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Conference Paper: A prospective randomized, open-label trial comparing the safety and efficacy of dose sparing intradermal 2010/2011 trivalent influenza vaccine delivered by two different devices

TitleA prospective randomized, open-label trial comparing the safety and efficacy of dose sparing intradermal 2010/2011 trivalent influenza vaccine delivered by two different devices
Authors
Issue Date2011
Citation
The 49th Annual Meeting of the Infectious Disease Society of America (IDSA 2011), Boston, MA., 20-23 October 2011. How to Cite?
AbstractBACKGROUND: We performed intradermal 2010/11 trivalent influenza vaccination (TIV) in adult subjects delivered by two different intradermal (ID) devices, using 20% and 60% of the standard dose and compared the immunogenicity and safety with full dose intramuscular (IM) immunization. METHODS: This is a prospective randomized trial conducted from December 2010 to March 2011, comprising chronically ill adults. Subjects were randomly assigned …
DescriptionPoster Abstract Session - Influenza Vaccines: no. 533
Persistent Identifierhttp://hdl.handle.net/10722/160319

 

DC FieldValueLanguage
dc.contributor.authorHung, IFNen_US
dc.contributor.authorLevin, Y-
dc.contributor.authorTo, KKW-
dc.contributor.authorChan, KH-
dc.contributor.authorLi, P-
dc.contributor.authorLi, C-
dc.contributor.authorTing, X-
dc.contributor.authorWong, TY-
dc.contributor.authorTong, T-
dc.contributor.authorYuen, KY-
dc.date.accessioned2012-08-16T06:07:59Z-
dc.date.available2012-08-16T06:07:59Z-
dc.date.issued2011en_US
dc.identifier.citationThe 49th Annual Meeting of the Infectious Disease Society of America (IDSA 2011), Boston, MA., 20-23 October 2011.en_US
dc.identifier.urihttp://hdl.handle.net/10722/160319-
dc.descriptionPoster Abstract Session - Influenza Vaccines: no. 533-
dc.description.abstractBACKGROUND: We performed intradermal 2010/11 trivalent influenza vaccination (TIV) in adult subjects delivered by two different intradermal (ID) devices, using 20% and 60% of the standard dose and compared the immunogenicity and safety with full dose intramuscular (IM) immunization. METHODS: This is a prospective randomized trial conducted from December 2010 to March 2011, comprising chronically ill adults. Subjects were randomly assigned …-
dc.languageengen_US
dc.relation.ispartofAnnual Meeting of the Infectious Disease Society of America, IDSA 2011en_US
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.titleA prospective randomized, open-label trial comparing the safety and efficacy of dose sparing intradermal 2010/2011 trivalent influenza vaccine delivered by two different devicesen_US
dc.typeConference_Paperen_US
dc.identifier.emailHung, IFN: ivanhung@hkucc.hku.hken_US
dc.identifier.emailTo, KKW: kelvinto@hkucc.hku.hk-
dc.identifier.emailChan, KH: chankh2@hkucc.hku.hk-
dc.identifier.emailLi, P: drckli@hku.hk-
dc.identifier.emailYuen, KY: kyyuen@hku.hk-
dc.identifier.authorityHung, IFN=rp00508en_US
dc.description.naturepostprint-
dc.identifier.hkuros203211en_US

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