Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06425224Phase 3Recruiting
Phase 3, randomised, double-blind trial (3 arms), sponsored by Boston Medical Corporation. Primary endpoint: Change in intravaginal latency time at 12 weeks. Started Jun 2022; 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.
See how Gosset can support your research on NCT06425224.