Drug intelligence / Profile preview

FOG-001 + leucovorin + 5-fluorouracil + oxaliplatin + bevacizumab

Development stage
Unknown
Lead developer
Parabilis Medicines
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Peptides, Monoclonal Antibodies → Antibody-Based Therapeutics, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

A combination regimen investigating **FOG-001**, a first-in-class Helicon peptide that acts as a competitive inhibitor of the protein-protein interaction between **β-catenin** and the **T-cell factor (TCF) family** of transcription factors, with standard chemotherapy agents **leucovorin**, **5-fluorouracil**, **oxaliplatin** (collectively known as FOLFOX), and the anti-angiogenic monoclonal antibody **bevacizumab**. FOG-001 disrupts Wnt/β-catenin pathway signaling, a mechanism frequently implicated in drug resistance and poor prognosis in colorectal cancer and other solid tumors. The regimen is designed for use in patients with advanced or metastatic solid tumors, primarily microsatellite-stable colorectal cancer, targeting both aberrant Wnt signaling and tumor angiogenesis. FOG-001 is developed by Parabilis Medicines and is currently in Phase 1/2 clinical trials in combination with FOLFOX and bevacizumab[1][3][5].

02

Targets

DNATCF/LEF (T-cell factor/Lymphoid enhancer-binding factor)CTNNB1 (Beta-catenin)VEGFA (Vascular endothelial growth factor A)TS (Thymidylate synthase)

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