Comparison of Rimegepant and Placebo for Pain in IBS

NCT06221111 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2026-05-22

Study results available
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Summary

The primary aim of this study is to evaluate the efficacy of rimegepant on abdominal pain scores in participants with non-constipation IBS.

Conditions

  • Irritable Bowel Syndrome

Interventions

DRUG

Rimegepant 75 MG [Nurtec]

placebo controlled trial

Sponsors & Collaborators

Principal Investigators

  • Michael Camilleri · Mayo Clinic

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-06
Primary Completion
2025-05-30
Completion
2025-06-03
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

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 NCT06221111 on ClinicalTrials.gov