A Study of MD-7246 to Treat Abdominal Pain in Patients With Diarrhea-predominant Irritable Bowel Syndrome

NCT03931785 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 515

Last updated 2021-03-12

Study results available
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Summary

To evaluate the safety and tolerability, treatment effect on abdominal pain, and dose response of MD-7246 administered orally to patients with diarrhea-predominant irritable bowel syndrome (IBS-D).

Conditions

  • Irritable Bowel Syndrome With Diarrhea (IBS-D)

Interventions

DRUG

MD-7246

Oral tablet

DRUG

Placebo

Matching oral tablet

Sponsors & Collaborators

  • Allergan Sales, LLC

    collaborator INDUSTRY
  • Ironwood Pharmaceuticals, Inc.

    lead INDUSTRY

Principal Investigators

  • Wilmin Bartolini, PhD · Ironwood Pharmaceuticals, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-01
Primary Completion
2020-02-26
Completion
2020-03-11
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03931785 on ClinicalTrials.gov