Welcome to our dedicated page for Sinovac Biotech news (Ticker: SVA), a resource for investors and traders seeking the latest updates and insights on Sinovac Biotech stock.
Sinovac Biotech, Ltd (symbol: SVA) is a leading China-based biopharmaceutical company dedicated to the research, development, manufacturing, and commercialization of vaccines aimed at protecting against human infectious diseases. Established with a strong commitment to public health, Sinovac's portfolio includes vaccines for hepatitis A and B, seasonal influenza, H5N1 avian influenza, H1N1 swine flu, and mumps. Additionally, the company produces an animal rabies vaccine for canines.
In 2009, Sinovac achieved a significant milestone by becoming the first company worldwide to receive approval for its H1N1 influenza vaccine, Panflu.1. This vaccine was manufactured for the Chinese central government under a government stockpiling program. Sinovac continues to be a key supplier for the government's H5N1 pandemic influenza vaccine stockpiling program.
Sinovac is also at the forefront of developing new vaccines, including those targeting enterovirus 71 (EV71) for hand, foot, and mouth disease (currently in Phase III clinical trials), pneumococcal conjugate, pneumococcal polysaccharides, and rubella. The company's extensive R&D efforts ensure a robust pipeline of vaccines designed to address emerging infectious diseases and public health threats.
Sinovac's products are essential for public health, contributing significantly to disease prevention and control. The company's commitment to innovation and quality has made it a trusted name in the biopharmaceutical industry, not just in China but globally.
Sinovac Biotech Ltd. (SVA) announced an amendment to its shareholder rights plan, extending its expiration from February 22, 2023, to February 22, 2024. The company, based in China, specializes in developing and manufacturing vaccines for infectious diseases, including COVID-19, hepatitis A, and enterovirus 71. Notably, Sinovac's COVID-19 vaccine, CoronaVac®, is approved in over 60 countries. The firm is committed to ongoing research and exploration of global market opportunities to enhance its product offerings.
Sinovac Biotech Ltd. (NASDAQ: SVA) reported its unaudited financial results for the first half of 2022, showing a significant decline in sales to $1.2 billion from $11.0 billion the previous year. Net income attributable to common shareholders was $481.6 million ($4.84 per share), down from $5.1 billion ($51.42 per share) in the same period last year. Despite the decline, Sinovac's non-COVID vaccine sales grew by 37%. The company is heavily investing in R&D for various COVID-19 vaccines and has gained multiple WHO approvals for its products, expanding its global market reach.
Sinovac Biotech Ltd. (NASDAQ: SVA) announced its live attenuated varicella vaccine received prequalification from the World Health Organization (WHO) on
Sinovac Biotech Ltd. (NASDAQ: SVA) announced its participation in CPHI Frankfurt from November 1-3, showcasing its extensive vaccine portfolio. The company will display its inactivated COVID-19 vaccine, CoronaVac®, among other products like the quadrivalent influenza vaccine and WHO prequalified vaccines. Chief Business Officer Helen Yang emphasized the significance of CPHI as a platform for business opportunities and new technologies. Sinovac aims to strengthen global partnerships and increase its market presence.
Sinovac Biotech Ltd. (NASDAQ: SVA) announced approval from the Chilean Public Health Institute for a phase II clinical trial of its inactivated Omicron strain COVID-19 vaccine and a trivalent COVID-19 vaccine. The trial aims to assess the immunogenicity and safety of booster doses in 826 vaccinated adults. This study marks the world's first investigation of a multivalent inactivated COVID-19 vaccine. Sinovac continues to progress in vaccine development and plans further collaboration with global partners.
Sinovac Biotech Ltd. (NASDAQ: SVA) has received approval from the Hong Kong Health Bureau for its COVID-19 vaccine, CoronaVac, for children aged 6 months to 3 years. This vaccine will adhere to a three-dose schedule, with no restrictions for immunosuppressed children. The vaccine has previously been authorized for minors and adults aged over 3 years since February 15, 2022, and is approved in 14 countries across Latin America, Asia, and Africa. The phase III clinical studies indicate a good safety profile and immunogenicity for the target age group.
Sinovac Biotech Ltd. (NASDAQ: SVA) announced the initiation of a phase III clinical trial for its inactivated quadrivalent influenza vaccine in Chile, collaborating with Pontificia Universidad Católica de Chile. The trial will recruit 1,600 volunteers to evaluate the vaccine's immunogenicity and safety. Participants aged 3 and above will receive either Sinovac's vaccine or a commercially available alternative. Observations will last 28 days post-inoculation. This trial aims to enhance the understanding of Sinovac's vaccine efficacy and safety.
Sinovac Biotech Ltd. (NASDAQ: SVA) announced that its COVID-19 vaccine, CoronaVac, received emergency use approval for children aged 3 to 5 from Brazil's Health Regulatory Agency (Anvisa) on July 13. The same dosage for minors 6 to 17 and adults will be used, with no restrictions for immunosuppressed children. This decision followed extensive evaluations involving data from multiple sources, including the Butantan Institute and real-life evidence from Chile. As of July 14, 2022, CoronaVac is approved for emergency use in minors across 14 countries.
Sinovac Biotech Ltd. (NASDAQ: SVA) announced that South Africa's Health Products Regulatory Authority granted conditional registration for its CoronaVac® vaccine for adults aged 18 and above, confirming its safety and efficacy. Previously given emergency use authorization on July 3, 2021, Sinovac has maintained compliance with safety monitoring and reporting obligations. The vaccine is now administered in two doses and has been supplied to over 60 countries, totaling nearly 2.9 billion doses.
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