5
项与 13价肺炎球菌多糖结合疫苗(北京科兴中维生物技术) 相关的临床试验 / Active, not recruiting临床1期 评价13价肺炎球菌多糖结合疫苗在2月龄(最小6周龄)健康婴儿和2 ~5岁(6岁生日前)健康幼儿中的安全性和免疫原性的随机、双盲、阳性对照Ⅰb期临床试验
主要目的:评价各年龄组受试者接种试验疫苗后的安全性。
次要目的:(1)评价各年龄组受试者接种试验疫苗后的安全性;(2)评价2月龄(最小6周龄)受试者接种试验疫苗基础免疫后30天针对所有血清型诱导的免疫反应;(3)评价2月龄(最小6周龄)受试者接种试验疫苗加强免疫后30天针对所有血清型诱导的免疫反应;(4)评价2~5岁(6岁生日前)受试者接种试验疫苗后30天针对所有血清型诱导的免疫反应。
A Randomized, Double Blinded, Positive Controlled Phase Ⅰb Clinical Trial in Participants Aged 2 Months (42-89 Days) and 2 to 5 Years to Evaluate the Safety and Immunogenicity of 13-valent Pneumococcal Polysaccharide Conjugate Vaccine
A phase 1b clinical trial of 13-valent Pneumococcal Polysaccharide Conjugate Vaccine (PCV13) developed by Sinovac Life Science Co., Ltd will be conducted in children aged 2 months (42-89 days) and 2 to 5 years. The objective of the study is to evaluate the safety and immunogenicity of Sinovac PCV13. The trial is a randomized, double blinded, positive controlled study.
An Open-label Combined Randomized Double-blind, Positive Control Clinical Trial in Subjects Aged 2 Months (Minimum 6 Weeks) and Above to Preliminary Evaluate the Safety and Immunogenicity of a 13-valent Pneumococcal Polysaccharide Conjugate Vaccine
This study is an open-label combined randomized double-blind, positive control phase Ⅰ clinical trial of the a 13-valent Pneumococcal Polysaccharide Conjugate Vaccine manufactured by Sinovac Research & Development Co., Ltd. The purpose of this study is to preliminary evaluate the safety and immunogenicity of the study vaccine
100 项与 13价肺炎球菌多糖结合疫苗(北京科兴中维生物技术) 相关的临床结果
100 项与 13价肺炎球菌多糖结合疫苗(北京科兴中维生物技术) 相关的转化医学
100 项与 13价肺炎球菌多糖结合疫苗(北京科兴中维生物技术) 相关的专利(医药)
100 项与 13价肺炎球菌多糖结合疫苗(北京科兴中维生物技术) 相关的药物交易