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OncoMatch/Clinical Trials/NCT07789210

A Single-Arm, Phase II, Multicenter Clinical Study of Neoadjuvant Encorafenib Plus Cetuximab N01 and mFOLFOX6 in Patients With Locally Advanced BRAF V600E-Mutant Colorectal Cancer With or Without Resectable Metastases

Is NCT07789210 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies Neoadjuvant therapy of encorafenib plus cetuximab N01 and mFOLFOX6 for colorectal cancer.

Phase 2RecruitingZhejiang UniversityNCT07789210Data as of Sep 2026Location: China

Treatment: Neoadjuvant therapy of encorafenib plus cetuximab N01 and mFOLFOX6This is a single-arm, multicenter, phase II clinical trial evaluating the safety and efficacy of neoadjuvant encorafenib plus cetuximab N01 and mFOLFOX6 in patients with locally advanced BRAF V600E-mutated colorectal cancer, with or without resectable metastases. Eligible patients will receive 8 weeks of neoadjuvant treatment with encorafenib, cetuximab N01, and mFOLFOX6, followed by tumor response assessment and radical surgery when appropriate. The primary endpoint is 18-month disease-free survival (DFS). Secondary endpoints include perioperative safety, objective response rate, pathological response rate, 1-year DFS, 3-year DFS, overall safety, and quality of life. This study aims to explore whether incorporating BRAF and EGFR targeted therapy into standard chemotherapy in the neoadjuvant setting can improve tumor control and long-term outcomes in this high-risk molecular subgroup of colorectal cancer.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Neoadjuvant therapy of encorafenib plus cetuximab N01 and mFOLFOX6

Cancer type

Colorectal Cancer

Biomarker criteria

Required: BRAF v600e

Required: KRAS wild-type

Required: NRAS wild-type

Required: Mismatch-repair proficient (pMMR / MSS)

Disease stage

Required: Stage T4N0-2M0, T3N2M0, T0-4N0-2M1A

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: targeted therapy

Previously received targeted drug therapy (including G12C inhibitors, bevacizumab, etc.)

Lab requirements

Blood counts

hemoglobin ≥ 90g/L; absolute neutrophil count ≥ 1.5 × 10^9/L; platelet count ≥ 75 × 10^9/L

Kidney function

serum creatinine ≤ 1.5x ULN or creatinine clearance rate ≥ 50ml/min

Liver function

total bilirubin (TBIL) ≤ 1.5x ULN (Gilbert syndrome ≤ 3x ULN); ALT and AST ≤ 2.5x ULN

Cardiac function

LVEF ≥ 50%

Blood routine examination criteria... Biochemical tests... Coagulation or thyroid function tests... Cardiac ultrasound evaluation: LVEF ≥ 50%

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

Frequently asked questions

Is NCT07789210 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior targeted therapy disqualifies patients from enrollment.

Does this trial require BRAF?

Yes, BRAF v600e is a required biomarker for enrollment.

Does this trial require KRAS?

Yes, KRAS wild-type is a required biomarker for enrollment.

Does this trial require MLH1?

Yes, MLH1 wild-type is a required biomarker for enrollment.

What disease stage is eligible?

Stage T4N0-2M0 or T3N2M0 or T0-4N0-2M1A is required.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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