OncoMatch/Clinical Trials/NCT05200442
A Study of VS-6766 and Cetuximab in Patients With Advanced Colorectal Cancer
Is NCT05200442 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including VS-6766/avutometinib and Cetuximab for colorectal cancer.
Treatment: VS-6766/avutometinib · Cetuximab — Doctors leading this study hope to learn about the safety of combining the study drug VS-6766 with another drug called cetuximab in colorectal cancer. This study is for individuals who have advanced colorectal cancer and their cancer has progressed while getting previous treatment or individuals who cannot take/tolerate previous treatments. If you choose to participate, your time in this research will last up to 24 months.
Check if I qualifyExtracted eligibility criteria
Cancer type
Colorectal Cancer
Biomarker criteria
Required: KRAS mutation
metastatic colorectal adenocarcinoma with kirsten rat sarcoma viral oncogene homolog (KRAS) mutations, detected by any Clinical Laboratory Improvement Amendments-certified method (tumor or ct-DNA)
Disease stage
Metastatic disease required
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: fluoropyrimidine (5-FU, capecitabine)
progression of disease on 5-FU or capecitabine
Must have received: platinum-based chemotherapy (oxaliplatin)
progression of disease on ... oxaliplatin
Must have received: topoisomerase inhibitor (irinotecan)
progression of disease on ... irinotecan
Must have received: anti-VEGF therapy (bevacizumab)
progression of disease on ... bevacizumab therapy or any other approved anti-VEGF therapy
Must have received: immunotherapy (anti-PD-L1, anti-CTLA4)
If participant has high levels of MicroSatellite Instability (MSI-H), they must have had recommended immunotherapy agent(s) i.e anti- programmed death ligand 1 (L)1 with or without anti-CTLA4 agents.
Cannot have received: (Lonsurf, regorafenib)
No prior Lonsurf or regorafenib treatment is allowed.
Cannot have received: MEK inhibitor
Must have not had any treatment with prior MEK (mitogen-activated protein kinase kinase) inhibitor
Cannot have received: anti-EGFR therapy
Must have not had any treatment with prior ... anti-EGFR (antineoplastic epidermal growth factor receptor)
Cannot have received: KRAS inhibitor
Must have not had any treatment with prior ... KRAS ... inhibitor therapy
Cannot have received: SOS1 inhibitor
Must have not had any treatment with prior ... SOS1 ( Son of sevenless 1) ... inhibitor therapy
Cannot have received: SHP2 inhibitor
Must have not had any treatment with prior ... SHP2 (Src homology-2 domain-containing protein tyrosine phosphatase-2) inhibitor therapy
Cannot have received: cytotoxic chemotherapy
Exception: within 2 weeks prior to entering the study
Participants should not have had chemotherapy ... within 2 weeks prior to entering the study.
Cannot have received: radiation therapy
Exception: within 2 weeks prior to entering the study
Participants should not have had ... radiotherapy ... within 2 weeks prior to entering the study.
Cannot have received: surgery
Exception: major surgery within 2 weeks prior to entering the study
Participants should not have had ... major surgery within 2 weeks prior to entering the study.
Cannot have received: allogeneic stem cell transplant
No prior allogeneic stem cell or solid organ transplantation.
Cannot have received: solid organ transplant
No prior allogeneic stem cell or solid organ transplantation.
Lab requirements
Blood counts
Must meet required clinical laboratory values set by study doctor
Kidney function
Must meet required clinical laboratory values set by study doctor
Liver function
Must meet required clinical laboratory values set by study doctor
Cardiac function
Must have adequate cardiac function as clinically confirmed by study doctor
Must meet required clinical laboratory values set by study doctor to show participant's health and organ function meets requirements to be in study. Must have adequate cardiac function as clinically confirmed by study doctor.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of Chicago Medical Center · Chicago, Illinois
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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