US2002052398A1PendingUtilityA1
Pharmaceutical composition of 6-amino EM-12
Priority: Mar 1, 1993Filed: Dec 12, 2001Published: May 2, 2002
Est. expiryMar 1, 2013(expired)· nominal 20-yr term from priority
Inventors:Robert D'Amato
A61P 9/08A61P 9/10A61P 35/04A61P 37/04A61P 3/10A61P 37/02A61P 43/00A61P 7/04A61P 7/06A61P 9/00A61P 35/00A61P 31/00A61P 29/00A61P 27/06A61P 31/22A61P 31/04A61P 27/00A61P 31/12A61P 31/10A61P 35/02A61P 27/02A61P 27/14A61P 33/02A61P 27/10A61K 31/445A61P 17/00A61K 31/19A61P 19/02A61P 19/08A61P 1/00A61P 17/06A61P 19/00A61P 17/02A61K 31/454A61K 31/4035A61K 31/535C07D 403/02A61K 31/40A61K 31/44A61K 31/33A61K 31/185
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Claims
Abstract
The present invention comprises a group of compounds that effectively inhibit angiogenesis. More specifically, thalidomide and various related compounds such as thalidomide precursors, analogs, metabolites and hydrolysis products have been shown to inhibit angiogenesis and to treat disease states resulting from angiogenesis. Importantly, these compounds can be administered orally.
Claims
exact text as granted — not AI-modified1 . A method of treating an eye condition associated with angiogenesis in a human or animal comprising administering to said human or animal an angiogenesis inhibiting amount of EM-138,
2 . The method of claim 1 wherein the eye condition is selected from the group consisting of diabetic retinopathy, retinopathy of prematurity, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, epidemic keratoconjunctivitis, Vitamin A deficiency, contact lens overwear, atopic keratitis, superior limbic keratitis, pterygium keratitis sicca, myopia, Terrien's marginal degeneration, mariginal keratolysis, radial keratotomy, macular degeneration, post-laser complications, chronic retinal detachment; optic pits, hyperviscosity syndromes, chronic uveitis, chronic vitritis, ocular neovascular disease, age-related macular degeneration, presumed ocular histoplasmosis, infections causing retinitis or choroiditis, proliferative vitreoretinopathy, scleritis, Eales'disease, Best's disease, and trachoma.
3 . The method of claim 1 wherein the amount administered is between approximately 0.1 and approximately 300 mg/kg/day.
4 . The method of claim 3 wherein the amount administered is between approximately 0.5 and approximately 50 mg/kg/day.
5 . The method of claim 4 wherein the amount administered is between approximately 1 and approximately 10 mg/kg/day.
6 . The method of claim 1 wherein the compound is administered in the form of a tablet or capsule.
7 . The method of claim 1 wherein the compound is administered in the form of a lozenge, a cachet, a solution, a suspension, an emulsion, a powder, an aerosol, a suppository, a spray, a pastille,an ointment, a cream, a paste, a foam, a gel, a tamport, or a pessary.
8 . The method of claim 1 wherein the administration is oral, parenteral, transdermal, or topical.
9 The method of claim 1 wherein the administration is sublingual, buccal, rectal, vaginal, or nasal.
10 . A method of treating a non-tumor blood condition associated with angiogenesis in a human or animal comprising administering to said human or animal an angiogenesis inhibiting amount of EM-138,
11 . The method of claim 10 wherein the blood condition is selected from the group consisting of vein occlusion, artery occlusion, carotid obstructive disease, polyarteritis, atherosclerosis, Osler-Weber-Rendu disease, and sickle cell anemia.
12 . A method of treating an ulcerative disease associated with angiogenesis in a human or animal comprising administering to said human or animal an angiogenesis inhibiting amount of EM-38,
13 . The method of claim 12 wherein the ulcerative disease is selected from the group consisting of bacterial ulcers, fungal ulcers, Mooren's ulcer, Wegener's sarcoidosis, Stevens-Johnson disease, Behcet's disease, pemphigoid, and ulceritive colitis.
14 . A method of treating a skin condition associated with angiogenesis in a human or animal comprising administering to said human or animal an angiogenesis inhibiting amount of EM-138,
15 . The method of claim 14 wherein the skin condition is selected from the group consisting of acne, rosacea, chemical burns, and psoriasis.
16 . A method of treating an immune disease associated with angiogenesis in a human or animal comprising administering to said human or animal an angiogenesis inhibiting amount of EM-138,
acquired immune deficiency syndrome, and osteoarthritis.
18 . A method of treating an infection associated with angiogenesis in a human or animal comprising administering to said human or animal an angiogenesis inhibiting amount of EM-138,
19 . The method of claim 18 wherein the infection is selected from the group consisting of Herpes simplex infections, Herpes zoster infections, Mycobacteria infections, protozoan infections, toxoplasmosis, syphilis, and Bartonellosis.
20 . A method for inhibiting undesired angiogenesis in a human or animal wherein the angiogenesis is associated with a condition selected from the group consisting of trauma, sjogren's syndrome, phylectenulosis, sarcoid, pseudoxanthoma elasticum, Stargardt's disease, Paget's disease, Lyme's disease, par planitis, pyogenic granulomas, and lipid degeneration comprising administering to the human or animal an angiogenesis inhibiting amount of EM-138,
21 . A method of inhibiting undesired angiogenesis in a human or animal wherein the angiogenesis is associated with a condition selected from the group consisting of Crohn's disease and chronic inflammation comprising administering to the human or animal an angiogenesis inhibiting amount of EM-138,
22 . A method of inhibiting undesired angiogenesis in a human or animal wherein the angiogenesis is associated with abnormal amount of EM-138,Join the waitlist — get patent alerts
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