US2020147225A1PendingUtilityA1
Rifaximin complexes
Est. expiryDec 10, 2028(~2.4 yrs left)· nominal 20-yr term from priority
Inventors:Maruti GhagareSunilkumar Parasnath SarojDharmaraj Ramachandra RaoRajendra Narayanrao Kankan
A61K 47/6951A61P 1/18B82Y 5/00A61P 1/12A61K 47/40A61K 31/4184A61P 31/04A61K 47/58A61K 47/32A61K 9/2095A61P 1/00A61K 31/44A61K 31/437A61P 9/12A61P 13/08A61P 1/04Y02A50/473Y02A50/30
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Claims
Abstract
There is provided a complex comprising rifaximin and a complexing agent, wherein the complexing agent is a polyvinyl pyrrolidone (PVP) or a cyclodextrin. There is also provided a process for preparing the complex, a pharmaceutical composition including the complex and therapeutic uses of the complex.
Claims
exact text as granted — not AI-modified1 - 24 . (canceled)
25 . A method of treating bowel disorders comprising:
administering to a patient a therapeutically effective amount of a complex comprising rifaximin and a complexing agent, wherein the complex is in an amorphous form and exhibits enhanced solubility compared to a physical mixture of rifaximin and the complexing agent.
26 . The method of claim 25 , wherein the complex is a component of a tablet, a pellet, or a capsule.
27 . The method of claim 25 , wherein the bowel disorder is travelers' diarrhea.
28 . The method of claim 25 , wherein the bowel disorder is a bowel disease.
29 . The method of claim 25 , wherein the bowel disorder is irritable bowel syndrome, Crohn's disease, chronic pancreatitis, pancreatic insufficiency and/or colitis.
30 . The method of claim 25 , wherein the bowel disorder is microbe associated diarrhea.
31 . The method according to claim 25 , wherein the ratio of rifaximin to complexing agent ranges from 20:1 to 1:20 w/w.
32 . The method according to claim 25 , wherein the ratio of rifaximin to complexing agent ranges from 10:1 w/w to 1:2 w/w.
33 . The method according to claim 25 , wherein the rifaximin complex is administered with one or more pharmaceutically acceptable excipients.Cited by (0)
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