Study to Evaluate Subcutaneous (SC) VGA039 in Patients With Von Willebrand Disease (VWD)
Recruiting now · Phase 3
Conditions studied: Von Willebrand Disease (VWD)
In brief
This is a phase 3 study that will evaluate subcutaneous (SC) VGA039 in patients with von Willebrand Disease (VWD)
Key facts
- Study ID
- NCT07115004
- Run by
- Vega Therapeutics, Inc
- People needed
- 60
- Starts
- 2025-10-15
- Expected to finish
- 2028-10-01
- Last updated by the study team
- 2026-04-03
Who can join
Age: 12 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Science 37, Inc. (Virtual Clinical MetaSite) — Morrisville, North Carolina, United States (enrolling)
- Hemophilia Center of Western PA — Pittsburgh, Pennsylvania, United States (enrolling)
- UT Southwestern Children's Hospital — Dallas, Texas, United States (enrolling)
- Washington Center for Bleeding Disorders — Seattle, Washington, United States (enrolling)
- K Eristavi National Center of Experimental and Clinical Surgery (ქირურგიის ეროვნული ცენტრი) — Tbilisi, Georgia (enrolling)
- Frankfurt University Hospital (Universitätsmedizin Frankfurt) — Frankfurt, Germany (enrolling)
- Charlotte Maxeke Johannesburg Academic Hospital School of Pathology Clinical Haematologist — Johannesburg, South Africa (enrolling)
- Arkansas Children's Hospital — Little Rock, Arkansas, United States (enrolling)
- Luskin Orthopaedic Institute For Children — Los Angeles, California, United States (enrolling)
- UC Davis Medical Center — Sacramento, California, United States (enrolling)
- University of California San Francisco — San Francisco, California, United States (enrolling)
- Emory University Hospital — Atlanta, Georgia, United States (enrolling)
- Children's Healthcare of Atlanta — Atlanta, Georgia, United States (enrolling)
- University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
Full record on ClinicalTrials.gov
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