Drug intelligence / Profile preview

Helicon peptide

Development stage
Unknown
Lead developer
Parabilis Medicines
Modality
Peptides, PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

Helicon peptides are a proprietary class of stabilized helical peptides developed by Parabilis Medicines (formerly FogPharma). These peptides are engineered to target intracellular proteins that are typically considered "undruggable" by binding to large, flat protein surfaces with high affinity and selectivity. The Helicon platform enables the development of both direct inhibitors, such as FOG-001 (which targets the β-catenin/TCF4 interaction), and targeted protein degraders (TPD). Specifically, Helicon peptide degraders have been designed to selectively target the agonist-bound, transcriptionally active conformation of the Androgen Receptor (ARON) for ubiquitin-proteasome-mediated degradation, offering a novel therapeutic strategy for castration-resistant prostate cancer.

Brand names
Helicon
Other names
Heliconsstabilized helical peptides
02

Targets

ERG (ETS-related gene transcription factor ERG)TCF4 (Transcription factor 4)AR (Adrenergic receptors)CTNNB1 (Beta-catenin)

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