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    Find the latest Drugs in Development and Pipeline Prospector News of Errant Gene Therapeutics.

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    Errant Gene Therapeutics Pushing Clinical Trial of Potentially Curative Treatment for Beta-Thalassemia and Eventually Sickle Cell Disease

    Details:

    The EHA abstract, submitted by Simona Raso, reports that 2 out of 3 Thalassemia patients treated with EGT’s autologous CD34+ cells have sustained dramatic reduction in blood transfusions after 8 and 5 years, respectively.


    Lead Product(s): Autologous CD34+ cells,TNS9.3.55

    Therapeutic Area: Genetic Disease Product Name: Undisclosed

    Highest Development Status: Phase IProduct Type: Cell and Gene therapy

    Partner/Sponsor/Collaborator: Memorial Sloan Kettering Cancer Center

    Deal Size: Not Applicable Upfront Cash: Not Applicable

    Deal Type: Not Applicable January 11, 2021

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