A Study of Marstacimab for Severe Hemophilia A

This study is for men aged 12 to 74 with severe hemophilia A (a rare bleeding disorder where blood doesn't clot normally) who are currently taking emicizumab. The purpose is to understand the safety of switching from emicizumab to a new medicine called marstacimab. Researchers will look for any side effects (adverse events) that happen while taking marstacimab. You would be eligible if you have severe hemophilia A (FVIII activity <1%) without inhibitors (antibodies that can make treatments less effective) and have been on emicizumab for at least 6 months. The study is currently unclear about its recruitment status and plans to enroll about 15 participants.

Study design
This is an open-label study, meaning you and your doctors will know which treatment you are receiving. It is not randomized, and about 10-15 participants will be included.
What's involved
You would take marstacimab once weekly by injection under the skin for about 4 months, after a 14-day break from emicizumab. The total study duration for each participant is about 6 months.
Compensation
Not stated in the trial record.
Follow-up
Your safety will be monitored for at least 28 days after your last dose of marstacimab.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06703606

A Study to Learn About How Changing Therapy From Emicizumab to Marstacimab Affects People With the Severe Hemophilia A.

Recruiting
PHASE1Ages 12–74InterventionalTreatment
Pfizer
~15 participants
Updated 2026-06-03 on ClinicalTrials.gov
What's tested:MARSTACIMAB

At a glance

Recruiting sites
7 of 7 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of marstacimab-related adverse events (AEs)
Measured over Approximately 178 days: from the time the participant provides informed consent, through and including a minimum of 28 calendar days after last dose of study treatment
+1 more outcome measured
Severe Hemophilia A
7 sites across 6 states
North Carolina2
California1
Gujarat1
Maharashtra1
İzmir1
İ̇stanbul1
  • Pfizer CT.gov Call Center · STUDY_DIRECTOR · Pfizer

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  • Incidence of marstacimab-related adverse events (AEs)Approximately 178 days: from the time the participant provides informed consent, through and including a minimum of 28 calendar days after last dose of study treatment
  • Incidence of marstacimab-related serious AEs (SAEs)Approximately 178 days: from the time the participant provides informed consent, through and including a minimum of 28 calendar days after last dose of study treatment