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A Study of Recombinant Von Willebrand Factor (rVWF) in Pediatric and Adult Participants With Severe Von Willebrand Disease (VWD)

Completed · Phase 3 · NCT03879135

Conditions: Von Willebrand Disease (VWD)

At a glance

Research payments reported, 2025
$66,261
U.S. investigators named
6
Sites paid
6
Planned or actual enrollment
38

About the trial

Sponsor
Baxalta now part of Shire (with Takeda Development Center Americas, Inc.)
Tested
rVWF (biological), rFVIII (biological)
Dates
Started 2019-04-01; completion 2025-01-30
Results posted
Yes

The main aim of the study is to check effectiveness of rVWF (vonicog alfa) prophylaxis based on the annualized bleeding rate (ABR) of spontaneous (not related to trauma) bleeding episodes in pediatric and adult participants during the first 12 months on study treatment. The participants will be treated with rVWF for a maximum of 3 years. Their von Willebrand Disease will be treated according to Investigational product (IP) dosing directions.

From ClinicalTrials.gov, last updated 2025-09-03. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Takeda Pharmaceuticals U.S.A., Inc. reported $66,261 in research payments for this study in 2025 (31 payments).

Products named: Vonvendi

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.