the inventors prepared 5 μM (i.e., 1.75 μg / mL) vinpocetine stock solutions, the solvent of which is physiological saline, stored at -80°C, and diluted to 1 μM, 0.1 μM, and 0.01 μM, respectively, with physiological saline before administration experiments. In the preparation process of vinpocetine eye drops, normal physical solubility-improving methods such as heating and stirring may be used, or the solubility may be increased by adjusting the pH using an acid, and finally the pH may be adjusted to 7.31. The above vinpocetine eye drops are transparent and stable at room temperature.

[0272] The animal groups were as follows: 1. Form Deprivation Group (FDM) (1) Form deprivation + vehicle injection group: one eye was subjected to an eye mask and the wearing eye was injected with saline vehicle for 2 weeks, sample size = 20.

[0273] (2) Form blockade + drug injection group: One eye was fitted with an eye mask and the wearing eye was injected with vinpocetine (0.01 μM: 0.1 mL / day) for 2 weeks, sample size = 15. One eye was fitted with an eye mask and the wearing eye was injected with vinpocetine (0.1 μM: 0.1 mL / day) for 2 weeks, sample size = 20. One eye was fitted with an eye mask and the wearing eye was injected with vinpocetine (1.00 μM: 0.1 mL / day) for 2 weeks, sample size = 22. (3) Form deprivation + positive control group: one eye was given an eye mask and atropine (0.1%: 0.1 mL / day) was injected into the wearing eye for two weeks, sample size = 15.

[0274] 2. Lens Induction Group (LIM): (1) Lens induction + vehicle injection group: one eye was fitted with a -4D lens and the fitted eye was injected with saline vehicle for 1 week, sample size = 10.

[0275] (2) Lens guidance + drug injection group: One eye was fitted with a -4D lens and the wearing eye was injected with vinpocetine (0.01 μM: 0.1 mL / day) for one week, sample size=12. One eye was fitted with a -4D lens and the fitted eye was injected with vinpocetine (0.1 μM: 0.1 mL / day) for one week, sample size=12. One eye was fitted with a -4D lens and the wearing eye was injected with vinpocetine (1.00 μM: 0.1 mL / day) for one week, sample size=13. (3) Lens induction + positive control group: one eye wore an eye mask and the wearing eye was injected with atropine (0.1%: 0.1 mL / day) for one week, sample size = 11.

[0276] However, the difference between the solvent control group and the experimental group is that it does not contain any active ingredient.

[0277] Measurement of refraction and ocular parameters of enrolled animals: In the same efficacy experiment, all animals were measured at the same time, and the first measurement was at 3 weeks of age, i.e., before administration. The refraction and axial parameters of the animals in the FDM group were measured before the experiment, 1 week after administration, and 2 weeks after administration, and the animals in the LIM group were measured before the experiment, 3 days after administration, and 7 days after administration. The refraction was measured using an eccentric infrared photoretinoscope (EIR) constructed by our laboratory, and each eye was measured three times and the average was used to obtain the final result. The axial parameters of the guinea pigs were measured using the A-mode probe of a CinescanA / B ultrasound diagnostic device (Quantel Medical, France, model number Aviso), with an ultrasonic frequency of 11 MHz, and the ultrasonic propagation speeds of the different refractive media of the eyeball were set as follows: anterior chamber 1557.5 m / s, crystalline lens 1723.3 m / s, and vitreous body 1540 m / s, respectively. Measurements included vitrous chamber depth (VCD) and axial length (AL). Approximately 2 minutes before measurement, 0.5% proparacaine hydrochloride eye drops (Alcon, Belgium) were used to anesthetize the guinea pig's measurement eye, and each eye was measured six times, with the average being used as the final result.

[0278] Measurement of choroidal blood flow and thickness: After the end of the experiment for the animals in the FDM group after one week of continuous administration and two weeks of administration, and after the end of the experiment for the animals in the LIM group after seven days of administration, choroidal blood flow parameters and choroidal thickness were measured, respectively. For the measurement of choroidal blood flow parameters and thickness, a commercially available OCTA (Spectralis HRA+OCT, OCTA, Heidelberg, Germany), which has been improved to better fit the animal's eyeball, was used. Before the measurement, the guinea pig was sufficiently anesthetized (a mixture of ketamine hydrochloride 60 mg / kg and xylazine hydrochloride 9 mg / kg, intraperitoneal injection), and later an OCTA image of the guinea pig was obtained, and the measurement results were quantified by a self-made program (MatLab R2017a, MathWorks), thereby realizing real-time quantitative detection of the blood flow and thickness of the choroid of the guinea pig (Sen Zhang, Invest Ophthalmol Vis Sci. 2019 Jul 1; 60(8): 3074-3083).

[0279] Example 2: Effect of local administration of vinpocetine to the eye The experimental method is the same as in Example 1. For the FDM group, the refraction, vitreous cavity and ocular axis of both eyes of all the test animals are measured before administration, 1 week after administration and 2 weeks after administration, respectively, and for the LIM group, the refraction, vitreous cavity and ocular axis of both eyes of all the test animals are measured before administration, 3 days after administration and 7 days after administration, respectively. All data are analyzed using repeated measures analysis of variance, and p value < 0.05 indicates significant difference, and p < 0.01 indicates highly significant difference.

