SER150 vs Placebo in Diabetic Kidney Disease

NCT ID: NCT04881123

Last Updated: 2024-06-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-08-18
• Study Completion Date: 2024-06-06

Brief Summary

This study is to assess the efficacy and safety of SER150 administered for 24 weeks as a 15 mg twice a day BID dose (except on Day 168 15 mg QD) in participants with type 2 diabetes (T2D) and albuminuria in treatment with either an angiotensin converting enzyme inhibitor (ACEi) or an angiotensin receptor antagonist (ARB).

Detailed Description

This is a randomized, double-blind, placebo-controlled, parallel groups, multicenter pivotal study assessing the efficacy and safety of 15 mg BID (except on Day 168 15 mg QD) of SER150 in well-controlled adult T2D participants with stable concomitant medications, diabetic kidney disease (DKD) and albuminuria in treatment with an ACEi or an ARB.

The randomized treatment period will be 24 weeks followed by a 4-weeks follow-up.

Conditions

Diabetic Kidney Disease

Study Design

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

Study Groups

SER150

Randomized participants will receive SER150, 15 mg, orally, BID (except on Day 168 where participants will only receive a 15 mg single dose (QD) in the morning)

Group Type: EXPERIMENTAL

SER150

Intervention Type: DRUG

Dosage Level(s): 30 mg (1 capsule of 15 mg twice a day - morning and evening) (except on Day 168 where participants will only receive a single dose (QD) in the morning)

Placebo

Randomized participants will receive matching placebo, orally, BID (except on Day 168 where participants will only receive a 15 mg single dose (QD) in the morning)

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Dosage Level(s): Matched placebo (1 capsule twice a day - morning and evening) (except on Day 168 where participants will only receive a single dose (QD) in the morning)

Interventions

SER150

Dosage Level(s): 30 mg (1 capsule of 15 mg twice a day - morning and evening) (except on Day 168 where participants will only receive a single dose (QD) in the morning)

Intervention Type: DRUG

Placebo

Dosage Level(s): Matched placebo (1 capsule twice a day - morning and evening) (except on Day 168 where participants will only receive a single dose (QD) in the morning)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Participant has had stable T2D for 3 months prior to screening
• Participant has albuminuria defined by urine UACR ≥ 200 mg/g creatinine as a mean of three independent samples of first urine void of the day
• Participant is receiving stable antidiabetic treatment. Antidiabetic treatment includes all drugs given for the treatment of T2D
• Participant is in treatment with ACEi or ARB, with eGFRcrea lower than 75 mL/minute /1.73 m^2 and above 15 mL/minute/1.73 m^2 (CKD-EPI formula) and will not, in the opinion of the investigator, become a candidate for renal dialysis whilst on the study
• Participant is determined to be overtly healthy as determined by Investigator review of their medical history, physical examination, laboratory tests, and cardiac monitoring. It is anticipated that, whilst some of the participant's results may be different to that of a completely healthy individual, the Investigator will review the participant's individual results to ensure they are as healthy as can be expected give the participant's current health status
• Participant has ASA physical status, health class 2, 3 or 4
• Participant has blood pressure ≤ 160 mmHg systolic, and ≤ 100 mmHg diastolic
• Participant has normal electrocardiogram
• Participant has glycosylated hemoglobin (HbA1c) ≤ 10%
• Participant has prothrombin within normal values
• Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies

Exclusion Criteria

• Acute myocardial infarction within the last 3 months
• Stroke within the last 3 months
• Any major surgery in the last 3 months that in the opinion of the Investigator poses an increased bleeding risk.
• ACR ≤ 200 mg/g creatinine
• Urinary bladder infections within the last 3 months (all other urinary tract infections and vulvovaginitis are excluded)
• Recent history (within the last 6 months) or ongoing liver disease, including viral infections
• Participants with HIV
• Participants with known specific renal diseases different from DKD
• Any bleeding disorder or acute blood coagulation defect
• A history of gastric ulcers or any other organic lesion susceptible to bleeding
• Participant has had a confirmed COVID-19 infection by appropriate laboratory test (PCR or Rapid Antigen Test) within the last 4 weeks prior to screening or on admission
• Participant who had severe course of COVID-19
• Any other condition or clinically relevant abnormal findings in physical examination, laboratory results or ECG during screening period that, in the opinion of the Investigator, may compromise the safety of the participant in the study, reduce the participant's ability to participate in the study, or interfere with evaluation of the study drug
• Change in antidiabetic treatment during last 3 months
• Chronic treatment with nonsteroidal anti-inflammatory drugs or other anti-inflammatory compounds during the last month
• Treatment with anticoagulant drugs
• Participation in another clinical trial of an investigational small molecule, antibody (or medical advice) within 30 days (or 5 half-lives of the drug, whichever is longer [if known]) prior to the start of IP administration on Day 2 (or within 6 months prior to the start of IP administration on Day 1 if the investigational drug was a biologic).
• Alanine aminotransferase or aspartate aminotransferase values exceeding 5 x upper limit of normal (ULN)
• Alkaline phosphatase and/or total bilirubin values exceeding 1.5 x ULN
• HbA1c > 10%
• eGFRcrea ≥75 mL/minute/1.73 m^2 and ≤ 15 mL/minute/1.73 m^2
• Allergy to the active substance or any of the excipients of the drug product
• Pregnant or lactating women

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Serodus AS

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Liverpool Hospital

Liverpool, New South Wales, Australia

The AIM Centre (Hunter Diabetes Centre)

Merewether, New South Wales, Australia

Royal North Shore Hospital

Saint Leonards, New South Wales, Australia

Princess Alexandra Hospital

Brisbane, Queensland, Australia

Southern Adelaide Diabetes and Endocrine Services

Adelaide, South Australia, Australia

SA Endocrine Research

Keswick, South Australia, Australia

St Vincent's Hospital

Fitzroy, Victoria, Australia

Sunshine Hospital

Saint Albans, Victoria, Australia

Pacific Clinical Research Clinic Rotorua

Rotorua, Bay of Plenty, New Zealand

PCRN Silverdale Medical Centre

Silverdale, Hibiscus Coast, New Zealand

Lakeland Clinical Trials Waikato

Hamilton, Waikato Region, New Zealand

New Zealand Clinical Research (NZCR)

Christchurch, , New Zealand

Countries

Australia; New Zealand

Other Identifiers

SER150 CL-009

Identifier Type: -

Identifier Source: org_study_id