RecruitingPhase 3NCT07428499
Rare condition
Hereditary angioedema type 2
3
studies recruiting now
as of 7 Sept 2026
21
studies registered in total
as of 7 Sept 2026
20
countries with a recruiting site
as of 7 Sept 2026
4 Mar 2026
most recent study posted
among recruiting studies
Recruiting trials
RecruitingPhase 3NCT06960213
STOP-HAE: A Phase 3 Study of ADX-324 in HAE
RecruitingNCT07448181
Real-life Ecological Momentary Assessment of Lived Burden in Hereditary AngioEdema
Showing the 3 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
Search all Hereditary angioedema type 2 studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Hereditary angioedema type 2
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (SERPING1).
Treatments being studied
12 approved treatments and 9 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.
Approved: Berotralstat Hydrochloride (Orladeyo)Approved: Stanozolol (Stromba)Approved: Human C1-Esterase Inhibitor (Cetor)Approved: Flutemetamol F 18 (Vizamyl)Approved: Lanadelumab (Takhzyro)Approved: SebetralstatApproved: EcallantideApproved: Conestat Alfa (Ruconest)Approved: IcatibantApproved: Icatibant Acetate (Firazyr)Approved: DonidalorsenApproved: Berotralstat
Phase 3Avoralstat
Phase 3Sodium Chloride (Aqsia (balanced salt soln))
Phase 2Navenibart
Phase 2Hyaluronidase (Human Recombinant) (Cumulase)
Phase 1Digoxin (Digamex)
Phase 1Feniralstat
Phase 1Rosuvastatin
Phase 1Cyclosporine (Capimune)
+ 1 more in development
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).