The Plecanatide Irritable Bowel Syndrome With Constipation Study (IBS-C)
NCT01722318 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 428
Last updated 2019-05-28
Summary
This is a randomized, 12-week, double-blind, placebo-controlled, dose-ranging study in patients with IBS-C.
Conditions
- Irritable Bowel Syndrome Characterized by Constipation
Interventions
- DRUG
-
Plecanatide
- DRUG
Sponsors & Collaborators
-
Bausch Health Americas, Inc.
lead INDUSTRY
Principal Investigators
-
Philip B Miner, MD · Oklahoma Foundation for Digestive Research
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-11-30
- Primary Completion
- 2014-04-30
- Completion
- 2014-10-31
Countries
- United States
Study Locations
More Related Trials
-
Efficacy of an Encapsulated Probiotic Bifidobacterium Infantis 35624 in Irritable Bowel Syndrome
NCT00135031 ·Status: COMPLETED ·Phase: PHASE3
-
Rifaximin 3 Times/Day (TID) for Non-Constipation Irritable Bowel Syndrome (IBS)
NCT00724126 ·Status: COMPLETED ·Phase: PHASE3
-
A Trial for New Treatment of Adult Participants With Irritable Bowel Syndrome
NCT03721107 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety and Efficacy of RDX5791 for the Treatment of Constipation Predominant Irritable Bowel Syndrome (IBS-C)
NCT01340053 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Effect of ASP0456 in Patients With Constipation Predominant Irritable Bowel Syndrome
NCT01714843 ·Status: COMPLETED ·Phase: PHASE2
-
Randomized, Double-blind, Dose-range-finding, Phase 2 Study of Linaclotide Administered to Patients With Irritable Bowel Syndrome With Constipation (IBS-C)
NCT00460811 ·Status: COMPLETED ·Phase: PHASE2
-
Irritable Bowel Syndrome Evaluation and Treatment in Primary Care
NCT01641341 ·Status: COMPLETED ·Phase: PHASE4
-
A Trial of Linaclotide 290 μg in Patients With Irritable Bowel Syndrome With Constipation (IBS-C)
NCT03573908 ·Status: COMPLETED ·Phase: PHASE3
-
Constipation Associated With Irritable Bowel Syndrome (IBS-C)
NCT00796354 ·Status: COMPLETED ·Phase: PHASE3
-
A Safety and Efficacy Study of a Range of Linaclotide Doses Administered Orally to Children Ages 7-17 Years, With Irritable Bowel Syndrome With Constipation
NCT02559817 ·Status: TERMINATED ·Phase: PHASE2
-
Rifaximin 3 Times/Day (TID) for Non-Constipation Irritable Bowel Syndrome (IBS)
NCT00731679 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of the Effect of SYN-010 on Subjects With IBS-C
NCT02495623 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability and Pharmacodynamics of DDP733 for IBS-c
NCT00215566 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Lubiprostone in Patients With Irritable Bowel Syndrome With Constipation
NCT00399542 ·Status: COMPLETED ·Phase: PHASE3
-
Olorinab in Irritable Bowel Syndrome With Predominant Constipation (IBS-C) and Irritable Bowel Syndrome With Predominant Diarrhea (IBS-D)
NCT04043455 ·Status: TERMINATED ·Phase: PHASE2
-
Study of LX1031 in Subjects With Non-Constipating Irritable Bowel Syndrome
NCT00813098 ·Status: COMPLETED ·Phase: PHASE2
-
A Study To Investigate The Effect Of PD-217,014 On Abdominal Pain/Discomfort In Patients With IBS.
NCT00139672 ·Status: COMPLETED ·Phase: PHASE2
-
Neomycin and Rifaximin Plus Neomycin in Treating Methane Positive Constipation Predominant Irritable Bowel Syndrome
NCT00945334 ·Status: COMPLETED ·Phase: NA
-
Saccharomyces Boulardii CNCM I-745 in Irritable Bowel Syndrome
NCT07168434 ·Status: RECRUITING ·Phase: PHASE3
-
Post-marketing Surveillance of Linaclotide Tablet in Patients With Irritable Bowel Syndrome With Constipation or Chronic Constipation (Excluding Constipation Due to Organic Diseases)
NCT03471728 ·Status: COMPLETED
-
Pregabalin on Colonic Motor and Sensory Function in Constipation Predominant Irritable Bowel Syndrome
NCT01331213 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of Lubiprostone on Small Bowel Contractions in Female Patients With Constipation Irritable Bowel Syndrome (C-IBS)
NCT01085643 ·Status: COMPLETED ·Phase: NA
-
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
NCT02621892 ·Status: COMPLETED ·Phase: PHASE3
-
Study of the Research Medicine CIN-103 in Adults With Irritable Bowel Syndrome With Predominant Diarrhea (IBS-D).
NCT06153420 ·Status: TERMINATED ·Phase: PHASE2
-
Diarrhea Predominant Irritable Bowel Syndrome in Females
NCT00461526 ·Status: COMPLETED ·Phase: PHASE2