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OncoMatch/Clinical Trials/Amivantamab

EGFR/MET bispecific antibody

Amivantamab (Rybrevant) Clinical Trials

14 recruiting trials·Johnson & Johnson / Janssen

Amivantamab (Rybrevant, JNJ-61186372) is a bispecific antibody targeting EGFR and MET, combining receptor downregulation with immune cell-directing (ADCC/ADCP) activity in a mechanism distinct from small-molecule TKIs. It received initial FDA approval in 2021 for EGFR exon 20 insertion–mutant advanced NSCLC after platinum-based chemotherapy based on the CHRYSALIS trial. In 2024, two additional FDA approvals expanded its use: amivantamab plus lazertinib (Lazcluze) for first-line EGFR-mutant (exon 19 deletion or L858R) advanced NSCLC based on MARIPOSA, and amivantamab plus carboplatin-pemetrexed for first-line EGFR exon 20 insertion NSCLC based on PAPILLON. A subcutaneous formulation was approved in December 2025 to reduce IV infusion burden. Active trials explore post-osimertinib combinations informed by the completed MARIPOSA-2 trial, and evaluation in MET-amplified or MET exon 14–skipping NSCLC. Eligibility varies by indication: EGFR exon 20 insertion or standard sensitizing EGFR mutation (del19/L858R) required depending on the trial.

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Lung Cancer — Non-Small Cell (NSCLC)
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Recruiting Amivantamab trials

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How OncoMatch helps you find Amivantamab trials

01

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OncoMatch reads the eligibility criteria for every Amivantamab trial and extracts structured requirements — biomarkers, stage, prior therapy — from protocol text.

02

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03

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Each trial shows which criteria you meet, which you don't, and which need more information. Bring the shortlist to your oncologist.

Lung Cancer — Non-Small Cell (NSCLC) trials →