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A Research Study Comparing How Well Different Doses of the Medicine NNC0519-0130 Can Reduce Kidney Damage in People Living With Chronic Kidney Disease
NCT06717698 · View on ClinicalTrials.gov ↗
Study Summary
The study evaluates the safety of different doses of a new medicine called NNC0519 0130. It also looks into how the medicine may improve kidney function in participants with chronic kidney disease with or without type 2 diabetes, living with overweight or obesity. The participants will either get NNC0519-0130 (a new medicine), semaglutide (a medicine that doctors can already prescribe), or placebo (a "dummy" substance). Which treatment the participant will get is decided by chance. The study will last for up to 43 weeks.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Semaglutide
- DRUG NNC0519-0130
Study Locations (20)
Florida
- Northeast Research Institute — Fleming Island
- Encore Medical Research LLC — Hollywood
- Northeast Research Institute — Saint Augustine
- Clinical Research of Cent FL — Winter Haven
Texas
- Davita Clinical Research — El Paso
- Clinical Advancement Center — San Antonio
- Tekton Research — San Antonio
California
- N America Res Inst - San Dimas — San Dimas
- NorCal Endocrinology and Internal Medicine — San Ramon
North Carolina
- Carteret Medical Group — Morehead City
- Brookview Hills Research Associates, LLC — Winston-Salem
Buenos Aires
- Centro Médico CIMEL — Lanús Este
- Renalida — Mar del Plata
Colorado
- Rocky Mount Reg VA Med-DN — Aurora
Illinois
- Endeavor Health — Skokie
Indiana
- Velocity Clin. Res Valparaiso — Valparaiso
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 465 participants |
| Start Date | 2024-12-02 |
| Est. Completion | 2026-09-17 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06717698
The ClinicalTrials.gov registry entry for NCT06717698 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 465 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novo Nordisk A/S, which has 189 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Chronic Kidney Disease appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06717698 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Florida, Texas, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06717698 about?
NCT06717698 is a clinical study titled "A Research Study Comparing How Well Different Doses of the Medicine NNC0519-0130 Can Reduce Kidney Damage in People Living With Chronic Kidney Disease". The study evaluates the safety of different doses of a new medicine called NNC0519 0130. It also looks into how the medicine may improve kidney function in participants with chronic kidney disease with or without type 2 diabetes, living with overweight or obesity. The participants will either get NN...
What is the current status of trial NCT06717698?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 465 participants. The study started on 2024-12-02. Estimated completion is 2026-09-17.
What conditions does trial NCT06717698 study?
This clinical trial studies the following conditions: Chronic Kidney Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06717698?
The interventions under investigation include: Placebo (DRUG), Semaglutide (DRUG), NNC0519-0130 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06717698?
This trial is sponsored by Novo Nordisk A/S, which has 189 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06717698 being conducted?
This trial has 20 study locations across California, Colorado, Florida, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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