drugset / Trial / NCT03801148

A Study to Compare the Bioavailability (BA) of Dexlansoprazole Delayed-release Capsules

NCT03801148

Phase 1 Completed 122 enrolled Takeda
RandomizedCrossoverOpen-labelOther

Summary

The purpose of this study is to assess the BA of 30 or 60 milligram (mg) dexlansoprazole capsule manufactured at TOB (Takeda GmbH Plant Oranienburg) to the corresponding 30 or 60 mg dexlansoprazole manufactured at TPC (Takeda Pharmaceutical Company Ltd.).

Timeline

Start
2019-01-10
Primary completion
2019-02-25
Completion
2019-04-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexlansoprazole Other / unclassified 30 mg Oral
Subject Dexlansoprazole Other / unclassified 60 mg Oral

Indications

No indication recorded.