A Study of HMB-002 for Von Willebrand Disease
This study is testing a new medication called HMB-002 for people with Von Willebrand Disease (VWD), including Types 1, 2, and 3. The main goal is to see how safe HMB-002 is and how well your body tolerates it. Researchers will also look at how the drug moves through your body (pharmacokinetics) and what effects it has (pharmacodynamics). You might receive HMB-002 alone or with another treatment called factor concentrate. To join, you need to be between 16 and 69 years old, weigh 50 to 120 kg, and have a confirmed diagnosis of VWD. The study is currently evaluating safety and dosage.
- Study design
- This is a Phase 1/2, open-label study with three parts, designed to test different doses and how HMB-002 is given. It plans to enroll 108 participants.
- What's involved
- Depending on the part of the study, your participation could last approximately 12, 17, or 21 weeks. You will receive HMB-002 as an injection under the skin.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your safety will be monitored for up to 113 days after treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study Assessing HMB-002 in Participants With Von Willebrand Disease
At a glance
Conditions
NCT06754852
Where you'd take part
This study runs at 25 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Arkansas Children's Hospital
Little Rock, Arkansasno site contact published
Not yet recruiting
Basingstoke and North Hampshire Hospital
Basingstoke, Hampshire, United Kingdomno site contact published
Recruiting
Children's Hospital of Los Angeles
Los Angeles, Californiano site contact published
Not yet recruiting
Emory Children's Center
Atlanta, Georgiano site contact published
Not yet recruiting
Fiona Stanley Hospital
Murdoch, Perth, Australiano site contact published
Not yet recruiting
Hemophilia Center of Western Pennsylvania
Pittsburgh, Pennsylvaniano site contact published
Not yet recruiting
Innovative Hematology, Inc./Indiana Hemophilia and Thrombosis Center
Indianapolis, Indianano site contact published
Recruiting
Mayo Clinic - Rochester
Rochester, Minnesotano site contact published
Not yet recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
What this trial measures
- Incidence of Treatment emergent adverse events (TEAE)up to Day 113