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. 2024 Jan 3;5(2):100630. doi: 10.1016/j.jtocrr.2023.100630

Table 2.

Ongoing Clinical Trials of MET Inhibitors in NSCLC

Category Agents Trial ID Research Time Sample size Trial Descriptions Phase Primary End Point
MET TKI Ib Capmatinib NCT04677595 2021–2025 35 METex14 advanced NSCLC II ORR
Savolitinib NCT04923945 2021–2024 163 METex14 locally advanced or metastatic NSCLC III ORR
Savolitinib + osimertinib NCT05015608 2021–2024 250 MET amplified advanced NSCLC III PFS
NCT05261399 2022–2026 324 EGFR-mutated locally advanced or metastatic NSCLC with MET overexpression and/or amplification after Osimertinib resistance III PFS
Gumarontinib NCT04270591 2019–2023 183 c-MET+ advanced NSCLC Ib/II ORR
Bozitinib NCT04258033 2020–2024 185 c-MET+ locally advanced/metastatic NSCLC II ORR
Bozitinib NCT03175224 2017–2026 497 MET-altered (MET fusion, METex14, and MET amplification) NSCLC I/II The MTD and the incidence of DLTs; ORR
Ia Ensartinib ChiCTR2100048767 2021–2024 42 METex14 advanced or metastatic NSCLC II ORR
II Cabozantinib NCT01639508 2012–2026 86 MET overexpression, amplification, or mutation in NSCLC II ORR
Antibody Amivantamab NCT02609776 2016–2024 751 Previously treated METex14 unresectable or metastatic NSCLC I Number of participants with DLTs, AEs and SAEs
Amivantamab+ NCT05488314 2022–2025 161 METex14 or MET amplified metastatic NSCLC I/II Number of participants with Aes, DLTs and ORR
Capmatinib
ADC Telisotuzumab Vedotin NCT03539536 2018–2025 270 Previously treated c-Met+ locally advanced or metastatic NSCLC II ORR; Number of participants with Aes
NCT05513703 2022–2027 70 Previously untreated MET amplified advanced/metastatic nonsquamous NSCLC II ORR
RC108 NCT04617314 2021–2025 32 c-Met + advanced malignant solid tumors I Number of participants with AEs;
Maximum tolerated dose

ADC, antibody-drug conjugate; AE, adverse event; DLT, dose limited toxicity; ICI, immune checkpoint inhibitor; ID, identification; METex14, MET exon 14; MTD, maximum tolerated dose; ORR, objective response rate; PFS, progression-free survival; RR, response rate; SAE, serious adverse event; TKI, tyrosine kinase inhibitor.