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HMBeacon: A Phase 2 Study to Evaluate ALN-6400 in Adult and Adolescent Female Patients With VWD and HMB
Sponsor: Alnylam Pharmaceuticals
Summary
The purpose of this study is to evaluate the safety, tolerability, efficacy, and pharmacodynamics (PD) of multiple doses of ALN-6400 in adult and adolescent patients with VWD and HMB
Official title: HMBeacon: A Phase 2, Randomized, Double-blind Study of the Safety, Tolerability, Efficacy, and Pharmacodynamics of Multiple Dose ALN-6400 in Adult and Adolescent Female Patients With Von Willebrand Disease (VWD) and Heavy Menstrual Bleeding (HMB)
Key Details
Gender
FEMALE
Age Range
16 Years - 45 Years
Study Type
INTERVENTIONAL
Enrollment
24
Start Date
2026-07-30
Completion Date
2028-11-29
Last Updated
2026-08-12
Healthy Volunteers
No
Interventions
ALN-6400
ALN-6400 will be administered subcutaneously (SC).
Locations (4)
Clinical Trial Site
Los Angeles, California, United States
Clinical Trial Site
Orange, California, United States
Clinical Trial Site
Miami, Florida, United States
Clinical Trial Site
Lexington, Kentucky, United States