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A Post Approval Commitment Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of KOVALTRY in Chinese Children, Adolescents /Adults With Severe Hemophilia A

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Trial Profile

A Post Approval Commitment Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of KOVALTRY in Chinese Children, Adolescents /Adults With Severe Hemophilia A

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 20 Apr 2025

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At a glance

  • Drugs Octocog alfa (Primary)
  • Indications Haemophilia A
  • Focus Therapeutic Use
  • Sponsors Bayer; Bayer HealthCare

Most Recent Events

  • 27 Mar 2024 Status changed from recruiting to completed.
  • 17 May 2023 Planned End Date changed from 12 Aug 2024 to 19 Sep 2028.
  • 17 May 2023 Planned primary completion date changed from 12 Aug 2024 to 19 Sep 2028.

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