[0280] Test Results: 1. Vinpocetine alone does not significantly reduce the incidence or progression of FDM-induced myopia (F 3,73=14.66, p<0.001). One week after administration of the FDM group, the induced myopia in the saline injection group was -4.94±2.35D, and two weeks later, the induced myopia in the same group was -6.74±1.90D, and both the depth of the vitreous cavity and the axial length were extended accordingly, indicating that the model was successfully created. After one week of continuous administration of 1 μM vinpocetine, the myopia of FDM and the corresponding extension of the axial length and the depth of the vitreous cavity were effectively inhibited, specifically, FDM+vehicle (Vehicle) vs. FDM+VPN (1 μM) was -4.94±2.35 vs. -2.44±1.88D, p<0.01, the refractive inhibition rate was 50.5%, and the depth of the vitreous cavity was also inhibited accordingly, indicating that the model was successfully created. Vehicle vs. FDM+VPN (1 μM) was 0.11±0.04 vs. 0.06±0.05 mm, p<0.01, the inhibition rate of vitreous cavity depth was 45.0%, and the axial length was also inhibited; FDM+vehicle vs. FDM+VPN (1 μM) was 0.11±0.05 vs. 0.07±0.05 mm, p=0.09, the inhibition rate of axial length was 39.8%. In addition, the corresponding indicators and results of myopia treatment by the medium concentration vinpocetine group also suggest that vinpocetine and its related compounds can be used for the treatment of myopia. In addition, the inventors found that the low concentration vinpocetine group (only 0.01 μM) had no statistically significant difference between the two efficacy measurement points, but the process of negative refraction and the extension of vitreous cavity depth tended to be inhibited compared to the negative control group. Comparing the myopia treatment results with the positive control group, after one week of administration, the model induced myopia in the 0.1% atropine group was -3.20±1.73D, the refraction suppression rate was 35.2%, the vitreous cavity depth was 0.08±0.05mm, the suppression rate of the vitreous cavity depth was 31.5%, and the axial length was 0.08±0.05, the suppression rate of the axial length was 32.1%. From the above results, it can be seen that the efficacy of high concentration vinpocetine in preventing and controlling myopia is superior to atropine, and the efficacy of myopia treatment with medium concentration vinpocetine is similar to that of atropine (Figure 1A-C).

[0281] After two weeks of continuous administration of vinpocetine, myopia in the FDM model was also effectively suppressed: FDM+vehicle vs. FDM+VPN (1 μM) -6.74 ± 1.90 vs. -3.36 ± 2.21 D, p<0.001, the suppression rate of refraction was 50.1%, and in some animals the refraction was almost unchanged compared to the previous measurement, and the depth of the vitreous cavity was suppressed accordingly: FDM+vehicle vs. FDM+VPN (1 μM) 0.16 ± 0.07 vs. 0.09 ± 0.05 mm, p<0.001, the suppression rate of the vitreous cavity depth was 43.4%, and the axial length was suppressed accordingly, and the FDM+vehicle vs. ) vs. FDM+VPN (1 μM) was 0.16 ± 0.06 vs. 0.08 ± 0.05 mm, p < 0.001, the inhibition rate of axial length was 48.2%, the myopia induced by 0.1% atropine in this case was -3.38 ± 2.79 D, the inhibition rate of refraction was 49.8%, the depth of the vitreous cavity was 0.10 ± 0.05 mm, the inhibition rate of the depth of the vitreous cavity was 38.2%, the axial length was 0.10 ± 0.05 mm, the inhibition rate of the axial length was 41.0% (Figure 1A-C), and the phenomenon of pupil dilation was observed in the animals during the use of atropine.

[0282] In addition, as can be seen from Figure 1, vinpocetine has a positive dose-response relationship in the treatment of the form deprivation myopia model, and as the dosage increases, the myopia treatment effect increases, and the same inhibitory effect is shown on the axial length and vitreous cavity depth. Compared with the control group, vinpocetine can significantly inhibit the negative refractive index of form deprivation myopia, and significantly inhibit the elongation of the axial length and the elongation of the vitreous cavity depth of form deprivation myopia. At the same time, vinpocetine's comprehensive performance in treating myopia in the FDM model is also superior to atropine, especially in the inhibitory effect on the process of negative refractive index.

[0283] 2. Vinpocetine can effectively inhibit the occurrence and progression of LIM-induced myopia (F 3,43= 4.073, p = 0.012). Three days after the experiment in the LIM group, the induced myopia was -3.25 ± 1.20 D in the saline injection group, and after 7 days, the induced myopia was -3.93 ± 1.26 D, with both the vitreous cavity depth and axial length increasing or decreasing accordingly. Three days after administration of 1 μM vinpocetine, myopia in the LIM model was effectively suppressed (LIM+vehicle vs. LIM+VPN (1 μM) -3.25±1.20 vs. -2.00±0.82 D, p<0.05), with a 38.5% reduction in refractive index and a corresponding reduction in vitreous cavity depth (LIM+vehicle vs. LIM+VPN (1 μM) 0.07±0.03 vs. 0.03±0.03 mm, p<0.01), with a 58.8% reduction in vitreous cavity depth and axial length. The myopia was suppressed according to the concentration of vinpocetine, LIM + vehicle (Vehicle) vs. LIM + VPN (1 μM) was 0.08 ± 0.02 vs. 0.04 ± 0.02 mm, p < 0.001, the suppression rate of axial length was 55.5%, the myopia induced by 0.1% atropine in this case was -2.34 ± 0.73 D, the suppression rate of refraction was 30.0%, the depth of the vitreous cavity was 0.04 ± 0.03 mm, the suppression rate of the depth of the vitreous cavity was 47.3%, the axial length was 0.04 ± 0.02 mm, the suppression rate of the axial length was 47.4%. This shows that all myopia treatment indexes of the high concentration (1 μM) vinpocetine group are better than atropine. Compared to the negative control group, all three vinpocetine groups, high, medium, and low concentrations, showed myopia treatment effects (Figure 2 A-C).

