| Eligibility |
Inclusion Criteria:
1. Male or female = 18 and = 75 years of age.
2. Body mass index (BMI) = 19 and = 42 kg/m2 at screening.
3. sUA levels = 7.5 mg/dL during screening and at check-in (Day -1).
4. Patients must meet the American College of Rheumatology scoring criteria for the
classification of primary gout (Neogi et al 2015).
5. Patients must be able to take gout flare prophylaxis with colchicine 0.6 mg QD
throughout the study as the primary method to prevent disease flare. If colchicine is
not tolerated or contraindicated, naproxen 250 mg BID with or without H2 antagonists
will be employed as a second line gout flare prophylactic agent. Gout flare
prophylaxis will be initiated at the Day -1 visit in patients who are sUA-lowering
agent naïve. For patients that discontinue an sUA-lowering agent(s) (ie, washout from
current therapy) during the screening period, gout flare prophylaxis should be
initiated at the time of discontinuation of the sUA-lowering agent(s).
6. Is a nonsmoker or light smoker (smokes fewer than 10 cigarettes per day).
7. Female patients either will be postmenopausal (female patients who state they are
postmenopausal should have had cessation of menses for > 1 year and have serum
follicle-stimulating hormone [FSH] levels > 40 mIU/mL and serum estradiol < 20 pg/mL);
or surgically sterile (including bilateral tubal ligation, salpingectomy [with or
without oophorectomy], surgical hysterectomy, or bilateral oophorectomy [with or
without hysterectomy]) for at least 3 months prior to screening; or will agree to use,
from the time of check-in (Day -1) until 90 days following the last dose of study
drug, the following forms of contraception: double-barrier method, hormonal
contraceptives, barrier with spermicide, diaphragm or cervical cap with spermicide,
intrauterine device, oral, implantable, or injectable contraceptives, or a sterile
sexual partner. All female patients, except those with documented surgical
hysterectomy in medical history, will have a negative urine pregnancy test result
prior to enrollment in the study.
8. Male patients either will be surgically sterile or agree to use, from the time of
check-in (Day -1) until 90 days following the last dose of study drug, the following
forms of contraception: male condom with spermicide and a female partner who is
sterile or agrees to use hormonal contraceptives, female condom with spermicide,
diaphragm or cervical cap with spermicide, intrauterine device, oral, implantable, or
injectable contraceptives. Male patients will refrain from sperm donation from the
time of check-in (Day -1) until 90 days following the last dose of study drug.
9. Is capable of understanding the written informed consent, provides signed and
witnessed written informed consent, and agrees to comply with protocol requirements.
Cohorts 1 through 3:
10. Patients who are not taking any UA-lowering medications within 2 weeks prior to the
dose of study drug. Patients may discontinue sUA-lowering agents (ie, washout from
current therapy) during the screening period. In the cases of a patient who must
discontinue sUA-lowering agents or a patient not previously taking sUA-lowering agents
during the screening period, gout flare prophylaxis should be initiated with
colchicine 0.6 mg QD as the primary method to prevent disease flare and be continued
during the study period. If colchicine is not tolerated or contraindicated, naproxen
250 mg BID with or without H2 antagonists will be employed as a second line gout flare
prophylactic agent.
Cohort 4:
11. Patient has been on a stable dose of allopurinol as existing urate-lowering therapy
for at least 3 months prior to Day 1.
Exclusion Criteria:
1. Female patient is pregnant, planning to get pregnant, or lactating/breastfeeding.
2. Has a history or presence of CS cardiovascular, renal, pulmonary, hepatic, gallbladder
or biliary tract, hematologic, gastrointestinal, endocrine, immunologic, dermatologic,
neurologic, or psychiatric disease, which in the investigator's opinion would not be
suitable for the study.
3. Serum creatinine level > 1.5 mg/dL and/or estimated glomerular filtration rate (eGFR)
= 60 mL/min/1.73 m2 calculated using the Chronic Kidney Disease Epidemiology
Collaboration (CKD-EPI) equation (Levey et al 2009; National Institute of Diabetes and
Digestive and Kidney Diseases, Estimating Glomerular Filtration Rate) at screening.
4. History of stomach or intestinal surgery (except cholecystectomy, appendectomy, and/or
hernia repair will be allowed).
5. History of prescription drug abuse, illicit drug use, or alcohol abuse according to
medical history within 6 months prior to the screening visit or any alcohol use for at
least 48 hours prior to dosing on Day 1.
6. Positive test for human immunodeficiency virus (HIV).
7. Positive test for hepatitis B virus or hepatitis C virus (HCV) consistent with current
infection. Confirmatory tests will be allowed at the discretion of the investigator to
rule out false positives.
8. Clinically significant abnormal liver function test at screening or check-in (Day -1),
defined as aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 1.5 ×
upper limit of normal (ULN) or total bilirubin > ULN; or a history of CS acute or
chronic hepatitis (including infectious, metabolic, autoimmune, genetic, ischemic, or
other forms), hepatocirrhosis, or hepatic tumors.
9. Positive screen for alcohol or drugs of abuse (except for patients with a positive
drug screen if it is a result of a prescribed medication from their physician) at
screening or check-in (Day -1).
10. History of a gout flare that is resolved within 14 days prior to the first dose of
study drug on Day 1 (exclusive of chronic synovitis/arthritis). If a gout flare occurs
during screening, patients may be rescreened after a period of at least 14 days has
passed following the flare.
11. Has a known hypersensitivity to URAT1 inhibitors, XOIs, or related compounds.
12. Receipt of any other investigational product within 30 days prior to the first dose of
study drug on Day 1 or planning to take an investigational agent during the study.
13. Use of drugs or nutrients known to significantly modulate cytochrome P450 (CYP)3A
activity starting from 14 days prior to the first dose of study drug on Day 1 until
EOS (any strong or moderate inhibitors or inducers of CYP3A4, including but not
limited to the following: inhibitors such as ketoconazole, miconazole, itraconazole,
fluconazole, atazanavir, erythromycin, clarithromycin, ranitidine, cimetidine,
verapamil, and diltiazem; and inducers such as rifampicin, rifabutin, glucocorticoids,
carbamazepine, phenytoin, phenobarbital, and St. John's wort).
14. Participated in strenuous exercise from 48 hours prior to check-in (Day -1) or during
the study through EOS.
15. Has donated or lost a significant volume (> 500 mL) of blood or plasma within 30 days
prior to check-in (Day -1).
16. Malignancy within 5 years prior to the screening visit (excluding basal cell
carcinoma).
17. Has problems understanding the protocol requirements, instructions, study-related
restrictions, and/or problems understanding the nature, scope, and potential
consequences of participating in this clinical study.
18. Is unlikely to comply with the protocol requirements, instructions, and/or
study-related restrictions (eg, uncooperative attitude, unavailable for follow up,
and/or improbability of completing the clinical study).
Cohorts 1 through 3:
19. Concomitant use of or treatment with any prescription drugs, herbal products,
vitamins, minerals, and over-the-counter (OTC) medications that are known to lower sUA
levels (eg, allopurinol, febuxistat, probenecid, lesinurad, and peglodicase) within 14
days prior to check-in (Day -1). Exceptions may be made on a case-by-case basis (such
as chronic use of low dose aspirin) following discussion and agreement between the
investigator and sponsor.
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