RecruitingPhase 3NCT07743671

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

A Phase 3, Randomized, Double-blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Engasertib in Subjects With Moderate to Severe Hereditary Hemorrhagic Telangiectasia (HHT)


Sponsor

Vaderis Therapeutics AG

Enrollment

240 participants

Start Date

Aug 14, 2026

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Engasertib and a drug called Placebo for people with hereditary hemorrhagic telangiectasia. The study is currently recruiting participants at 4 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEngasertib

Engasertib will be administered as oral capsules.

DRUGPlacebo

Placebo will be administered as oral capsules.


Locations(4)

The University of Chicago Medical Center (UCMC)

Chicago, Illinois, United States

Innovative Hematology, Inc.,

Indianapolis, Indiana, United States

Mayo Clinic

Rochester, Minnesota, United States

Washington University School of Medicine

St Louis, Missouri, United States

View Full Details on ClinicalTrials.gov

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NCT07743671


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