drugset / Trial / NCT02064907

Bioavailability, Safety, and Pharmacodynamics of Dexlansoprazole Delayed-Release Orally Disintegrating Tablets in Healthy Participants

NCT02064907

Phase 1 Completed 52 enrolled Takeda
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to assess the pharmacokinetics (PK) and Pharmacodynamics (PD) of dexlansoprazole delayed-release orally disintegrating (OD) tablets administered on the tongue and swallowed without water.

Timeline

Start
2014-02
Primary completion
2014-03
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexlansoprazole Other / unclassified 60 mg Oral

Indications

No indication recorded.