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A Phase 1/2 Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of HMB-002 in Participants with Von Willebrand Disease Open


A study to evaluate the effectiveness of HMB-002 as a prophylactic treatment option to prevent and reduce the frequency of bleeding events in participants with Von Willebrand Disease.

Study Details
Internal Title: Hemab - HMB-002-102 (Velora Pioneer)

PCH IRB Number: IRB-26-012
Clinical Trials Government Identifier: NCT06754852

Diagnoses & Treatments: Von Willebrand Disease, VWD, HMB-002, bleeding events, Velora Pioneer

Study Type: Clinical Trial

Eligibility: 18 to 65 years old, Type 1, 1C, 2A VWD; minimum annualized treated bleeding event of 3

Enrollment Status: Open

Phase: I/II


Coordinator Contact: Mark Tracy
Contact Email:


Principal Investigator