About: Evaluation of a Single Vaccination of One of Three Ascending Dose Levels of a 4-Antigen Staphylococcus Aureus Vaccine (SA4Ag) and a Single Dose Level of a 3-Antigen Staphylococcus Aureus Vaccine (SA3Ag) in Healthy Adults Aged 65 to <86 Years

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About: Evaluation of a Single Vaccination of One of Three Ascending Dose Levels of a 4-Antigen Staphylococcus Aureus Vaccine (SA4Ag) and a Single Dose Level of a 3-Antigen Staphylococcus Aureus Vaccine (SA3Ag) in Healthy Adults Aged 65 to <86 Years Goto Sponge NotDistinct Permalink

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clinical trial

Attributes	Values
rdf:type	Item
description	clinical trial (en) ensayu clínicu (ast) klinisch onderzoek (nl) клінічне випробування (uk)
rdfs:label	Evaluation of a Single Vaccination of One of Three Ascending Dose Levels of a 4-Antigen Staphylococcus Aureus Vaccine (SA4Ag) and a Single Dose Level of a 3-Antigen Staphylococcus Aureus Vaccine (SA3Ag) in Healthy Adults Aged 65 to <86 Years (en)
skos:prefLabel	Evaluation of a Single Vaccination of One of Three Ascending Dose Levels of a 4-Antigen Staphylococcus Aureus Vaccine (SA4Ag) and a Single Dose Level of a 3-Antigen Staphylococcus Aureus Vaccine (SA3Ag) in Healthy Adults Aged 65 to <86 Years (en)
name	Evaluation of a Single Vaccination of One of Three Ascending Dose Levels of a 4-Antigen Staphylococcus Aureus Vaccine (SA4Ag) and a Single Dose Level of a 3-Antigen Staphylococcus Aureus Vaccine (SA3Ag) in Healthy Adults Aged 65 to <86 Years (en)
title	wds:Q63841139-8C1BF444-402A-4255-9073-36FB10FBF88B
title	A Phase 1/2 Placebo-controlled, Randomized, Double-blind Trial To Evaluate The Safety, Tolerability, And Immunogenicity Of 3 Ascending Dose Levels Of A 4-antigen Staphylococcus Aureus Vaccine (sa4ag) And A Single Dose Level Of A 3-antigen Staphylococcus Aureus Vaccine (sa3ag) In Healthy Adults Aged 65 To <86 Years (en)
end time	wds:Q63841139-7250C634-9B7B-4A1C-8A03-862E611E753B
end time	2013-05-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q63841139-D7FB4E51-9C99-4ACD-ABA9-9AA9C723E9E4
instance of	clinical trial
start time	wds:Q63841139-580B91D4-07B2-4D41-B36A-D200E05A6607
start time	2012-08-01 00:00:00Z (xsd:dateTime)
research site	wds:Q63841139-33DD7F19-9AA6-4183-8F85-78EF2F99FB6A wds:Q63841139-69089107-4BCC-486D-8A0E-2485C4556D88 wds:Q63841139-8BBA77B8-9457-41F5-ABAA-074A2179EA23
research site	Vanderbilt University Medical Center PMG Research Benchmark Research (United States)
minimum age	wds:Q63841139-864D01A9-AB1A-40F3-B5BB-DC4F2978BF8E
minimum age	65 (xsd:decimal)
number of participants	wds:Q63841139-20F0BD14-8739-4535-8ECB-D3A2B8A99729
number of participants	284 (xsd:decimal)
maximum age	wds:Q63841139-A6287DC9-C899-425A-8C3A-6915803106F2
maximum age	85 (xsd:decimal)
study type	wds:Q63841139-6CC94F53-27F5-43BD-AE77-800EED72DB34
study type	interventional study
ClinicalTrials.gov ID	wds:Q63841139-4712753F-8A47-48B0-ABAB-A85B493E97C2
ClinicalTrials.gov ID	NCT01643941
clinical trial phase	wds:Q63841139-D979E4F2-04A2-4935-B2B8-918A5449FAA2
clinical trial phase	phase I clinical trial
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q63841139

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