[0284] After 7 days of administration of vinpocetine, the myopia in LIM model was also effectively suppressed.By comparing the change trend of the process of negative refractive index in different experimental groups during the entire administration period, it was found that vinpocetine can significantly slow down the rate of myopia progression in the lens-induced myopia model. The results of refraction were -3.93±1.26 vs. -2.61±1.17D for LIM+vehicle vs. LIM+VPN (1 μM), p<0.05, with a 36.3% reduction in refraction and a corresponding reduction in vitreous cavity depth, 0.09±0.04 vs. 0.05±0.02mm for LIM+vehicle vs. LIM+VPN (1 μM), p<0.001, with a 49.8% reduction in vitreous cavity depth and a corresponding reduction in axial length, LIM+vehicle vs. LIM+VPN (1 μM). 1μM) was 0.10±0.04 vs. 0.05±0.02mm, p<0.001, and the inhibition rate of axial length was 53.8%. In this case, the myopia induced by 0.1% atropine was -2.61±1.17D, the inhibition rate of refraction was 33.4%, the depth of the vitreous cavity was 0.05±0.03mm, the inhibition rate of the depth of the vitreous cavity was 45.7%, the axial length was 0.06±0.03mm, and the inhibition rate of the axial length was 41.8% (Figure 2A-C). During the use of atropine, the phenomenon of pupil dilation was observed in the animals. This shows that the overall performance of high-concentration vinpocetine in the treatment of LIM model myopia is superior to (high-concentration) atropine, especially when evaluating the drug development potential of both in terms of drug safety and efficacy.

[0285] In addition, as can be seen from Figure 2, different concentrations of vinpocetine have a positive dose-response relationship in the treatment of the lens-induced myopia model. At the same time, vinpocetine can achieve a very high inhibitory effect in the early stage of myopia, and can continue to maintain this inhibitory effect, that is, the excellent efficacy of vinpocetine in preventing and controlling myopia is not related to the severity of myopia or the rate at which the refractive index becomes negative. In addition, compared with the saline group, all vinpocetine treatment groups have significantly inhibited the process of lens-induced myopia becoming negative throughout the entire administration period, postponed the onset and progression of myopia, and significantly inhibited the elongation of axial length and the increase in vitreous cavity depth in lens-induced myopia.

[0286] Data from two commonly accepted animal models for evaluating the efficacy of myopia show that vinpocetine exhibits excellent myopia treatment effects in both cases, and the degree of inhibition and retardation of the process of negative refraction is consistent with the corresponding inhibition of axial elongation and inhibition of the increase in vitreous cavity depth, proving that vinpocetine treats myopia mainly by controlling axial elongation and the increase in vitreous cavity depth. The inventors have unexpectedly found that when vinpocetine is used alone, the efficacy of vinpocetine in treating myopia, especially axial myopia, is superior to that of high-concentration atropine (0.1% atropine). It is worth noting that the above-mentioned therapeutic effect of vinpocetine on myopia is independent of the gender, age, type of myopia, myopia progression rate and myopia severity of the subjects.

[0287] No abnormalities in the eyes were observed during the administration period of the test animals in any of the vinpocetine groups, no obvious changes in pupil size were observed in the test eyes of the young guinea pigs during the local administration period of vinpocetine, and no allergic phenomena were observed. At the same time, no individual showed common clinical adverse events of vinpocetine or toxic reactions such as weight loss during the administration period of the test animals in any of the vinpocetine groups.

[0288] Considering the pharmacodynamic outcome evaluation and safety of long-term continuous administration, vinpocetine can be used to prevent, treat and control myopia, especially in the prevention and control of childhood and juvenile myopia.

[0289] Example 3: Mechanism of myopia treatment with vinpocetine It is well known that vinpocetine has the effect of improving blood circulation. The inventors use the method of Example 1 to measure the signal changes of choroidal thickness ChT and choroidal blood flow ChBP index in FDM (1 week and 2 weeks after administration) and LIM (1 week after administration) at different times during the administration period. Compared with the vehicle injection group, the therapeutically effective amount of vinpocetine only slightly increases the increase in choroidal thickness and choroidal blood flow perfusion, and it is found that there is no statistical significance (in the FDM model, ChBP:F 3,59 = 1.294, p = 0.285, Fig. 3A and B. In the LIM model, ChBP:F 3,44= 0.383, p = 0.766, Figure 4 A and B). In addition, a comprehensive study of the drug's inhibitory effects on myopia treatment indicators such as refractive index and axial length, and the effects of vinpocetine on choroidal thickness increase and choroidal blood perfusion at the corresponding time points revealed the following: The actual efficacy of the drug in treating myopia and controlling the progression of myopia and the assumed mechanism of action of vasodilation (increased choroidal blood flow) are not logically related, and the relevant measurement data of the form blockade group after one week of administration are contradictory; that is, vinpocetine at different concentrations can effectively suppress indicators such as negative refraction and increased vitreous cavity depth, showing a significant myopia treatment effect and a positive dose-response relationship, but the effect of vinpocetine on choroidal blood flow perfusion shows a negative dose-response relationship, and the effect of vinpocetine at each concentration on choroidal blood flow perfusion is closer to the trend of the negative control group compared to the atropine group. In particular, the high-concentration vinpocetine group (1 μM) had the worst effect on improving choroidal blood flow, but had the best efficacy in inhibiting the process of myopia leading to negative refractive power (Figures 1A and 1B and Figure 3B). Furthermore, after 2 weeks, the myopia treatment effect of medium-concentration vinpocetine (0.1 μM) in the form blockade group on the axial parameters was similar to that of atropine, but its choroidal vascular dilation effect was inferior to that of atropine (Figures 1B and 1C and Figure 3B).

