drugset / Trial / NCT06883305

A Study to Investigate the Efficacy and Safety of Tezepelumab in Adult Participants With Moderate to Very Severe COPD (D5241C00006)

NCT06883305

Phase 3 Recruiting 990 enrolled AstraZeneca Amgen · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Tezepelumab in Adults with Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD)

Timeline

Start
2025-03-18
Primary completion
2029-03-13
Completion
2029-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Tezepelumab Monoclonal antibody Subcutaneous