drugset / Trial / NCT05776069

Study of VGA039 in Healthy Volunteers and Patients With Von Willebrand Disease (VIVID)

NCT05776069 ↗

Phase 1/2 Recruiting 116 enrolled Vega Therapeutics, Inc
RandomizedSequentialDouble-blindTreatment

Summary

The VIVID study is structured in a master protocol format comprised of multiple parts that evaluate intravenous (IV) and subcutaneous (SC) VGA039 in healthy volunteers and subjects with von Willebrand Disease (VWD) and other bleeding disorders.

Timeline

Start
2023-03-16
Primary completion
2029-12
Completion
2029-12

Drugs

EvaluationDrugModalityDoseRoute
Subject VGA039 Unknown — Intravenous