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A Multicenter, Non-randomized, Open-label, Multiple Dose Escalation Study to Evaluate the Safety and Tolerability of Subcutaneous BAY1093884 in Males With Severe Hemophilia

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Trial Profile

A Multicenter, Non-randomized, Open-label, Multiple Dose Escalation Study to Evaluate the Safety and Tolerability of Subcutaneous BAY1093884 in Males With Severe Hemophilia

Status: Withdrawn prior to enrolment
Phase of Trial: Phase I

Latest Information Update: 04 Nov 2021

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At a glance

  • Drugs Befovacimab (Primary)
  • Indications Haemophilia A; Haemophilia B
  • Focus Adverse reactions
  • Sponsors Bayer

Most Recent Events

  • 21 Oct 2019 Planned initiation date changed from 30 Sep 2019 to 28 Oct 2019.
  • 21 Oct 2019 Status changed from not yet recruiting to withdrawn prior to enrolment.
  • 10 Sep 2019 Planned initiation date changed from 2 Sep 2019 to 30 Sep 2019.

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