US2021137895A1PendingUtilityA1
Compositions and Methods of Treating Cardiac Fibrosis with Ifetroban
Assignee: CUMBERLAND PHARMACEUTICALS INCPriority: May 16, 2014Filed: Jan 17, 2021Published: May 13, 2021
Est. expiryMay 16, 2034(~7.8 yrs left)· nominal 20-yr term from priority
A61K 31/422A61K 9/0019A61K 9/4858C07D 413/04A61K 9/2059A61P 9/00A61K 31/421C07D 493/08A61K 9/00A61P 43/00C07D 263/30C07D 407/04
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Claims
Abstract
The present invention is directed to methods of treating, preventing, and/or ameliorating fibrosis syndrome, and in particular cardiac fibrosis, by administration of a therapeutically effective amount of ifetroban, or a pharmaceutically acceptable salt thereof.
Claims
exact text as granted — not AI-modified1 . A method of treating pulmonary arterial hypertension in a human in need of treatment thereof, comprising administering a therapeutically effective amount of a [1S-(1α,2α,3α,4α)]-2-[[3-[4-[(Pentylamino)carbonyl]-2-oxazolyl]-7-oxabicyclo[2.2.1]hept-2-yl]methyl]-benzenepropanoic acid (ifetroban) or a pharmaceutically acceptable salt thereof to the mammal human.
2 . (canceled)
3 . (canceled)
4 . (canceled)
5 . (canceled)
6 . (canceled)
7 . The method of claim 1 wherein the therapeutically effective amount is from 10 mg to 1000 mg per day.
8 . The method of claim 7 , wherein the ifetroban or the pharmaceutically acceptable salt thereof is administered orally, intranasally, rectally, vaginally, sublingually, buccally, parenterally, or transdermally.
9 - 19 . (canceled)
20 . The method of claim 1 , wherein the pharmaceutically acceptable salt of ifetroban is ifetroban sodium.
21 . The method of claim 7 , wherein the therapeutically effective amount is from 100 mg to 500 mg per day.
22 . The method of claim 20 , wherein the ifetroban sodium is in an oral solid dosage form.
23 . The method of claim 7 , wherein the therapeutically effective amount is 250 mg per day.
24 . The method of claim 8 , wherein the ifetroban or the pharmaceutically acceptable salt thereof is administered orally.
25 . The method of claim 22 , wherein the therapeutically effective amount is 250 mg per day.
26 . The method of claim 1 , wherein the pulmonary arterial hypertension is associated with systemic sclerosis.Cited by (0)
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