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Clinical Trial of Omalizumab for Allergen Sensitized and Exposed Individuals With COPD (COPD-OMA)

Status: Recruiting
Location: See all (23) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This research is being done to test if a drug called omalizumab can help people with Chronic Obstructive Pulmonary Disease (COPD) and allergies. Each participant will be in the study for about 16 months, including 1-3 months of screening, 12 months of receiving the study drug at a clinic, and a follow-up call one month after your final clinic visit.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: f
View:

• Able and willing to provide informed consent.

• Age \>40 years at screening.

• Combustible tobacco cigarette exposure \>10 pack-years.

• Self-report of physician diagnosis of COPD and currently on dual or triple long-acting inhaled therapy (ICS/LABA/LAMA, ICS/LABA, LABA/LAMA).

• COPD Assessment Test (CAT) score of \>15 OR history of at least one documented moderate (requiring treatment with oral corticosteroids) or severe (requiring ED visit or hospitalization) COPD exacerbation in the past year.

• Participants of childbearing potential must have negative pregnancy test upon study entry.

• Female (and male) participants with reproductive potential must agree to use FDA approved methods of contraception for duration of study.

• Post-bronchodilator FEV1/FVC ratio \< 0.7 and FEV1% predicted \< 80%.

• Sensitization to one or more of five common indoor allergens including cat, dog, mouse, cockroach, dust mite defined with positive skin prick test (SPT) (SPT wheal size at least 3 mm greater than negative control). Positive specific IgE testing within 12 months of randomization to cat, dog, mouse, cockroach, or dust mite will be accepted in lieu of skin prick test if SPT is not interpretable or SPT cannot be safely performed.

• Exposure to the same allergen to which individual is sensitized based on measurement in home settled dust (1 U/g cockroach, 1 μg/g mouse, 2 μg/g dust mite, (Der f 1), 8 μg/g for cat and dog).

Locations
United States
Alabama
University of Alabama
NOT_YET_RECRUITING
Birmingham
Arizona
University of Arizona- Tuscon
NOT_YET_RECRUITING
Tucson
California
University of San Francisco
NOT_YET_RECRUITING
San Francisco
Colorado
National Jewish Health
NOT_YET_RECRUITING
Denver
Florida
University of Florida
NOT_YET_RECRUITING
Jacksonville
Iowa
University of Iowa
NOT_YET_RECRUITING
Iowa City
Illinois
Northwestern University
NOT_YET_RECRUITING
Chicago
Rush University Medical Center
NOT_YET_RECRUITING
Chicago
University of Illinois at Chicago
NOT_YET_RECRUITING
Chicago
Kansas
University of Kansas Medical Center
NOT_YET_RECRUITING
Kansas City
Maryland
Johns Hopkins University
RECRUITING
Baltimore
Michigan
University of Michigan
NOT_YET_RECRUITING
Ann Arbor
Henry Ford Health
NOT_YET_RECRUITING
Detroit
North Carolina
Duke University Medical Center
NOT_YET_RECRUITING
Durham
New York
Columbia University
NOT_YET_RECRUITING
New York
Cornell University
NOT_YET_RECRUITING
New York
Mount Sinai, Icahn School of Medicine
NOT_YET_RECRUITING
New York
Pennsylvania
Temple University
NOT_YET_RECRUITING
Philadelphia
University of Pittsburgh
NOT_YET_RECRUITING
Pittsburgh
Tennessee
Vanderbilt University Medical Center
NOT_YET_RECRUITING
Nashville
Texas
Baylor College of Medicine
NOT_YET_RECRUITING
Houston
Vermont
University of Vermont
NOT_YET_RECRUITING
Colchester
Washington
Pacific Northwest Airways - VA Puget Sound Healthcare System, Seattle
NOT_YET_RECRUITING
Seattle
Contact Information
Primary
Kayla Long
klong33@jhu.edu
410-502-9048
Backup
Heather Hazucha
hhazuch1@jhu.edu
410-502-0585
Time Frame
Start Date: 2026-02-12
Estimated Completion Date: 2031-05
Participants
Target number of participants: 334
Treatments
Active_comparator: Omalizumab injection
Active treatment is omalizumab injection, dosed using standardized weight and total IgE based table, as used for asthma treatment
Placebo_comparator: Placebo injection
Placebo for omalizumab used in the study will be commercially packaged 0.9% Sodium Chloride Injection, USP (e.g., normal saline). The injection volumes of normal saline administered will be calculated based upon the volume of active omalizumab expected to be administered based upon weight and total IgE level.
Sponsors
Collaborators: National Institute of Allergy and Infectious Diseases (NIAID), Genentech, Inc., American Lung Association Asthma Clinical Research Centers, American Lung Association
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov

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