Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of amivantamab, a bispecific monoclonal antibody, and tepotinib, a small molecule tyrosine kinase inhibitor. Amivantamab targets both the epidermal growth factor receptor (EGFR) and the mesenchymal-epithelial transition (MET) receptor, while tepotinib is a highly selective MET inhibitor. The combination is primarily being investigated in clinical trials sponsored by the M.D. Anderson Cancer Center for the treatment of patients with non-small cell lung cancer (NSCLC) harboring MET alterations, such as MET exon 14 skipping mutations or MET amplification. By simultaneously targeting EGFR and MET through multiple mechanisms, this regimen aims to provide more robust inhibition of oncogenic signaling and overcome potential resistance mechanisms in MET-driven lung cancers.
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 amivantamab + tepotinib.