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Clinical Trials associated with Tetanus Vaccine,Adsorbed (Sinovac Life Sciences)评价吸附破伤风疫苗用于18~44岁成人安全性和免疫原性的随机、双盲、阳性对照Ⅰ期临床试验和Ⅲ期临床试验
[Translation] A randomized, double-blind, positive-controlled phase I and phase III clinical trial to evaluate the safety and immunogenicity of adsorbed tetanus vaccine in adults aged 18 to 44 years
I期:评价试验疫苗应用于18~44岁成人的安全性,为后续Ⅲ期临床试验的开展提供安全性证据
III期:评价试验疫苗应用于18~44岁成人的免疫原性,以验证试验疫苗非劣效于阳性对照疫苗。
[Translation] Phase I: Evaluate the safety of the trial vaccine in adults aged 18 to 44, and provide safety evidence for the subsequent Phase III clinical trial
Phase III: Evaluate the immunogenicity of the trial vaccine in adults aged 18 to 44, to verify that the trial vaccine is non-inferior to the positive control vaccine.
Randomized, Double-blind, Controlled Phase Ⅰ and Phase Ⅲ Clinical Trial to Evaluate the Safety and Immunogenicity of Tetanus Vaccine, Adsorbed in 18~44 Years Old Population
This is a randomized, double-blind, positive controlled design clinical trial of tetanus vaccine, adsorbed manufactured by Sinovac Life Sciences Co., Ltd.The purpose of this study is to evaluate the safety and immunogenicity of tetanus vaccine, adsorbed in 18
44 years old population.
100 Clinical Results associated with Tetanus Vaccine,Adsorbed (Sinovac Life Sciences)
100 Translational Medicine associated with Tetanus Vaccine,Adsorbed (Sinovac Life Sciences)
100 Patents (Medical) associated with Tetanus Vaccine,Adsorbed (Sinovac Life Sciences)
100 Deals associated with Tetanus Vaccine,Adsorbed (Sinovac Life Sciences)