Study of of URC102 to Assess the Efficacy and Safety in Gout Patients

NCT ID: NCT04804111

Last Updated: 2021-03-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 171 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-01-21
• Study Completion Date: 2020-11-29

Brief Summary

To confirm the safety and efficacy (dose response and optimal dose according to the serum uric acid response rate) of URC102 when orally-administered to patients with gout and gout-related hyperuricemia in comparison with placebo.

Therapeutic dose-finding study, Placebo-controlled, randomized, double-blind, multicenter, phase 2 clinical trial.

Detailed Description

Placebo-controlled, randomized, double-blind, multicenter, phase 2 clinical trial.

Conditions

Gout

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Placebo

maintain the initial dose, without increasing the dose.

Group Type: PLACEBO_COMPARATOR

arm 0

Intervention Type: DRUG

placebo group

URC102 3mg

Administer 3 mg of URC102 for 12 weeks

Group Type: ACTIVE_COMPARATOR

arm 1

Intervention Type: DRUG

3 mg of the URC102 group

URC102 6mg

Administer 3 mg of URC102 for 1 week and 6 mg of URC102 for 11 Weeks.

Group Type: ACTIVE_COMPARATOR

arm 2

Intervention Type: DRUG

6 mg of the URC102 group

URC102 9mg

Administer 3 mg of URC102 for 1 week and 6 mg of URC102 for 1 Weeks, maintain 9 mg of URC102 dose

Group Type: ACTIVE_COMPARATOR

arm 3

Intervention Type: DRUG

9 mg of the URC102 group

Febuxostat 80 mg

maintain the initial dose, without increasing the dose.

Group Type: OTHER

arm 4

Intervention Type: DRUG

Febuxostat 80 mg

Interventions

arm 0

placebo group

Intervention Type: DRUG

arm 1

3 mg of the URC102 group

Intervention Type: DRUG

arm 2

6 mg of the URC102 group

Intervention Type: DRUG

arm 3

9 mg of the URC102 group

Intervention Type: DRUG

arm 4

Febuxostat 80 mg

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subjects who are aged ≥19 and <70 years at the time of providing written informed consent

2. Subjects who are diagnosed with gout according to American College of Rheumatology (1977) criteria for the classification of acute arthritis of primary gout.

3. Subjects who have the ability and willingness to actively conduct TLC recommended in this study

4. Subjects who provided written informed consent to voluntarily participate in the study

1. sUA ≥ 7.0 mg/dL at Visit 2

Exclusion Criteria

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1. Subjects who have medical history or comorbidity as follow; (1) Active malignancy or history of malignancy within the past 5 years at the time of screening (2) Urolithiasis (3) Clinically important allergic disease (anaphylactic shock, etc.) (4) Lesch-Nyhan syndrome (5) Hereditary problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption (6) Ischemic heart diseases or congestive heart failure (7) Organ transplantation (recipient or scheduled to receipt)

2. Subjects who have comorbidity or abnormality of lab results as follows; (1) Uncontrolled diabetes mellitus with drug therapy

• HbA1c ≥ 9% or
• Fasting plasma glucose (FPG) ≥160 mg/dL (2) Uncontrolled hypertension with treatment
• Systolic blood pressure (SBP) ≥180 mmHg or
• Diastolic blood pressure (DBP) ≥ 110 mmHg (3) Uncontrolled dyslipidemia with treatment
• Total cholesterol ≥ 250 mg/dL (at least 8 hours of fasting) (4) Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≥ 2 X upper limit of normal (ULN) or Total bilirubin ≥ 1.5 X ULN (5) eGFR* < 60 mL/min/1.73m2 * eGFR (MDRD equation) GFR(ml/min/1.73m2) = 186 × (SCr)-1.154 × (age)-0.203 × (0.742 if female) × (1.210 if African American) (6) Uncontrolled thyroid function with treatment (thyroid-stimulating hormone (TSH) ≥ 1.5 X UNL

3. Subjects who are judged by the investigator to have a clinical cardiovascular disease that may affect the study based on the 12-lead ECG obtained at screening or those suspected to be at such risk

4. Patients who have received or plan to receive any XOI or uricosuric agents within 3 weeks prior to study treatment

5. Patients who have received or plan to receive diuretics or any medication action on human Uric Acid Transporter 1(hURAT1) such as indomethacin, pyrazinamide, fenofibrate, atorvastatin, amlodipine, losartan, captopril, enalapril, salicylates etc. within 2 weeks prior to study treatment However, those who have been on stable doses as below are allowed to participate in the study, if the administration method and dosage remain the same during the study period (1) Diuretics (thiazide only or thiazide-based combination, etc.) and antihypertensive agents (losartan etc.) used for the treatment of hypertension (2) Fenofibrate or lipid lowering drugs (atorvastatin) used for hyperlipidemia (3) Salicylates (aspirin)

6. Patients who have been administered or plan to administer Mercaptopurine, Azathioprine, Theophyline within 1 week or within more than 5 times of its half-life prior to the Visit 1

7. HIV Ag/Ab, HBs Ag or HCV Ab positive at screening

8. Subjects who have known hypersensitivity or allergy to IPs (URC102 or febuxostat) or any components in their formulations

9. Subjects who have childbearing or nursing

10. Subjects who agree to use methods of birth control* during the study period and for up to 7 days after the final administration of the IP

• Methods of birth control: ① intrauterine device or birth control implant, ② dual protection (condom with spermicide and contraceptive diaphragm or contraceptive sponge or cervical cap ③ surgical sterilization (vasectomy or tubal ligation or etc.)

11. Subjects who have been administered any other IP or investigational device by participating in other studieswithin 4 weeks or within more than 5 times of its halflife prior to the Visit 1

12. Subjects who have a history of drug or alcohol abuse within 5 years prior to the Visit 1

13. Subjects who have any other reason that may affect the study or those who are judged by the investigator to be ineligible for participation in the study

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 69 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

JW Pharmaceutical

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

JW Pharmaceutical

Seoul, , South Korea

Chung-Ang University Hospital

Seoul, , South Korea

Countries

South Korea

References

Jun JB, Lee HS, Kim SH, Lee SG, Lim DH, Kim J, Park YB, Lim MJ, Hong SJ, Choi HJ, Lee SS, Kim HA, Hwang J, Suh CH, Han S, Choe JY, Yoo WH, Song JS. Efficacy and safety of epaminurad, a potent hURAT1 inhibitor, in patients with gout: a randomized, placebo-controlled, dose-finding study. Arthritis Res Ther. 2025 May 26;27(1):113. doi: 10.1186/s13075-025-03577-w.

Reference Type: DERIVED

PMID: 40420308 (View on PubMed)

Other Identifiers

JWP-URC-203

Identifier Type: -

Identifier Source: org_study_id