A Phase Ⅱ Study of RC108 in Combination With Furmonertinib for the First-line Treatment of EGFR-Mutated Combined MET-Positive Unresectable Locally Advanced or Recurrent Metastatic NSCLC

Evaluate the efficacy and safety of RC108 in combination with Furmonertinib against Furmonertinib for treatment of EGFR mutation combined with MET-positive unresectable locally advanced or recurrent metastatic NSCLC

Trial Details

NCT ID
NCT06962865
Phase
PHASE2
Sponsor
RemeGen Co., Ltd.
Status
RECRUITING
Cancer Type
Non-Small Cell (NSCLC) Lung Cancer
Interventions
  • RC108
  • Furmonertinib Mesilate Tablets Monotherapy
Locations (sample)
  • Beijing, China|39.9075,116.39723
  • Beijing, China|39.9075,116.39723
  • Binzhou, China|37.36667,118.01667
  • Changchun, China|43.88,125.32278
  • Changsha, China|28.19874,112.97087

Key Eligibility Criteria

  • Voluntarily participate in the study and signed the ICF;
  • Male or female, aged 18-75 years;
  • All participants to be enrolled must be diagnosed with histopathologically or cytologically confirmed, unresectable locally advanced (stage IIIB/II…
  • For previously locally advanced or recurrent metastatic disease not treated with systemic antitumor therapy;

For full eligibility, visit ClinicalTrials.gov.

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