drugset / Trial / NCT06981078

A Study to Assess the Efficacy and Safety of Verekitug in Participants With COPD

NCT06981078 ↗

Phase 2 Active not recruiting 666 enrolled Upstream Bio Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the efficacy and safety of verekitug (UPB-101) in participants with moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD), an inflammatory lung disease.

Timeline

Start
2025-07-02
Primary completion
2027-10
Completion
2027-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Verekitug Monoclonal antibody 100 mg Subcutaneous
Subject Verekitug Monoclonal antibody 400 mg Subcutaneous