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10.3760/cma.j.cn112150-20200803-01084 http://scihub22266oqcxt.onion/10.3760/cma.j.cn112150-20200803-01084 32907278!ä!32907278 Warning: Undefined variable $yww in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 538 Warning: Undefined variable $yww in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 538       Zhonghua+Yu+Fang+Yi+Xue+Za+Zhi 2020 ; 54 (9): 915-917 Nephropedia Template TP {{tp|p=32907278|t=2020. Conduct vaccines clinical trials and optimize the immunization strategies |pdf=|usr=}}{{32907278}} gab.com Text Conduct vaccines clinical trials and optimize the immunization strategies JO: Zhonghua Yu Fang Yi Xue Za Zhi http://www.kidney.de/pget.php?&tw=1&pmid=32907278 #FOAvip Development of an effective vaccine requires a long and complicated process. Preclinical studies and phase ?, ?, ? clinical trials mainly focused on the assessment of the vaccine's safety (tolerability), immunogenicity and efficacy before license. After license, it is necessary to further evaluate the actual effectiveness and safety in the general population through phase ? clinical trials and optimize the immunization strategies with the disease's epidemiology data. In this special issue, published several articles, which reported the main results of pre-license clinical trials and post-marketing evaluation of various vaccines, it was extremely useful to support vaccine licensing and market use. We encourage the continuous clinical studies and post-marketing evaluation of vaccines, including the novel corona virus-19 vaccines, to provide technical support for the population use, under the situation of COVID-19 pandemic. Twit Text FOAVip Conduct vaccines clinical trials and optimize the immunization strategies ????Zhonghua Yu Fang Yi Xue Za Zhi http://www.kidney.de/pget.php?&tw=1&pmid=32907278 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32907278 #FOAvip English Wikipedia <ref>{{Cite pmid|32907278}}</ref> Conduct vaccines clinical trials and optimize the immunization strategies #MMPMID32907278 Yin ZD Zhonghua Yu Fang Yi Xue Za Zhi 2020[Sep]; 54 (9): 915-917 PMID32907278show ga Development of an effective vaccine requires a long and complicated process. Preclinical studies and phase ?, ?, ? clinical trials mainly focused on the assessment of the vaccine's safety (tolerability), immunogenicity and efficacy before license. After license, it is necessary to further evaluate the actual effectiveness and safety in the general population through phase ? clinical trials and optimize the immunization strategies with the disease's epidemiology data. In this special issue, published several articles, which reported the main results of pre-license clinical trials and post-marketing evaluation of various vaccines, it was extremely useful to support vaccine licensing and market use. We encourage the continuous clinical studies and post-marketing evaluation of vaccines, including the novel corona virus-19 vaccines, to provide technical support for the population use, under the situation of COVID-19 pandemic. |*Vaccines[MESH] |COVID-19[MESH] |COVID-19 Vaccines[MESH] |Clinical Trials as Topic/*organization & administration[MESH] |Coronavirus Infections/epidemiology/prevention & control[MESH] |Humans[MESH] |Immunization/*methods[MESH] |Pandemics/prevention & control[MESH] |Pneumonia, Viral/epidemiology/prevention & control[MESH] Conduct vaccines clinical trials and optimize the immunization strate(epmc).pdf DeepDyve Pubget Overpricing