Overview
This is a multicenter, randomized, double-blind, Phase 2b/3 study to evaluate the efficacy and safety of ABP-671. Part 1 of the study will compare the efficacy and safety of different doses and regimens of ABP-671 with placebo and allopurinol. Part 2 of the study will compare the dosing regimen(s) of ABP-671 selected from Part 1 with placebo in participants who have not been enrolled for Part 1.
Eligibility
Inclusion Criteria:
- Male and female participants aged ≥19 and <70 years of age at the time of informed consent.
- A body mass index (BMI) of ≥18 kg/m2 to ≤40 kg/m2.
- Diagnosis of gout per American College of Rheumatology/European Alliance of
Associations for Rheumatology 2015 Gout Classification Criteria and must meet the
criteria as follows:
- At Screening, participants with gout on ULT (including allopurinol) must be willing to discontinue ULT.
- At Screening, participants with gout who are not currently treated with any UA lowering therapy must have an sUA ≥7.5 mg/dL (≥0.450 mmol/L).
- At the confirmatory sUA visit, all participants must have an sUA ≥7.0 mg/dL (≥0.420
mmol/L).
- Women of childbearing potential (WOCBP) must be surgically sterile (eg, hysterectomy,
bilateral salpingectomy, or bilateral oophorectomy) or willing to use acceptable and
highly effective double contraception from Screening until at least 30 days after the
last dose of the study drug. Double contraception is defined as a condom AND one other
form of the following:
- Established hormonal contraception (with approved oral contraceptive pills, long-acting implantable hormones, injectable hormones);
- A vaginal ring or an intrauterine device OR
- Documented evidence of surgical sterilization at least 6 months prior to Screening (eg, tubal occlusion, hysterectomy, bilateral salpingectomy, or bilateral oophorectomy for women or vasectomy for men [with appropriate post-vasectomy documentation of the absence of sperm in semen] provided the male partner is the sole partner). The absence of records will not exclude screening the participant; if medical records cannot be obtained, serum pregnancy testing will be conducted to confirm the participant is not pregnant.
Note: Women not of childbearing potential must be postmenopausal for ≥12 months.
Postmenopausal status will be confirmed through follicle stimulating hormone (FSH)
concentration testing.
-Men must be surgically sterile (>30 days since vasectomy), abstinent, or if engaged in
sexual relations with a female partner of childbearing potential, the participant must use
an acceptable form of contraception from Screening until at least 30 days after the last
dose of the study drug. Acceptable methods of contraception include the use of condoms in
addition to the use of an effective contraceptive for the female partner that includes
approved oral contraceptive pills, long-acting implantable hormones, injectable hormones, a
vaginal ring, or an intrauterine device. Participants who practice abstinence (abstinence
from penile-vaginal intercourse) are eligible when this is in line with their preferred and
usual lifestyle. In addition, men must not donate sperm for at least 30 days after the last
dose of the study drug.
Exclusion Criteria:
- History of rheumatoid arthritis or other autoimmune disease.
- Clinically significant hepatic, cardiovascular, renal, neoplastic, psychiatric, or
hematological disorders such as polycythemia vera, sickle cell disease, or
myelodysplastic disorder.
- Positive test result for HIV, hepatitis B surface antigen, or hepatitis C virus
antibody. Active hepatitis C virus infection is defined as a participant with a
positive hepatitis C antibody and detectable hepatitis C viral load RNA.
- Participants who, in the opinion of the Investigator, have a high genetic risk of
allopurinol hypersensitivity syndrome unless they have been found to be negative for
Human leukocyte antigen (HLA)-B*5801, either clinically by prior exposure to
allopurinol or by laboratory evaluation.
- Liver function tests >2x the laboratory upper limit of normal (ULN) range of aspartate
aminotransferase, alkaline phosphatase, or alanine aminotransferase; total bilirubin
>1.5x ULN at Screening.
- Inadequate renal function with serum creatinine >1.5 mg/dL (>0.133 mmol/L) or
estimated glomerular filtration rate (eGFR) < 60 mL/min/m2 (by the 2021 Chronic Kidney
Disease Epidemiology Collaboration creatinine-based eGFR equation).
- History of malignancy within the previous 5 years; with the exception of non-melanoma
skin cancer that has been treated with no evidence of recurrence, treated cervical
dysplasia, or treated in situ grade 1 cervical cancer.
- History within the last 12 months of unstable angina, New York Heart Association
functional class III or IV heart failure, myocardial infarction, stroke, venous
thromboembolism, or a history of percutaneous coronary intervention.
- Uncontrolled hypertension (systolic BP ≥160 mmHg and/or diastolic BP ≥90 mmHg). If BP
is controlled while taking antihypertensive medication, the participant must be on
stable dose for previous 2 months.
- Active liver disease or impaired hepatic function as assessed by liver function tests.
- Received any investigational therapy within 30 days or 5 half-lives (whichever is
longer) prior to Screening.
- Any other medical or psychological condition, that, in the opinion of the Investigator
and/or Medical Monitor, might create undue risk to the participant, interfere with the
participant's ability to comply with the protocol requirements to complete the study,
or potentially compromise the results or interpretation of the study.
- Pregnant, breastfeeding, or planning a pregnancy during the study or ≤30 days after
the last dose of the study drug.
- Intolerant or unwilling to take colchicine or naproxen.