This After Market Study is Seeing if Dupilumab Plus Usual Standard of Care (SOC) is Better Than Usual Care Alone for Adult Participants After a Severe Chronic Obstructive Pulmonary Disease (COPD) Flare-Up Requiring Hospitalization
- Sponsor
- Regeneron Pharmaceuticals
- Study ID
- NCT07587658
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
- Chronic Obstructive Pulmonary Disease (COPD)
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- dupilumab — DRUGAdministered per the protocol
- Placebo — DRUGAdministered per the protocol
Study Details
This study is researching a drug called dupilumab, referred to as "study drug". The study is focused on people diagnosed with COPD to determine if the study drug, in addition to standard of care treatment for COPD, might reduce the reoccurrence of a COPD exacerbation (a "flare-up") happening within the study treatment duration (around 90 days). The study is looking at another research question: • What side effects may happen from taking the study drug
Key Dates
- Start date
- Jun 30, 2026
- Status verified
- Apr 2026
- Primary completion
- Jul 30, 2028
- Completion
- Jul 30, 2028
Study Design
- Enrollment
- 754 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: dupilumab
- Placebo Comparator: Placebo
Primary Outcome Measure
Time to first all-cause event [ Time Frame: Through day 90 ]
Central Contacts
- Clinical Trials Administrator844-734-6643
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