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J2S-MC-GZMT: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Brenipatide in the Treatment of Adult Participants with IBS-C

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524974-41-00
Enrollment
70
Registered
2026-08-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritable Bowel Syndrome - Constipation

Brief summary

Percentage of Participants with a Weekly Composite Clinical Response for at Least 50 Percent (%) of Weeks

Interventions

DRUGBrenipatide
DRUGPlacebo to match LY

Sponsors

Eli Lilly & Co.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percentage of Participants with a Weekly Composite Clinical Response for at Least 50 Percent (%) of Weeks—

Outcome results

None listed

Source: EU CTIS · Data processed: Aug 12, 2026