Pharmacokinetics of Lanraplenib in Adults With Impaired Renal Function

Status Completed

Clinical Trial Summary

The primary objective of this study is to evaluate the pharmacokinetics (PK) of lanraplenib in participants with impaired renal function relative to matched healthy controls. Participants in this study will be enrolled using an adaptive design that includes up to 3 enrolled cohorts. Based on safety and/or PK data in Cohort 1, participants will be enrolled in adaptive Cohorts 2 and/or 3.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02959138
Study type	Interventional
Source	Gilead Sciences
Contact
Status	Completed
Phase	Phase 1
Start date	November 21, 2016
Completion date	October 5, 2018

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