Clinical Trial

A Trial to Assess the Efficacy and Safety of Engasertib in Participants With Moderate to Severe Hereditary Hemorrhagic Telangiectasia (HHT)

Not Yet Recruiting Phase 3
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Summary
The primary objective of this trial is to assess the efficacy of engasertib 40 mg once daily (QD) in reducing the frequency of epistaxis compared to placebo QD during 28 weeks of double-blind treatment in participants with moderate to severe HHT.
Trial Details
NCT Number NCT07743671
Lead Sponsor Vaderis Therapeutics AG
Conditions Hereditary Hemorrhagic Telangiectasia
Enrollment 240 participants
Start Date 2026-09
Primary Completion 2028-06 (estimated)
Study Completion 2028-06 (estimated)
Updated on ClinicalTrials.gov 2026-08-04