Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is an investigational multi-component cancer immunotherapy regimen combining two tumor antigen peptides (MAGE-3.A1 and NA17.A2), three immune-stimulatory cytokines (interleukin-2, interferon-alpha, granulocyte-macrophage colony-stimulating factor), and the topical immune response modifier imiquimod. The MAGE-3.A1 peptide is derived from the melanoma-associated antigen 3 (MAGE-3) and is presented by HLA-A1 molecules to activate cytotoxic T lymphocytes against tumor cells expressing this antigen[3][5][6]. NA17.A2 is another tumor-associated peptide targeting a different epitope. IL-2, IFN-alpha, and GM-CSF are cytokines that enhance T-cell proliferation, activation, dendritic cell maturation, and overall antitumor immunity. Imiquimod acts as a toll-like receptor 7 agonist to further stimulate local immune responses at the site of administration. This combination aims to induce robust cellular immunity against tumors—primarily melanoma—by promoting both specific cytotoxic T cell responses against defined tumor antigens and general immune activation.
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 MAGE-3.A1 peptide + NA17.A2 peptide + IL-2 + IFN-α + GMCSF + imiquimod.