Guest guest Posted August 15, 2006 Report Posted August 15, 2006 Ran across this today- I know in the past a few people acked about Hep C _______Summary_______________________________________________ Expert Opinion on Pharmacotherapy May 2006, Vol. 7, No. 7, Pages 953-964 (doi:10.1517/14656566.7.7.953) Nitazoxanide, a broad-spectrum thiazolide anti-infective agent for the treatment of gastrointestinal infections Hemphill & #8203; & #8204;1, Joachim Mueller & #8203; & #8204;2 & Marco Esposito & #8203; & #8204;3 1ProfessorGroup Leader, Institute of Parasitology, University of Berne, Längass-Strasse 122, CH-3012 Berne, Switzerland. hemphill@... 2PhDBiochemistSenior Research Fellow, Institute of Parasitology, University of Berne, Längass-Strasse 122, CH-3012 Berne, Switzerland 3Dr. Vet. MedPhD Candidate, Institute of Parasitology, University of Berne, Längass-Strasse 122, CH-3012 Berne, Switzerland. hemphill@... † Author for correspondence Colonisation of the gastrointestinal tract by anaerobic bacteria, protozoa, trematodes, cestodes and/or nematodes and other infectious pathogens, including viruses, represents a major cause of morbidity and mortality in Africa, South America and southeast Asia, as well as other parts of the world. Nitazoxanide is a member of the thiazolide class of drugs with a documented broad spectrum of activity against parasites and anaerobic bacteria. Moreover, the drug has recently been reported to have a profound activity against hepatitis C virus infection. In addition, nitazoxanide exhibits anti-inflammatory properties, which have prompted clinical investigations for its use in Crohn's disease. Studies with nitazoxanide derivatives have determined that there must be significantly different mechanisms of action acting on intracellular versus extracellular pathogens. An impressive number of clinical studies have shown that the drug has an excellent bioavailability in the gastrointestinal tract, is fast acting and highly effective against gastrointestinal bacteria, protozoa and helminthes. A recent Phase II study has demonstrated viral response (hepatitis C) to monotherapy, with a low toxicity and an excellent safety profile over 24 weeks of treatment. Pre-clinical studies have indicated that there is a potential for application of this drug against other diseases, not primarily affecting the liver or the gastrointestinal tract. Quote
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