Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MELITAC 12.1 is a synthetic peptide cancer vaccine designed to stimulate immune responses against melanoma. It consists of an emulsion containing a mixture of 12 class I MHC-restricted melanoma peptides and a class II MHC-restricted tetanus toxoid helper peptide, formulated with the adjuvant Montanide ISA-51[1][4]. The vaccine aims to induce CD8+ T cell responses targeting multiple melanoma antigens, thereby enhancing anti-tumor immunity[5]. It has been studied in combination with immunostimulatory agents such as toll-like receptor agonists (e.g., polyICLC) and IDO1 inhibitors (e.g., epacadostat)[2][5]. The primary indication is for the treatment of advanced or high-risk melanoma, including cutaneous malignant and mucosal subtypes[3][6]. Initial development was by Oncovir; later development has involved Incyte Corporation and academic centers such as the University of Virginia[2][3][6].
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 MELITAC 12.1.