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Clinical Trial Summary

To learn if avutometinib in combination with defactinib and cetuximab can help to control unresectable, anti-EGFR-refractory, advanced colorectal cancer.


Clinical Trial Description

The primary objective is to assess the antitumor activity of the treatment combinations based on Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Secondary Objectives: 1. Assess impact of treatment combinations on survival 2. Characterize the safety profile of the treatment combinations (DLTs) 3. Evaluate the pharmacodynamics of the avutometinib combination with defactinib plus cetuximab. 4. Evaluate for pERK and Ki67 inhibition Exploratory Objectives - Assess blood- and tissue-based predictive biomarkers of activity upon treatment with cetuximab plus avutometinib plus defactinib - Demonstrate feasibility of establishing patient-derived xenograft (PDX) models in matched patients with cetuximab-refractory mCRC to evaluate for biomarkers of response and mechanisms of resistance. - Explore mechanisms of resistance to cetuximab plus avutometinib and defactinib ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06369259
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Christine Parseghian, MD
Phone (713) 795-9280
Email cparseghian@mdanderson.org
Status Not yet recruiting
Phase Phase 2
Start date October 31, 2024
Completion date February 1, 2028

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