IP Library Granted Patent US 7,776,899
Granted Patent B2
US 7,776,899 · App. 10/700,274 · Granted Aug 17, 2010

Methods for treatment of erectile dysfunction

Assignee: Repros Therapeutics Inc.
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Quick Facts
Patent No.
US 7,776,899
App. No.
10/700,274
Granted
Aug 17, 2010
Kind
B2
Abstract

Improved drug compositions and methods useful in the treatment of male erectile dysfunction. An optimized mixture of the drugs phentolamine mesylate, papaverine hydrochloride, and alprostadil in a buffer containing L-arginine and glycine is to be injected into the penile tissue to produce an erection in otherwise impotent men.

Claims (13)

1. A method for the treatment of male erectile dysfunction which comprises administering to a male in need thereof a pharmacologically effective amount of a composition comprising an α-adrenergic blocker selected from phentolamine mesylate or phentolamine hydrochloride and a prostaglandin being alprostadil in a buffer, wherein the buffer comprises L-arginine and glycine and has a pH range of from about 3 to about 5.

2. The method of claim 1 wherein the α-adrenergic blocker is phentolamine mesylate, or any pharmaceutically acceptable salt thereof.

3. The method of claim 1 wherein the α-adrenergic blocker is phentolamine mesylate, or any pharmaceutically acceptable salt thereof and the prostaglandin is alprostadil, and wherein the composition is administered in one or more dosages.

4. The method of claim 1 wherein the buffer comprises glycine and L-arginine in a weight ratio of about 1:20.

5. The method of claim 1 wherein the buffer further comprises benzyl alcohol and mannitol and has a pH range of from about 3 to about 5.

6. The method of claim 3 wherein a weight ratio of phentolamine mesylate: alprostadil is about 0.5:0.005 to about 5: 0.20.

7. The method of claim 3 wherein a weight ratio of phentolamine mesylate: alprostadil is about 1:0.01.

8. The method of claim 3 wherein a dosage of phentolamine mesylate and alprostadil is less than 40 μg/ml alprostadil and less than 10 mg/ml phentolamine.

9. The method of claim 8 wherein the dosage of phentolamine mesylate and alprostadil are in the range of about 1.25-5 mg/ml phentolamine and about 5-20 μg/ml alprostadil.

10. The method of claim 8 wherein a dosage of phentolamine mesylate and alprostadil are about 1 mg/ml phentolamine and about 0.01 mg/ml alprostadil.

11. The method of claim 8 wherein the dosage of phentolamine mesylate and alprostadil is present in a total volume of 0.5 ml.

12. The method of claim 3 wherein the dosage of alprostadil is about 5 μg/ml in a total volume of 0.5 ml.

13. The method of claim 3 wherein a dosage of phentolamine is about 1.25 mg/ml in a total volume of 0.5 ml.

Assignments (1)
CHANGE OF NAME Recorded Nov 30, 2006
From: ZONAGEN, INC.
To: REPROS THERAPEUTICS INC.
Reel/Frame 018573/0121 →
Continuity (3)
Division 0949462700 · Jan 31, 2000
Division 0915467700 · Sep 17, 1998
Related Publication 20040102475A1 · May 27, 2004