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mFOLFOX 6

Chungnam National University Hospital · Phase 3 active Small molecule

mFOLFOX6 is a chemotherapy regimen that combines 5-fluorouracil, leucovorin, and oxaliplatin to inhibit DNA synthesis and induce apoptosis in cancer cells.

mFOLFOX6 is a chemotherapy regimen that combines 5-fluorouracil, leucovorin, and oxaliplatin to inhibit DNA synthesis and induce apoptosis in cancer cells. Used for Metastatic colorectal cancer, Adjuvant treatment of stage III colorectal cancer.

At a glance

Generic namemFOLFOX 6
Also known asOxaliplatino + l-leucovorin + 5 Fluorouracile
SponsorChungnam National University Hospital
Drug classCombination chemotherapy regimen
TargetThymidylate synthase (5-FU); DNA (oxaliplatin)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

mFOLFOX6 (modified FOLFOX6) is a combination chemotherapy regimen where 5-fluorouracil (5-FU) inhibits thymidylate synthase to disrupt DNA synthesis, leucovorin (folinic acid) enhances 5-FU activity by stabilizing its binding to the enzyme, and oxaliplatin is a platinum agent that forms DNA cross-links to trigger cell death. This triplet combination is designed to provide synergistic cytotoxic effects against rapidly dividing cancer cells.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results