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OncoMatch/Clinical Trials/NCT06116682

Targeted Treatment for Advanced Non-Small Cell Lung Cancer That Has Increased Copies of the MET Gene (An Expanded Lung-MAP Treatment Trial)

Is NCT06116682 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Amivantamab for lung non-small cell carcinoma.

Phase 2RecruitingSWOG Cancer Research NetworkNCT06116682Data as of Jun 2026

Treatment: AmivantamabThis phase II Expanded Lung-MAP treatment trial tests how well amivantamab-subcutaneous (SC) works in treating patients patients with MET amplification non-small cell lung cancer. Amivantamab-SC is a drug that reduces extra copies of the MET gene, a change present in your tumor. Giving amivantamab-SC may lower the chance of the growth or spread of advanced non-small cell lung cancer that has extra copies of the MET gene in the tumor.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Amivantamab

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: MET amplification

MET amplification determined by FMI tissue-based next generation sequencing (NGS) assay

Excluded: EGFR sensitizing mutation

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) EGFR sensitizing mutations

Excluded: EGFR T790M

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... EGFR T790M mutation

Excluded: MET exon 14 skipping

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... MET Exon-14 skipping mutant NSCLC

Excluded: ALK fusion

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... ALK gene fusion

Excluded: ROS1 rearrangement

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... ROS1 gene rearrangement

Excluded: RET rearrangement

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... RET gene rearrangement

Excluded: NTRK1 rearrangement

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... NTRK rearrangement

Excluded: NTRK2 rearrangement

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... NTRK rearrangement

Excluded: NTRK3 rearrangement

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... NTRK rearrangement

Excluded: HER2 (ERBB2) mutation

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... HER2 mutation

Excluded: KRAS activating mutation

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... KRAS activating mutations

Excluded: BRAF V600E

Participants must not have other known actionable oncogenic alterations, such as (but not limited to) ... BRAF V600E mutation

Disease stage

Required: Stage IV

Stage IV or recurrent Non-Small Cell Lung Cancer

Performance status

ZUBROD 0–2

Prior therapy

Min 1 prior line

Must have received: systemic therapy — stage iv or recurrent nsclc

Cannot have received: met tyrosine kinase inhibitor (tepotinib, capmatinib, crizotinib)

Lab requirements

Blood counts

Absolute neutrophil count ≥ 1.5 x 10^3/uL; Hemoglobin ≥ 10.0 g/dL; Platelets ≥ 75 x 10^3/uL

Kidney function

serum creatinine ≤ institutional ULN or calculated creatinine clearance ≥ 45 mL/min

Liver function

Total bilirubin ≤ 1.5 x institutional ULN unless history of Gilbert's disease (then ≤ 5 x ULN); AST and ALT ≤ 3 × institutional ULN (≤ 5 x ULN with liver metastasis)

Cardiac function

Participants with cardiac disease or history of cardiotoxic agents must be NYHA class 2B or better

Absolute neutrophil count ≥ 1.5 x 10^3/uL; Hemoglobin ≥ 10.0 g/dL; Platelets ≥ 75 x 10^3/uL; Total bilirubin ≤ 1.5 x institutional ULN unless history of Gilbert's disease (then ≤ 5 x ULN); AST and ALT ≤ 3 × institutional ULN (≤ 5 x ULN with liver metastasis); serum creatinine ≤ institutional ULN or calculated creatinine clearance ≥ 45 mL/min; NYHA class 2B or better if cardiac disease

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro · Jonesboro, Arkansas
  • University of Arkansas for Medical Sciences · Little Rock, Arkansas
  • Sutter Auburn Faith Hospital · Auburn, California
  • Alta Bates Summit Medical Center-Herrick Campus · Berkeley, California
  • Palo Alto Medical Foundation-Fremont · Fremont, California

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06116682 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior met tyrosine kinase inhibitor disqualifies patients from enrollment.

Does this trial require MET?

Yes, MET amplification is a required biomarker for enrollment.

Are patients with EGFR alterations eligible?

No. EGFR sensitizing mutation is an exclusion criterion.

Are patients with EGFR alterations eligible?

No. EGFR T790M is an exclusion criterion.

What disease stage is eligible?

Stage IV is required.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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