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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.

Phase 3RecruitingHoffmann-La RocheNCT06793215Data as of May 2026

Treatment: Divarasib · Pembrolizumab · Pemetrexed · Carboplatin · CisplatinThe 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).

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Extracted 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

No prior treatment (treatment-naive required)
Max 0 prior lines

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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