Study to Evaluate Pharmacokinetics of A Modified Release Formulation of PF-06650833 in Healthy Subjects

This is the third study of PF-06650833. The goals of the study are to assess the PK in
healthy subjects of single doses of modified release (MR) tablets of PF-06650833 when orally
administered under fasting and high fat meal fed conditions.

Inclusion Criteria:

1. Healthy female subjects of non childbearing potential and/or male subjects, between
the ages of 18 and 55 years

2. BMI of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs).

3. Personally signed and dated Informed Consent

4. Willing and able to comply with scheduled visits, treatment plan, laboratory tests,
and other study procedures.

Exclusion Criteria:

1. Clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal,
cardiovascular, hepatic, psychiatric, neurologic, or allergic disease

2. Any condition possibly affecting drug absorption

3. Positive urine drug screen.

4. Heavy smokers

5. History of regular heavy alcohol consumption within 6 months of Screening.

6. Treatment with an investigational drug within 30 days (or as determined by the local
requirement) or 5 half lives

7. Screening supine blood pressure <=100 mm Hg (systolic) or<=50 mm Hg (diastolic)
or>=140 mm Hg (systolic) or >=90 mm Hg (diastolic), following at least 5 minutes of
supine rest.

8. Screening pulse (HR) >100 bpm after at least 5 minutes of rest.

9. Single supine 12 lead ECG demonstrating QTc >450 msec or a QRS interval >120 msec at
Screening.

10. Abnormal chest X ray

11. History of TB or active or latent or inadequately treated infection, positive
Quantiferon TB test.

12. History of hepatitis or positive testing for human HIV,HepBsAg, HepBc Ab or HCVAb

13. Any medical history of disease [ie, Gilbert's disease] that has the potential to
cause a rise in total bilirubin over the ULN

14. Clinical laboratory abnormalities including:

- Creatine kinase >1.2 X ULN;

- CK MB > ULN;

- Serum myoglobin >1.2 X ULN;

- Cardiac Troponin I (cTn I) > ULN of the laboratory reference range;

- Serum aspartate transaminase (AST) or alanine transaminase (ALT) >=2 x ULN,
total serum bilirubin >=1.5 mg/dL;

- Subjects with benign ethnic neutropenia;

- Hemoglobin <=14 gm/dl (males) and <=13 gm/dL (females).

15. Nursing female subjects; male subjects with partners currently pregnant; male
subjects able to father children who are unwilling or unable to use a highly
effective method of contraception as outlined in this protocol for the duration of
the study and for 28 days after the last dose of investigational product or longer
based upon the compound's half life characteristics.

16. Use of prescription or nonprescription drugs and dietary supplements within 7 days or
5 half lives (whichever is longer) prior to the first dose of investigational product
until discharge from the study at the end of Period 2.

Herbal supplements and hormone replacement therapy must be discontinued 28 days prior
to the first dose of investigational product. Acetaminophen/paracetamol should not be
used. As an exception, ibuprofen may be used at doses of 200 to 400 mg orally every 6
hours as needed for up to 3 of 7 consecutive days.

17. Blood donation (excluding plasma donations) of approximately 1 pint (500 mL) or more
within 56 days prior to dosing.

18. History of sensitivity to heparin or heparin induced thrombocytopenia.

19. History of cancer (other than treated basal cell and squamous cell carcinoma of the
skin) in the previous 5 years.

20. Previous exposure to PF 06650833.

21. Unwilling or unable to comply with the Lifestyle guidelines

22. Subjects who are investigational site staff members directly involved in the conduct
of the study and their family members, site staff members otherwise supervised by the
Investigator, or subjects who are Pfizer employees directly involved in the conduct
of the study.

23. Other severe acute or chronic medical or psychiatric condition or laboratory
abnormality