Sinovac Obtains Initial Order of H1N1 Vaccine from Chinese Central Government
Sinovac initiated the production of H1N1 vaccine on June 15, 2009 andinitiated the clinical trial on July 22. On August 17, Sinovac announced itstop-line positive results of H1N1 vaccine clinical trials, in which thevaccine showed good safety and immunogenicity profiles after one shot.Following the positive results of an experts' evaluation conference organizedby the State Food and Drug Administration (SFDA), on September 3, 2009,Sinovac obtained the production license from the SFDA for PANFLU.1, Sinovac'sH1N1 vaccine.
Mr. Weidong Yin, Chairman, President and CEO of Sinovac, commented,"Sinovac has been aiming to provide Chinese children with international-quality vaccines and provide children throughout the world with vaccines madein China, and to fulfill our mission of supplying vaccines to eliminate humandiseases. Sinovac is very glad to be supplying our H1N1 vaccine to the Chinesegovernment and we are confident that we can complete the national H1N1 vaccinestockpiling task in a timely manner."
Sinovac Biotech Ltd. is a China-based biopharmaceutical company thatfocuses on the research, development, manufacture and commercialization ofvaccines that protect against human infectious diseases. Sinovac's vaccineproducts include Healive(R) (hepatitis A), Bilive(R) (combined hepatitis A andB), and Anflu(R) (influenza). Panflu(TM), Sinovac's pandemic influenza vaccine(H5N1), has already been approved for government stockpiling. Sinovac isdeveloping vaccines for enterovirus 71, universal pandemic influenza, Japaneseencephalitis, and human rabies. Its wholly owned subsidiary, Tangshan Yian, isconducting field trials for independently developed inactivated animal rabiesvaccines.
Safe Harbor Statement
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SOURCE Sinovac Biotech Ltd.
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