Astegolimab
DrugParticipants will receive SC astegolimab Q2W or Q4W
NCT Number: NCT05595642
This study will evaluate the efficacy and safety of astegolimab compared with placebo in participants with chronic obstructive pulmonary disease (COPD) who are former or current smokers and have a history of frequent exacerbations.
This study is active but is not currently recruiting participants.
40 year–80 year
All sexes
Interventional
Phase 3
AES - AS - Glenny Corp. S.A. Buenos Aires, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive SC astegolimab Q2W or Q4W
Participants will receive SC placebo Q2W
Time frame: 52 weeks
Time frame: 52 weeks
Time frame: Week 52
Time frame: Week 52
Time frame: Week 52
Time frame: Week 52
Time frame: 52 weeks
Hoffmann-La Roche
Industry
A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Astegolimab in Patients With Chronic Obstructive Pulmonary Disease
Acronym: ARNASA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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