Overview

Study to Evaluate the Effect of Hepatic Impairment on the Pharmacokinetics and Safety of Lorlatinib

Status:
Not yet recruiting
Trial end date:
2023-01-03
Target enrollment:
Participant gender:
Summary
This is a post approval requirement to study the effect of moderate and severe hepatic impairment on the pharmacokinetics of lorlatinib.
Phase:
Phase 1
Details
Lead Sponsor:
Pfizer