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Clinical Trial Summary

This study is a randomized, double-blind, placebo-controlled, dose-response study of BKR-017 and placebo that will be conducted at two investigative sites. The total duration of subject involvement is approximately 15 weeks; the screening period can be up to 3 weeks prior to the start of test period, followed by a 12-week test period. During the test period, subjects will self-administer three tablets of test product, two times daily: before breakfast and before bedtime.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04673656
Study type Interventional
Source BioKier Inc.
Contact
Status Completed
Phase N/A
Start date April 18, 2021
Completion date February 7, 2023

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