Xifaxan success in Phase III TARGET-3 trial for IBS-Diarrhea.- Salix
Salix Pharmaceuticals, Ltd. announced the successful outcome of TARGET 3 � a Phase III randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of repeat treatment with Xifaxan ( rifaximin 550 mg TID ) (three times daily) for 14 days in subjects with Irritable Bowel Syndrome with Diarrhea, or IBS-D, who respond to an initial treatment course with rifaximin 550 mg TID for 14 days.
In the study a statistically significant greater proportion of rifaximin treated subjects (as compared to placebo) responded to repeat treatment as assessed by the composite primary endpoint of IBS-related abdominal pain and stool consistency during the 4 week treatment-free follow-up period (Primary Evaluation Period, or PEP) in the Double Blind Repeat Treatment Phase.