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Clinical Study on the Safety and Efficacy of a Single Intravenous Dose of CRISPR/Cas9-Edited Autologous CD34+ Hematopoietic Stem/Progenitor Cells (BRL-101) in the Treatment of Sickle Cell Disease

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Trial Profile

Clinical Study on the Safety and Efficacy of a Single Intravenous Dose of CRISPR/Cas9-Edited Autologous CD34+ Hematopoietic Stem/Progenitor Cells (BRL-101) in the Treatment of Sickle Cell Disease

Status: Not yet recruiting
Phase of Trial: Phase I

Latest Information Update: 22 Mar 2024

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At a glance

  • Drugs BRL 101 (Primary)
  • Indications Sickle cell anaemia
  • Focus Adverse reactions; Therapeutic Use

Most Recent Events

  • 05 Mar 2024 New trial record

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