Skip to main content
Clinical Trials/NCT03407651
NCT03407651
Completed
Phase 2

Phase 2 Study to Evaluate the Pharmacokinetics, Efficacy and Safety of a Daily Subcutaneous Treatment Regimen With Marzeptacog Alfa (Activated) for Bleeding Prophylaxis in Adult Subjects With Hemophilia A and B Subjects With an Inhibitor

Catalyst Biosciences9 sites in 5 countries11 target enrollmentDecember 18, 2017

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hemophilia A With Inhibitor
Sponsor
Catalyst Biosciences
Enrollment
11
Locations
9
Primary Endpoint
Bleeding Episode Prevention Success
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Phase 2, multi-center, open-label study designed to evaluate the PK, bioavailability, PD, efficacy and safety of a daily subcutaneous [SC] treatment regimen with MarzAA for bleeding prophylaxis in 12 adult subjects with hemophilia A or B with an inhibitor and history of frequent spontaneous bleeding episodes.

Detailed Description

Multi-center, open-label Phase 2 study to evaluate the PK, bioavailability, PD, efficacy and safety of a daily SC treatment regimen with MarzAA for bleeding prophylaxis in adult subjects with hemophilia A or B with an inhibitor. The study will enroll and dose, both intravenously and subcutaneously, a total of 12 adult male subjects with severe congenital hemophilia A or B with an inhibitor, and history of frequent bleeding episodes during the 6 months prior to enrollment, as per the individual's bleeding and treatment records. Once a subject is enrolled into the trial, the study will be conducted in three parts (occurring consecutively): Part 1a (24 hours): Single IV administration of MarzAA; Part 1b (48 hours): Single SC administration of MarzAA; Part 2: Daily SC administration. Dose escalation in Part 2 will occur if breakthrough bleeding occurs. Subjects are treated for 50 days at the final dose level required.

Registry
clinicaltrials.gov
Start Date
December 18, 2017
End Date
April 13, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
Male

Investigators

Sponsor
Catalyst Biosciences
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Severe congenital hemophilia A or B with an inhibitor.
  • History of frequent spontaneous bleeding episodes.
  • Male, age 18 or older.
  • Affirmation of informed consent with signature confirmation before any trial-related activities.

Exclusion Criteria

  • Receiving prophylaxis treatment.
  • Previous participation in a clinical trial evaluating a modified rFVIIa agent.
  • Known positive antibody to FVII or FVIIa detected by central laboratory at screening.
  • Have a coagulation disorder other than hemophilia A or B.
  • Significant contraindication to participation.

Outcomes

Primary Outcomes

Bleeding Episode Prevention Success

Time Frame: Day 1 of final MarzAA dose level - Day 50

Annualized bleed rate (ABR; spontaneous and total) during Part 2 when on final MarzAA dose level versus recorded historical ABR. The analysis of the primary endpoint (annualized bleeding rate ABR for spontaneous and traumatic bleeds) of the final dose of MarzAA each subject was treated was based on the 1-sample test compared to a predefined rate assumed for the on-demand therapy. The latter was assumed to be 12 (or 1 bleed per month), which was the minimum ABR for each subject according to inclusion criterion 2 (defined as the H0), with no maximum value. A higher score indicated a worse outcome. ABR is on a scale of 0 to 365, with a lower score reflective of a lower number of bleeding events in a year.

Secondary Outcomes

  • Number of Events of Antibody Formation(From time of first dose of MarzAA until date of first occurrence of clinical event, assessed up to treatment Day 50)
  • Number of Events of an Antibody Response(From time of first dose of MarzAA until date of first occurrence of clinical event, assessed up to treatment Day 50.)
  • Occurrence of Breakthrough Bleeding(From Day 5 of dose level until occurrence of event)
  • Occurrence of Clinical Thrombotic Event(From date of first dose until date of first occurrence of clinical event, assessed up to treatment Day 50)
  • Coagulation Assessment - Prothrombin Time(From date of pre-dose to 24 hours (Part 1a), pre-dose to 48 hours (Part 1b), and pre-dose to Day 50 (Part 2))
  • Coagulation Assessment - Activated Partial Thromboplastin Time(From date of pre-dose to 24 hours (Part 1a), 48 hours (Part 1b), to Day 50/end of study (Part 2))
  • Coagulation Assessment - Fibrinogen(From date of pre-dose to 24 hours (Part 1a), 48 hours (Part 1b), or Day 50 (Part 2).)
  • Thrombogenicity Assessment(From time of pre-dose of MarzAA at Day 1 until date of first occurrence of thrombotic event, assessed up to treatment Day 50.)

Study Sites (9)

Loading locations...

Similar Trials