According to an internationally renowned consulting firm, IMS, a few days ago, China’s R&D investment in new special drugs reached US$2.7 billion between 2008 and 2010, and will increase by US$6 billion in the next five years. At the same time, relevant research institutions predict that the growth rate of China's pharmaceutical market in 2011 will reach 25%-27%, and the total market will exceed US$50 billion, making it the third largest pharmaceutical market in the world.

The reporter learned that there are 187 original innovative drugs currently in clinical research in China, of which 2/3 drugs are in Phase I clinical studies, and drugs in Phase II clinical studies and Phase III clinical studies account for 19% and 22%, respectively.

According to the above-mentioned IMS sources, among the 187 original innovative drugs, 70 drugs have compound patent protection in China, compared with 23 U.S. patents and 16 European patents.

In fact, the low gold content of China's new special drugs can not be ignored, and the reasons include many aspects. According to industry insiders, the development of a new drug in developed countries can be as low as $100 million, and as much as $1 billion. Once the new drug is successfully listed, its annual sales in the world can be as high as $5 billion or more; and in addition to the API market in China's pharmaceutical market, Outside of the international market, pharmaceutical preparations have been blocked. This has resulted in less annual sales of drugs with a level of more than RMB 100 million. The company's sales are not large enough, so it is impossible to invest huge R&D funds. On the other hand, China has 50 - There are relatively few large-scale pharmaceutical enterprises with a total value of 10 billion yuan, and even fewer mega-enterprises with a total value of more than 20 billion yuan. Enterprises lack sufficient pre-research and development funds.

Under this situation, in addition to increasing investment in new special drugs, government departments have encouraged the restructuring of products based on innovative drugs to become an important goal of the "12th Five-Year Plan" for China's biomedical industry. An authoritative source involved in the compilation of the "12th Five-Year Plan" for pharmaceuticals told reporters that during the "12th Five-Year Plan" period, China's pharmaceutical product structure will be adjusted from the "basic drug-based" transition to "mainly based on generic drugs." Ultimately, the model of "based on innovative drugs" will be achieved.

According to the authoritative sources, during the 12th Five-Year Plan period, major new drug creation projects will strive to independently create 30 innovative drugs, complete the transformation and re-innovation of about 200 major drug varieties, and at the same time basically establish a world-class drug innovation system. Cultivate a batch of new drug incubation bases, production and research alliances, and high-tech parks, focusing on breaking through 20-30 key technologies for new drug R&D and industrialization.

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