drugset / Trial / NCT00835211

Desmopressin Acetate 0.2 mg Tablets, Fasting

NCT00835211

Phase 1 Completed 48 enrolled Teva Pharmaceuticals USA
RandomizedCrossoverOpen-label

Summary

The objective of this study was to compare the single-dose relative bioavailability of TEVA and Aventis Pharmaceuticals (DDAVP®) 0.2 mg desmopressin acetate tablets following a 0.8 mg dose under fasting conditions.

Timeline

Start
2003-07
Primary completion
2003-08
Completion
2003-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Desmopressin Peptide 0.8 mg

Indications

No indication recorded.