Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06658535Phase 1Recruiting
Phase 1, open-label trial of perflenapent in respiratory distress syndrome (RDS) (3 cohorts), sponsored by NuvOx Therapeutics. Primary endpoint: Maximum Tolerated Dose at 28 days. Started Mar 2025; status: recruiting.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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