A Double-blind Study to Investigate Efficacy, Safety and Tolerability of BAY1142524 in Patients With Type II Diabetes and a Clinical Diagnosis of Diabetic Kidney Disease
- Conditions
- Diabetic Kidney Disease
- Interventions
- Drug: Placebo
- Registration Number
- NCT03412006
- Lead Sponsor
- Bayer
- Brief Summary
The purpose of the trial is the analysis of safety and efficacy of the chymase inhibitor BAY1142524 at a dose of 25 mg BID in comparison to placebo using a 6 months treatment period in type II diabetic patients with a clinical diagnosis of diabetic kidney disease. BAY1142524 or placebo will be given on top of evidence-based standard of care for diabetic kidney disease. Primary objective is the analysis of first signs of efficacy as determined by favourable changes in urinary albumin creatinine ratio. Secondary objective is the analysis of safety and tolerability as evidenced by the incidence and severity of adverse events. 64 valid patients have to complete treatment with verum and 32 valid patients have to complete treatment with placebo.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 152
- Patients with Type 2 Diabetes Mellitus and a clinical diagnosis of diabetic kidney disease (DKD) (as judged by the investigator) who have finished their up-titration with an angiotensin receptor blocker (ARB) or an ACEI (angiotensin-converting enzyme inhibitor) to their maximum tolerated dose at least 3 months prior to the screening visit, whereby the maximum tolerated dose has to be at least as high as the minimal recommended dose of an ARB or ACEI according to local and/or international guidelines. Patients have to be treated with an ARB or ACEI, but not with both simultaneously, without any adjustments to this therapy for at least 4 weeks prior to the screening visit.
- UACR >50 mg/g and <3000 mg/g in 2 out of 3 consecutive morning void samples at the screening and the baseline visit
- estimated glomerular filtration rate (eGFR) ≥30 mL/min/1.73 m*2 and <90 mL/min/1.73 m*2 (Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI]) at the screening visit and the baseline visit
- Non-DKD if it is the main diagnosis contributory to chronic kidney disease (CKD), as judged by the investigator
- Known bilateral clinical relevant renal artery stenosis (>75%)
- New York Heart Association (NYHA) Class IV
- Acute kidney injury or dialysis within the last 3 months before the screening visit
- Renal replacement therapy during study conduct
- Renal allograft in place or a scheduled kidney transplant during study conduct
- Stroke, transient ischemic cerebral attack, acute coronary syndrome, or hospitalization for heart failure in the last 3 months prior to screening visit
- Clinically relevant hepatic dysfunction
- Uncontrolled hypertension as evidenced by systolic blood pressure >160 mmHg, diastolic blood pressure >100 mmHg (mean of triplicate values at the screening or baseline visit)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Fulacimstat (BAY1142524) Fulacimstat (BAY1142524) Patients have to have a clinical diagnosis of diabetic kidney disease and have to be treated with standard of care for this condition Placebo Placebo Patients have to have a clinical diagnosis of diabetic kidney disease and have to be treated with standard of care for this condition
- Primary Outcome Measures
Name Time Method Change in urinary albumin to creatinine ratio (UACR) Baseline and at 6 months The ratio of albumin to creatinin will be determined in first morning void urine at baseline (before treatment start) and after 6 months of treatment
- Secondary Outcome Measures
Name Time Method Number of patients with serious adverse events From first intake of study drug up to 3 days after last administration of study drug Number of patients with treatment-emergent adverse event From first intake of study drug up to 3 days after last administration of study drug
Trial Locations
- Locations (27)
Med. Center Equita
🇧🇬Varna, Bulgaria
TAYS TKI Keskus Tutkimusvastaanotto
🇫🇮Tampere, Finland
The Nazareth Trust Hospital EMMS
🇮🇱Nazareth, Israel
Shamir Medical Center (Assaf Harofeh)
🇮🇱Zerifin, Israel
Med Centre Diamedical 2013
🇧🇬Dimitrovgrad, Bulgaria
Barzilai Medical Center
🇮🇱Ashkelon, Israel
Hadassah Hebrew University Hospital Ein Kerem
🇮🇱Jerusalem, Israel
A.O.U. di Padova
🇮🇹Padova, Veneto, Italy
MCOMH Preventsia-2000
🇧🇬Stara Zagora, Bulgaria
Pihlajalinna ITE Kuopio
🇫🇮Kuopio, Finland
Turun yliopistollinen keskussairaala, kantasairaala
🇫🇮Turku, Finland
DMC - Diabetes Medical Center
🇮🇱Tel Aviv, Israel
Nordsjællands Hospital
🇩🇰Hillerød, Denmark
Steno Diabetes Center Copenhagen
🇩🇰Gentofte, Denmark
Rigshospitalet
🇩🇰København, Denmark
Terveystalo Oulu
🇫🇮Oulu, Finland
Edith Wolfson Medical Center
🇮🇱Holon, Israel
A.O.U. Policlinico Federico II Napoli
🇮🇹Napoli, Campania, Italy
IRCCS Casa Sollievo della Sofferenza
🇮🇹Foggia, Puglia, Italy
Univ. Alma Mater - Dip. Medicina Spec, Diagnostica e Sperim
🇮🇹Bologna, Emilia-Romagna, Italy
Complexo Hospitalario Universitario de Ferrol
🇪🇸Ferrol, A Coruña, Spain
Hospital de Galdakao
🇪🇸Galdakao, Vizcaya, Spain
Hospital Fundació Puigvert
🇪🇸Barcelona, Spain
Centralsjukhuset Kristianstad
🇸🇪Kristianstad, Sweden
S3 Clinical Research Centers
🇸🇪Vällingby, Sweden
Akardo MedSite AB
🇸🇪Stockholm, Sweden
Universitetssjukhuset Örebro
🇸🇪Örebro, Sweden