Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2024-517606-29-00Phase 3Authorised
Phase 3, randomised, double-blind trial in central retinal artery occlusion (CRAO) comparing Tenecteplase + placebo with Acetylsalicylic acid + placebo (2 arms). Primary endpoint: Best-corrected visual acuity improvement at 30 days (ITT). Planned start Oct 2024; status: authorised.
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 2024-517606-29-00.