RecruitingPhase 1NCT05985954

Open-label Phase 1b Study of Ulixertinib and Cetuximab or Ulixertinib in Combination With Cetuximab and Encorafenib in Patients With Unresectable or Metastatic Colorectal Cancer Who Have Previously Received EGFR or BRAF-directed Therapy


Sponsor

M.D. Anderson Cancer Center

Enrollment

27 participants

Start Date

Jan 18, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To find the recommended dose of ulixertinib that can be given in combination with cetuximab and/or encorafenib to patients with unresectable/metastatic CRC and who have received EGFR or BRAF-directed therapy in the past.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests two targeted drug combinations — ulixertinib with cetuximab, and ulixertinib with cetuximab and encorafenib — in people with colorectal cancer that cannot be surgically removed or has spread, and who have already been treated with EGFR or BRAF-targeted therapies. **You may be eligible if...** - You have colorectal cancer that is unresectable (cannot be removed with surgery) or has spread to other parts of the body - You have already received prior treatment targeting EGFR or BRAF - You are able to provide informed consent **You may NOT be eligible if...** - You have not previously received EGFR or BRAF-directed therapy - Your cancer has not been confirmed as colorectal cancer - You have significant health conditions that would make you unable to tolerate the study drugs Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGCetuximab

Given by IV (vein)

DRUGUlixertinib

Given by PO

DRUGEncorafenib

Given by PO


Locations(1)

M D Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT05985954


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