Pseudo-von Willebrand disease

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At a Glance

Live from database

Regulatory Watchboard

7 events
Aug 2025Efficacy and Safety of BT200 (Rondaptivon Pegol) in Patients With Type 2B Von Willebrand Disease

Medical University of Vienna — PHASE2

TrialRECRUITING
Feb 2025A Study Assessing HMB-002 in Participants With Von Willebrand Disease

Hemab ApS — PHASE1, PHASE2

TrialRECRUITING
Aug 2024A Study of Bleeding and Treatment in Participants With Von Willebrand Disease

Hemab ApS

TrialRECRUITING
Jan 2022

Vonvendi: FDA approved

For use in adults (age 18 and older) diagnosed with von Willebrand disease (VWD) for routine prophylaxis to reduce the frequency of bleeding episodes in patients with severe Type 3 VWD receiving on-demand therapy

FDAcompleted
Dec 2021The Severe Von Willebrand Disease (sVWD) Patient Registry

VWD Connect Foundation

TrialRECRUITING
Jan 2007

Alphanate: FDA approved

For surgical and/or invasive procedures in patients with von Willebrand Disease (VWD) in whom desmopressin is either ineffective or contraindicated. It is not indicated for patients with severe VWD (Type 3) undergoing major surgery

FDAcompleted
Apr 1999

Humate-P: FDA approved

(1) In adult patients for treatment and prevention of bleeding in hemophilia A (classic hemophilia) and (2) in adult and pediatric patients for treatment of spontaneous and trauma-induced bleeding episodes in severe von Willebrand disease, and in mild and moderate von Willebrand disease where use of desmopressin is known or suspected to be inadequate.

FDAcompleted

Data from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Financial Assistance

3 programs

FINANCIAL LANDSCAPE SUMMARY

3

Total programs

3

Open now

3

Copay cards

Copay Assistance3

Humate-P

CSL Behring

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Vonvendi

Takeda Pharmaceuticals U.S.A., Inc.

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Alphanate

Grifols Biologicals Inc.

OpenContact for details

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Approved Treatments

3 FDA-approved

Vonvendi

(von Willebrand factor (recombinant))Orphan drug

Takeda Pharmaceuticals U.S.A., Inc.

Approved Jan 2022

Alphanate

(Antihemophilic factor (human))Orphan drug

Grifols Biologicals Inc.

Approved Jan 2007

Humate-P

(Antihemophilic factor/von Willebrand factor complex (human), dried, pasteurized)Orphan drug

CSL Behring

Approved Apr 1999

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Clinical Trial Landscape

No active clinical trials currently recruiting for Pseudo-von Willebrand disease.
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Recent News & Research

No recent news articles indexed yet for Pseudo-von Willebrand disease.
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Specialist Network

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