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A Phase I trial of lentiviral vector-based gene therapy-ET3 for the treatment of hemophilia A

Trial Profile

A Phase I trial of lentiviral vector-based gene therapy-ET3 for the treatment of hemophilia A

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 31 May 2020

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At a glance

  • Drugs Gene therapies (Primary)
  • Indications Haemophilia A
  • Focus Therapeutic Use

Most Recent Events

  • 31 May 2020 New trial record
  • 26 May 2020 According to an Expression Therapeutics media release, the United States Food and Drug Administration (FDA) has approved the Investigational New Drug Application (IND) for clinical testing of lentiviral vector-based gene therapy-ET3 for hemophilia A. The trial will be conducted at the Emory University and will enroll patients shortly.

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