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  • A Phase I, Open-label, Randomised, 3-way Crossover Study to Demonstrate Bioequivalence of a Single Oral Dose of Naproxen Administered as VIMOVO Manufactured at AstraZeneca AB Compared to that of VIMOVO Manufactured by Patheon Pharmaceuticals and a Marketed Enteric-coated Naproxen Formulation (Manufactured by Roche) in Healthy Volunteers

Disease
rheumatoid arthritis
Drug Name
Vimovo
Generic Name
naproxen/esomeprazole magnesium
Sponsor
AstraZeneca
Drug Status
Approved Medicine
Phase
I
Start Date
Mar 14, 2011
Study Name
D1120C00030
Study Id
D1120C00030
ClinicalTrials.gov ID
NCT01331993
Recruiting Status
Open
Protocol Status
Not Available
Report
Jan 23, 2012
  • D1120C00030.pdf (173 KB)

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