A study to Compare the Pharmacokinetics of PF-06882961 in Adult Participants With Varying
Degrees of Hepatic Impairment. A Phase 1, Non-Randomized, Open-Label, Single- Dose, Parallel Cohort Study to Compare the Pharmacokinetics of PF-06882961 in Adult Participants With Varying Degrees of Hepatic Impairment Relative to Participants Without Hepatic
Impairment.