Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**FT536 + amivantamab** is an investigational combination therapy being evaluated in Phase 1 clinical trials for the treatment of advanced solid tumors, particularly locally advanced or metastatic non-small cell lung cancer (NSCLC)[1]. FT536 is an off-the-shelf, allogeneic, chimeric antigen receptor (CAR)-engineered NK cell therapy, designed to enhance anti-tumor activity and persistence after infusion. Amivantamab is a fully human bispecific IgG1 monoclonal antibody that targets both epidermal growth factor receptor (EGFR) and mesenchymal-epithelial transition factor (MET), blocking ligand binding and receptor signaling, thus inhibiting cancer cell growth and survival. Amivantamab also mediates immune effector functions including antibody-dependent cell-mediated cytotoxicity (ADCC)[2]. The combination is being developed to leverage the synergistic effects of FT536’s innate immune action and amivantamab’s dual targeting and ADCC induction, particularly in NSCLC cohorts after lymphodepletion[1][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 FT536 + amivantamab.