RecruitingPhase 2NCT06411600

Combination Therapy for BRAF-V600E Metastatic CRCm

Bevacizumab Plus encoRAfenib-cetuximab in BRAF-V600E Mutated Metastatic Colorectal Cancer, a Phase II Study With a Safety lead-in Cohort, the BRAVE Trial


Sponsor

Vall d'Hebron Institute of Oncology

Enrollment

94 participants

Start Date

May 17, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The BRAVE is a phase II clinical trial aimed at evaluating the efficacy of the combination therapy of encorafenib, cetuximab, and bevacizumab in patients with metastatic colorectal cancer (CRC) harboring the BRAF-V600E mutation. This mutation is present in about 8-10% of CRC cases and is associated with poor prognosis and limited treatment options. The rationale behind this trial stems from preclinical studies suggesting that the overexpression and activation of vascular endothelial growth factor A (VEGFA) may contribute to resistance to BRAF inhibitors (BRAFi) in CRC. Thus, the trial hypothesizes that adding bevacizumab, an anti-angiogenic agent targeting VEGFA, to the combination of encorafenib and cetuximab may delay acquired resistance, leading to improved progression-free survival. The primary objective of the BRAVE is to evaluate the antitumor activity of the encorafenib-cetuximab-bevacizumab combination in patients who have experienced disease progression after one or two chemotherapy regimens for BRAF V600E-mutant metastatic CRC. This activity will be assessed based on the confirmed progression-free survival rate according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 criteria.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a targeted combination therapy for metastatic colorectal cancer that carries a specific genetic change called BRAF V600E mutation. The combination uses drugs that block the mutated BRAF protein and related pathways to slow or stop cancer growth. **You may be eligible if...** - You are 18 or older with metastatic colorectal cancer - Your tumor has been confirmed to have a BRAF V600E gene mutation - Your cancer is microsatellite stable (MSS), a specific molecular feature - You have had 1 or 2 prior chemotherapy regimens for metastatic disease - Your cancer has measurable or evaluable disease **You may NOT be eligible if...** - Your tumor does not have the BRAF V600E mutation - Your cancer is microsatellite instable (MSI-high) - You have had more than 2 prior lines of treatment in the metastatic setting - Your organ function does not meet the required levels 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGEncorafenib

Encorafenib is administered orally at a daily dose of 300 mg, typically in the form of four 75 mg capsules taken together.

DRUGCetuximab

Cetuximab is administered intravenously every two weeks at a dose of 500 mg/m².

DRUGBevacizumab

Bevacizumab is administered intravenously every two weeks at a dose of 5 mg/kg.


Locations(1)

Vall d'Hebron Hospital

Barcelona, Spain

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06411600


Related Trials