Status:

ACTIVE_NOT_RECRUITING

A Study to Learn About the Study Medicine -Hympavzi in Congenital Hemophilia Patients Without Inhibitors in Japan.

Lead Sponsor:

Pfizer

Conditions:

Hemophilia A or B

Eligibility:

All Genders

Brief Summary

A study to evaluate the safety of Hympavzi under the actual use in patients with congenital hemophilia who do not have inhibitors.

Detailed Description

The objective of this study is to assess the safety of this drug under actual usage conditions in patients with congenital hemophilia who do not have inhibitors. The observation period will be up to ...

Eligibility Criteria

Inclusion

  • Patients must meet all of the following inclusion criteria to be eligible for inclusion in the study:
  • Patients who have received at least one dose of this drug after the launch of this drug

Exclusion

    Key Trial Info

    Start Date :

    October 30 2025

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    December 13 2029

    Estimated Enrollment :

    50 Patients enrolled

    Trial Details

    Trial ID

    NCT07161687

    Start Date

    October 30 2025

    End Date

    December 13 2029

    Last Update

    November 20 2025

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Pfizer, Inc

    Tokyo, Japan