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The two co-primary endpoints required by the European Medicines Agency (EMA) were met in this trial, showing statistically significant improvements for linaclotide-treated patients for both abdominal pain/abdominal discomfort responder and IBS degree of ...
candidate linaclotide provided patients suffering from IBS and constipation (IBS-C) with significant relief from abdominal pain, discomfort, and associated symptoms, according to Phase III data reported by the drug’s developer, Ironwood Pharmaceuticals ...
(RTTNews) - Salix Pharmaceuticals Ltd. (SLXP: News ) Monday presented two analyses of data from its Phase 3 pivotal clinical trials, TARGET 1 and 2, demonstrating a 14-day course of XIFAXAN 550 mg or rifaximin taken three times daily achieved adequate ...
Xifaxan 550 mg also achieved statistical significance in the key secondary endpoint of providing relief from IBS-related bloating. The approval of Xifaxan 550 mg for the IBS indication would be a major boost for the company. We believe that the IBS ...
Napo has formed alliances with Direct Relief International and others to make crofelemer ... Crofelemer for diarrhea irritable bowel syndrome (CRO-IBS), Phase 2 - Crofelemer for acute infectious diarrhea (including cholera), Phase 2 (CRO-ID) - Crofelemer ...
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