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

Phase 1

Not yet recruiting

• Conditions: Severe Hemophilia A
• Interventions: Drug: MARSTACIMAB

• Registration Number: NCT06703606
• Lead Sponsor: Pfizer

Brief Summary

The purpose of the study is to learn about safety, how the body processes marstacimab and how it works in patients with severe hemophilia A. A rare bleeding disorder where the blood doesn't clot normally. This causes a person to bleed a lot, even from a small cut.
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Detailed Description

This is a non-randomized open-label study in approximately 10-15 adolescent and adult participants between ages 12 to \<75 years with severe hemophilia A (defined as FVIII activity \<1%) with or without inhibitors who are currently on treatment with emicizumab for ≥6 months. The study is designed to assess the safety and PK/PD during a 4-month treatment peri...

Basic Information
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Recruitment & Eligibility
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Study & Design

Study Timeline

• Status Verified: 2024-11
• Study First Submitted: 2024-11-21
• Study First Submitted QC: 2024-11-21
• Last Update Submitted: 2024-11-21
• Study First Posted: 2024-11-25
• Last Update Posted: 2024-11-25
• Study Start: 2024-12-24
• Primary Completion: 2025-07-25
• Study Completion: 2025-07-25

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Male
• Target Recruitment: 15

Inclusion Criteria

1. Male and 12 to <75 years of age with a minimum body weight of 35 kg at the time of signing the informed consent.
2. Diagnosis of severe hemophilia A (FVIII activity <1%) with or without inhibitors.
3. On emicizumab therapy at a standard clinical dose for ≥6 months.

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Exclusion Criteria

1. Previous or current treatment for or history of coronary artery diseases, venous or arterial thrombosis, or ischemic disease.
2. Any medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
3. Known hemostatic defect other than hemophilia A.
4. Current use of any prohibited concomitant medication(s) or unwillingness or inability to use a required concomitant medication(s).
5. Previous administration of an investigational product (drug or vaccine) within 30 days or 5 half-lives preceding the first dose of study intervention used in this study (whichever is longer). Participation in studies of other investigational products (drug or vaccine) at any time during participation in this study.
6. Platelet count <100,000/μl or hemoglobin <10 g/dL.
7. Clinically significant renal or hepatic function abnormality based on laboratory results at screening, or known kidney or liver disease.
8. CD4 cell count ≤200/μl if HIV positive.
9. Screening 12-lead ECG that demonstrates clinically significant abnormalities that, in the opinion of the investigator, may affect participant safety or interpretation of study results.
10. Known planned surgical procedure.
11. Hypersensitivity or allergic reaction to hamster protein or other components of the study intervention.
12. Investigator site staff directly involved in the conduct of the study and their family members, site staff otherwise supervised by the investigator, and sponsor and sponsor-delegate employees directly involved in the conduct of the study and their family members.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
MARSTACIMAB	MARSTACIMAB	Marstacimab 150 mg subcutaneous (SC) once weekly (QW)

Primary Outcome Measures

Name	Time	Method
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

Secondary Outcome Measures

Name	Time	Method
Plasma Concentration Versus Time of Marstacimab (Listings)	Day 1 up to day 135
Maximum Observed Plasma Concentration (Cmax) of Marstacimab	Day 1 up to day 135
Average Plasma Concentration (Cavg) of Marstacimab	Day 1 up to day 135
Minimum Observed Plasma Concentration (Cmin)	Day 1 up to day 135
Change from baseline in tissue factor pathway inhibitor (TFPI).	Baseline, Day 1 up to day 135
Change from baseline in prothrombin fragment 1+2 (PF 1+2)	Baseline, Day 1 up to day 135
Change from baseline in D-dimer	Baseline, Day 1 up to day 135
Change from baseline in TGA (thrombin generation assay).	Baseline, Day 1 up to day 135
Incidence of Anti-Drug Antibody (ADA)	Day 1 up to day 135
Incidence of clinically significant persistent neutralizing antibodies (NAb)	Day 1 up to day 135