[0290] In summary, the mechanism of action of vinpocetine in the treatment of myopia may not depend on dilating ocular blood vessels or improving ocular circulation or increasing choroidal blood flow, but may depend more on an as yet unknown (ocular) function whose corresponding biological target may even be in a competitive binding relationship with vinpocetine's known vasodilatory targets.

[0291] Example 4: Effect of systemic administration of vinpocetine on the progression of myopia The purpose of this study was to evaluate the effect of systemically administered vinpocetine (e.g., intravenous drip or intragastric administration) in the treatment of myopia, particularly in controlling the progression of myopia, and to comprehensively analyze the efficacy and safety of the drug based on indexes such as refraction, axial length, vitreous cavity depth, and body weight. In rats, the bioavailability of oral vinpocetine was 52% (Vereczkey et al., 1979a), and the LD 50 The value is about 500 mg / kg ( JPEG0007659940000002.jpg18170According to the safety evaluation data of vinpocetine on rodents published by the FDA, when administered intragastrically to animals of reproductive age, rats had no obvious abnormalities when administered 20mg / kg daily, and toxic reactions such as weight loss and reduced food intake occurred when administered 40mg / kg or more; rabbits had no obvious abnormalities when administered 75mg / kg daily, and toxic reactions such as weight loss and reduced food intake began to appear when administered 150mg / kg daily. Currently, the dosage forms of vinpocetine preparations sold in China include tablets and injections. The inventor believes that, taking into consideration the normal lifestyle of guinea pigs, the requirements for creating a form-blocking model, and the principle of drug compliance in future clinical use for myopia treatment, the efficacy of systemic administration of vinpocetine in the treatment of myopia using intragastric administration is approximately the same as or better than that of intravenous infusion. The single dose of vinpocetine administered intragastricly to guinea pigs should be determined by simultaneously referring to the oral bioavailability of vinpocetine in closely related species and the corresponding toxic dose of intragastric administration to rodents, and the dose should substantially maintain the normal physiological state of guinea pigs and not cause serious toxic reactions such as ataxia or clonic convulsions.

[0292] The inhibitory effect of the systemic administration of vinpocetine on the progression of myopia was evaluated by daily continuous administration, and the toxicity response of the dose was observed at the same time. The form deprivation myopia animal model and the method for evaluating the efficacy of vinpocetine in treating myopia used in this experiment are the same as those in other related examples (local administration) of this application, among which, the model preparation of the guinea pig form deprivation myopia model (FDM) and intragastric administration are both operated and performed with reference to the literature published by the inventor's laboratory (Pan Miaozhen, Proc Natl Acad Sci USA. 2021 Oct 26; 118 (43): e2104689118). Specifically, after removing individuals with obvious ocular disease or abnormality from healthy 3-week-old tricolor guinea pigs (regardless of male or female), the refraction (decentered infrared photoretinoscope) and eye axis (A mode) are measured to select animals with a refractive power between 3 and 8 diopters (D) and binocular anisometropia not exceeding 2D, which are randomly divided into the following three groups: form deprivation (FDM) + solvent control (vehicle) group, FDM + low-dose vinpocetine group (VPN) group, and FDM + high-dose VPN group, with the average body weights of the animals in the three groups before administration being substantially the same and not statistically significantly different from each other. At 8:00 a.m. on the first day of the experiment, the creation of a form deprivation (FD) myopia model in guinea pigs begins. The mask method was used to create the form deprivation myopia model, and the hood was made by the inventor using a 10-inch milky white non-toxic latex balloon. The right eye of the guinea pig model was covered with the hood (experimental eye) and the left eye was not covered with the hood (contralateral eye). FD induction was continuously performed throughout the entire drug efficacy experiment period of intragastric administration of vinpocetine, and the hood was temporarily removed only when eye measurements (e.g., refractive index measurement) were performed. The position of the hood was checked at 8:00 a.m., 12:00 p.m., 7:00 p.m., and before administration every day after the drug efficacy experiment began, and the hood was removed if the hood fell off three or more times. From the day of model creation, the solvent or drug corresponding to the FDM model was administered between 9:00 a.m. and 10:00 a.m. every day. The administration method was intragastric administration, and the dosage was 50 mg / kg / d (low dose) and 100 mg / kg / d (high dose), respectively. The actual administration was calculated based on the average body weight of the animals in each group, and the intragastric administration amount for the solvent group was 5 mL / kg / d. Administer once daily for two consecutive weeks.The refraction and axial parameters of the test animals were measured at the start of the efficacy experiment of the model, and after 1 week and 2 weeks. All data collection and processing methods were the same as those published in the literature by the inventor's laboratory (Sen Zhang, Invest Ophthalmol Vis Sci. 2019 Jul 1; 60(8): 3074-3083; Pan Miaozhen, Proc Natl Acad Sci USA. 2021 Oct 26; 118(43): e2104689118), and statistics were based on the difference between the experimental eye and the contralateral eye of the same test subject. At the same time, the body weight of all test subjects was recorded during the experimental period. The preparation method of vinpocetine intragastric administration liquid used by the inventor in this example is as follows: It has been reported that the solubility of vinpocetine in 0.5% methylcellulose at room temperature reaches 200 mg / mL (Waidyanatha S et al, Systemic exposure of vinpocetine in pregnant Sprague Dawley rats following repeated oral exposure: An investigation of fetal transfer, Toxicol Appl Pharmacol, 338: 83-92, 15 Nov 2017). Under the condition that no other pharmaceutical additives or other compounds are added, the inventors directly dissolve the powder of vinpocetine compound completely in 0.5% methylcellulose solvent (sterile water + methylcellulose) to formulate 10 mg / mL and 20 mg / mL vinpocetine formulations (intragastric administration liquid) respectively. At room temperature, the formulation has an overall appearance of clear, transparent, uniform, and no visible suspended matter. In the manufacturing process of the formulation, conventional physical and chemical solubility enhancing means such as heating, stirring, and pH adjustment may be used as necessary, and the compound will not precipitate before administration of the formulation.

