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RECRUITING
NCT07575308
PHASE2

HMBeacon: A Phase 2 Study to Evaluate ALN-6400 in Adult and Adolescent Female Patients With VWD and HMB

Sponsor: Alnylam Pharmaceuticals

View on ClinicalTrials.gov

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

DRUG

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