Drug intelligence / Profile preview

abiraterone acetate + docetaxel + prednisone

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Targeted Protein Degraders (TPDs) → Small Molecules, Prodrugs/Conditional Activator Small Molecules → Small Molecules, Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Multivalent & Scaffold-Based Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

abiraterone acetate + docetaxel + prednisone is a combination regimen used experimentally for the treatment of metastatic castration-sensitive and castration-resistant prostate cancer, especially in high-risk or de novo metastatic settings. **Abiraterone acetate** is a selective, irreversible inhibitor of the enzyme CYP17A1, leading to androgen biosynthesis inhibition. **Docetaxel** is a taxane-class chemotherapy that disrupts microtubule function, inducing cell death. **Prednisone** is a synthetic corticosteroid that serves as an anti-inflammatory and is used to counteract some side effects of the other drugs and, in abiraterone therapy, to suppress adrenocorticotropic hormone feedback. The three agents, when combined, target androgen production, mitotic division, and hormonal pathways, with evidence suggesting improved radiographic progression-free survival in metastatic castration-sensitive prostate cancer over standard of care. This regimen has been evaluated in studies such as the phase 1b COU-AA-206 study and the phase 3 PEACE-1 study, but is not yet a universally established or FDA-approved standard for use as a triplet outside of clinical trials for prostate cancer[1][4].

Brand names
TaxotereZytiga
Other names
docetaxel + prednisone + abiraterone acetate
02

Targets

CYP17A1 (Steroid 17-alpha-hydroxylase/C17,20 lyase)GR (Glucocorticoid receptor)Microtubule

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