首页> 外文OA文献 >Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years : 7-year follow-up of the phase 3, double-blind, randomised controlled VIVIANE study
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Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years : 7-year follow-up of the phase 3, double-blind, randomised controlled VIVIANE study

机译:25岁以上女性使用人乳头瘤病毒16/18 AS04辅助疫苗的功效,安全性和免疫原性:3期,双盲,随机对照VIVIANE研究的7年随访

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摘要

Acknowledgments The VIVIANE study was funded and coordinated by GlaxoSmithKline Biologicals SA, which also covered all costs associated with development and publication of this report. We thank all study participants and their families. We gratefully acknowledge the work of the central and local study coordinators, and staff members of the sites who participated in this study. Writing support services were provided by Mary Greenacre (An Sgriobhadair, Isle of Barra, UK), on behalf of GSK Vaccines; editing and publication coordination services were provided by Jérôme Leemans (Keyrus Biopharma, Lasne, Belgium), Stéphanie Delval (XPE Pharma and Science, Wavre, Belgium), and Matthieu Depuydt (Business Decision Life Sciences, Brussels, Belgium), on behalf of GSK Vaccines
机译:致谢VIVIANE研究由葛兰素史克(GlaxoSmithKline Biologicals SA)资助和协调,该研究还涵盖了与开发和发布本报告相关的所有费用。我们感谢所有的研究参与者及其家人。我们衷心感谢中央和地方研究协调员以及参与本研究的站点工作人员的工作。玛丽·格林纳克雷(Mary Greenacre)(英国,巴拉岛的安哥里达哥都航空)代表GSK疫苗提供了写作支持服务; JérômeLeemans(比利时Lasne的Keyrus Biopharma),StéphanieDelval(比利时Wavre的XPE Pharma and Science)和Matthieu Depuydt(比利时布鲁塞尔的商业决策生命科学)提供了编辑和出版协调服务。疫苗

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