Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A multi-antigenic peptide-based cancer vaccine composed of synthetic peptides derived from three melanocyte differentiation antigens—MART‑1 (Melanoma Antigen Recognized by T cells 1 or Melan-A), gp100 (Glycoprotein 100 or PMEL), and Tyrosinase. These antigens are highly expressed in both cutaneous and uveal melanomas. The vaccine is designed to stimulate an immune response against tumor cells expressing these antigens by presenting the selected HLA-A2-restricted epitopes to cytotoxic T lymphocytes. It is typically administered with immunological adjuvants such as GM-CSF and PF3512676 in Montanide ISA oil to enhance immunogenicity. Developed primarily for the treatment of melanoma, this approach aims to induce antigen-specific T cell responses targeting malignant melanocytes[2][3][4][5].
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 Multi-epitope peptide melanoma vaccine.