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A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
NCT05878769 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Astegolimab
Study Locations (20)
Florida
- St Francis Medical Institute ClinEdge PPDS — Clearwater
- Finlay Medical Research Corporation — Greenacres City
- Flourish Research - Leesburg - PPDS — Leesburg
- Advanced Pulmonary Research Institute — Loxahatchee Groves
- San Marcus Research Clinic Inc. — Miami
- Finlay Medical Research Corporation — Miami
- Oceane7 Medical & Research Center, Inc. — Miami
- Research Institute of South Florida Inc — Miami
- Diverse Clinical Research, LLC — Miami
- Central Florida Pulmonary Group, PA — Orlando
- Florida Institute for Clinical Research, LLC — Orlando
Alabama
- UAB Lung Health Center — Birmingham
- SEC Clinical Research LLC - Dothan 2 - ClinEdge - PPDS — Dothan
- Jasper Summit Research LLC — Jasper
- Pulmonary Associates of Mobile PC — Mobile
California
- Kern Allergy and Medical Research — Bakersfield
- Cadena Care Institute, LLC — Poway
- Apex Clinical Research — San Diego
Arizona
- Pulmonary Associates Deer Valley Office — Phoenix
- AES - DRS - Synexus Clinical Research US, Inc. - Tucson — Tucson
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,000 participants |
| Start Date | 2023-06-28 |
| Est. Completion | 2027-06-30 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05878769
The ClinicalTrials.gov registry entry for NCT05878769 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoffmann-La Roche, which has 758 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chronic Obstructive Pulmonary Disease appearing as the primary indexed condition, and to 1 intervention — of which Astegolimab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05878769 reports 20 study locations spanning 4 distinct geographic areas — top geographies include Florida, Alabama, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05878769 about?
NCT05878769 is a clinical study titled "A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)". 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.
What is the current status of trial NCT05878769?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 2,000 participants. The study started on 2023-06-28. Estimated completion is 2027-06-30.
What conditions does trial NCT05878769 study?
This clinical trial studies the following conditions: Chronic Obstructive Pulmonary Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05878769?
The interventions under investigation include: Astegolimab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05878769?
This trial is sponsored by Hoffmann-La Roche, which has 758 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05878769 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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