OncoMatch

OncoMatch/Clinical Trials/NCT06412198

A Multicenter Phase 1b/2 Study of Adagrasib, Cetuximab, and Cemiplimab for Metastatic Colorectal Cancer Harboring KRAS G12C Mutations

Is NCT06412198 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including Cetuximab and Cemiplimab for metastatic colorectal cancer.

Phase 1/2RecruitingM.D. Anderson Cancer CenterNCT06412198Data as of May 2026

Treatment: Cetuximab · Cemiplimab · AdagrasibTo learn if the drug combination of adagrasib, cetuximab, and cemiplimab can help to control metastatic CRC with KRAS G12C mutations.

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Extracted eligibility criteria

Cancer type

Colorectal Cancer

Biomarker criteria

Required: KRAS G12C mutation

KRASG12C mutation

Disease stage

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: chemotherapy — metastatic

Participants must have received at least one prior line of chemotherapy for metastatic disease with progression on treatment or intolerance to therapy.

Cannot have received: anti-PD-1 therapy

Prior PD1 or CTLA4 inhibition therapy

Cannot have received: anti-CTLA-4 therapy

Prior PD1 or CTLA4 inhibition therapy

Cannot have received: KRAS inhibitor

Prior KRASG12C inhibition therapy

Lab requirements

Blood counts

Absolute neutrophil count ≥ 1,000/mm3; Platelet count ≥ 100,000/mm3; Hemoglobin ≥ 9 g/dL, in the absence of transfusions for at least 2 weeks

Kidney function

Calculated creatinine clearance (Cockcroft-Gault) ≥ 60mL/min at screening

Liver function

Total bilirubin ≤ 1.5x ULN (if associated with Gilbert's disease or UGT1A1*28 homozygosity, ≤ 3x ULN); AST and ALT ≤ 3.0x ULN (if associated with liver metastases ≤5x ULN)

Laboratory values within the screening period: Absolute neutrophil count ≥ 1,000/mm3; Platelet count ≥ 100,000/mm3; Hemoglobin ≥ 9 g/dL, in the absence of transfusions for at least 2 weeks; Total bilirubin ≤ 1.5x ULN (if associated with Gilbert's disease or UGT1A1*28 homozygosity, ≤ 3x ULN); AST and ALT ≤ 3.0x ULN (if associated with liver metastases ≤5x ULN); Calculated creatinine clearance (Cockcroft-Gault) ≥ 60mL/min at screening

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

US trial sites

  • Massachusetts General Hospital Cancer Center · Boston, Massachusetts
  • MD Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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