drugset / Trial / NCT00840866

Cefprozil 500 mg Tablets Under Fed Conditions

NCT00840866 ↗

Phase 1 Completed 39 enrolled Teva Pharmaceuticals USA
RandomizedCrossoverOpen-labelOther

Summary

The objective of this study is to compare the relative bioavailability of cefprozil 500 mg tablets with that of Cefzil 500 mg tablets in healthy, non-smoking adults under non-fasting conditions.

Timeline

Start
2003-09
Primary completion
2003-09
Completion
2003-09

Outcome

Met primary endpoint

registry Ratio of the T/R geometric mean x 100 104 (90% CI 99 to 109) NCT00840866 ↗

registry Ratio of the T/R geometric mean x 100 99.9 (90% CI 98.6 to 101) NCT00840866 ↗

registry Ratio of the T/R geometric mean x 100 99.8 (90% CI 98.5 to 101) NCT00840866 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject CEFPROZIL ANHYDROUS, (E)- Small molecule 500 mg —

Indications

No indication recorded.