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Xifaxan rifaximin: Additional Phase III data

Additional data from the double-blind, international Phase III TARGET 3 trial in 636 patients with IBS-D showed that retreatment with thrice-daily 550 mg oral Xifaxan met the secondary composite endpoint of a greater proportion of responders based on both IBS-related abdominal pain and stool consistency during the first 6-week treatment phase and who continued to respond without recurrence through week 12 independent of any additional treatment vs. placebo (p=0.0419). A treatment phase comprised a 2-week

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