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Clinical Trial Summary

This study will evaluate the pharmacokinetics of Lu AF35700 after a single dose tablet to subjects with renal impairment (kidney insufficiency) and compare that with healthy subjects


Clinical Trial Description

If the initial data shows a substantial effect in subjects with severe renal impairment, the study will be expanded to include subjects with intermediate level (mild and moderate) of renal impairment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03241147
Study type Interventional
Source H. Lundbeck A/S
Contact
Status Terminated
Phase Phase 1
Start date July 25, 2017
Completion date July 24, 2019

See also
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