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A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
Condition: Chronic Obstructive Pulmonary Disease · Sponsor: Hoffmann-La Roche
About this study
The purpose of this study is to assess the long-term safety and to explore the efficacy of astegolimab in participants with chronic obstructive pulmonary disease (COPD) who have completed the 52-week placebo-controlled treatment period in parent studies GB43311 or GB44332.
This description comes directly from the study's public registry record.
Talk to the study team
Reference Study ID Number: GB43374 https://forpatients.roche.com/ No attachments to email below. · 888-662-6728 · global-roche-genentech-trials@gene.com
Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
Always discuss trial participation with your own doctor first.
Locations (486)
| UAB Lung Health Center | Birmingham, Alabama, United States | Recruiting |
| SEC Clinical Research LLC - Dothan 2 - ClinEdge - PPDS | Dothan, Alabama, United States | Recruiting |
| Jasper Summit Research LLC | Jasper, Alabama, United States | Recruiting |
| Pulmonary Associates of Mobile PC | Mobile, Alabama, United States | Recruiting |
| Pulmonary Associates Deer Valley Office | Phoenix, Arizona, United States | Recruiting |
| AES - DRS - Synexus Clinical Research US, Inc. - Tucson | Tucson, Arizona, United States | Recruiting |
| Kern Allergy and Medical Research | Bakersfield, California, United States | Recruiting |
| Cadena Care Institute, LLC | Poway, California, United States | Recruiting |
| Apex Clinical Research | San Diego, California, United States | Completed |
| St Francis Medical Institute ClinEdge PPDS | Clearwater, Florida, United States | Recruiting |
| Finlay Medical Research Corporation | Greenacres City, Florida, United States | Recruiting |
| Flourish Research - Leesburg - PPDS | Leesburg, Florida, United States | Recruiting |
+ 474 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05878769