US2018237429A1PendingUtilityA1
Compositions, formulations and methods for treating ocular diseases
Est. expiryMar 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
A61K 31/426A61K 31/513A61K 31/4439C07D 277/56A61K 31/497A61P 27/00C07D 417/04C07D 417/12A61K 9/0051C07D 277/30A61K 31/427C07D 277/64A61K 47/40A61K 2039/505C07K 16/22C07D 277/60A61K 31/496A61K 31/506A61K 38/179A61K 9/0019A61K 31/433A61K 47/6951A61K 39/3955A61P 27/02A61K 31/428C07D 277/28A61K 31/538A61K 2039/54A61K 47/26A61K 39/395
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Claims
Abstract
Disclosed herein are compounds effective for activation of Tie-2 and inhibition of HPTP-beta. The compounds can provide effective therapy for conditions associated with angiogenesis, for example, ocular conditions. Formulations for increased solubility are disclosed. Combination therapy with antibodies and PK/PD data are also disclosed.
Claims
exact text as granted — not AI-modified1 - 54 . (canceled)
55 . A method of treating glaucoma, the method comprising administering to a subject in need thereof a therapeutically-effective amount of a Tie-2 activator.
56 . The method of claim 55 , wherein the Tie-2 activator binds HPTP-beta.
57 . The method of claim 55 , wherein the Tie-2 activator inhibits HPTP-beta.
58 . The method of claim 55 , wherein the Tie-2 activator comprises an amino acid backbone.
59 . The method of claim 55 , wherein the administering is subcutaneous.
60 . The method of claim 55 , wherein the administering is topical.
61 . The method of claim 55 , wherein the administering is to the eye of the subject.
62 . The method of claim 55 , wherein the Tie-2 activator is formulated as a drop.
63 . The method of claim 55 , wherein the Tie-2 activator is formulated as a drop, wherein the drop is administered to an eye of the subject.
64 . The method of claim 55 , wherein the therapeutically-effective amount is from about 0.1 mg to about 100 mg.
65 . The method of claim 55 , wherein the therapeutically-effective amount is from about 0.5 mg to about 30 mg.
66 . The method of claim 55 , wherein the therapeutically-effective amount is from about 0.05 mg to about 1.5 mg.
67 . The method of claim 55 , wherein the subject is human.Join the waitlist — get patent alerts
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