Overview

Safety and Efficacy Study of MBX-102 in Treatment of Hyperuricemia in Patients With Gout

Status:
Completed
Trial end date:
2011-11-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the study is to evaluate the safety and effectiveness of MBX-102 compared to placebo when given orally once daily for 4 weeks for the treatment of hyperuricemia in patients with gout.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
CymaBay Therapeutics, Inc.
Treatments:
Colchicine
Criteria
Inclusion Criteria:

- Read and sign the informed consent after the elements of consent have been fully
explained and all questions have been addressed, prior to any study procedures.

- Known gout patient (per criteria of the American Rheumatism Association for the
classification of the acute arthritis of primary gout in Appendix 3)

- the sUA must be ≥ 8.0 mg/dL and ≤12 mg/dL

- if on ULT, the patients must agree to temporarily discontinue their existing ULT
and the sUA must be ≥ 8.0 mg/dL and ≤12 mg/dL after wash-out at Week -1

- Male or female, 18-75 years of age at Screening Visit

- All female patients must be surgically sterile or post-menopausal (at least 45 years
of age with no history of menses for at least 2 years; or any age with no history of
menses for at least 6 months and serum FSH ≥ 40 mIU/mL) or have a partner who has
undergone vasectomy or must agree to use two medically accepted methods of
contraception including a barrier method (see the list in Appendix 4) for the entire
duration of the study unless reporting complete sexual abstinence.

- Female patients must not be pregnant or lactating

- Male patients with a female partner of child-bearing potential must agree to use
condom or the partner must use a medically acceptable method of contraception for the
entire duration of the study.

- Patients must have an estimated CrCl ≥ 60 mL/min as calculated by the Cockcroft-Gault
method

- Serum creatinine value must be ≤ 1.1 mg/dL in females and ≤ 1.3 mg/dL in males

- Patients must have liver function tests ≤ 1.5X ULN for AST, ALT and T-bilirubin, ≤ 2X
ULN for ALP, ≤ 3X ULN for GGT; and ≤ 3X ULN for CK

- All other clinical laboratory parameters must be within normal limits or considered
not clinically significant for participation in this study

- Electrocardiogram (ECG) must be normal, or if abnormal, considered not clinically
significant for participation in this study

- Patients must have a systolic blood pressure ≤ 160 mm Hg and a diastolic blood
pressure ≤ 90 mm Hg; known hypertensive patients controlled with medication other than
thiazide diuretics (BP reading as above) may be included

Exclusion Criteria:

- Known or suspected secondary hyperuricemia (e.g. due to myeloproliferative disorder,
or organ transplant).

- Known patient with xanthinuria

- History of documented or suspected kidney stones

- Over producers of uric acid as evidenced by 24-hour urinary uric acid > 800 mg (on
normal unrestricted diet)

- Known infection with the human immunodeficiency virus (HIV) or history of viral
hepatitis type B or C

- History of illicit drug or alcohol abuse within last 1 year

- History of significant pulmonary disease, upper GI bleeding, documented peptic ulcer
disease (unless known H. pylori infection treated successfully without recurrence), or
nephrotic syndrome within last 3 years

- All patients must not have had a stroke, TIA, acute myocardial infarction, congestive
heart failure (NYHA Class II-IV), angina pectoris, coronary intervention procedure
(including but not limited to angioplasty, stent placement, coronary
revascularization), lower extremity bypass procedure, systemic or intracoronary
fibrinolytic therapy within last 5 years

- Malignancy within the last 5 years (except resected basal cell carcinoma)

- Body mass index (BMI) > 42 kg/m2

- Current or expected requirement for anticoagulant therapy (except for ≤ 325 mg/day
aspirin and/or Plavix® 75 mg/day)

- Rheumatoid arthritis or other autoimmune disease requiring ongoing treatment

- Current or expected treatment with potent CYP3A4 inhibitors (See in Appendix 6),
ranolazine, digoxin, cyclosporine, cyclophosphamide and other cytotoxic agents,
sulphonylurea, thiazolidinedione, diuretic, atypical antipsychotic agents, and
phenytoin

- Chronic treatment with non-steroidal anti-inflammatory drugs (NSAIDs use to treat
acute flares are permitted)

- Current or expected treatment with systemic corticosteroids (except topical,
ophthalmic, intra-articular, or inhaled at a dose < 1600 μg/day) other than to treat
acute flares

- Known hypersensitivity to colchicine

- Treatment with any other investigational therapy within the 30 days prior to the
Screening Visit, or patients who received at least one dose of blinded study drug
while enrolled in any previous MBX-102 trial

- Any other condition that compromises the ability of the patient to provide informed
consent or to comply with the objectives and procedures of this protocol, as judged by
the investigator and/or medical monitor