Drug intelligence / Profile preview

CF10

Development stage
Preclinical
Lead developer
Wake Forest University School of Medicine
Modality
Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intraperitoneal, Intravenous
01

Overview

**CF10** is an investigational, second-generation polymeric fluoropyrimidine developed from the F10 platform. It is a chemically modified oligonucleotide composed of fluorodeoxyuridylate monomers in a single-stranded DNA-based polymer designed to generate the active fluoropyrimidine metabolite FdUMP more directly than 5-fluorouracil. CF10 produces dual antitumor activity through potent inhibition of thymidylate synthase and trapping of DNA topoisomerase I cleavage complexes, causing thymidine depletion, replication stress, DNA damage, and cancer-cell death. It originated at Wake Forest University School of Medicine and is being advanced by Deep Creek Pharma as a late-preclinical candidate for colorectal cancer, including metastatic and 5-fluorouracil-refractory disease, with additional preclinical work in pancreatic ductal adenocarcinoma, small cell lung cancer, and acute myeloid leukemia.

Other names
AraC-FdUMP [10]AraC-FdUMP[10]Capped F10
02

Targets

TOP1 (DNA Topoisomerase I)TS (Thymidylate synthase)

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