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Prospective, Multinational, Non-interventional Post-authorisation Study to Document the Long-term Immunogenicity, Safety, and Efficacy of Human-cl rhFVIII (Simoctocog Alfa) in Patients With Haemophilia A Treated in Routine Clinical Practice

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Trial Profile

Prospective, Multinational, Non-interventional Post-authorisation Study to Document the Long-term Immunogenicity, Safety, and Efficacy of Human-cl rhFVIII (Simoctocog Alfa) in Patients With Haemophilia A Treated in Routine Clinical Practice

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 07 Jul 2022

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At a glance

  • Drugs Simoctocog alfa (Primary)
  • Indications Haemophilia A
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Octapharma

    • Most Recent Events

    • 04 Jul 2022 According to OctaPharma media release, data from this study will be featured in poster presentations and two Supported Symposia during ISTH 2022 Congress major international meeting.
    • 26 Aug 2020 Status changed from active, no longer recruiting to completed.
    • 27 Jul 2020 Planned End Date changed from 1 Jul 2020 to 1 Aug 2020.

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