[0293] The experimental results show that the changes in refraction and ocular axis parameters of the animals in the negative control group are all consistent with the predictions for the myopia model, proving that the model of form deprivation myopia was successfully created in this experiment and can be used to evaluate the efficacy of the test drug. As shown in Figure 5, throughout the treatment period, whether judging from refraction or ocular axis parameters, the vinpocetine systemic administration group tends to treat myopia and inhibit the progression of myopia compared to the solvent control group. At the same time, the weight gain of the vinpocetine group is obviously inhibited. Let us take the low-concentration intragastric administration group as an example. After one week of administration, the body weight of the 50 mg / kg vinpocetine group was significantly lower than that of the vehicle group, FDM+vehicle (Vehicle) vs. FDM+VPN (50 mg / kg) 208.5±14.9 vs. 188.0±22.9 mg, p<0.05, with a mean body weight reduction of 9.9%. After two weeks of administration, the body weight gain of the 50 mg / kg vinpocetine group was significantly inhibited, FDM+vehicle (Vehicle) vs. FDM+VPN (50 mg / kg) 229.6±21.4 vs. 210.2±21.9 mg, p<0.05, with a mean body weight reduction of 8.4%. This shows that a daily administration dose of 50 mg / kg already causes substantial toxicity in the experimental animals, and that further increases in the dose of vinpocetine will increase the risk of toxicity to the test individuals. However, it should be emphasized that the inventors have found that intragastric administration of vinpocetine has a definite dose-response relationship for the treatment of myopia, particularly in the inhibition of myopia progression. That is, as the intragastric dose increases, the efficacy of systemic administration of vinpocetine in the treatment of myopia becomes more evident. Compared to the administration of a dose of 50 mg / kg, intragastric administration of 100 mg / kg further inhibits the degree of negative refraction and the elongation of the axial length of the test individual.In terms of refraction and axial parameters for the animals in the three groups at the end of treatment, refraction was −6.59±1.42 vs. −5.71±2.41 vs. −5.223±2.20 D for FDM+Vehicle vs. FDM+VPN (50 mg / kg) vs. FDM+VPN (100 mg / kg), and vitreous cavity depth was −6.59±1.42 vs. −5.71±2.41 vs. −5.223±2.20 D for FDM+Vehicle vs. FDM+VPN (50 mg / kg) vs. FDM+VPN (100 mg / kg). +VPN (50mg / kg) vs. FDM+VPN (100mg / kg) were 0.12±0.05 vs. 0.13±0.07 vs. 0.10±0.06mm, and axial length was 0.14±0.05 vs. 0.13±0.05 vs. 0.11±0.05mm for FDM+Vehicle vs. FDM+VPN (50mg / kg) vs. FDM+VPN (100mg / kg). From the above results, the following conclusions can be drawn: Systemic administration of vinpocetine may also inhibit myopia progression and achieve significant myopia treatment effects, but systemic administration should be at a higher dose or for a longer administration time compared to local administration. With regard to safety evaluation, plans to use direct systemic administration of vinpocetine (e.g., direct intravenous infusion or oral tablet) to treat myopia result in certain side effects (e.g., weight loss or increased risk of miscarriage), and therefore a local administration mode is more recommended since treating a patient's myopia with systemic administration modes such as oral administration of vinpocetine carries additional clinical risks.

[0294] This shows that vinpocetine can be used to prevent and treat myopia, whether administered systemically or locally. Compared with systemic administration, local administration of vinpocetine is a better choice for preventing and controlling the progression of myopia. It should be understood that the results of this example are not inconsistent with the conclusion of the present application, and further suggest the following. When directly administering vinpocetine to prevent, control and treat myopia, it is preferable to use a safer, more efficient and convenient local administration method (preferably ocular administration), but this does not exclude the use of a systemic administration route, for example, by using a specific drug targeting technology to effectively reduce the drug toxicity of systemic administration, while at the same time bioaccumulating the vinpocetine drug in the eye to realize a safe, efficient and convenient systemic administration method to treat or inhibit myopia.

[0295] Example 5: Treatment of myopia with salmeterol and tiotropium bromide The efficacy of the drug was evaluated using the form deprivation myopia model of guinea pigs described in the present invention. The refraction and ocular axis of all individuals were measured, and animals that did not meet the conditions were removed. After that, the animals were randomly divided into the following five groups: a vinpocetine monotherapy group, a salmeterol + tiotropium bromide + vinpocetine combination therapy group, a salmeterol + tiotropium bromide combination therapy group, a negative control group (solvent group), and a 0.1% atropine group (positive control group). The concentrations of salmeterol (S) and tiotropium bromide (T) used were 1×10 -5 M and 1×10 -6 M, and the concentration of vinpocetine used is 1 μM whether administered alone or in combination. At 8 am on the first day of the experiment, the guinea pigs were subjected to morphological deprivation, and the right eye was covered (experimental eye) and the left eye was not covered (contralateral eye) using the mask method. From the day of model creation, the solvent or drug corresponding to the experimental eye was administered every day from 9 to 10 am, and the drug was injected subconjunctivally near the eyeball, with the injection volume being 100 μL, once a day for two consecutive weeks. The refraction and axial parameters of the animals were measured before and after the efficacy experiment, and all data collection and processing methods were the same as in other embodiments of the present invention, and statistics were based on the difference between the experimental eye and the contralateral eye of the same subject.

