CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 218 enrolled
Drug / intervention
Plecanatide +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03596905
NCT03596905Phase 2Completed

A Randomized, Double-blind, Placebo-Controlled, Dose Ranging, Parallel-Group Study of the Efficacy and Safety of Plecanatide in Children 6 to <18 Years of Age With Irritable Bowel Syndrome With Constipation (IBS-C)

Bausch Health Americas, Inc.·interventional·Posted Jul 24, 2018·Updated Dec 31, 2025

In Brief

A Phase 2 clinical trial evaluating Plecanatide and Matching placebo for Irritable Bowel Syndrome With Constipation. Completed, enrolled 218 participants across 35 sites.

Detailed Summary

The goal of this clinical trial is to learn if plecanatide can improve bowel function and relieve symptoms of irritable bowel syndrome with constipation (IBS-C) in children and adolescents aged 6 to \<18 years. The main questions it aims to answer are: * Does plecanatide increase the number of spontaneous bowel movements (SBMs) compared to placebo? * Is plecanatide safe and well tolerated in this pediatric population? Researchers will compare plecanatide at different doses to a placebo (a look-alike substance with no active drug) to see if plecanatide improves bowel function. Participants will: * Take plecanatide or placebo orally once daily for 4 weeks * Complete daily symptom diaries * Attend clinic visits for assessments and safety checks

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedJul 24, 2018
Enrollment StartJun 30, 2018
Primary CompletionNov 25, 2024
TodayJul 2, 2026
Enrollment to primary: 6.4 yearsPosted 7.9 years ago

Interventions

Plecanatidedrug

Taken orally daily for 4 weeks

Matching placebodrug

Taken orally daily for 4 weeks