Condition
Hereditary Hemorrhagic Telangiectasia clinical trials and research
As of November 12, 2026, Find a Trial lists 6 Hereditary Hemorrhagic Telangiectasia clinical trials that are recruiting, at sites in 6 countries (most in United States (2), Germany (2), Australia (1)). By phase: Phase 3 (1), Phase 1/2 (1). Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 6Clinical trials
- 6Countries
Newest Hereditary Hemorrhagic Telangiectasia clinical trials
| Study | Phase | Where | Status | Registered |
|---|---|---|---|---|
| Body donation in HHT | — | Essen, North Rhine-Westphalia | Recruiting | Sep 17, 2026 |
| Engasertib for moderate to severe HHT: see if daily 40 mg helps with nosebleeds | Phase 3 | Chicago, Illinois and 3 other locations | Recruiting | Aug 4, 2026 |
| DIAG723 in Adults With HHT | Phase 1/2 | Camperdown, New South Wales and 10 other locations | Recruiting | Jun 3, 2026 |
| Registry for patients with Hereditary Hemorrhagic Telangiectasia | — | Birmingham, Alabama and 15 other locations | Recruiting | Feb 14, 2024 |
| Evaluating Antiplatelet and Anticoagulation Therapy in Hereditary Hemorrhagic Telangiectasia | — | Angers and 17 other locations | Recruiting | Dec 7, 2022 |
| Examining the role of hypoxia in hereditary hemorrhagic telangiectasia | — | Essen, North Rhine-Westphalia | Recruiting | Jul 14, 2020 |
All recruiting trials (6)
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Body donation in HHT
This study tests whether donated human tissue with and without vascular malformations from people with hereditary hemorrhagic telangiectasia can be analyzed to better understand the disease.
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Engasertib for moderate to severe HHT: see if daily 40 mg helps with nosebleeds
This trial tests whether taking engasertib once daily for 28 weeks reduces nosebleed frequency in adults with hereditary hemorrhagic telangiectasia compared with placebo.
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DIAG723 in Adults With HHT
A first-in-human study tests DIAG723 versus placebo in adults with hereditary hemorrhagic telangiectasia to see if it is safe and possibly helpful.
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Registry for patients with Hereditary Hemorrhagic Telangiectasia
This study is collecting information from people with Hereditary Hemorrhagic Telangiectasia to better understand the condition and help improve treatments in the future.
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Evaluating Antiplatelet and Anticoagulation Therapy in Hereditary Hemorrhagic Telangiectasia
This study is testing how well people with Hereditary Hemorrhagic Telangiectasia can handle new blood-thinning treatments compared to not using them, to find out which ones work best for them.
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Examining the role of hypoxia in hereditary hemorrhagic telangiectasia
This study looks at how low oxygen levels might affect people with hereditary hemorrhagic telangiectasia (HHT) and how it could change the way the disease develops.
Related topics
Quick answers
How many Hereditary Hemorrhagic Telangiectasia clinical trials are recruiting right now?
6, as of November 12, 2026. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 6 countries. The most sites are in United States (2 trials), Germany (2 trials), Australia (1 trial), Canada (1 trial), New Zealand (1 trial). Each study page lists its sites and which ones are recruiting.
What phases are they in?
Phase 3: 1, Phase 1/2: 1. Trials with no phase listed are usually device, behavioural or observational studies.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.