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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
2026-05-22
Completion Date
2028-11-29
Last Updated
2026-05-14
Healthy Volunteers
No
Interventions
ALN-6400
ALN-6400 will be administered subcutaneously (SC).
Locations (1)
Clinical Trial Site
Miami, Florida, United States