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CompletedNCT00913887

To Demonstrate the Relative Bioavailability of Diclofenac Sodium 75 mg Enteric-Coated Tablets Under Non-Fasting Conditions

A Relative Bioavailability Study of Diclofenac Sodium 75 mg Enteric-Coated Tablets Under Non-Fasting Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Sandoz · Industry
Sex
Male
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

To demonstrate the relative bioavailability of Diclofenac Sodium 75 mg enteric-coated tablets under non-fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGDiclofenac Sodium 75 mg Tablets Under Fasting Conditions (Geneva Pharmaceutical)
DRUGDiclofenac Sodium 75 mg Tablets Under Fed Conditions (Geneva Pharmaceutical)
DRUGVoltaren 75 mg Tablets Under Fed Conditions (Geigy Pharmaceuticals)

Timeline

Start date
1994-04-01
Primary completion
1994-05-01
Completion
1994-05-01
First posted
2009-06-04
Last updated
2017-03-28

Source: ClinicalTrials.gov record NCT00913887. Inclusion in this directory is not an endorsement.

To Demonstrate the Relative Bioavailability of Diclofenac Sodium 75 mg Enteric-Coated Tablets Under Non-Fasting Conditio (NCT00913887) · Clinical Trials Directory