OncoMatch/Clinical Trials/NCT06793215
A Study Evaluating the Efficacy and Safety of Divarasib and Pembrolizumab Versus Pembrolizumab and Pemetrexed and Carboplatin or Cisplatin in Participants With Previously Untreated, KRAS G12C-Mutated, Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer
Is NCT06793215 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments for non-small cell lung cancer.
Treatment: Divarasib · Pembrolizumab · Pemetrexed · Carboplatin · Cisplatin — The purpose of this study is to evaluate the efficacy and safety of divarasib and pembrolizumab compared with pembrolizumab and pemetrexed and carboplatin or cisplatin, for the first-line treatment of adult participants with KRAS G12C-mutated, advanced or metastatic non squamous non-small cell lung cancer (NSCLC).
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Small Cell Lung Carcinoma
Biomarker criteria
Required: KRAS G12C mutation
Documentation of the presence of a KRAS G12C mutation
Required: PD-L1 (CD274) expression status known (status known)
Documentation of known PD-L1 expression status in tumor tissue
Disease stage
Metastatic disease required
advanced or metastatic non squamous NSCLC that is not eligible for curative surgery and/or definitive chemoradiotherapy
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: KRAS G12C inhibitor
Prior treatment with KRAS G12C inhibitors
Cannot have received: pan-KRAS/RAS inhibitor
Prior treatment with ... pan-KRAS/RAS inhibitors
Cannot have received: systemic therapy
Any anti-cancer systemic therapy, including hormonal therapy, within 21 days prior to randomization
Cannot have received: radiation therapy
Radiation therapy including palliative RT to bone metastases within 2 weeks prior to randomization and RT to the lung >30Gy within 6 months prior to randomization
Cannot have received: immune checkpoint inhibitor
Treatment with systemic immunosuppressive or immunostimulatory medications, including CD137 agonists and immune checkpoint inhibitors
Cannot have received: allogeneic stem cell or solid organ transplantation
Prior allogeneic stem cell or solid organ transplantation
Lab requirements
Blood counts
Adequate end-organ function
Kidney function
Adequate end-organ function
Liver function
Adequate end-organ function
Adequate end-organ function
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Alaska Oncology and Hematology · Anchorage, Alaska
- Marin Cancer Care Inc · Greenbrae, California
- Hoag Memorial Hospital · Newport Beach, California
- BioResearch Partner · Hialeah, Florida
- Ascension Sacred Heart · Pensacola, Florida
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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