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Clinical Trials in the EU / 2026-525480-41-00
Authorised Phase II

J2S-MC-GZMV: A Phase 2, Multicenter, Randomized, Double-Blind, 52-week Study to Investigate the Efficacy and Safety of Brenipatide Compared With Placebo for the Treatment of Adult Participants With Moderate-to-Severe Chronic Obstructive Pulmonary Disease (COPD)

2026-525480-41-00 · tracked via the Priya Life Science EU tracker
Sponsor
Eli Lilly & Co.
Sponsor type
Pharmaceutical company
Therapeutic area
Respiratory Tract Diseases
Decision date
15/09/2026
Enrollment target
81
Sites
Denmark, Czechia

Condition studied

Pulmonary Disease, Chronic Obstructive

Investigational medicinal product(s)

BrenipatideBrenipatidePlacebo to match TestBrenipatideBrenipatide

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Change from Baseline in Pre-Bronchodilator (BD) Forced Expiratory Volume in 1 Second (FEV₁)

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-525480-41-00 on CTIS ↗ ← All trials in the EU