IP Library Patent Application 17144548
Patent Application
App. No. 17/144,548

COMBINATIONS OF POSITIVE ALLOSTERIC MODULATORS AND NICOTINIC ACETYLCHOLINE RECEPTOR AGONISTS FOR TREATING OCULAR CONDITIONS

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Quick Facts
Patent No.
US None
App. No.
17/144,548
Abstract

Described herein are methods and pharmaceutical formulations for treating dry eye disease, increasing tear production, and reducing ocular discomfort.

Claims (41)

1 - 91 . (canceled)

92 . A method of treating keratitis, dry eye disease, increasing tear production, or reducing ocular discomfort in an individual in need thereof, comprising administering

a first dose, and optionally one or more subsequent doses, of an effective amount of a nicotinic acetylcholine receptor (nAChR) agonist, or a pharmaceutically acceptable salt thereof, and

a first dose, and optionally one or more subsequent doses, of an effective amount of a positive allosteric modulator (PAM), or a pharmaceutically acceptable salt thereof,

into a nasal cavity of the individual in need thereof;

wherein the nAChR agonist, or a pharmaceutically acceptable salt thereof, is varenicline, or a pharmaceutically acceptable salt thereof, or compound 1 having the structure

or a pharmaceutically acceptable salt thereof.

93 . The method of claim 92 , wherein keratitis is neurotrophic keratitis.

94 . A method of treating keratitis, dry eye disease, increasing tear production, or reducing ocular discomfort in an individual in need thereof, comprising administering

an effective amount of a positive allosteric modulator (PAM), or a pharmaceutically acceptable salt thereof, into a nasal cavity of the individual in need thereof.

95 . The method of claim 92 , wherein 5-4000 micrograms of the nAChR agonist, or a corresponding amount of a pharmaceutically acceptable salt thereof, per dose is administered to the individual.

96 . The method of claim 92 , wherein the nAChR agonist, or a pharmaceutically acceptable salt thereof, is administered in a pharmaceutical formulation for nasal administration comprising between 1 mg/mL and 40 mg/mL of nAChR agonist, or a corresponding amount of a pharmaceutically acceptable salt thereof.

97 . The method of claim 92 , wherein the nAChR agonist, or a pharmaceutically acceptable salt thereof, is administered in a pharmaceutical formulation for nasal administration, and the total volume of the pharmaceutical formulation administered per dose of the nAChR agonist, or a pharmaceutically acceptable salt thereof, to the individual is 50 microliters-250 microliters.

98 . The method of claim 92 , wherein the individual has undergone Lasik surgery within 2 weeks or is scheduled to undergo Lasik surgery within 2 weeks.

99 . The method of claim 92 , wherein the nAChR agonist is varenicline, or a pharmaceutically acceptable salt thereof.

100 . The method of claim 92 , wherein the nAChR agonist is compound 1, or a pharmaceutically acceptable salt thereof.

101 . The method of claim 92 , wherein the PAM is selected from the group consisting of 17-beta-Estradiol, (R)-7-bromo-N-(piperidin-3-yl)benzo[b]thiophene-2-carboxamide, ivermectin, galantamine, genistein, 5-hydroxyindole, 4BP-TQS, A-86774, CCMI, levamisole, morantel, LY-2087101, mecamylamine, menthol, NS206, NS1738, NS9283, PNU-120596, RO5126946, TBS-345, dFBR, and HEPES, or a pharmaceutically acceptable salt of any of the foregoing.

102 . The method of claim 92 , wherein the PAM is (R)-7-bromo-N-(piperidin-3-yl)benzo[b]thiophene-2-carboxamide, or a pharmaceutically acceptable salt thereof.

103 . The method of claim 92 , wherein the individual in need thereof has a blood plasma Cmax of the nAChR agonist, or a pharmaceutically acceptable salt thereof, of less than 5 ng/mL.

104 . The method of claim 92 , wherein the effective treatment of the individual is indicated by one or more of the tests selected from the group consisting of

a) Eye Dryness score test on a visual analog scale,

b) Schirmer's test,

c) Corneal Fluorescein Staining test, and

d) Ocular Surface Disease Index test.

