Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07575906Phase 1Completed
Phase 1, randomised, double-blind trial comparing Placebo with PF-08057418 (2 arms). Primary endpoint: Number of Participants with Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) at 10 weeks. Started May 2026; status: completed.
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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