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Clinical Trial Summary

Randomized, open label, single dose, 2-way crossover study to investigate the bioequivalence of a new fixed dose combination (FDC) tablet of nifedipine GITS and candesartan with the corresponding loose combination under fed conditions.


Clinical Trial Description

Clinical pharmacology ;


Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT01350609
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 1
Start date April 2011
Completion date September 2011

See also
  Status Clinical Trial Phase
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