Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Recombinant MAGE-3.1 antigen is a tumor-specific melanoma-associated antigen produced using recombinant DNA technology. It is designed as a therapeutic cancer vaccine to stimulate the immune system to recognize and attack cells expressing the MAGE (Melanoma Antigen Gene) family proteins, particularly in melanoma and other tumors that express this antigen. Vaccination with recombinant MAGE-3.1 antigen aims to induce a host immune response against tumor cells bearing the MAGE-A family antigens, potentially leading to tumor regression or disease control[8][6]. The drug has been evaluated in clinical trials for its safety, immunogenicity, and anti-tumor activity in patients with advanced or metastatic melanoma[6]. Its mechanism of action involves presenting the specific tumor-associated peptide (MAGEA1) to the immune system, thereby promoting an anti-tumor T-cell response.
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 recombinant MAGE-3.1 antigen.