TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ZYTIGA

ABIRATERONE ACETATE
Oncology Approved 2011-04-28
5
Indications
--
Phase 3 Trials
3
Priority Reviews
14
Years on Market

Details

Status
Prescription
First Approved
2011-04-28
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: ABIRATERONE ACETATE

ZYTIGA Approval History

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What ZYTIGA Treats

2 indications

ZYTIGA is approved for 2 conditions since its original approval in 2011. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Metastatic Castration-Resistant Prostate Cancer
  • Metastatic Castration-Sensitive Prostate Cancer
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

ZYTIGA FDA Label Details

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Indications & Usage

FDA Label (PDF)

ZYTIGA is indicated in combination with prednisone for the treatment of patients with Metastatic castration-resistant prostate cancer (CRPC) Metastatic high-risk castration-sensitive prostate cancer (CSPC) ZYTIGA is a CYP17 inhibitor indicated in combination with prednisone for the treatment of patients with metastatic castration-resistant prostate cancer (CRPC). metastatic high-risk castration-sensitive prostate cancer (CSPC).

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.