Drug intelligence / Profile preview

P-bi-TAT

Development stage
Preclinical
Lead developer
NanoPharmaceuticals
Modality
Small Molecules, Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Subcutaneous
01

Overview

P-bi-TAT is an investigational **anticancer thyrointegrin antagonist** being developed by NanoPharmaceuticals. It is a **PEGylated small-molecule conjugate** composed of two tetraiodothyroacetic acid molecules linked to polyethylene glycol, giving a molecular weight greater than 3000 Da. The agent is designed to bind the **integrin alphaV beta3** receptor on tumor cells and tumor vasculature, where it antagonizes thyroid hormone analog signaling and modulates cancer-relevant transcriptional programs. In preclinical studies, P-bi-TAT has shown antitumor activity in glioblastoma multiforme, pancreatic cancer, and other human cancer models, including effects on cancer stemness, proliferation, survival, angiogenesis, and tumor energy metabolism, with reported downregulation of genes involved in electron transport and oxidative phosphorylation. It has also been described as crossing the blood-brain barrier, supporting potential use in brain cancers such as glioblastoma.

Other names
polyethylene glycol conjugated bivalent tetraiodothyroacetic acidPEGylated bivalent tetrac
02

Targets

αVβ1 (Integrin alpha-V beta-1)TTR (Transthyretin)GPIIb/IIIa (Integrin alpha-IIb/beta-3)αVβ3 (Integrin αVβ3)ITGA5:ITGB1 (Integrin α5β1)αVβ6 (Integrin αVβ6)αVβ5 (Integrin αVβ5)

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