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.

NCT06754852

A Study Assessing HMB-002 in Participants With Von Willebrand Disease

Recruiting
PHASE1Ages 16–69InterventionalTreatment
Hemab ApS
~108 participants
Updated 2026-06-30 on ClinicalTrials.gov
What's tested:HMB-002 (Part A)HMB-002 (Part B)HMB-002 with Concomitant Factor Concentrate (Part C) (Not Applicable in US)

At a glance

Recruiting sites
6 of 25 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of Treatment emergent adverse events (TEAE)
Measured over up to Day 113
Von Willebrand Disease (VWD)
Von Willebrand Disease (VWD), Type 1
Von Willebrand Disease (VWD), Type 2
Von Willebrand Disease (VWD), Type 3

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.

Opens a ready-to-send draft in your own email app — review before sending.

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Eligibility criteria

Inclusion

Cohorts A1 and A2: Participants with Type 1 VWD, only.
Cohorts A3 and A4: Participants with Type 1 VWD (including Type 1C) and Type 2A VWD 7. Residual VWF activity of ≤ 50 IU/dL and FVIII activity ≤ 70 IU/dL during screening.
  • Incidence of Treatment emergent adverse events (TEAE)up to Day 113