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NCT07519395: BALANCE

A Study to Investigate Abdominal Symptoms With Camlipixant Compared With Placebo in Adults With Irritable Bowel Syndrome - Diarrhea (IBS-D) and Irritable Bowel Syndrome - Mixed (IBS-M)

Not yet recruiting Phase 2 Last updated 9 April 2026
What this trial tests

Phase 2 trial testing Placebo in Irritable Bowel Syndrome in 420 participants. Not yet recruiting.

Timeline
6 April 2026
Primary endpoint
5 March 2027
9 July 2027

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingtriple
Primary purposetreatment
Enrollment420
Start date6 April 2026
Primary completion5 March 2027
Estimated completion9 July 2027

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 18 to 80, any sex, with Irritable Bowel Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is designed to evaluate the efficacy and safety of camlipixant in adults with IBS-D and IBS-M. The study has two parts. After the first part, some participants will be randomly chosen again to either get a higher dose or stop the drug.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Camlipixant

Trials testing the same drug.

Other recruiting trials for Irritable Bowel Syndrome

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07519395.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing