Drug intelligence / Profile preview

BEA-28

Development stage
Preclinical
Lead developer
Beactica Therapeutics
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
01

Overview

BEA-28 is a first-in-class, cereblon-recruiting small molecule targeted protein degrader (PROTAC) that degrades TEAD (TEA Domain) transcription factors, which are key effectors of the Hippo-YAP/TAZ signaling pathway. Developed by Beactica Therapeutics using its Eclipsor platform, BEA-28 is designed to remove TEAD proteins and all their functions rather than simply blocking a binding pocket. This mechanism is particularly suited for treating cancers where Hippo pathway dysregulation drives tumor growth, immune evasion, or resistance to targeted therapies. In preclinical studies, BEA-28 has demonstrated robust tumor regression in xenograft models of mesothelioma and KRAS-mutant lung cancer, and has shown the ability to reverse acquired resistance to KRAS inhibitors in cellular models. Beactica is advancing BEA-28 as a preclinical candidate with plans for biomarker-selected combination strategies involving checkpoint inhibitors and KRAS inhibitors.

02

Targets

CRBN (Cereblon)TEAD4

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