A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
Purpose
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.
Condition
- Chronic Obstructive Pulmonary Disease
Eligibility
- Eligible Ages
- Between 40 Years and 90 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Completion of the 52-week treatment period in either parent GB43311 or GB44332
Exclusion Criteria
- Withdrawal of consent and/or premature discontinuation from parent study - Any permanent discontinuation of study drug in parent study - Significant non-compliance in the parent study, specifically defined as missing scheduled visits, per investigator's judgment - Any new diagnosis of asthma according to the Global Initiative for Asthma guidelines or other accepted guidelines since enrolling in the parent study - Any new clinically significant pulmonary disease other than COPD (e.g., pulmonary fibrosis, sarcoidosis, chronic pulmonary embolism or primary pulmonary hypertension, alpha-1-antitrypsin deficiency) since enrolling in the parent study - Any new unstable cardiac disease, myocardial infarction, or New York Heart Association Class III or IV heart failure since enrolling in the parent study
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Open-Label Extension |
Eligible participants from parent studies GB43311 and GB44332 will receive subcutaneous (SC) astegolimab every 2 weeks (Q2W) until the end of the study |
|
Recruiting Locations
Birmingham, Alabama 35205-2610
Dothan, Alabama 36305
Jasper, Alabama 35501
Mobile, Alabama 36608-3135
Phoenix, Arizona 85027-5163
Tucson, Arizona 85741-3118
Bakersfield, California 93301-4205
Poway, California 92064-2419
Clearwater, Florida 33765
Greenacres City, Florida 33467-2979
Leesburg, Florida 34748-5077
Loxahatchee Groves, Florida 33470-9272
Miami, Florida 33014
Miami, Florida 33126-1941
Miami, Florida 33144-2155
Miami, Florida 33173
Miami, Florida 33175-3434
Orlando, Florida 32803
Orlando, Florida 32825-4454
Winter Park, Florida 32789-4681
Stonecrest, Georgia 30038-2649
Chicago, Illinois 60611
Hammond, Indiana 46324-2213
New Orleans, Louisiana 70115-3628
Bangor, Maine 04401-5691
Fall River, Massachusetts 02723-1511
Farmington Hills, Michigan 48336-2817
Flint, Michigan 48504-4730
Southfield, Michigan 48075
Troy, Michigan 48085
Chesterfield, Missouri 63017-3625
Saint Charles, Missouri 63301
St Louis, Missouri 63110
St Louis, Missouri 63141
Las Vegas, Nevada 89101-3485
Las Vegas, Nevada 89106-4159
Reno, Nevada 89502-1576
Charlotte, North Carolina 28277
Denver, North Carolina 28037-7929
Gastonia, North Carolina 28054
Greensboro, North Carolina 27403-4443
Shelby, North Carolina 28150-3803
Winston-Salem, North Carolina 27103-4029
Edmond, Oklahoma 73034-3258
Portland, Oregon 97220
DuBois, Pennsylvania 15801-2277
Pittsburgh, Pennsylvania 15241
Columbia, South Carolina 29204
Gaffney, South Carolina 29340-4737
North Charleston, South Carolina 29406
Rock Hill, South Carolina 29732
Chattanooga, Tennessee 37421
Hendersonville, Tennessee 37075-3085
Corsicana, Texas 75110-2471
Houston, Texas 77008-1772
Houston, Texas 77030-4202
Houston, Texas 77089-6097
McKinney, Texas 75069
Sherman, Texas 75090
Colchester, Vermont 05446-3052
Charlottesville, Virginia 22903
Everett, Washington 98208
Greenfield, Wisconsin 53228
Guaynabo, Puerto Rico 00968
More Details
- NCT ID
- NCT05878769
- Status
- Recruiting
- Sponsor
- Hoffmann-La Roche
Study Contact
Reference Study ID Number: GB43374 https://forpatients.roche.com/888-662-6728
global-roche-genentech-trials@gene.com