About: Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants

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clinical trial

Attributes	Values
rdf:type	Item
description	clinical trial (en) ensayo clínico (es) ensayu clínicu (ast) klinisch onderzoek (nl) клінічне випробування (uk)
rdfs:label	Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (en) Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (nl)
skos:prefLabel	Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (en) Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (nl)
name	Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (en) Study of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (nl)
title	wds:Q95056252-761D206D-9151-40AA-9DCC-6C484E612539
title	Safety and Immunogenicity of a Pneumococcal Conjugate Vaccine When Administered Concomitantly With Routine Pediatric Vaccines in Healthy Toddlers and Infants (en)
end time	wds:Q95056252-F7C9EDB7-8B01-469F-86D3-6D73D66693CA
end time	2022-06-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q95056252-A8873D43-5DD4-410E-90CC-5206A1FE4906
instance of	clinical trial
start time	wds:Q95056252-7C1FAE69-E11E-4C5B-B0E4-8B743ED30E4A
start time	2020-05-18 00:00:00Z (xsd:dateTime)
country	wds:Q95056252-549A8AA2-22EF-48E7-804D-4F1A05BD2928
country	United States of America
research intervention	wds:Q95056252-6EEDAE14-2714-4E1B-99DE-B5BE2B89551A
research intervention	heptavalent pneumococcal conjugate vaccine
medical condition	wds:Q95056252-81B975BB-5A16-4673-9C86-79C265C4F2B0 wds:Q95056252-93BA03F8-520F-4040-A6F6-24228157CC60 wds:Q95056252-E882DDC5-5F78-451C-8FDC-CE9B064878D1
sponsor	wds:Q95056252-4A8C3794-4320-4E89-A507-1554796B1B18
medical condition	diphtheria rubella hepatitis B
sponsor	Sanofi
number of participants	wds:Q95056252-745D16B4-469F-409E-B08E-45F1E558C8C1
number of participants	840 (xsd:decimal)
maximum age	wds:Q95056252-C33C2F6A-996A-49B1-9FE3-C67DDA9D3FB0
maximum age	15 (xsd:decimal)
study type	wds:Q95056252-DC098B1F-E9F4-4579-A384-1975F55E2015
study type	interventional study
ClinicalTrials.gov ID	wds:Q95056252-E227952F-7CE4-4C28-8757-D0C75A09E3F3
ClinicalTrials.gov ID	NCT04398706
clinical trial phase	wds:Q95056252-45C42AC1-4DA0-4485-AD21-DCCDC34306DD
clinical trial phase	phase II clinical trial
research subject recruitment status	wds:Q95056252-FDB97BCF-ACBB-43FF-9F33-209CCC6CC49A
research subject recruitment status	recruiting
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q95056252

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