IP Library Granted Patent US 8,486,960
Granted Patent B2
US 8,486,960 · App. 13/530,025 · Granted Jul 16, 2013

Formulations and methods for vascular permeability-related diseases or conditions

Inventors: David M. Kleinman (Rochester, NY); Thierry Nivaggioli (Atherton, CA); Mary E. Gerritsen (San Mateo, CA); David A. Weber (Danville, CA)
Assignee: Santen Pharmaceutical Co., Ltd.
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Quick Facts
Patent No.
US 8,486,960
App. No.
13/530,025
Granted
Jul 16, 2013
Kind
B2
Abstract

Described herein are formulations and methods for treating, inhibiting, preventing, delaying onset, or causing regression of a disease or condition relating to vascular permeability.

Claims (11)

1. A method to decrease vascular permeability in a subject in need thereof, comprising administering a therapeutic agent to the subject at a dose of no greater than an amount equivalent to 2 mg/kg of rapamycin,

wherein the subject in need thereof has a disease or condition selected from the group consisting of blepharitis, eyelid swelling, conjunctival edema, contact lens induced conjunctivitis, pinguecula, hordeolum, and chalazion,

and the therapeutic agent is rapamycin, or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein the subject is a human subject.

3. The method of claim 1 , wherein the disease or condition is blepharitis.

4. The method of claim 1 , wherein the therapeutic agent is rapamycin.

5. The method of claim 1 , wherein the therapeutic agent is administered to the subject in need thereof at a dose of no greater than an amount equivalent to 0.5 mg/kg of rapamycin.

6. The method of claim 1 , wherein the therapeutic agent is administered to the subject in need thereof at a dose of no greater than an amount equivalent to 0.27 mg/kg of rapamycin.

7. The method of claim 1 , wherein the therapeutic agent is administered to the subject in need thereof at a dose of no greater than an amount equivalent to 0.07 mg/kg of rapamycin.

8. The method of claim 1 , wherein the therapeutic agent is administered to the subject in need thereof at a dose of no greater than an amount equivalent to 0.014 mg/kg of rapamycin.

9. The method of claim 1 , wherein the therapeutic agent is rapamycin, and the rapamycin is administered in a formulation containing about 2% w/w rapamycin, about 4% w/w ethanol, and about 94% w/w PEG 400.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2012
From: KLEINMAN, DAVID M.; NIVAGGIOLI, THIERRY; GERRITSEN, MARY E.; WEBER, DAVID A.
To: MACUSIGHT, INC.
Reel/Frame 028538/0104 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2012
From: MACUSIGHT, INC.
To: SANTEN PHARMACEUTICAL CO., LTD.
Reel/Frame 028539/0252 →
Continuity (3)
Continuation 11726813 · Mar 23, 2007
Provisional Application 60785814 · Mar 23, 2006
Related Publication 20120329759A1 · Dec 27, 2012