Rare condition

Von Willebrand disease type 2A

ORPHA:166084 ↗Gene VWFClinical subtype

2

studies recruiting now

as of 7 Sept 2026

3

studies registered in total

as of 7 Sept 2026

3

countries with a recruiting site

as of 7 Sept 2026

24 Sept 2024

most recent study posted

among recruiting studies

Recruiting trials

Showing the 2 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.

Search all Von Willebrand disease type 2A studies

Where 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 Von Willebrand disease type 2A

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 (VWF).

Treatments being studied

3 approved treatments and 3 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.

Approved: Von Willebrand Factor Human (Von willebrand factor human component of voncento)Approved: Human Coagulation Factor Viii (Hemofil m)Approved: Vonicog Alfa (Veyvondi)
Phase 3Octocog Alfa (Advate)
Phase 3Tranexamic Acid (Cyklo-f heavy period relief)
Phase 2Rondaptivon Pegol

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).