About: Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients

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About: Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients 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	Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients (en) Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients (nl)
skos:prefLabel	Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients (en) Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients (nl)
name	Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients (en) Zidovudine / Lamivudine + Nevirapine Twice Daily, Versus Tenofovir + Lamivudine + Nevirapine Once Daily in ARV-Naive Patients (nl)
title	wds:Q65545410-7C95E750-B3ED-457A-87A9-3188B29F1C99
title	Multicenter, Randomized, Open-Label Trial, Assessing the Efficacy of Zidovudine, Lamivudine and Nevirapine Combination Administered Twice Daily, Versus the Association of Tenofovir, Lamivudine and Nevirapine, Once Daily, in Antiretroviral Naive HIV-1 Infected Patients (en)
instance of	wds:Q65545410-E23F8823-809A-4910-8ED7-01F862B05934
instance of	clinical trial
start time	wds:Q65545410-25EE7DAD-8737-4E88-B4C6-6C3B4EAD1203
start time	2005-04-01 00:00:00Z (xsd:dateTime)
country	wds:Q65545410-D76366C6-1147-48E6-A884-1CD1740BF369
country	France
research intervention	wds:Q65545410-744B9203-0148-4BCE-928B-B9A73BB3A3AA wds:Q65545410-D428508F-0ADB-4B74-83D9-249262B7548C
research intervention	wd:Q198504 wd:Q263713
minimum age	wds:Q65545410-69E8DCC3-4AD0-4266-A74B-3E7E1E38D4D0
minimum age	18 (xsd:decimal)
sponsor	wds:Q65545410-6CB38258-DC9B-4A2B-B031-2700BFB6A6F3
sponsor	Medex
number of participants	wds:Q65545410-8B82E5B6-B69A-45F3-A0EE-2632C75192FE
number of participants	250 (xsd:decimal)
study type	wds:Q65545410-A7188D4D-1B95-41BB-A71B-FC1D28393D51
study type	interventional study
ClinicalTrials.gov ID	wds:Q65545410-D4E869A5-350F-4EAE-B3EF-9EFAF01842C2
ClinicalTrials.gov ID	NCT00199979
clinical trial phase	wds:Q65545410-65293011-7BB5-4710-A621-8AFF9FEC25B6
clinical trial phase	phase III clinical trial
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q65545410

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