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Clinical Trial Active — Not Recruiting Phase I NCT02609776

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

Study of Amivantamab, a Human Bispecific EGFR and cMet Antibody, in Participants With Advanced Non-Small Cell Lung Cancer — Active Not Recruiting • Phase I • Oncology •…

📅 06 Jul 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase I
NCT ID
NCT02609776
Start
2016-05-24
Completion
2026-12-31
ClinicaliQ Trial Snapshot
  • Study of Amivantamab, a Human Bispecific EGFR and cMet Antibody, in Participants With Advanced Non-Small Cell Lung Cancer — Active Not Recruiting • Phase I • Oncology • NCT02609776.
  • Trial testing new cancer drug amivantamab alone and combined with existing treatments in advanced lung cancer patients to find safe, effective doses.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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What This Trial Is Studying

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). Conditions: Non-Small-Cell Lung Cancer Interventions: Amivantamab, Amivantamab, Lazertinib, Carboplatin, Pemetrexed Lead Sponsor: Janssen Research…

Full Trial Details
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Eligibility criteria, protocol, and results when available
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