RecruitingPhase 2NCT07575308

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

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)


Sponsor

Alnylam Pharmaceuticals

Enrollment

24 participants

Start Date

Jul 30, 2026

Study Type

INTERVENTIONAL

Conditions

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


Eligibility

Sex: FEMALEMin Age: 16 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called ALN-6400 for people with heavy menstrual bleeding (hmb) and von willebrand disease (vwd). The study is currently recruiting participants at 4 locations. People eligible for this study include women aged 16 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGALN-6400

ALN-6400 will be administered subcutaneously (SC).


Locations(11)

Clinical Trial Site

Orange, California, United States

Clinical Trial Site

San Diego, California, United States

Clinical Trial Site

San Francisco, California, United States

Clinical Trial Site

Miami, Florida, United States

Clinical Trial Site

Lexington, Kentucky, United States

Clinical Trial Site

Pittsburgh, Pennsylvania, United States

Clinical Trial Site

Nijmegen, Netherlands

Clinical Trial Site

Stockholm, Sweden

Clinical Trial Site

Bradford, United Kingdom

Clinical Trial Site

Oxford, United Kingdom

Clinical Trial Site

Truro, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT07575308


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