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NOT YET 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

2026-05-22

Completion Date

2028-11-29

Last Updated

2026-05-14

Healthy Volunteers

No

Interventions

DRUG

ALN-6400

ALN-6400 will be administered subcutaneously (SC).

Locations (1)

Clinical Trial Site

Miami, Florida, United States