Phase IIb Clinical Trial for the Efficacy and Safety by CU01-1001 for 24 Weeks in Type 2 DM Patients With Albuminuria

NCT ID: NCT05718375

Last Updated: 2023-02-08

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 240 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-01-25
• Study Completion Date: 2024-09-30

Brief Summary

To evaluate the efficacy and safety of CU01-1001 administered for 24 weeks in type 2 diabetic nephropathy patients with albuminuria.

Conditions

Diabetic Nephropathies

Study Design

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

Study Groups

CU01-1001 (low dose)

1 Tab/3 times/day (CU01-1001 120 mg, Breakfast and Dinner; Placebo 120 mg, Lunch)

Group Type: EXPERIMENTAL

CU01-1001

Intervention Type: DRUG

CU01-1001

Placebo

Intervention Type: DRUG

Placebo

CU01-1001 (high dose)

1 Tab/3 times/day (CU01-1001 120 mg, Breakfast, Lunch, and Dinner)

Group Type: EXPERIMENTAL

CU01-1001

Intervention Type: DRUG

CU01-1001

Placebo

1 Tab/3 times/day (Placebo, Breakfast, Lunch, and Dinner)

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo

Interventions

CU01-1001

CU01-1001

Intervention Type: DRUG

Placebo

Placebo

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male/female patients aged 30 years or above

2. Patients diagnosed as type 2 diabetes prior to screening

3. Patients receiving ACE inhibitors (angiotensin-converting-enzyme inhibitor) or ARB (angiotensin II receptor blockers) for at least 8 weeks prior to screening

4. Patients who experienced albuminuria (albumin to creatinine ratio) 200~1,000 mg/g Cr) at least twice prior to 24weeks including screening results

5. Patients with blood pressure ≤ 140/90mmHg at screening

6. Patients with 25 ≤ GFR (glomerular filtration rate) ≤ 75ml/min/1.73m2 at screening

7. Patients with 6.5% < HbA1c ≤ 9% at screening

Exclusion Criteria

1. Patients with past medical history of acute renal failure within 12weeks prior to screening; or Increase in SCr ≥ 0.3 mg/dL within 48 hours; or an increase in SCr ≥ 1.5-fold from baseline (the lowest value) within 12 weeks; or urine output <0.5mg/kg/hour for 6 hours

2. NYHA class III~IV

3. Patients with medical history related liver disease and hepatic function as follows: ALT (alanine aminotransferase) or AST (aspartate aminotransferase) >3 X institutional upper limit of normal (ULN), or Total bilirubin >3 X institutional upper limit of normal (ULN)

4. Patients with malabsorption due to organic gastrointestinal disorder or chronic gastroenterological disorders at screening (short-bowel syndrome, active Crohn's disease, and ulcerative colitis, etc.)

5. Patients with acute disease (including infectious diseases) at screening and who are thought to be unable to participate in the clinical study)

6. Within 12 weeks of the informed consent, patients who had the diagnosis and procedures of the following cardiovascular diseases: cardiac failure (NYHA class III and IV), unstable angina pectoris, myocardial infarction, transient ischemic attack, cerebro-vascular accident, history of peripheral vascular disease or coronary artery bypass surgery, and percutaneous transluminal coronary angioplasty

7. Patients with history of alcohol or drug abuse

8. Patients with any allergic reaction to the investigational product or its components

9. Patients who are planning to receive dialysis or renal transplantation within 36 weeks (9 months) in the future

10. Patients who are expected to have lower compliance with protein-limited diets and the use of the study drug

11. Women who are pregnant or breastfeeding a baby

12. Women who are able to become pregnant and do not agree to use acceptable contraception as defined by the protocol; however, women of childbearing potential who have not gone sterility procedures can participate in the study only for negative pregnancy test, and should agree to maintain effective contraception (implants of intrauterine device or intrauterine system, double barrier contraception (condom, diaphragm, sponge or cervical cap with spermicide), oral contraceptives, sterilization, and total abstinence) throughout the study

13. Patients who participated in other clinical study within 12 weeks of the participation in this study

14. Patients who are not eligible for this study participation in the judgment of the principal investigator or sub-investigator

• Minimum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Curacle Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

KyuChang Won

Role: PRINCIPAL_INVESTIGATOR

Yeongnam University Medical Center

HyeJin Yoo

Role: PRINCIPAL_INVESTIGATOR

Koera University Guro Hospital

Jun Hwa Hong

Role: PRINCIPAL_INVESTIGATOR

Eulji University Hospital

Young Min Cho

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Medical Center

Locations

Yeongnam University Medical Center

Daegu, , South Korea

Site Status: RECRUITING

Countries

South Korea

Central Contacts

Hyunjeong Kim

Role: CONTACT

hjkim02@curacle.com

+82-2-3487-0077

Facility Contacts

KyuChang Won

Role: primary

+82-53-620-3846

Other Identifiers

CU01-1001-DN-P2b

Identifier Type: -

Identifier Source: org_study_id