Bioequivalence Study of Lisinopril Tablets 40 mg Under Fasting Condition

Update Il y a 4 ans
Reference: NCT01735318

Woman and Man

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Extract

This is a randomized, balanced, open Label, two-treatment, two-period, two-sequence, single dose, crossover pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fasting condition in normal, healthy, adult, male and female human subjects.


Inclusion criteria

  • Fasting

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