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NCT number NCT03424135
Study type Interventional
Source Bayer
Contact Bayer Clinical Trials Contact
Phone (+) 1-888-8422937
Email clinical-trials-contact@bayer.com
Status Not yet recruiting
Phase Phase 1
Start date February 25, 2018
Completion date August 5, 2018

Clinical Trial Summary

To evaluate the relative bioavailability of naproxen sodium/diphenhydramine hydrochloride (DHP HCL) 220/25 mg soft capsules (Test) versus naproxen sodium/DPH HCl 220/25 mg tablets (Reference) after a single oral administration (2 x naproxen sodium 220 mg and DPH HCl 25 mg combination product) under fed conditions in healthy adult subjects.

To assess the safety and tolerability of the investigational products in terms of adverse events (AEs) and clinical parameters (systolic/diastolic blood pressure, pulse rate, physical examination, clinical and laboratory testing).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


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