The collaboration between WuXi STA and Ascletis began in 2012, and the approval of Ganovo® marks a critical milestone in the history of the “MAH” policy in China. WuXi STA is now the first Contract Development and Manufacturing Organization (CDMO) in China to support the launch of an innovative drug using the Marketing Authorization Holder (MAH) pilot program.

Ganovo® is the first Direct-acting Anti-viral Agent (DAA) developed by a domestic company in China and has been selected as a National Science and Technology Major Project for “Innovative Drug Development”.

WuXi STA supported the process optimization and process validation of Ganovo® Active Pharmaceutical Ingredient (API), as well as the Ganovo®NDA submission and approval – via its process development and manufacturing technology platform, and global standard quality systems.

In December 2017, WuXi STA’s Jinshan API manufacturing site successfully passed the pre-approval inspection by CNDA as part of the Ganovo® NDA application process. As a pioneer of “MAH”, WuXi STA is helping many innovative drug development partners in China, including Ascletis, to optimize their manufacturing processes, significantly reduce commercial production costs, mitigate business risk, and improve operational efficiency. 

"The successful development of Ganovo® fulfilled our commitment to deliver affordable innovative drugs for the Chinese patients." said Jinzi J. Wu, Ph.D., Ascletis' founder, President and CEO. "We sincerely appreciate the dedicated support from WuXi STA over the past six years, which was crucial to the approval of Ganovo®.”

“Congratulations to our partner Ascletis for reaching this milestone. The strong support received from the Chinese government for new drugs and the successful implementation of ‘MAH’ pilot was integral to reaching this milestone. We now look forward to enabling more partners to launch their innovative medicines both in China and internationally for benefit of patients around the world.” said Dr. Minzhang Chen, CEO of WuXi STA.