drugset / Trial / NCT01278797

Telmisartan and Amlodipine Versus Monocomponent Tablets

NCT01278797

Phase 1 Completed 28 enrolled Boehringer Ingelheim
RandomizedCrossoverSingle-blindBasic science

Summary

This study will be an open-label, randomized, two-treatment, two-period, two-sequence crossover study to evaluate the bioequivalence of the amlodipine component of Boehringer Ingelheim Pharma GmbH \& Co. KGs 80 mg telmisartan/10 mg amlodipine fixed dose combination tablet to the corresponding mono-component amlodipine tablets, 10 mg (Pfizers Norvasc).

Timeline

Start
2011-01
Primary completion
2011-02
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Amlodipine Other / unclassified 10 mg
Comparator Telmisartan Other / unclassified 80 mg

Indications