Efficacy and Safety of Extended Release and Immediate Release Febuxostat in Participants With Gout

The drug being tested in this study is called febuxostat. Febuxostat is being tested to
decrease and maintain serum urate in people who have gout. This study will look at serum
urate levels in people who take febuxostat extended release (XR) capsules compared to
febuxostat immediate release (IR) capsules and placebo.

The study will enroll approximately 1750 patients. Participants will be randomly assigned
(by chance) to one of the five treatment groups—which will remain undisclosed to the patient
and study doctor during the study (unless there is an urgent medical need):

- Febuxostat 40 mg XR

- Febuxostat 80 mg XR

- Febuxostat 40 mg IR

- Febuxostat 80 mg IR

- Placebo (dummy inactive pill) - this is a tablet that looks like the study drug but has
no active ingredient.

All participants will be asked to take one capsule at the same time each day throughout the
study, and will be asked to call an interactive voice response system any time they are
having a gout flare up. In addition to study medication, participants will also take 0.6 mg
of colchicine every day or every other day, or naproxen 250 mg twice a day and lansoprazole
15 mg once a day to prevent gout flare ups.

This multi-centre trial will be conducted in the United States. The overall time to
participate in this study is up to approximately 4 months and participants will make up to 7
visits to the clinic.

Inclusion Criteria:

1. In the opinion of the investigator, the participant is capable of understanding and
complying with protocol requirements.

2. The participant or, when applicable, the participant's legally acceptable
representative signs and dates a written, informed consent form and any required
privacy authorization prior to the initiation of any study procedure.

3. Has a history or presence of gout defined as having one or more of the American
Rheumatism Association (ARA) criteria for the diagnosis of gout:

1. A tophus proven to contain urate crystals by chemical or polarized light
microscopic means, AND/OR;

2. Characteristic urate crystals in the joint fluid, AND/OR;

3. History of at least 6 of the following clinical, laboratory, and x-ray
phenomena:

i. more than one attack of acute arthritis, ii. maximum inflammation developed within
1 day, iii. monoarticular arthritis, iv. redness observed over joints, v. first
metatarsophalangeal joint painful or swollen, vi. unilateral first
metatarsophalangeal joint attack, vii. unilateral tarsal joint attack, viii. tophus
(proven or suspected), ix. Hyperuricemia, x. asymmetric swelling within a joint on
x-ray, xi. subcortical cysts without erosions on x-ray; xii. joint fluid culture
negative for organisms during attack.

4. Is male or female at least 18 years of age, inclusive.

5. A female participant of childbearing potential who is sexually active with a
nonsterilized male partner agrees to use routinely adequate contraception from
signing of informed consent throughout the duration of the study.

6. Have a serum urate (sUA) level ≥8.0 mg/dL at the Day -4 Visit or at the retest visit.

7. Has an estimated Glomerular Filtration Rate (eGRF) ≥15 mL/min using the Modification
of Diet in Renal Disease (MDRD) formula at the Screening visit (Day -21 for
participants on urate lowering therapy (ULT) and Day -4 for participants not on ULT)
or at the retest visit.

8. Has at least one gout flare within 12 months prior to Screening visit.

Exclusion Criteria:

1. Has received any investigational compound within 30 days prior to Screening.

2. Is an immediate family member, study site employee, or is in a dependant relationship
with a study site employee who is involved in conduct of this study (eg, spouse,
parent, child, sibling) or may consent under duress.

3. Is breastfeeding or pregnant.

4. Has secondary hyperuricemia (eg, due to myeloproliferative disorder).

5. Has a history of xanthinuria.

6. Has received ULT (ie, allopurinol, probenecid, etc.) within 20 days prior to Day
1/Randomization Visit.

7. Has a known hypersensitivity to febuxostat or any components of their formulation;
has a known hypersensitivity to naproxen, any other nonsteroidal anti-inflammatory
drug (NSAID), aspirin, lansoprazole, colchicine or any components in their
formulation.

8. Has active peptic ulcer disease.

9. Has a history of cancer (other than basal cell carcinoma of the skin) within 5 years
prior to the Screening Visit.

10. Has alanine aminotransferase (ALT) and aspartate aminotransferase (AST) values >2 x
the upper limit of normal (ULN).

11. Has rheumatoid arthritis which requires treatment.

12. Has a significant medical condition and/or conditions that would interfere with the
treatment, safety, or compliance with the protocol.

13. Has experienced a myocardial infarction (MI), stroke, hospitalized unstable angina,
cardiac or cerebrovascular revascularization procedure or hospitalized transient
ischemic attack (TIA) - except in participants who have severe renal impairment.

14. Participants with severe renal impairment had a MI or stroke within 90 days prior to
initial screening visit or has a MI or stroke during the screening period prior to
Day 1/Randomization Visit.

15. Participant consumes >14 alcoholic beverages/week. Has a history of alcoholism or
illicit drug abuse within 5 years.

16. Has participated in another investigational study within the 30 days prior to the
Screening Visit.

17. Has a known history of infection with hepatitis B, hepatitis C, or human
immunodeficiency virus.

18. Is required to take excluded medications.