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    GammaDelta Therapeutics Receives FDA Clearance of IND Application for GDX012

    Details:

    GammaDelta plans to initiate a Phase 1 clinical trial for patients with measurable residual disease (MRD) positive AML. Expected to begin later in 2021 as a multicentre study in the US, the trial will evaluate safety, tolerability and anti-leukemic activity of GDX012.


    Lead Product(s): GDX012

    Therapeutic Area: Oncology Product Name: GDX012

    Highest Development Status: IND EnablingProduct Type: Cell and Gene therapy

    Partner/Sponsor/Collaborator: Not Applicable

    Deal Size: Not Applicable Upfront Cash: Not Applicable

    Deal Type: Not Applicable May 20, 2021

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