Status:
COMPLETED
SER150 vs Placebo in Diabetic Kidney Disease
Lead Sponsor:
Serodus AS
Conditions:
Diabetic Kidney Disease
Eligibility:
All Genders
18-85 years
Phase:
PHASE2
PHASE3
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 albuminu...
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-control...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
August 18 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 6 2024
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT04881123
Start Date
August 18 2021
End Date
June 6 2024
Last Update
June 21 2024
Active Locations (12)
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1
Liverpool Hospital
Liverpool, New South Wales, Australia, 2170
2
The AIM Centre (Hunter Diabetes Centre)
Merewether, New South Wales, Australia
3
Royal North Shore Hospital
Saint Leonards, New South Wales, Australia, 2065
4
Princess Alexandra Hospital
Brisbane, Queensland, Australia, 4102