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 therapy** consisting of three agents: - **Lifileucel** is an autologous tumor-infiltrating lymphocyte (TIL) cell therapy, where T cells are harvested from a patient’s tumor, expanded ex vivo, and reinfused to target a broad range of patient-specific tumor neoantigens. - **Nivolumab** is a fully human monoclonal antibody targeting the programmed death 1 (PD-1) immune checkpoint receptor, blocking its interaction with ligands PD-L1/PD-L2 and thereby enhancing T-cell activation and anti-tumor immunity. - **Relatlimab** is a monoclonal antibody targeting lymphocyte-activation gene 3 (LAG-3), a negative immune checkpoint regulator, relieving inhibition of T lymphocytes and promoting anti-tumor response. The combination aims to leverage adoptive cell therapy with checkpoint inhibition for synergistic activation of the immune response, primarily evaluated in advanced melanoma refractory to other immunotherapies[2][3][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 lifileucel + nivolumab + relatlimab.