This study is open to adults with chronic kidney disease at risk of progression. People with and without type 2 diabetes can take part in this study. The study is open to people who take other medicines called angiotensin converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARB). People who already take empagliflozin or any other sodium-glucose cotransporter-2 inhibitor (SGLT2i) can also join. The study is also open to people who currently do not take any of these treatments. The purpose of this study is to find out whether a medicine called BI 690517 helps people with chronic kidney disease when taken in combination with a study medicine called empagliflozin. Worsening of kidney function increases the risk for kidney failure, cardiovascular disease, and heart disease. This study has 2 parts. In the first part, participants get empagliflozin or placebo matching BI 690517 for at least 6 weeks. Participants continue taking ACEi or ARB throughout the study if such treatments are indicated. In the second part, participants are divided into 2 groups by chance. One group takes BI 690517 tablets and the other group takes placebo tablets. Placebo tablets look like BI 690517 tablets but do not contain any medicine. Participants take 1 tablet once a day in addition to empagliflozin for the duration of the study. The doctors document when participants experience worsening of their kidney disease, go to hospital due to heart failure, or die of cardiovascular problems during the study. The time to these events is compared between the 2 treatment groups to see whether the treatment works. The study continues until the required number of events have occurred which is about 3 to 4 years. During this time, participants visit the study site about 4 times within the first 6 months. Then they visit the study site every 6 months. At the visits, doctors regularly check participants' health, take blood and urine samples, measure blood pressure and weight, check kidney function, and take note of any unwanted effects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
11,000
Apogee Clinical Research
Huntsville, Alabama, United States
RECRUITINGSouthwest Kidney Institute
Surprise, Arizona, United States
RECRUITINGFlorida Kidney Physicians LLC
Jacksonville Beach, Florida, United States
RECRUITINGTotal Research Group, LLC
Miami, Florida, United States
Time to first occurrence of the primary composite outcome of: (i) Kidney disease progression*; or (ii) Hospitalization for heart failure; or (iii) Cardiovascular death.
Kidney disease progression is defined as kidney failure or a sustained decline of ≥40% in estimated Glomerular Filtration Rate (eGFR) from randomization
Time frame: up to 4 years
Key secondary outcome: Annual rate of change in eGFR from 3 month visit until last scheduled visit (i.e. chronic eGFR slope)
Time frame: up to 4 years
Time to first event of kidney failure, hospitalization for heart failure or cardiovascular death
Time frame: up to 4 years
Time to kidney disease progression
Time frame: up to 4 years
Occurrences of hospitalizations for heart failure (first and any subsequent, combined) or cardiovascular death
Time frame: up to 4 years
Occurrences of hospitalizations from any cause (first and any subsequent, combined)
Time frame: up to 4 years
Time to first event of kidney disease progression or cardiovascular death
Time frame: up to 4 years
Time to death from any cause
Time frame: up to 4 years
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East Coast Institute For Research LLC
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RECRUITINGKootenai Research Services
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RECRUITING...and 338 more locations