IP Library Patent Application 18485082
Patent Application
App. No. 18/485,082

USE OF DEXPRAMIPEXOLE FOR THE TREATMENT OF MODERATE TO SEVERE ASTHMA

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Patent No.
US None
App. No.
18/485,082
Abstract

Disclosed herein are methods of treating moderate to severe asthma of the eosinophilic phenotype in a human subject in need thereof with a daily dose of about 75 mg to about 300 mg of dexpramipexole or pharmaceutical acceptable salt thereof, and treating severe asthma of the eosinophilic phenotype in a human subject in need thereof with a daily dose of about 150 mg to about 300 mg of dexpramipexole or pharmaceutical acceptable salt thereof.

Claims (31)

1 - 72 . (canceled)

73 . A method of improving the mean forced expiratory volume in 1 second (FEV 1 ) in a human subject in need thereof comprising orally administering to the subject from about 75 mg to about 300 mg of dexpramipexole or a pharmaceutically acceptable salt thereof.

74 . The method of claim 73 , wherein FEV 1 is increased by about 5% to about 10% following administration.

75 . The method of claim 73 , wherein FEV 1 is increased by about 10% to about 20% following administration.

76 . The method of claim 73 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered once daily.

77 . The method of claim 73 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered twice per day.

78 . The method of claim 73 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 150 mg/day.

79 . The method of claim 73 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 300 mg/day.

80 . The method of claim 78 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a dose of about 75 mg twice per day.

81 . The method of claim 79 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a dose of about 150 mg twice per day.

82 . A method of treating human disease with an eosinophilic phenotype in a human subject in need thereof comprising orally administering to the subject from about 75 mg to about 300 mg of dexpramipexole or a pharmaceutically acceptable salt thereof.

83 . The method of claim 82 , wherein the method results in a reduction of the level of blood absolute eosinophil counts in the subject compared to the level prior to the administration of dexpramipexole to the subject.

84 . The method of claim 82 , wherein the level of blood absolute eosinophil counts in the subject is reduced by about 90%.

85 . The method of claim 82 , wherein the level of blood absolute eosinophil counts in the subject is reduced by about 80%.

86 . The method of claim 82 , wherein the level of blood absolute eosinophil counts in the subject is reduced by about 70%.

87 . The method of claim 82 , wherein the level of blood absolute eosinophil counts in the subject is reduced by about 60%.

88 . The method of claim 82 , wherein the level of blood absolute eosinophil counts in the subject is reduced by about 50%.

89 . The method of claim 82 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered once daily.

90 . The method of claim 82 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered twice per day.

91 . The method of claim 82 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 150 mg/day.

92 . The method of claim 82 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 300 mg/day.

93 . The method of claim 91 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a dose of about 75 mg twice per day.

94 . The method of claim 92 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a dose of about 150 mg twice per day.

95 . A method of reducing an exacerbation rate in a human subject exhibiting an eosinophilic phenotype comprising orally administering to the subject from about 75 mg to about 300 mg of dexpramipexole or a pharmaceutically acceptable salt thereof.

96 . The method of claim 95 , wherein the exacerbation rate is reduced to less than 2 per year.

97 . The method of claim 95 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered once daily.

98 . The method of claim 95 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered twice per day.

99 . The method of claim 95 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 150 mg/day.

100 . The method of claim 95 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 300 mg/day.

101 . The method of claim 99 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a dose of about 75 mg twice per day.

102 . The method of claim 100 , wherein dexpramipexole or a pharmaceutically acceptable salt thereof is administered at a dose of about 150 mg twice per day.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2025
From: KNOPP BIOSCIENCES LLC
To: ARETEIA THERAPEUTICS, INC.
Reel/Frame 073532/0950 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2025
From: PRUSSIN, CALMAN PHILIP
To: KNOPP BIOSCIENCES, LLC
Reel/Frame 073533/0559 →