drugset / Trial / NCT00828932

Pharmacokinetic Properties of Lorcaserin in Subjects With Hepatic Impairment

NCT00828932

Phase 1 Completed 24 enrolled Eisai Inc.
NaSingle-groupOpen-labelOther

Summary

The purpose of this study is to evaluate and establish whether lorcaserin dose adjustment is required in patients with mild or moderate hepatic impairment.

Timeline

Start
2008-08
Primary completion
2008-12
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Lorcaserin Small molecule 10 mg

Indications

No indication recorded.