[0296] The experimental results showed that the changes in refraction and axial parameters of the animals in the negative control group were in line with the expectations of the myopia model, and the positive control drug atropine showed the expected efficacy in the experiment, proving that the myopia model was successfully created in this experiment and can be used to evaluate the efficacy of the test drug. After the administration intervention, there was no statistically significant difference in either refraction or axial parameters between the salmeterol + tiotropium bromide combination treatment group and the negative control group. The specific data is that after 2 weeks of administration, refraction was significantly higher in FDM + vehicle (Vehicle) vs. FDM + S + T (salmeterol, 10 -5 M+tiotropium, 10 -6M) was -6.00±1.61 vs. -5.09±1.80D, p>0.05, and vitreous cavity depth ... -5 M+tiotropium, 10 -6 M) was 0.12±0.05 vs. 0.12±0.06 mm, p>0.05, and axial length was significantly improved in FDM+vehicle vs. FDM+S+T (salmeterol, 10 -5 M+tiotropium, 10 -6 M) was 0.13±0.04 vs. 0.13±0.08 mm, p>0.05. The above results fully demonstrate that salmeterol and tiotropium bromide have no therapeutic effect on myopic individuals and cannot effectively control the progression of myopia. Compared with the negative control group, the vinpocetine alone (1 μM) treatment group and the 0.1% atropine group at the end of the two-week treatment are consistent with the myopia treatment results of other examples of the present invention, both of which significantly inhibit the negative refraction, the elongation of the axial length, and the increase in the depth of the vitreous cavity in myopic individuals (for example, as shown in Figure 6, there is a statistically significant difference between the vinpocetine (1 μM) treatment group and the solvent control group). No abnormalities were observed in the ocular tissue in the vinpocetine-treated group, while pupil dilation was observed in the atropine group, and the relevant indexes of the corneal curvature (RCC), anterior chamber depth (ACD) and lens thickness (LT) of the test animals in the two groups were not affected by the drug (see Figure 6). Therefore, under the premise of simultaneously meeting the ocular safety requirements for administration to young individuals, vinpocetine, as the sole active ingredient, main active ingredient or direct active ingredient, can effectively prevent and control myopia, and significantly inhibit, control and delay the progression of myopia.

[0297] Furthermore, the therapeutic effects of the combined salmeterol + tiotropium bromide + vinpocetine treatment group and vinpocetine alone (1 μM) were similar, and there was no statistically significant difference between the two in the indices of refraction, axial length, and vitreous cavity depth in a guinea pig myopia model throughout the entire administration period, suggesting that neither salmeterol nor tiotropium bromide exhibits a synergistic or enhancing effect on myopia treatment with vinpocetine. A comprehensive analysis showed that the efficacy of the combination of salmeterol + tiotropium bromide + vinpocetine was not significantly different from that of vinpocetine alone for myopia treatment. Combined with the fact that the salmeterol + tiotropium bromide treatment group had no significant pharmacological effect on myopia, it was found that in the combination of salmeterol + tiotropium bromide + vinpocetine, only vinpocetine exerted a myopia treatment effect, that is, vinpocetine can be used as the sole active ingredient, main active ingredient, or direct active ingredient to prevent and control myopia, and can effectively control the progression of myopia. The treatment of myopia by the single use of vinpocetine is superior to the drug combination treatment group in this example in terms of safety, efficacy, and drug development potential.

[0298] Example 6: Vinpocetine can effectively prevent and control myopia when administered non-invasively (in eye drop form) The purpose of this experiment is to evaluate the effect of vinpocetine on myopia by a non-invasive administration route, and all test drugs are prepared as eye drops. The efficacy is evaluated using the guinea pig form-deprived myopia model described in the present invention, and the refraction and eye axis of all individuals are measured. After removing animals that do not meet the conditions, the animals are randomly divided into the following four groups: a low concentration vinpocetine (1 μM) group, a high concentration vinpocetine (5 μM) group, a negative control group (solvent group), and a 0.1% atropine group (positive control group). At 8 am on the first day of the experiment, the guinea pigs were deprived of form, and the right eye was covered (experimental eye) and the left eye was not covered (opposite eye) using the mask method. From the day the model was created, the solvent or drug was administered to all experimental eyes at 9-10 am and 14-15 pm every day, and administered directly by eye drops. The single dose of eye drops was 25 μL for each dose, and administered twice a day for two consecutive weeks. Before and after the efficacy test, the refraction and ocular axis parameters of the animals were measured, and all data collection and processing methods were the same as in other examples of the present invention, and statistics were based on the difference between the experimental eye and the contralateral eye of the same subject. The vinpocetine eye drops and atropine eye drops used in this example were both prepared by the inventors using 0.9% saline, and no other active substances or additives were added to the eye drops.

[0299] The experimental results showed that the changes in refractive index and axial parameters of the animals in the negative control group were consistent with expectations for the myopia model, and the positive control drug atropine showed the expected efficacy in the experiment, proving that the myopia model was successfully created in this experiment and can be used to evaluate the efficacy of vinpocetine (ophthalmic solution formulation).

