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