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Tech Sheet: Dr. Reddy’s Abiraterone Acetate API offerings

Abiraterone Acetate API

Abiraterone is an orally active inhibitor of the steroidal enzyme CYP17A1 (17 alpha-hydroxylase/C17,20 lyase). It inhibits CYP17A1 selectively and irreversibly via a covalent binding mechanism. Abiraterone is a CYP17 inhibitor indicated in combination with prednisolone to treat patients with metastatic castration-resistant prostate cancer (CRPC) and Metastatic high-risk castration-sensitive prostate cancer (CSPC).

Abiraterone Acetate (Zytiga, Janssen Biotech Inc.) was approved by the Food and Drug Administration (FDA) on April 28, 2011, for Prostate Cancer treatment. In December 2012, FDA expanded Zytiga’s use for late-stage Prostate Cancer. In February 2018, the FDA approved Abiraterone Acetate tablets with prednisone for metastatic high-risk castration sensitive prostate cancer (CSPC).

As of February 2008, Abiraterone is approved in various countries worldwide for different indications.

Key takeaways of Dr. Reddy’s Abiraterone Acetate API:

  • Enough capacity to cater to current market requirements.
  • Quality – in line with ICH guidelines.
  • Earliest generic API manufacturer of abiraterone globally.
  • Country-specific regulatory filings
  • GTI & Nitrosamine free.

To know more about our offerings , please read the technical sheet on Abiraterone Acetate by filling the contact form below.

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免责声明

本目錄中的任何信息(包括對任何產品或服務的任何引用)均不構成銷售要約,或被解釋為代表銷售要約。受有效專利保護的產品不提供或供應用於商業用途。但是,只要存在此類監管豁免,就可以出於監管提交的目的提供此類產品的研究數量。買方應對各自市場的專利方案進行獨立評估,並承擔所有與專利相關的責任。在印度受有效專利保護的產品不可用於商業用途,但可用於第 107A 節。

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