Atlas Trials

A 12-Week Study With a 4-Week Randomized Withdrawal Period to Evaluate the Efficacy and Safety of Tenapanor for the Treatment of IBS-C

Clinical trial NCT02621892 · COMPLETED

Trial details

NCT number
NCT02621892
Sponsor
Ardelyx
Status
COMPLETED
Phase
Phase 3
Study type
INTERVENTIONAL
Constipation Predominant Irritable Bowel Syndrome
Start date
2015-10-01
Primary completion
2017-03-01
Enrollment
606

View on ClinicalTrials.gov

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