Pharmacokinetics of Lu AF35700 in Subjects With Renal Impairment

Status Terminated

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

Clinical Trial Details

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

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