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 combination drug regimen consisting of: - **autogene cevumeran**, a personalized mRNA-based neoantigen vaccine designed to stimulate an immune response against patient-specific tumor antigens[4] - **atezolizumab**, a monoclonal antibody that targets and inhibits PD-L1, a checkpoint protein on tumor cells[4] - **folinic acid (leucovorin)**, a vitamin used to increase the effectiveness of fluorouracil[5] - **fluorouracil**, a pyrimidine analog and antimetabolite that inhibits thymidylate synthase, impairing DNA synthesis[5] - **irinotecan**, a topoisomerase I inhibitor that induces DNA strand breaks[5] - **oxaliplatin**, a platinum-based chemotherapeutic that forms DNA crosslinks, triggering apoptosis[5] The regimen combines an individualized immunotherapy (autogene cevumeran), a checkpoint inhibitor (atezolizumab), and standard cytotoxic chemotherapy (FOLFIRINOX: folinic acid, fluorouracil, irinotecan, oxaliplatin). Its mechanism aims to induce robust tumor-specific T cell responses, block immune suppression via PD-L1, and directly kill proliferating cancer cells by impairing DNA replication and synthesis[4][5][2].
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 autogene cevumeran + atezolizumab + folinic acid + fluorouracil + irinotecan + oxaliplatin.