Drug intelligence / Profile preview

nab-17-AAG

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Small Molecules, Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

nab-17-AAG is a **nanoparticle albumin-bound formulation** of 17-allylamino-17-demethoxygeldanamycin (17-AAG), a semi-synthetic derivative of geldanamycin and a potent inhibitor of the molecular chaperone **HSP90 (Heat Shock Protein 90)**. 17-AAG induces the degradation of client proteins involved in cell growth and survival, leading to cell cycle arrest and apoptosis in cancer cells. The **nab- formulation** is designed to improve the solubility and delivery of 17-AAG, potentially enhancing its therapeutic index and allowing intravenous administration. The core mechanism is inhibition of HSP90, leading to destabilization of oncogenic signaling proteins such as AKT, HER2, EGFR, and others. 17-AAG and its formulations have been evaluated primarily for **solid tumors** including hormone-refractory prostate cancer, neuroblastoma, and gallbladder cancer, but clinical studies have not led to regulatory approval.

Other names
nab-paclitaxel-17-allylamino-17-demethoxygeldanamycinnab-paclitaxel17-allylamino-17-demethoxygeldanamycinnab-paclitaxel 17-allylamino-17-demethoxygeldanamycinnanoparticle albumin-bound 17-AAG
02

Targets

HSP90 (Heat shock protein 90 chaperone complex)VDAC (Voltage-dependent anion channel)HSP90AA1 (Heat shock protein HSP90-alpha)

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