Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GDX012 is an investigational, allogeneic, non-engineered cell therapy composed of highly enriched variable delta 1 (Vδ1) gamma-delta (γδ) T cells derived from healthy donor blood. It is being developed for the treatment of certain cancers, primarily acute myeloid leukemia (AML), especially in patients with measurable residual disease after standard-of-care treatment. The therapy leverages the unique properties of Vδ1 γδ T cells, which can recognize and kill cancer cells through their specific receptors without requiring genetic engineering. These cells are expanded ex vivo to create an "off-the-shelf" product intended to provide anti-leukemic activity by targeting molecular patterns associated with cancer cell dysregulation. GDX012 has received FDA orphan drug designation for AML and is currently in phase I clinical trials to assess safety, tolerability, pharmacokinetics, and anti-leukemic efficacy[1][3][4][5][7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on allogeneic variable delta 1 gamma-delta T cells.