Recruiting
Phase 3

Marstacimab

Sponsor:

Pfizer

Code:

NCT05145127

Conditions

Hemophilia A

Hemophilia B

Eligibility Criteria

Sex: Male

Age: 1 - 70+

Healthy Volunteers: Not accepted

Interventions

PF-06741086

Study Details

Brief summary:

Study B7841007 is an open-label extension study to assess the long-term safety, tolerability, and efficacy of prophylaxis treatment with marstacimab in participants who did not require "Early Termination" from the Phase 3 Study B7841005 and from the Phase 3 Study B7841008.

Study B7841005: approximately 145 adolescent and adult participants 12 to <75 years of age with severe hemophilia A or moderately severe to severe hemophilia B (defined as FVIII activity <1% or FIX activity ≤2%, respectively) with or without inhibitors are expected to be enrolled in Study B7841005 during which they will receive prophylaxis (defined as treatment by SC injection of marstacimab).

Study B7841008: this is an ongoing Phase 3, open-label study in pediatric participants <18 years of age with severe hemophilia A (FVIII Coagulation Factor Activity <1%) or moderately severe to severe hemophilia B (FIX Coagulation Factor Activity ≤2%). A sequential approach will be used in enrolling at least 100 pediatric participants, at least 20 of which will be aged ≥12 to <18 years and at least 80 participants will be aged ≥1 to <12 years. At the start of study B7841008, the dosing and data available in adolescent and adult participants in Study B7841005 supported the initiation of B7841008 study in participants aged ≥12 to <18 years. Subsequently, additional safety and efficacy data from adolescent participants in Study B7841005 became available for benefit/risk assessment in support of dosing participants aged ≥6 to <12 years. Based on the positive benefit/risk assessment conducted by both internal Pfizer review and eDMC review, dosing of the ≥6 to <12 years age group was initiated in June 2023 in B7841008 Study. Data from participants ≥6 years from B7841008 Study and Study B7841005 will support the dosing of participants aged ≥1 to <6 years.

All participants will be provided the prefilled pen (PFP) for administration of marstacimab in the study. Use of the prefilled syringe (PFS) will be permitted at the investigator's discretion for those participants who have difficulty with administration of the PFP. Additionally, participants will be provided the PFS for use in this study in countries where the PFS is anticipated to be the only presentation available commercially. An optional, open-label, single arm, substudy using the PFP was completed in the first 23 participants rolled over from Study B7841005 who agreed to participate in the substudy.

Conditions

Hemophilia A

Hemophilia B

Study ID

NCT05145127

Start date

Nov 17, 2021

Status verified date

Jun, 2026

Completion date

Jul 31, 2030

Anticipated

Primary completion date

Jul 31, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 1 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • All participants will have a minimum body weight as defined by parent studies
  • Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.
  • Participants have successfully completed participation in parent studies, defined as did not require "Early Termination"

Exclusion Criteria:

  • Previous or current treatment for or history of coronary artery disease, venous or arterial thrombosis (CTCAE Grade >3), or ischemic disease (except catheter-associated thrombosis)
  • Abnormal renal function as defined by eGFR <30 mL.min/1.73 m(2)
  • Known planned surgical procedure during the planned study period
  • Unstable hepatic function as determined by the Investigator clinical assessment and review of the participant's most recent laboratory results, which would make the participant inappropriate for the study
  • For participants known to be HIV+, worsening disease status as determined by the Investigator clinical assessment and review of participant's most recent laboratory results, to include recent locally available CD4 count (if available), which would make the participant inappropriate for the study
  • Regular, concomitant therapy with immunomodulatory drugs (eg, IVIG, and routine systemic corticosteroids, rituximab)
  • Ongoing or planned use of immune tolerance induction or prophylaxis with FVIII or FIX replacement during the study
  • Participation in other study involving investigational drug(s) or investigational vaccine(s) within 30 days or 5 half-lives prior to or during study participation, with the exception of participation in parent studies
  • Investigator site staff or Pfizer employees directly involved in the conduct of the study, site staff otherwise supervised by the Investigator, and their respective family members

Study Design

Enrollment

245 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: PF-06741086

For participants aged ≥12 years 300 milligrams(mg) subcutaneous (sc) loading dose followed by 150 mg sq once weekly (qw). 300 mg sc qw is prescribed for participants who meet dose escalation criteria.

For participants aged ≥6 to <12 years is marstacimab 150 mg SC for initial loading dose followed by 75 mg SC QW. 150 mg sc qw is prescribed for participants who meet dose escalation criteria.

Interventions

PF-06741086

For participants aged ≥12 years 300 milligrams(mg) subcutaneous (sc) loading dose followed by 150 mg sq once weekly (qw). 300 mg sc qw is prescribed for participants who meet dose escalation criteria.

For participants aged ≥6 to <12 years is marstacimab 150 mg SC for initial loading dose followed by 75 mg SC QW. 150 mg sc qw is prescribed for participants who meet dose escalation criteria.

Primary outcome measure

  • Number of subject reporting Adverse Events [ Time Frame: Baseline up to 7 years ]
  • Number of subjects reporting Serious Adverse Events [ Time Frame: Baseline up to 7 years ]
  • Incidence and severity of thrombotic events [ Time Frame: Baseline up to 7 years ]
  • Incidence and severity of thrombotic microangiopathy [ Time Frame: Baseline up to 7 years ]
  • Number of subjects reporting Disseminated intravascular coagulalopathy/consumption coagulopathy [ Time Frame: Baseline up to 7 years ]
  • Incidence of clinically significant persistent NAb against marstacimab [ Time Frame: Baseline up to 7 years ]
  • Incidence and severity of injection site reaction [ Time Frame: Baseline up to 7 years ]
  • Clinically significant changes in vital signs from baseline [ Time Frame: Baseline up to 7 years ]
  • Incidence of clinically significant laboratory value abnormalities [ Time Frame: Baseline up to 7 years ]
  • Incidence of severe hypersensitivity and anaphylactic reactions [ Time Frame: Baseline up to 7 years ]

Central Contacts and Locations

Central contacts

Pfizer CT.gov Call Center

1-800-718-1021ClinicalTrials.gov_Inquiries@pfizer.com

Locations

Northwell Health HTC

Recruiting

New Hyde Park, New York, United States, 11040

The Feinstein Institutes for Medical Research

Recruiting

Philadelphia, Pennsylvania, United States, 19195

Washington Institute for Coagulation d/b/a WACBD

Recruiting

Seattle, Washington, United States, 98101

Stollery Children's Hospital

Recruiting

Edmonton, Alberta, Canada, T6G 2B7

Hamilton Health Sciences - McMaster University Medical Centre

Recruiting

Hamilton, Ontario, Canada, L8N 3Z5

Hamilton Health Sciences - McMaster University Medical Centre

Recruiting

Hamilton, Ontario, Canada, L8N3Z5

More Information

Sponsor

Pfizer

Last update posted

Jul 1, 2026

Last verified

Jun, 2026

Keywords

  • Factor VIII Inhibitor
  • Factor IX Inhibitor
  • PF-06741086
  • Marstacimab
  • Anti-TFPI

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Pfizer on 2026-07-01.