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.
A Study to Learn About How Changing Therapy From Emicizumab to Marstacimab Affects People With the Severe Hemophilia A.
At a glance
Conditions
Where it's being run
7 sites across 6 statesStudy leadership
- Pfizer CT.gov Call Center · STUDY_DIRECTOR · Pfizer
Who to contact
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What this trial measures
- 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