A Study to Find Out How EMPAgliflozin is Tolerated and if it Helps Children and Adolescents With Chronic KIDNEY Disease (EMPA-KIDNEY® Kids)
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Boehringer Ingelheim
- Study ID
- NCT07107945
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 2 Years - 17 Years
- Healthy Volunteers
- Not accepted
Interventions
- Empagliflozin — DRUGEmpagliflozin
- Placebo — DRUGPlacebo
Study Details
This study is open to children aged 2 to 17 with chronic kidney disease (CKD). The purpose of this study is to find out if a medicine called empagliflozin helps children and adolescents with CKD. Other goals of the study are to find out how empagliflozin is tolerated and handled by the body in children and adolescents with CKD. Participants are put into 2 groups randomly, which means by chance. One group takes empagliflozin and the other group takes placebo. Placebo looks like empagliflozin but does not contain any medicine. Participants are twice as likely to be in the empagliflozin group. Participants take empagliflozin or placebo as tablets once a day for 6 months. After 6 months, participants in both groups take empagliflozin as tablets once a day for 1 year. Participants are in the study for a little over a year and a half. During this time, they visit the study site about 15 times and get at least 5 phone or video calls from the site staff. At the visits, the doctors take blood and urine samples from the participants. The doctors also regularly check participants' health and take note of any unwanted effects.
Key Dates
- Start date
- Dec 9, 2025
- Status verified
- Jun 2026
- Primary completion
- Jun 26, 2028
- Completion
- Jun 25, 2029
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Empagliflozin treatment arm
- Placebo Comparator: Placebo arm
Primary Outcome Measure
Change from Day 1 to the Week 24 visit in urine albumin-creatinine (UACR) [mg/g] [ Time Frame: Up to week 24 ]
Central Contacts
- Boehringer Ingelheim1-800-243-0127
Locations (30)
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