IP Library Patent Application 19190263
Patent Application
App. No. 19/190,263

AQUEOUS OPHTHALMIC SOLUTIONS OF PHENTOLAMINE AND MEDICAL USES THEREOF

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Patent No.
US None
App. No.
19/190,263
Abstract

The invention provides aqueous ophthalmic solutions of phentolamine or pharmaceutically acceptable salts thereof, medical kits, and methods for using such ophthalmic solutions to improve visual performance in a patient. Exemplary aqueous ophthalmic solutions include those containing phentolamine mesylate, mannitol, sodium acetate, and water.

Claims (60)

1 . An aqueous ophthalmic solution comprising:

a. about 0.1% (w/v) to about 4% (w/v) of phentolamine or a pharmaceutically acceptable salt thereof;

b. at least one polyol compound selected from the group consisting of mannitol, glycerol, propylene glycol, ethylene glycol, sorbitol, and xylitol;

c. about 0.1 mM to about 10 mM of at least one buffer;

d. water; and

e. optionally one or more of a poly (C 2-4 alkylene) glycol polymer, dextran, pharmaceutically acceptable carrier, pharmaceutically acceptable salt, cellulose agent, carbohydrate, alkali metal halide, alkaline earth metal halide, boric acid, cyclodextrin, dextrose, glycerin, urea, viscosity modifying agent, solubilizing agent, surfactant, demulcent polymer, wetting agent, or water-miscible solvent;

wherein said aqueous ophthalmic solution has a pH of about 4.0 to about 7.5; and said aqueous ophthalmic solution has a temperature of 2-8° C.

2 . The aqueous ophthalmic solution of claim 1 , wherein the at least one polyol has a concentration of from about 1% (w/v) to about 6% (w/v) in the aqueous ophthalmic solution.

3 . The aqueous ophthalmic solution of claim 1 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is present in the solution in an amount of from about 0.5% (w/v) to about 2% (w/v); and the at least one polyol compound is present in the solution in an amount of from about 2% (w/v) to about 5% (w/v).

4 . The aqueous ophthalmic solution of claim 3 , wherein the at least one polyol compound is mannitol.

5 . The aqueous ophthalmic solution of claim 4 , wherein the solution has a pH of 4.5 to 5.5.

6 . The aqueous ophthalmic solution of claim 5 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is phentolamine mesylate.

7 . The aqueous ophthalmic solution of claim 1 , wherein the solution consists essentially of:

a. about 0.1% (w/v) to about 4% (w/v) of phentolamine or a pharmaceutically acceptable salt thereof;

b. least one polyol compound selected from the group consisting of mannitol, glycerol, propylene glycol, ethylene glycol, sorbitol, and xylitol;

c. about 0.1 mM to about 10 mM of at least one buffer;

d. water; and

e. optionally one or more of a poly (C 2-4 alkylene) glycol polymer, dextran, pharmaceutically acceptable carrier, pharmaceutically acceptable salt, cellulose agent, carbohydrate, alkali metal halide, alkaline earth metal halide, boric acid, cyclodextrin, dextrose, glycerin, urea, viscosity modifying agent, solubilizing agent, surfactant, demulcent polymer, wetting agent, or water-miscible solvent.

wherein said aqueous ophthalmic solution has a pH of about 4.0 to about 7.5; and said aqueous ophthalmic solution has a temperature of 2-8° C.

8 . The aqueous ophthalmic solution of claim 7 , wherein the at least one polyol has a concentration of from about 1% (w/v) to about 6% (w/v) in the aqueous ophthalmic solution.

9 . The aqueous ophthalmic solution of claim 7 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is present in the solution in an amount of from about 0.5% (w/v) to about 2% (w/v); and the at least one polyol compound is present in the solution in an amount of from about 2% (w/v) to about 5% (w/v).

10 . The aqueous ophthalmic solution of claim 9 , wherein the at least one polyol compound is mannitol.

11 . The aqueous ophthalmic solution of claim 10 , wherein the solution has a pH of 4.5 to 5.5.

12 . The aqueous ophthalmic solution of claim 11 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is phentolamine mesylate.

13 . An aqueous ophthalmic solution, comprising:

a. about 0.1% (w/v) to about 4% (w/v) of phentolamine or a pharmaceutically acceptable salt thereof;

b. at least one polyol compound selected from the group consisting of mannitol, glycerol, propylene glycol, ethylene glycol, sorbitol, and xylitol;

c. about 0.1 mM to about 10 mM of at least one buffer;

d. water; and

e. optionally one or more of an alkali metal halide or alkaline earth metal halide;

wherein said aqueous ophthalmic solution has a pH of about 4.0 to about 7.5; and said aqueous ophthalmic solution has a temperature of 2-8° C.

