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Clinical Trial Summary

The objectives of this study are to evaluate the safety, efficacy, and dose response of two delayed release formulations of linaclotide (DR; DR formulation 1 is DR1; DR formulation 2 is DR2) administered orally to patients with irritable bowel syndrome with constipation (IBS-C). Additional objectives include understanding how the two DR formulations compare with each other and with the FDA-approved 290 μg LINZESS® (the immediate release [IR] formulation of linaclotide).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02559206
Study type Interventional
Source Ironwood Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 2
Start date October 22, 2015
Completion date September 30, 2016

See also
  Status Clinical Trial Phase
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