US2020157158A1PendingUtilityA1

Modulation of Wnt5a to Treat Glaucoma

Assignee: UNIV CALIFORNIAPriority: Aug 20, 2017Filed: Jan 26, 2020Published: May 21, 2020
Est. expiryAug 20, 2037(~11.1 yrs left)· nominal 20-yr term from priority
Inventors:Lu Chen
A61K 2039/54A61K 9/0048A61K 2039/505A61K 38/18A61P 27/06C07K 2317/76C12N 2310/14C07K 16/22C12N 15/113A61K 38/08A61K 9/0019C07K 14/4703A61K 9/06C12N 15/111C07K 7/06A61K 31/335A61K 48/00A61P 27/00A61K 31/713A61K 38/00A61K 39/395A61K 9/10A61K 9/08
56
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

Glaucoma or pathogenic intraocular pressure is treated by locally administering to an eye in need thereof formulations of a Wnt5a inhibitor.

Claims

exact text as granted — not AI-modified
1 . A method of treating glaucoma or pathogenic intraocular pressure, comprising locally administering to an eye in need thereof a Wnt5a inhibitor. 
     
     
         2 . The method of  claim 1  wherein the administering step comprises delivery by eye drop or by intracameral, subconjuctival injection or intravitreal injection. 
     
     
         3 . The method of  claim 1  wherein the administration is topical, and the inhibitor is administered in form of a topical ophthalmic gel, ointment, suspension or solution. 
     
     
         4 . The method of  claim 1  wherein the inhibitor is selected from an antibody, an siRNA, an small interfering peptide, and a small molecule inhibitor. 
     
     
         5 . The method of  claim 2  wherein the inhibitor is selected from an antibody, an siRNA, an small interfering peptide, and a small molecule inhibitor. 
     
     
         6 . The method of  claim 3  wherein the inhibitor is selected from an antibody, an siRNA, an small interfering peptide, and a small molecule inhibitor. 
     
     
         7 . The method of  claim 1  wherein the inhibitor is an anti-Wnt5a antibody. 
     
     
         8 . The method of  claim 1  wherein the inhibitor is an anti-Wnt5a siRNA 
     
     
         9 . The method of  claim 1  wherein the inhibitor is an anti-Wnt5a small interfering peptide 
     
     
         10 . The method of  claim 1  wherein the inhibitor is an anti-Wnt5a small molecule inhibitor selected from t-butyloxycarbonyl-modified Wnt5A hexapeptide (Box5) and 6,7-dihydro-10alpha-hydroxy radicicol. 
     
     
         11 . The method of  claim 1  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning Para 31. 
     
     
         12 . The method of  claim 2  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         13 . The method of  claim 3  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         14 . The method of  claim 4  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         15 . The method of  claim 5  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         16 . The method of  claim 6  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         17 . The method of  claim 7  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         18 . The method of  claim 8  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         19 . The method of  claim 9  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         20 . The method of  claim 10  further comprising detecting a resultant decrease in the eye of a parameter of glaucoma selected from pathogenic intraocular pressure (IOP), corneal edema, retinal ganglion cell (RGC) death, and retinal nerve fiber layer (RNFL) thinning. 
     
     
         21 . An ophthalmic formulation of a Wnt5a-specific inhibitor selected from an antibody, an siRNA, an small interfering peptide, and a small molecule inhibitor, in unit dosage form for treating glaucoma or pathogenic intraocular pressure, wherein optionally:
 in the form of a topical ophthalmic gel, ointment, suspension or solution;   the dosage form is an inhibitor-loaded contact lens, eye drop, depot or bollus;   packaged in an eye drop dispenser;   loaded in a syringe configured for intracameral injection, subconjuctival injection or intravitreal injection; and/or   further comprising excipients and features suitable for direct, topical delivery to the eye, selected from the group consisting of opthalmically suitable clarity, pH buffer, tonicity, viscosity, stability and sterility.

Join the waitlist — get patent alerts

Track US2020157158A1 — get alerts on status changes and closely related new filings.

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