Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Hereditary angioedema type 3

MONDO:0012526

Hereditary angioedema type 3 (HAE 3) is a form of hereditary angioedema characterized by acute edema in subcutaneous tissues, viscera and/or the upper airway.

Also known as: F12 hereditary angioedema, HAE 3, HAE-III, angioedema, hereditary, 3, hereditary angioedema caused by mutation in F12, hereditary angioedema type 3, hereditary angioneurotic edema type 3, hereditary angioneurotic oedema type 3

2 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Cardiovascular disorder (1051) Disease (680) Inflammatory disease (332) Hereditary disease (176) Vascular disorder (135) Skin disorder (132) Dermatitis (62) Hereditary angioedema (57) Urticaria (27) Angioedema (17)
Not yet finished but already full! 1 Completed 1
Sort by
  • New pill could stop dangerous swelling attacks in hereditary angioedema

    Symptom relief ENROLLING_BY_INVITATION

    This study tests a pill called deucrictibant for quickly treating swelling attacks in people with hereditary angioedema (HAE), including life-threatening throat swelling. About 150 adults who have had HAE attacks before will take the drug as needed and be monitored for safety and…

    Phase: PHASE2, PHASE3 • Sponsor: Pharvaris Netherlands B.V. • Aim: Symptom relief

    Last updated Jul 23, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space