105 . A pharmaceutical formulation for local administration into the nasal cavity of an individual comprising a nAChR agonist, or a pharmaceutically acceptable salt thereof, and a PAM, or a pharmaceutically acceptable salt thereof,

wherein the nAChR agonist, or a pharmaceutically acceptable salt thereof, is varenicline, or a pharmaceutically acceptable salt thereof, or compound 1 having the structure

or a pharmaceutically acceptable salt thereof, formulated for nasal administration.

106 . The pharmaceutical formulation of claim 105 , comprising 5-4000 micrograms of the nAChR agonist, or a corresponding amount of a pharmaceutically acceptable salt thereof, per dose.

107 . The pharmaceutical formulation of claim 105 , wherein the pharmaceutical formulation comprises between 1 mg/mL and 40 mg/mL of nAChR agonist, or a corresponding amount of a pharmaceutically acceptable salt thereof.

108 . The pharmaceutical formulation of claim 105 , wherein the nAChR agonist is varenicline, or a pharmaceutically acceptable salt thereof.

109 . The pharmaceutical formulation of claim 105 , wherein the nAChR agonist is compound 1, or a pharmaceutically acceptable salt thereof.

110 . The pharmaceutical formulation of claim 105 , wherein the PAM is selected from the group consisting of 17-beta-Estradiol, (R)-7-bromo-N-(piperidin-3-yl)benzo[b]thiophene-2-carboxamide, ivermectin, galantamine, genistein, 5-hydroxyindole, 4BP-TQS, A-86774, CCMI, levamisole, morantel, LY-2087101, mecamylamine, menthol, NS206, NS1738, NS9283, PNU-120596, RO5126946, TBS-345, dFBR, and HEPES, or a pharmaceutically acceptable salt of any of the foregoing.

111 . The pharmaceutical formulation of claim 105 , wherein the PAM is (R)-7-bromo-N-(piperidin-3-yl)benzo[b]thiophene-2-carboxamide or NS9283, or a pharmaceutically acceptable salt of either of the foregoing.

112 . The pharmaceutical formulation of claim 105 , wherein the pharmaceutical formulation is a liquid, suspension, aerosol, gel, ointment, dry powder, cream, paste, balm, or nasal spray.

113 . The pharmaceutical formulation of claim 105 , wherein the pharmaceutical formulation is administered into the nasal cavity by a syringe, dropper, bottle nebulizer, atomization pump, inhaler, powder spray device, vaporizer, patch, medicated stick, pipette, or jet of liquid.

114 . The pharmaceutical formulation of claim 105 , for use in treating keratitis, dry eye disease, increasing tear production, or improving ocular discomfort in an individual in need thereof.

115 . The pharmaceutical formulation of claim 114 , wherein keratitis is neurotrophic keratitis.

116 . A kit comprising a nAChR agonist, or a pharmaceutically acceptable salt thereof, and a PAM, or a pharmaceutically acceptable salt thereof,

for use in treating keratitis, dry eye disease, increasing tear production, or improving ocular discomfort in an individual in need thereof;

wherein the nAChR agonist, or the pharmaceutically acceptable salt thereof, is varenicline, or a pharmaceutically acceptable salt thereof, or compound 1 having the structure

or a pharmaceutically acceptable salt thereof.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Feb 3, 2023
From: ORBIMED ROYALTY & CREDIT OPPORTUNITIES III, LP
To: OYSTER POINT PHARMA INC.
Reel/Frame 062582/0873 →
PATENT SECURITY AGREEMENT Recorded Aug 5, 2021
From: OYSTER POINT PHARMA, INC.
To: ORBIMED ROYALTY & CREDIT OPPORTUNITIES III, LP
Reel/Frame 057104/0189 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2021
From: NAU, JEFFREY ALAN
To: OYSTER POINT PHARMA, INC.
Reel/Frame 054862/0181 →