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Clinical Trial Summary

This study is being conducted to evaluate in participants with diarrhea-predominant Irritable Bowel Syndrome (IBS-D) the abdominal pain response to BOS-589 after 4 weeks of treatment and to evaluate the overall safety and tolerability of BOS-589 in the treatment of IBS-D during 4 weeks of treatment, relative to placebo (PBO).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03977155
Study type Interventional
Source Boston Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date June 4, 2019
Completion date May 6, 2020

See also
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