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Trials / Completed

CompletedNCT01358383

Assessment of Pharmacokinetics of a Single Oral Dose of VIMOVO in Healthy Adult Volunteers

A Phase I, Open-label, Single-center Study to Assess the Pharmacokinetics of a Single Oral Dose of VIMOVO (250 mg Naproxen/20 mg Esomeprazole)in Healthy Adult Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
28 (actual)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is an assessment of Pharmacokinetics of a single oral dose of VIMOVO in healthy adult volunteers.

Detailed description

A Phase I, Open-label, Single-center Study to Assess the Pharmacokinetics of a Single Oral Dose of VIMOVO (250 mg Naproxen/20 mg Esomeprazole)in Healthy Adult Subjects

Conditions

Interventions

TypeNameDescription
DRUGnaproxen250mg, oral dose
DRUGesomeprazole20mg, oral dose

Timeline

Start date
2011-05-01
Primary completion
2011-06-01
Completion
2011-06-01
First posted
2011-05-23
Last updated
2012-06-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01358383. Inclusion in this directory is not an endorsement.

Assessment of Pharmacokinetics of a Single Oral Dose of VIMOVO in Healthy Adult Volunteers (NCT01358383) · Clinical Trials Directory