US2021221836A1PendingUtilityA1
Idiopathic pulmonary fibrosis-detection, monitoring, prediction methods
Est. expiryOct 31, 2032(~6.3 yrs left)· nominal 20-yr term from priority
A61M 15/00C07H 19/056G01N 2800/122A61K 9/0078A61K 31/7008A61M 2202/064A61K 31/7016C07H 5/10C07B 2200/13A61M 15/0085A61K 9/0075G01N 2333/4724G01N 33/6893A61K 31/7056C07H 3/04
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Claims
Abstract
Provided is a compound of the general formula (I):The compound of formula (I) is suitable for treating pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a mammal. Also provided is a method for treatment of pulmonary fibrosis, such as Idiopathic pulmonary fibrosis in a human subject having a galectin-3 level indicative of pulmonary fibrosis or exacerbation of symptoms as well as a method for making said compound.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A compound of the general formula (I):
2 . The compound of claim 1 selected from bis (3-deoxy-3-(3-fluorophenyl-1H-1,2,3-triazol-1-yl)-β-D-galactopyranosyl) sulfane as the free form.
3 . A pharmaceutical composition comprising the compound of formula (I) of claim 1 and optionally a pharmaceutically acceptable additive.
4 . A method for treatment of pulmonary fibrosis comprising administering to a mammal in need thereof an amount of the compound of formula (I) of claim 1 effective to treat said pulmonary fibrosis.
5 . The method of claim 4 , wherein said compound is administered by the pulmonary route.
6 . The method of claim 4 , wherein the mammal is a human subject diagnosed with pulmonary fibrosis.
7 . The method of claim 4 , wherein the mammal is a human subject diagnosed with idiopathic pulmonary fibrosis.
8 . The method of claim 6 , wherein the human subject has an indicative level of galectin-3 of at least about 10 ng/ml.
9 . The method of claim 8 , wherein the human subject has an indicative level of galectin-3 of at least about 22 ng/ml.Join the waitlist — get patent alerts
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