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非在研适应症- |
最高研发阶段批准上市 |
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首次获批日期2021-07-12 |
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非在研适应症- |
最高研发阶段批准上市 |
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首次获批日期2021-02-05 |
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非在研适应症- |
最高研发阶段申请上市 |
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A Randomized, Double-blind, Positive Controlled Phase Ib Clinical Trial to Evaluate the Safety and Immunogenicity of 24-valent Pneumococcal Conjugate Vaccine in Children Aged 2 (Minimum 42 Days)-23 Months
A Phase 1b clinical trial of 24-valent pneumococcal conjugate vaccine (PCV24) developed by Sinovac Life Science Co., Ltd will be conducted in pediatric population aged 2 months (minimum 42 days)-23 months.
The objective of the study is to evaluate the safety and immunogenicity of Sinovac PCV24. The trial is a randomized, double-blind, positive controlled phase Ib clinical trial.
A Phase Ⅲ Clinical Study to Evaluate the Safety and Immunogenicity of 13-Valent Pneumococcal Conjugate Vaccine (PCV13) in Healthy Infants
A Phase Ⅲ clinical trial of 13-valent pneumococcal conjugate vaccine (PCV13) developed by Sinovac Life Science Co., Ltd will be conducted in pediatric population aged 2 months (minimum 6 weeks)-5 years (before 6th birthday). The objective of the study is to evaluate the immunogenicity and safety of Sinovac PCV13.
评价b型流感嗜血杆菌结合疫苗在1~49岁健康人群中的安全性和免疫原性的开放性结合随机、盲法、阳性对照Ⅰa期临床试验
主要目的:评价Hib结合疫苗在1至49周岁人群中的安全性;
次要目的:1.评价Hib结合疫苗在1至49周岁人群中的安全性;2.评价Hib结合疫苗在1至5周岁人群中的免疫原性;
100 项与 北京科兴中维生物技术有限公司 相关的临床结果
0 项与 北京科兴中维生物技术有限公司 相关的专利(医药)
100 项与 北京科兴中维生物技术有限公司 相关的药物交易
100 项与 北京科兴中维生物技术有限公司 相关的转化医学