ClinicalTrials.gov record
Completed Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT02932618

Public ClinicalTrials.gov record NCT02932618. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 7:50 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official 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) of rVWF in Children Diagnosed With Severe Von Willebrand Disease

Study identification

NCT ID
NCT02932618
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Baxalta now part of Shire
Industry
Enrollment
47 participants

Conditions and interventions

Interventions

  • Antihemophilic Factor (Recombinant) Biological
  • Vonicog alfa Biological

Biological

Eligibility (public fields only)

Age range
Up to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 5, 2017
Primary completion
Apr 16, 2026
Completion
Apr 16, 2026
Last update posted
May 14, 2026

2017 – 2026

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
University of Colorado Hemophilia & Thrombosis Center Aurora Colorado 80045
Children's National Medical Center Washington D.C. District of Columbia 20010
University of Florida College of Medicine Jacksonville Florida 32610
Bleeding and Clotting Disorders Institute Peoria Illinois 61615
Indiana Hemophilia and Thrombosis Center Indianapolis Indiana 46260
University of Nebraska Medical Center Omaha Nebraska 68198
St. Jude Affiliate Clinic at Novant Health Charlotte North Carolina 28204
Comprehensive Cancer Center of Wake Forest Unversity Winston-Salem North Carolina 27157
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229
Rainbow Babies and Children's Hospital Cleveland Ohio 44106
Nationwide Children's Hospital Columbus Ohio 43205
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104
Medical University of South Carolina Charleston South Carolina 29425
Texas Children's Cancer and Hematology Center Houston Texas 77030
Texas Children's Hospital Houston Texas 77030
Comprehensive Center for Bleeding Disorders Milwaukee Wisconsin 53225

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02932618, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 14, 2026 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02932618 live on ClinicalTrials.gov.

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