Efficacy and Safety of Plecanatide in Children 6 to <18 Years of Age With Irritable Bowel Syndrome With Constipation (IBS-C)
- Conditions
- Irritable Bowel Syndrome With Constipation
- Interventions
- Drug: Matching placebo
- Registration Number
- NCT03596905
- Lead Sponsor
- Bausch Health Americas, Inc.
- Brief Summary
This study of the efficacy and safety of Plecanatide in children 6 to \<18 Years of Age with Irritable Bowel Syndrome with Constipation (IBS-C)
- Detailed Description
The purpose of this study is to evaluate the safety, efficacy and pharmacokinetic (PK) parameters of plecanatide of once daily oral 4 dose levels of plecanatide (0.5, 1.0, 2.0, or 3.0 mg) for 4 weeks as treatment in children 6 to \<18 years of age with IBS-C.
The study will include a 28-day Screening/Baseline Period, a 4 week treatment period, and a 2-week post-treatment follow-up period. Patients/caregivers will visit the clinic 4 times during the study.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 210
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Matching placebo Matching placebo Matching placebo Taken orally daily for 4 weeks Group A: 6 to 11 years old Group B: 12 to \< 18 years old 0.5 mg plecanatide Plecanatide Plecanatide 0.5 mg Taken orally once daily for 4 weeks Group A: 6 to 11 years old 1.0 mg plecanatide Plecanatide Plecanatide 1.0 mg Taken orally daily for 4 weeks Group A: 6 to 11 years old Group B: 12 to \< 18 years old 2.0 mg plecanatide Plecanatide Plecanatide 2.0 mg Taken orally daily for 4 weeks Group B: 12 to \< 18 years old 3.0 mg plecanatide Plecanatide Plecanatide 3.0 mg Taken orally daily for 4 weeks Group B: 12 to \< 18 years old
- Primary Outcome Measures
Name Time Method Change from baseline in weekly SBM frequency over the 4 Week Treatment Period compared to placebo and across treatment groups 4 Week
- Secondary Outcome Measures
Name Time Method Change from baseline in frequency and severity of abdominal pain/discomfort 4 Week Change from baseline in frequency of BMs and CSBMs 4 Week Change from baseline in stool consistency (BSFS or mBSFS-C) 4 Week
Trial Locations
- Locations (1)
Synergy Research Site
🇺🇸Newport News, Virginia, United States