For Healthcare Professionals

Phase II of Neoadjuvant and Adjuvant Capmatinib in NSCLC

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About the study

The purpose of this study is to determine if neoadjuvant capmatinib can improve outcomes in participants with stages I-IIIA non-small cell lung cancer with MET exon 14 mutations and/or high MET amplification beyond those achieved with surgery, chemotherapy, and radiation.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Histologically confirmed NSCLC stage IB-IIIA, N2 and selected IIIB (T3N2 or T4N2)
  2. Participant must have either MET exon 14 mutations and/or high level MET amplification
  3. Participants must be eligible for surgery and scheduled for surgical resection within approximately 2 weeks after the last does of neoadjuvant study treatment.

EXCLUSION CRITERIA

Exclusion Criteria:


  1. Participants with unresectable or metastatic disease. All participants should have brain imaging (either MRI brain or CT brain with contrast) prior to enrollment to exclude brain metastasis.
  2. Prior treatment with any MET inhibitor or HGF-targeting therapy
  3. Major surgery (e.g., intra-thoracic, intra-abdominal or intra-pelvic) within 4 weeks prior to starting study treatment, or who have not recovered from side effects of such procedure.
  4. Prior systemic anti-cancer therapy (chemotherapy, immunotherapy, biologic therapy, vaccine) or investigational agents for NSCLC within the past 3 years.
  5. History of or current interstitial lung disease or pneumonitis

Other protocol-defined inclusion/exclusion criteria may apply at the end


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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Non-small Cell Lung Cancer

Age (in years)

18 - 90

Phase

Phase 2

Participants needed

3

Est. Completion Date

Aug 6, 2026

Treatment type

Interventional


Sponsor

Novartis

ClinicalTrials.gov identifier

NCT04926831

Study number

CINC280AUS12

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