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Clinical Trial Summary

Primary Objective: To study the effect of mild, moderate and severe renal impairment on the pharmacokinetics (PK) of Venglustat following a single dose. Secondary Objective: To assess the tolerability of Venglustat given as a single dose in subjects with mild, moderate and severe renal impairment in comparison with matched subjects with normal renal function.


Clinical Trial Description

Approximately 41 days, including a 21-day screening period, a 1-day treatment period, followed by a 9-day period of plasma sampling for assessment of primary endpoints. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03687554
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 1
Start date October 5, 2018
Completion date February 27, 2019

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