Method for treating eye disease or conditions affecting the posterior segment of the eye
Described is the use of prodrug for the manufacture of a medicament useful for treating an ocular disease affecting the posterior segment of the eye, in a subject in need thereof, wherein the prodrug is a composition injected into the vitreous body, and the frequency of injections does not exceed one injection per month.
1. A method for treating an ocular disease affecting the posterior segment of the eye selected from the group consisting of Exudative Age Related Macular Degeneration, Choroidal Neovascular Membranes and Cystoid Macular Edema, Inflammatory Disorders, Uveitic Retinal Disease, Vascular Disorders, Diabetic Retinopathy, Diabetic Macular Edema, Arterial Occlusion, Venous Occlusion, Heredo Retinal Dystrophies, and Stargardt's Disease, in a subject in need thereof,
wherein a composition comprising about 0.01% to 10% w/w of a prodrug of a drug suitable for the treatment of said ocular disease, and medium chain triglycerides, is injected into the vitreous body, and the frequency of injections does not exceed one injection per month, said prodrug sustainingly releasing a drug in vivo,
said release occurring by biological reactions at affected tissues of the posterior segment of the eye,
the prodrug being a C4-C16 alkyl ester or ether of the drug,
the drug being an anti-inflammatory selected from the group consisting of alclometasone dipropionate, amcinonide, amcinafel, amcinafide, beclamethasone, betamethasone, betamethasone dipropionate, betamethasone valerate, clobetasone propionate, chloroprednisone, clocortelone, cortisol, cortisone, cortodoxone, difluorosone diacetate, descinolone, desonide, defluprednate, dihydroxycortisone, desoximetasone, dexamethasone, deflazacort, diflorasone, diflorasone diacetate, dichlorisone, esters of betamethasone, fluazacort, flucetonide, flucloronide, fludrotisone, fluorocortisone, flumethasone, flunisolide, fluocinonide, fluocinolone, fluocinolone acetonide, flucortolone, fluperolone, fluprednisolone, fluoroandrenolone acetonide, fluocinolone acetonide, flurandrenolide, fluorametholone, fluticasone propionate, hydrocortisone, hydrocortisone butyrate, hydrocortisone valerate, hydrocortamate, loteprendol, medrysone, meprednisone, methylprednisone, methylprednisolone, mometasone furoate, paramethasone, paramethasone acetate, prednisone, prednisolone, prednidone, triamcinolone acetonide, triamcinolone hexacatonide, and triamcinolone, salts, derivatives, and a mixture thereof, and
the prodrug is not hexadecyloxypropylcyclic cidofovir or 1-O-hexadecylpropanediol-3-phosphoganciclovir.
2. The method according to claim 1 , wherein two months after one injection of said prodrug, the drug cannot be detected in the vitreous or the molar ratio of the prodrug to the drug, in the vitreous, is more than 60.
3. The method according to claim 1 , wherein the molar ratio of the prodrug to the drug, in the retina, two months after one injection of said prodrug, is less than 60.
4. The method according to claim 1 , wherein the molar ratio of the prodrug to the drug, in the choroid, two months after one injection of said prodrug, is less than 60.
5. The method according to claim 1 , wherein the prodrug is injected in the vitreous in an amount enabling the sustained release of a therapeutically amount of said drug for a duration of at least one month.
6. The method according to claim 1 , wherein the prodrug is injected at most once every two months.
7. The method according to claim 1 , wherein the prodrug is in combination with any suitable excipient or carrier suitable for ophthalmic use.
8. The method according to claim 1 wherein the prodrug is within an emulsion.
9. The method according to claim 1 , wherein the prodrug is injected in the vitreous in an amount enabling the sustained release of a therapeutically amount of said drug for a duration of at least two months.
10. The method according to claim 1 , wherein the prodrug is injected at most once every two months.