14 . The aqueous ophthalmic solution of claim 13 , wherein the at least one polyol has a concentration of from about 1% (w/v) to about 6% (w/v) in the aqueous ophthalmic solution.

15 . The aqueous ophthalmic solution of claim 13 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is present in the solution in an amount of from about 0.5% (w/v) to about 2% (w/v); and the at least one polyol compound is present in the solution in an amount of from about 2% (w/v) to about 5% (w/v).

16 . The aqueous ophthalmic solution of claim 15 , wherein the at least one polyol compound is mannitol.

17 . The aqueous ophthalmic solution of claim 16 , wherein the solution has a pH of 4.5 to 5.5.

18 . The aqueous ophthalmic solution of claim 17 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is phentolamine mesylate.

19 . An aqueous ophthalmic solution, consisting essentially of:

a. about 0.1% (w/v) to about 4% (w/v) of phentolamine or a pharmaceutically acceptable salt thereof;

b. at least one polyol compound selected from the group consisting of mannitol, glycerol, propylene glycol, ethylene glycol, sorbitol, and xylitol;

c. about 0.1 mM to about 10 mM of at least one buffer;

d. water; and

e. optionally one or more of an alkali metal halide or alkaline earth metal halide;

wherein said aqueous ophthalmic solution has a pH of about 4.0 to about 7.5; and said aqueous ophthalmic solution has a temperature of 2-8° C.

20 . The aqueous ophthalmic solution of claim 19 , wherein the at least one polyol has a concentration of from about 1% (w/v) to about 6% (w/v) in the aqueous ophthalmic solution.

21 . The aqueous ophthalmic solution of claim 19 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is present in the solution in an amount of from about 0.5% (w/v) to about 2% (w/v); and the at least one polyol compound is present in the solution in an amount of from about 2% (w/v) to about 5% (w/v).

22 . The aqueous ophthalmic solution of claim 21 , wherein the at least one polyol compound is mannitol.

23 . The aqueous ophthalmic solution of claim 22 , wherein the solution has a pH of 4.5 to 5.5.

24 . The aqueous ophthalmic solution of claim 23 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is phentolamine mesylate.

25 . An aqueous ophthalmic solution, consisting of:

a. about 0.1% (w/v) to about 4% (w/v) of phentolamine or a pharmaceutically acceptable salt thereof;

b. at least one polyol compound selected from the group consisting of mannitol, glycerol, propylene glycol, ethylene glycol, sorbitol, and xylitol;

c. about 0.1 mM to about 10 mM of at least one buffer;

d. water; and

e. optionally one or more of an alkali metal halide or alkaline earth metal halide;

wherein said aqueous ophthalmic solution has a pH of about 4.0 to about 7.5; and said aqueous ophthalmic solution has a temperature of 2-8° C.

26 . The aqueous ophthalmic solution of claim 25 , wherein the at least one polyol has a concentration of from about 1% (w/v) to about 6% (w/v) in the aqueous ophthalmic solution.

27 . The aqueous ophthalmic solution of claim 25 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is present in the solution in an amount of from about 0.5% (w/v) to about 2% (w/v); and the at least one polyol compound is present in the solution in an amount of from about 2% (w/v) to about 5% (w/v).

28 . The aqueous ophthalmic solution of claim 27 , wherein the at least one polyol compound is mannitol.

29 . The aqueous ophthalmic solution of claim 28 , wherein the solution has a pH of 4.5 to 5.5.

30 . The aqueous ophthalmic solution of claim 29 , wherein the phentolamine or a pharmaceutically acceptable salt thereof is phentolamine mesylate.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2026
From: MEYER, ALAN R.
To: OCULARIS PHARMA, LLC
Reel/Frame 074673/0812 →
SECURITY INTEREST Recorded Apr 21, 2026
From: OPUS GENETICS, INC.
To: OPCM SA LLC, AS PURCHASER AGENT FOR THE SECURED PARTIES
Reel/Frame 075478/0138 →
MERGER Recorded Oct 9, 2025
From: OCULARIS PHARMA, LLC
To: OCUPHIRE PHARMA, INC.
Reel/Frame 073068/0845 →
CHANGE OF NAME Recorded Oct 9, 2025
From: OCUPHIRE PHARMA, INC.
To: OPUS GENETICS, INC.
Reel/Frame 073069/0550 →
CHANGE OF NAME Recorded Sep 5, 2025
From: OCUPHIRE PHARMA, INC.
To: OPUS GENETICS, INC.
Reel/Frame 072819/0171 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 5, 2025
From: MEYER, ALAN R.
To: OCULARIS PHARMA, LLC
Reel/Frame 072819/0162 →
MERGER Recorded Sep 5, 2025
From: OCULARIS PHARMA, LLC
To: OCUPHIRE PHARMA, INC.
Reel/Frame 072819/0167 →