Rademikibart Add-on Treatment of an Acute Asthma Exacerbation (Seabreeze STAT Asthma)
A Phase 2, Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled Trial to Evaluate the Efficacy and Safety of Rademikibart as an Add-on Treatment for Acute Exacerbation in Adult and Adolescent Participants With Asthma and Type 2 Inflammation
Sponsor: Connect Biopharm LLC
A observational or N/A phase clinical study on Asthma Acute, this trial is actively recruiting participants. The trial is conducted by Connect Biopharm LLC and has accumulated 7 data snapshots since 2025. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Study Description(click to expand)This is a Phase 2, randomized, double-blind, placebo-controlled, parallel-group, interventional trial in participants with an acute asthma exacerbation with type 2 inflammation to compare rademikibart plus standard therapy to standard therapy alone (plus placebo), targeting an acute asthma exacerbation in the urgent healthcare setting.
This is a Phase 2, randomized, double-blind, placebo-controlled, parallel-group, interventional trial in participants with an acute asthma exacerbation with type 2 inflammation to compare rademikibart plus standard therapy to standard therapy alone (plus placebo), targeting an acute asthma exacerbation in the urgent healthcare setting.
Status Flow
Change History
7 versions recorded-
Apr 28, 2026 — Present [daily]
Recruiting
Phase: PHASE2 → None
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Feb 2026 — Apr 2026 [monthly]
Recruiting PHASE2
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Dec 2025 — Feb 2026 [monthly]
Recruiting PHASE2
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Nov 2025 — Dec 2025 [monthly]
Recruiting PHASE2
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Oct 2025 — Nov 2025 [monthly]
Recruiting PHASE2
▶ Show 2 earlier versions
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Jun 2025 — Oct 2025 [monthly]
Recruiting PHASE2
Status: Not Yet Recruiting → Recruiting
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May 2025 — Jun 2025 [monthly]
Not Yet Recruiting PHASE2
First recorded
Eligibility Summary
This is a Phase 2, randomized, multicenter study in adult and adolescent participants with asthma and type 2 inflammation
Contact Information
- Connect Biopharm LLC
For direct contact, visit the study record on ClinicalTrials.gov .