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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.

Phase 1/2RecruitingUniversity of ChicagoNCT05200442Data as of May 2026

Treatment: VS-6766/avutometinib · CetuximabDoctors 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.

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Extracted 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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