Drug intelligence / Profile preview

mFOLFIRI

Development stage
Phase 4
Lead developer
University of Utah
Modality
Small Molecules
Administration
Intravenous
01

Overview

mFOLFIRI is a modified chemotherapy regimen consisting of leucovorin (folinic acid), fluorouracil (5-FU), and irinotecan. It is a variation of the standard FOLFIRI regimen, typically modified by omitting the bolus dose of fluorouracil to improve the safety profile and reduce hematologic toxicities such as neutropenia. mFOLFIRI is widely utilized in the treatment of gastrointestinal cancers, most notably metastatic colorectal cancer, where it serves as a standard-of-care backbone. Its mechanism involves the inhibition of topoisomerase I by irinotecan and the inhibition of thymidylate synthase by fluorouracil, with leucovorin acting as a biochemical modulator to enhance the efficacy of fluorouracil.

Other names
modified FOLFIRIleucovorin + fluorouracil + irinotecan
02

Targets

DNATOP1 (DNA Topoisomerase I)TS (Thymidylate synthase)

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