A prospective, randomised, partially-blinded, placebo-controlled, phase III, multicentre trial to assess safety, tolerability and imunogenicity of liquid influenza virus vaccine, trivalent, types A & B, live cold-adapted (liquid CAIV-T) administered concomitantly with live, attenuated, poliovirus vaccine in healthy children

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dc.contributor.authorBreiman, Robert F.-
dc.contributor.authorBrooks, Abdullah-
dc.contributor.authorNaheed, Aliya-
dc.date.accessioned2014-02-19T09:00:17Z-
dc.date.available2014-02-19T09:00:17Z-
dc.date.issued2001-
dc.identifier.urihttp://hdl.handle.net/123456789/4924-
dc.format.extent1996675 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoenen
dc.relation.ispartofseriesICDDRB Research Protocolen
dc.relation.ispartofseriesno. 2001-011en
dc.subjectClinical Protocolsen
dc.subjectVaccinationen
dc.subjectChilden
dc.subjectProspective Studiesen
dc.titleA prospective, randomised, partially-blinded, placebo-controlled, phase III, multicentre trial to assess safety, tolerability and imunogenicity of liquid influenza virus vaccine, trivalent, types A & B, live cold-adapted (liquid CAIV-T) administered concomitantly with live, attenuated, poliovirus vaccine in healthy childrenen
dc.typeOtheren
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