[0300] Through non-invasive administration, vinpocetine eye drops can effectively inhibit the occurrence and progression of myopia (refraction is F 2,42 = 9.115, p < 0.001, and the vitreous cavity was 2,42 = 6.243, p = 0.04, and the eye axis is F 2,42=8.986, p<0.001), and there is a dose-response relationship, i.e., the higher the administered concentration, the better the myopia (eye) treatment effect, and there is a statistically significant difference in the ocular axis parameter indexes during myopia treatment between different concentrations of vinpocetine drug groups. Due to the model construction method, the eye structure of guinea pigs (the eyeball is more protruding than that of humans and does not close its eyes spontaneously), and the animals blink normally, the effective therapeutic dose of the drug actually obtained by eye drop administration in each test eye is less than the dose of the same amount of eye periocular injection, and the total amount of eye drop administered to the test animals every day is also less than the injection dose in Example 2. Therefore, in this example, whether it was the low-concentration vinpocetine eye drop group or the 0.1% atropine group, the efficacy (refractive index) of direct administration of eye drops was inferior to the therapeutic effect on myopia of periocular injection administration. The specific results are shown in FIG. 7. In the high-concentration group, after two weeks of continuous administration of 5 μM vinpocetine, the increase in FDM myopia and the corresponding extension of the ocular axis and vitreous cavity depth were effectively suppressed. Specifically, the results for FDM+vehicle (Vehicle) vs. FDM+VPN (5 μM) were -6.56±1.70 vs. -3.80±1.16D, p<0.001, and the refraction suppression rate was 42.1. %, and there was a corresponding reduction in vitreous cavity depth, FDM+vehicle vs. FDM+VPN (5 μM), 0.14±0.05 vs. 0.09±0.04 mm (actual values: 0.0869±0.0448 mm, rounded), p<0.01, for a 38.6% reduction in vitreous cavity depth, and there was a corresponding reduction in axial length, FDM+vehicle vs. FDM+VPN (5 μM), 0.16±0.04 vs. 0.09±0.04 mm (actual values: 0.0925±0.0406 mm, rounded), p<0.001, for a 41.4% reduction in axial length. The low concentration 1 μM vinpocetine treatment group was also able to effectively control myopia progression, with FDM+vehicle vs. FDM+VPN (1 μM) -6.56±1.70 vs. -4.81±1.72 D, p<0.05, and a refractive inhibition rate of 26.7%.Comparing the progression of myopia with the negative control group, the model-induced myopia of the 0.1% atropine eye drop group after two weeks of administration was -3.93 ± 1.75 D, the refraction suppression rate was 40.0%, the vitreous cavity depth was 0.11 ± 0.05 mm (actual value was 0.1107 ± 0.0502 mm, rounded), the suppression rate of the vitreous cavity depth was 21.8%, and the axial length was 0.11 ± 0.05 mm (actual value was 0.1093 ± 0.0530 mm, rounded), the suppression rate of the axial length was 30.7%. During the administration period of the atropine group, adverse events of pupil dilation occurred, but no obvious ocular abnormalities were observed in the vinpocetine group. Whether atropine or vinpocetine was used for myopia intervention, the corneal curvature, anterior chamber, and crystalline lens of the test individuals were not affected (see Figure 7). In the laboratory to which the inventor belongs, no therapeutic effect was observed in a guinea pig myopia model with atropine at 0.01%, which is currently widely used as a concentration for clinical trials, under the same administration conditions as in this example (myopia model, administration method, administration frequency, administration amount, etc. are the same), and 0.01% atropine had no significant intervention effect, whether in refractive index or axial parameter index, which may be related to the short retention time on the ocular surface after administration of the ophthalmic solution to animals. Therefore, in terms of efficacy and safety, the risk-benefit ratio of administration of vinpocetine to myopic individuals is superior to atropine (for example, when vinpocetine is used during the daytime, there is no phenomenon such as photophobia caused by pupil dilation caused by atropine at the same time as treating myopia), and it is particularly suitable for the treatment of myopia in children and adolescents and the prevention and control of myopia in school-age groups.

[0301] This example proves that when vinpocetine eye drops are administered by eye drop, it can significantly inhibit the negative refraction of myopia, and significantly inhibit the extension of myopic axial length and the increase of vitreous cavity depth, just like when it is administered by subconjunctival injection near the eyeball.Such administration methods also have a positive dose-response relationship, that is, the higher the dose of vinpocetine, the more obvious the effect of treating myopia.At the same time, when administered non-invasively, the comprehensive performance of vinpocetine in treating myopia is better than that of the positive control atropine, especially in terms of the effect of controlling the progression of myopia.

[0302] Example 7: Apovincaminic acid (AVA), a metabolite of vinpocetine, can effectively prevent and control myopia The efficacy of the guinea pig model of myopia described in the present invention was evaluated by measuring the refraction and ocular axis of all the animals, and after removing the animals that did not meet the conditions, the animals were randomly divided into three groups, namely, apovincaminic acid alone group, negative control group (solvent group) and 0.1% atropine group (positive control group), in which the concentration of apovincaminic acid (AVA) was 1 μM. The method of preparing the model of myopic individuals was the same as in other examples of the present invention, and all groups were administered by subconjunctival injection near the eyeball, with the injection volume of 100 μL, and administered once daily for one week. The refraction and ocular axis parameters of the animals were measured before and after the efficacy experiment, and all data collection and processing methods were the same as in other examples of the present invention, and statistics were based on the difference between the experimental eye and the contralateral eye of the same subject. The AVA injection and atropine injection used in this example were both prepared by the inventors themselves using 0.9% saline, and no other active substances or additives were added.

