Drug intelligence / Profile preview

Abiraterone Acetate Tablets (II)

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Small Molecules, Nanoparticles → Drug Delivery Systems
Administration
Oral
01

Overview

Abiraterone Acetate Tablets (II) is an improved nanocrystal formulation of abiraterone acetate, a small molecule prodrug that inhibits the enzyme CYP17 (17α-hydroxylase/C17-20 lyase). This enzyme is a critical component of the androgen biosynthesis pathway in the testes, adrenal glands, and prostate tumor tissues. This specific formulation, developed by Ding-Wei Ye and colleagues, utilizes nanocrystal technology and the absorption enhancer Sodium N-[8-(2-hydroxy-benzoyl) amino] caprylate (SNAC) to improve oral bioavailability and reduce pharmacokinetic variability. These improvements allow for a significantly lower therapeutic dose (300 mg daily) compared to the 1000 mg daily dose required for the originator product (Zytiga), while maintaining equivalent efficacy in treating metastatic castration-resistant prostate cancer (mCRPC). The formulation also minimizes the food effect, allowing for administration without dietary restrictions.

Other names
nanocrystal abiraterone acetateabiraterone acetate nanocrystal formulationabiraterone acetate + SNAC
02

Targets

CYP17A1 (Steroid 17-alpha-hydroxylase/C17,20 lyase)CYP1A2 (Cytochrome P450 1A2)CYP2C19 (Cytochrome P450 2C19)CYP2C8 (Cytochrome P450 2C8)CYP2C9 (Cytochrome P450 family 2 subfamily C member 9)CYP2D6 (Cytochrome P450 2D6)

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