About: Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination     Goto   Sponge   NotDistinct   Permalink

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clinical trial

AttributesValues
rdf:type
description
  • clinical trial (en)
  • ensayu clínicu (ast)
  • klinisch onderzoek (nl)
  • клінічне випробування (uk)
  • կլինիկական փորձարկում (hy)
rdfs:label
  • Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination (en)
  • Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination (nl)
skos:prefLabel
  • Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination (en)
  • Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination (nl)
name
  • Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination (en)
  • Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination (nl)
title
title
  • A Phase 1, Single and Multiple-Dose, Open-Label Study in Healthy Subjects to Assess the Effect of the Acid Reducing Agents, Omeprazole (OME) and Famotidine (FAM), on the Pharmacokinetics (PK) of Cenicriviroc Mesylate (CVC) (en)
end time
end time
instance of
instance of
start time
start time
country
country
research site
research site
research intervention
research intervention
minimum age
minimum age
number of participants
number of participants
maximum age
maximum age
study type
study type
ClinicalTrials.gov ID
ClinicalTrials.gov ID
  • NCT02684799
clinical trial phase
clinical trial phase
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