Drug intelligence / Profile preview

narmafotinib + mFOLFIRINOX

Development stage
Unknown
Lead developer
Amplia Therapeutics
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral (narmafotinib), Intravenous (mFOLFIRINOX: Oxaliplatin, Irinotecan, Leucovorin, 5-fluorouracil)
01

Overview

Narmafotinib + mFOLFIRINOX is an investigational combination regimen composed of **narmafotinib** (AMP945), a selective, orally bioavailable focal adhesion kinase (FAK) inhibitor, and **mFOLFIRINOX**, a chemotherapy protocol consisting of oxaliplatin, irinotecan, leucovorin, and 5-fluorouracil administered in modified doses. Narmafotinib acts by inhibiting FAK, a non-receptor tyrosine kinase that plays a central role in tumor cell survival, proliferation, migration, and resistance to chemotherapy, as well as modulating the tumor microenvironment by reducing fibrosis and immunosuppression. mFOLFIRINOX is used as a cytotoxic backbone, targeting rapidly dividing cancer cells through multiple mechanisms. The primary indication under investigation is **metastatic pancreatic cancer**, with clinical evaluation in Phase 1 and 2 trials. The combination aims to improve chemotherapy response and progression-free survival in a disease with historically limited treatment efficacy[2][3][5].

02

Targets

TOP1 (DNA Topoisomerase I)DNAFAK (Focal adhesion kinase)TS (Thymidylate synthase)

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