Connect Biopharma announced the initiation of its Phase 2 Seabreeze STAT Asthma study (NCT06940141), following written agreement on the final study protocol from the U.S. Food and Drug Administration. This study will evaluate rademikibart as an adjunct to standard of care for acute exacerbations in adults and adolescent participants with asthma and type 2 inflammation.
The study is designed to enroll approximately 160 participants globally who are experiencing an acute asthma exacerbation. Participants will receive either a single dose of rademikibart or placebo, administered subcutaneously.
The primary endpoint is the safety and efficacy of rademikibart as an adjunct to standard of care, measured by the treatment failure rate over 28 days following an acute exacerbation. Topline data from this study are expected in the first half of 2026.
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