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China Clears GSK’s Relenza For Clinical Trials By Chinese Firms

This article was originally published in PharmAsia News

Executive Summary

China's State FDA has cleared for clinical testing GlaxoSmithKline's Relenza (zanamivir) antiviral for treating avian flu. The drug is being developed under a licensing agreement in China between Nanjing Simcere Dongyuan Pharmaceutical and Nanjing EffactPharm Drug Development along with the Shanghai Institute of Materia Medica. Simcere has marketing rights from GSK in China, Indonesia, Thailand, Vietnam and other developing countries. (Click here for more

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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