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Clinical Trial Summary

This is an open-labeled (laboratory blinded), randomized, two period, single-center, crossover, comparative study, where each participant will be randomly assigned to the reference (Zestril®, 20 mg) or the test (Lisinopril, 20 mg) formulation in each period of study (sequences Test-Reference (TR) or Reference-Test (RT)), in order to evaluate if both formulations are bioequivalent


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05061901
Study type Interventional
Source Pharmtechnology LLC
Contact Veronika Kumpel
Phone 80173094418
Email [email protected]
Status Not yet recruiting
Phase Phase 1
Start date October 6, 2021
Completion date November 6, 2021

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