Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GM-K562 is an autologous cancer vaccine developed by the Dana-Farber Cancer Institute for the treatment of advanced chronic lymphocytic leukemia (CLL) following reduced-intensity allogeneic stem cell transplantation. The vaccine is a cellular immunotherapy consisting of lethally irradiated autologous CLL tumor cells mixed with K562 cells that have been genetically modified to secrete granulocyte-macrophage colony-stimulating factor (GM-CSF). GM-CSF acts as an immune adjuvant to recruit and activate antigen-presenting cells, which then process and present the patient-specific tumor antigens from the autologous cells to the immune system. This approach aims to enhance the graft-versus-leukemia (GVL) effect and expand leukemia-reactive T cells while minimizing graft-versus-host disease (GVHD). It was evaluated in a Phase 1 clinical trial (NCT00442130) led by Dr. Catherine Wu.
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 autologous GM-K562 vaccine.