Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a **cell-based cancer immunotherapy** composed of autologous (patient-derived) myeloma cells admixed with an allogeneic (donor-derived) cell line genetically engineered to secrete **granulocyte macrophage colony-stimulating factor** (GM-CSF). The GM-CSF-producing cell line enhances the immune stimulation at the vaccination site by recruiting and activating dendritic cells, which present tumor antigens from the autologous myeloma cells to the patient’s immune system, aiming to induce tumor-specific CD4+ and CD8+ T cell responses. The most commonly used bystander cell line in clinical trials is the GM-CSF–secreting K562 cell line. This combinatorial approach leverages patient-specific tumor antigens (from autologous cancer cells) together with “off-the-shelf” immune activation (via the engineered cell line). It has been assessed in trials for hematologic malignancies and solid tumors, often as adjuvant therapy to stem cell transplantation or combined with chemotherapy or immunomodulation.
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 myeloma cells + allogeneic granulocyte macrophage colony-stimulating factor producing cell line.