A Study To Describe The Effect Of Impaired Hepatic Function Of The Pharmacokinetics Of Palbociclib

This is a 4-cohort single period study. The four cohorts will consist of healthy volunteers,
and subjects with mild, moderate, and severely impaired hepatic function. Each cohort will
receive the same treatment consisting of a single oral 75mg dose of palbociclib administered
with food. Serial PK samples will be drawn up to 120 hours post dose for the cohort
consisting of healthy volunteers, and will continue until up to 192 hours post-dose for the
cohorts of hepatic impairment subjects.

Inclusion Criteria:

- Body Mass Index (BMI) of 18 to 40 kg/m2; and a total body weight >50 kg (110 lbs)

- Evidence of a personally signed and dated informed consent document indicating that
the subject has been informed of all pertinent aspects of the study

- Subjects who are willing and able to comply with all scheduled visits, treatment plan,
laboratory tests, and other study procedures

Exclusion Criteria:

- Any condition possibly affecting drug absorption (eg, gastrectomy)

- A positive urine drug screen

- Pregnant female subjects; breastfeeding female subjects; female subjects of
childbearing potential; male subjects with partners currently pregnant; male subjects
of childbearing potential who are unwilling or unable to use a highly effective method
of contraception for the duration of the study and for 90 days after the last dose of
investigational product

- History of sensitivity to heparin or heparin-induced thrombocytopenia

- Blood donation of approximately 1 pint (500 mL) or more within 56 days prior to dosing

- Unwilling or unable to comply with the Lifestyle Guidelines described in this protocol

- Use of tobacco or nicotine products in excess of 5 cigarettes per day (or equivalent)

- History of sensitivity to palbociclib