US2020368212A1PendingUtilityA1
Rifaximin
Est. expirySep 22, 2026(~0.2 yrs left)· nominal 20-yr term from priority
Y02A50/30A61P 1/18A61P 1/12C07D 498/22A61P 1/00A61K 31/437A61P 31/04A61P 1/04
64
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Claims
Abstract
Amorphous rifaximin, methods of making it, and pharmaceutical compositions containing it. Also described are methods of converting amorphous rifaximin to crystalline rifaximin and vice versa.
Claims
exact text as granted — not AI-modified1 .- 22 . (canceled)
23 . A pharmaceutical composition comprising amorphous rifaximin, silicon dioxide, disodium edetate, hydroxypropyl methyl cellulose, microcrystalline cellulose, sodium starch glycolate, and glycerol palmitostearate.
24 . The pharmaceutical composition of claim 23 , wherein the amorphous rifaximin is characterized by the XRPD pattern shown in FIG. 1 .
25 . The pharmaceutical composition of claim 23 , wherein the pharmaceutical composition is in tablet form.
26 . A method of treating a bowel related disorder in a patient in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 23 to the patient.
27 . The method of claim 26 , wherein the bowel related disorder is selected from the group consisting of irritable bowel syndrome, traveler's diarrhea, Crohn's disease, chronic pancreatitis, pancreatic insufficiency, and colitis.Join the waitlist — get patent alerts
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