US2016220541A1PendingUtilityA1

Compositions, formulations and methods for treating ocular diseases

Assignee: AERPIO THERAPEUTICS INCPriority: Mar 15, 2013Filed: Apr 14, 2016Published: Aug 4, 2016
Est. expiryMar 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
C07D 277/30C07K 16/22A61K 31/428A61K 31/496A61K 31/513C07D 417/12A61K 31/4439C07D 277/56A61K 31/538A61K 31/426C07D 277/64A61K 38/179A61K 31/433C07D 417/04A61K 39/395A61K 47/40C07D 277/60A61P 27/00A61P 27/02A61K 47/6951A61K 31/506A61K 9/0051A61K 2039/505A61K 31/497A61K 2039/54A61K 9/0019A61K 31/427A61K 47/26C07D 277/28A61K 39/3955
63
PatentIndex Score
0
Cited by
0
References
0
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-modified
1 - 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, or a pharmaceutically-acceptable salt thereof. 
     
     
         56 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof binds HPTP-beta. 
     
     
         57 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof inhibits HPTP-beta. 
     
     
         58 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof is a phosphate mimetic. 
     
     
         59 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof comprises an amino acid backbone. 
     
     
         60 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof comprises a sulfamic acid. 
     
     
         61 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof is administered subcutaneously. 
     
     
         62 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof is administered topically. 
     
     
         63 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof is administered to an eye of the subject. 
     
     
         64 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof is formulated as a drop. 
     
     
         65 . The method of  claim 55 , wherein the Tie-2 activator or the pharmaceutically-acceptable salt thereof is formulated as a drop, wherein the drop is administered to an eye of the subject. 
     
     
         66 . The method of  claim 55 , wherein the therapeutically-effective amount is from about 0.1 mg to about 100 mg. 
     
     
         67 . The method of  claim 55 , wherein the therapeutically-effective amount is from about 0.5 mg to about 30 mg. 
     
     
         68 . The method of  claim 55 , wherein the therapeutically-effective amount is from about 0.05 mg to about 1.5 mg. 
     
     
         69 . The method of  claim 55 , wherein the therapeutically-effective amount is about 0.05 mg. 
     
     
         70 . The method of  claim 55 , wherein the therapeutically-effective amount is about 30 mg. 
     
     
         71 . The method of  claim 55 , wherein the therapeutically-effective amount is about 15 mg. 
     
     
         72 . The method of  claim 55 , wherein the subject is human.

Join the waitlist — get patent alerts

Track US2016220541A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.