[0303] The experimental results showed that the changes in refractive index and axial parameters of the animals in the negative control group were consistent with the expectations of the myopia model, and the positive control drug atropine showed the expected efficacy in the experiment, proving that the myopia model was successfully created in this experiment and can be used to evaluate the efficacy of AVA. The experimental results demonstrated that AVA, a metabolite of vinpocetine, can effectively inhibit the occurrence and progression of FDM-induced myopia (refraction is F 2,36 = 7.914, p = 0.001, and the vitreous cavity was 2,36 = 3.904, p = 0.029, and the eye axis is F 2,36 = 4.539, p = 0.017). After one week of continuous administration of 1 μM AVA, the increase in myopia and the corresponding increase in the ocular axis and vitreous cavity depth were effectively suppressed (see FIG. 8), specifically, FDM + vehicle (Vehicle) vs. FDM + AVA (1 μM) was -4.39 ± 1.73 vs. -2.65 ± 1.18 D, p < 0.01, the refractive inhibition rate was 39.6%, and the vitreous cavity depth was correspondingly suppressed, and FDM + Vehicle (Vehicle) vs. FDM + AVA (1μM) 0.09±0.04 vs. 0.06±0.02mm, p<0.05, inhibition rate of vitreous cavity depth 34.7%, axial length also inhibited, FDM + Vehicle (Vehicle) vs. FDM + AVA (1μM) 0.10±0.04 vs. 0.07±0.03mm, p<0.01, inhibition rate of axial length 36.4%. In the atropine group, pupil dilation occurred during the administration period, but no abnormality was observed in the AVA group. From the above results, it can be seen that AVA, a metabolite of vinpocetine, has a remarkable therapeutic effect in the prevention, control and treatment of myopia.

[0304] In summary, vinpocetine can not only significantly delay the process of the refraction becoming negative in myopic individuals or individuals prone to myopia, but also significantly inhibit the increase in the depth of the vitreous cavity and the elongation of the eye axis, significantly improve the symptoms associated with myopic disease, and obtain the effects of preventing, treating, and controlling the progression of myopia, and no abnormalities were observed in the eyes of all test individuals during the administration period, and no obvious changes were observed in the pupil size of the test eyes during the administration period. Therefore, vinpocetine can be used to prevent, control, and treat myopia, postpone the onset and progression of myopia, and control the progression of myopia, especially for the treatment, prevention, control, or improvement of pediatric and juvenile myopia, or simple axial myopia, or progressive myopia, or primary myopia, and their associated symptoms.

Claims

1. A drug or preparation for preventing or treating myopia, comprising an effective amount of vinpocetine, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a metabolite thereof, apovincaminic acid, or a crystalline compound thereof, or a combination of these substances as an active ingredient, A drug or formulation, characterized in that vinpocetine, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a metabolite thereof apovincaminic acid, or a crystalline compound thereof, or a combination of these substances, is the sole active ingredient, the main active ingredient, or the direct active ingredient of the drug or formulation, the myopia is simple myopia, and the drug or formulation does not contain a beta-adrenergic receptor agonist.

2. The drug or preparation according to claim 1, characterized in that the simple myopia is simple axial myopia or childhood and juvenile myopia.

3. The drug or preparation according to claim 2, characterized in that the pediatric and juvenile myopia is pediatric and juvenile myopia in the age group of 3 to 26 years.

4. The drug or preparation according to claim 3, wherein the pediatric and juvenile myopia aged 3 to 26 years is pediatric and juvenile axial myopia aged 3 to 26 years.

5. The drug or formulation according to any one of claims 1 to 4, characterized in that the concentration of vinpocetine, or a solvate thereof, or a pharma- ceutically acceptable salt thereof, or a metabolite thereof apovincaminic acid, or a crystalline compound thereof, or a combination of these substances in the drug or formulation is 0.01 μM to 1000 μM.

6. The drug or formulation according to any one of claims 1 to 4, wherein the drug or formulation is administered ophthalmically, by injection, intranasally or orally.

7. The drug or formulation according to claim 5, wherein the drug or formulation is administered ophthalmically, by injection, intranasally or orally.

8. 7. The drug or formulation of claim 6, wherein the drug or formulation is in the form of an ophthalmic administration formulation selected from the group consisting of eye drops, eye ointments, spray-type eye drops, intraocular implants, eye gels, eye pads, ocular microspheres, ophthalmic sustained release formulations, periocular injections, and intraocular injections.

9. 8. The drug or formulation of claim 7, wherein the drug or formulation is in the form of an ophthalmic administration formulation selected from the group consisting of eye drops, eye ointments, spray-type eye drops, intraocular implants, eye gels, eye pads, ocular microspheres, ophthalmic sustained release formulations, periocular injections, and intraocular injections.

10. The drug or formulation according to any one of claims 1 to 4, characterized in that the treatment of myopia is to control the progression of myopia or inhibit the increase in axial elongation or vitreous cavity depth in a myopic individual.

11. 6. The drug or formulation of claim 5, wherein the treatment of myopia is to control the progression of myopia or inhibit the increase in axial elongation or vitreous cavity depth in a myopic individual.

12. 9. The drug or formulation of claim 8, wherein the treatment of myopia is to control the progression of myopia or inhibit the increase in axial elongation or vitreous cavity depth in a myopic individual.

13. The drug or formulation of claim 9, wherein the treatment of myopia is characterized by controlling the progression of myopia or inhibiting the increase in axial elongation or vitreous cavity depth in a myopic individual.

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