drugset / Trial / NCT02609776

Study of Amivantamab, a Human Bispecific EGFR and cMet Antibody, in Participants With Advanced Non-Small Cell Lung Cancer

NCT02609776 ↗

Phase 1 Active not recruiting 751 enrolled Janssen Research & Development, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of study is to evaluate the safety, pharmacokinetics, and preliminary efficacy of Amivantamab as a monotherapy and in combination with lazertinib, and to determine the recommended Phase 2 dose (RP2D) (monotherapy), recommended Phase 2 combination dose (RP2CD) (combination therapy), and to determine recommended Phase 2 Dose (RP2q3W) with combination chemotherapy (Amivantamab in combination with standard of care carboplatin and pemetrexed) in 21 day treatment cycle for participants with advanced non-small cell lung cancer (NSCLC).

Timeline

Start
2016-05-24
Primary completion
2026-12-31
Completion
2027-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Amivantamab Monoclonal antibody 140 mg —
Subject Amivantamab Monoclonal antibody 1050 mg —
Subject Amivantamab Monoclonal antibody 1400 mg —
Subject Lazertinib Small molecule — —
Background Carboplatin Small molecule — Intravenous
Background Pemetrexed Small molecule — Intravenous