A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)

Last updated:
2026-09-12
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View trial details

Overview

Official protocol title:

A PHASE 3, PROSPECTIVE, MULTICENTER, UNCONTROLLED, OPEN-LABEL CLINICAL STUDY TO DETERMINE THE EFFICACY, SAFETY, AND TOLERABILITY OF RVWF WITH OR WITHOUT ADVATE IN THE TREATMENT AND CONTROL OF BLEEDING EPISODES, THE EFFICACY AND SAFETY OF RVWF IN ELECTIVE AND EMERGENCY SURGERIES, AND THE PHARMACOKINETICS (PK) OR RVWF IN CHILDREN DIAGNOSED WITH SEVERE VON WILLEBRAND DISEASE

Intervention/treatment:
BAX 111 / ADVATE
Medical condition:
VON WILLEBRAND DISEASE
Protocol code:
071102
Control number:
208143
Status:
Closed
Approved:
September 13, 2017
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02932618
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
Birth to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Takeda Contact
Role
CONTACT
Phone:
1-877-825-3327
Sponsor
BAXALTA INNOVATIONS GMBH
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