Methods of treating retinal diseases
A method of treating or inhibiting degeneration of a retina of a subject in need thereof comprising administering an effective amount of a compound of metipranolol, or a metabolite thereof, to an organ, a tissue, or the subject, wherein the degeneration of the retina is caused by an ocular disease. In some embodiments, the compound, or a metabolite thereof, is administered topically, orally, or parenterally. In some embodiments, a drug delivery vehicle comprising a dosage of the compound, or the metabolite of, is delivered parenterally via intravitreal injection. In further embodiments, the dosage may range from 0.5 μg/day-15 μg/day.
1. A method of treating or inhibiting degeneration of a retina of a subject in need thereof comprising administering a dosage of an effective amount of desacetylmetipranolol to the eye of the subject, wherein the degeneration of the retina is caused by an ocular disease selected from the group consisting of diabetic retinopathy and choroidal neovascularization, wherein the dosage of the effective amount of desacetylmetipranolol is administered parenterally to the eye of the subject by direct injection.
2. The method of claim 1 , wherein the dosage of the effective amount of desacetylmetipranolol is within a drug delivery vehicle comprising biocompatible polymers or copolymers configured to release the effective amount of desacetylmetipranolol in a controlled manner and wherein the drug delivery vehicle is delivered via intravitreal injection.
3. The method of claim 2 , wherein the dosage of the effective amount of desacetylmetipranolol of the drug delivery vehicle ranges from 0.5 μg/day to 15 μg/day.
4. The method of claim 2 , wherein the drug delivery vehicle is bioerodible.
5. The method of claim 2 , wherein the drug delivery vehicle is an intravitreal insert.
6. The method of claim 2 , wherein the drug delivery vehicle is an amorphous mass.
7. A method of treating or inhibiting dystrophy of rods and cones of a retina of a subject in need thereof comprising administering a dosage of an effective amount of desacetylmetipranolol to the eye of the subject.
8. The method of claim 7 , wherein the dosage of the effective amount of desacetylmetipranolol is within a drug delivery vehicle comprising biocompatible polymers or copolymers configured to release the effective amount of desacetylmetipranolol in a controlled manner and wherein the drug delivery vehicle is delivered via intravitreal injection.
9. The method of claim 7 , wherein the dosage of the effective amount of desacetylmetipranolol of the drug delivery vehicle ranges from 0.5 μg/day-15 μg/day.
10. The method of claim 7 , wherein the drug delivery vehicle is bioerodible.
11. The method of claim 7 , wherein the drug delivery vehicle is an intravitreal insert.
12. The method of claim 7 , wherein the drug delivery vehicle is an amorphous mass.