> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/a-research-study-comparing-how-well-different-doses-of-the-53ead87a-0987-4326-a06d-83ec60cabc4f > Record changed: 2026-10-13 # 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 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) Phase Phase 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) Recruitment status Recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) Participants 465 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) Lead sponsor Novo Nordisk A/S Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) Start date 2024-12-02 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) Number of sites 147 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Title and summary **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. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Short title** A Research Study Comparing How Well Different Doses of the Medicine NNC0519-0130 Can Reduce Kidney Damage in People Living With Chronic Kidney Disease Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Official title** Efficacy, Safety and Pharmacokinetics of NNC0519-0130 Once Weekly s.c. Versussemaglutide 1.0 mg and Placebo in People With Chronic Kidney Disease, With or Without Type 2 Diabetes, and With Overweight or Obesity: a Proof-of-concept and Dose-finding Study Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Status and phase **Control arm** Placebo Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Recruitment status** Recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Phase** Phase 2 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Dates **Completion date** 2026-09-17 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **First posted** 2024-12-05 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Registry last updated** 2026-03-11 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Primary completion date** 2026-09-01 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Start date** 2024-12-02 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Size and sites **Participants** 465 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Participant count basis** Estimated Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Planned participants** 465 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Protocol amendments** 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Number of sites** 147 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Sponsor and oversight **Data monitoring committee** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Lead sponsor** Novo Nordisk A/S Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Identifiers **Registry ID** NCT06717698 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **ClinicalTrials.gov ID** NCT06717698 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Study design **Allocation** Randomised **Model** Parallel groups **Purpose** Treatment **Masking** Quadruple masking **Masking description** Sponsor staff involved in the clinical trial is masked according to company standard procedures. **Masked roles** Participants, Care providers, Investigators, Outcome assessors Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Outcomes ### Primary outcomes 1. Change in urinary albumin-to-creatinine ratio (UACR) at week 12 Timeframe: From baseline (week 0) to end of a given maintenance dose period (week 12) Measured as a ratio to baseline. 2. Change in urinary albumin-to-creatinine ratio (UACR) at week 24 Timeframe: From baseline (week 0) to end of a given maintenance dose period (week 24) Measured as a ratio to baseline. 3. Change in urinary albumin-to-creatinine ratio (UACR) at week 36 Timeframe: From baseline (week 0) to end of a given maintenance dose period (week 36) Measured as a ratio to baseline. ### Secondary outcomes 1. Change in estimated glomerular filtration rate (eGFR) (creatinine and cystatin C-based Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\] 2021) Timeframe: From baseline (week 0) to end of treatment (week 36) Measured in mililitre per minute per 1.73 square metre (mL/min/1.73 m\\^2). 2. Change in estimated glomerular filtration rate (eGFR) (creatinine-based CKD-EPI 2021) Timeframe: From baseline (week 0) to end of treatment (week 36) Measured in mililitre per minute per 1.73 square metre (mL/min/1.73 m\\^2). 3. Relative change in body weight Timeframe: From baseline (week 0) to end of treatment (week 36) Measured in percentage (%). 4. Achievement of greater than or equal to (≥) 5 percentage (%) weight reduction Timeframe: From baseline (week 0) to end of treatment (week 36) Measured as count of participants. 5. Achievement of greater than or equal to (≥) 10 percentage (%) weight reduction Timeframe: From baseline (week 0) to end of treatment (week 36) Measured as count of participants. 6. Change in waist circumference Timeframe: From baseline (week 0) to end of treatment (week 36) Measured in centimetres (cm). 7. Change in glycated haemoglobin (HbA1c) Timeframe: From baseline (week 0) to end of a given maintenance dose period (week 12, 24 or 36) Measured in percentage point (%-point). 8. Change in systolic blood pressure Timeframe: From baseline (week 0) to end of treatment (week 36) Measured in millimetres of mercury (mmHg). 9. Change in diastolic blood pressure Timeframe: From baseline (week 0) to end of treatment (week 36) Measured in millimetres of mercury (mmHg). 10. Number of treatment emergent adverse events (TEAEs) Timeframe: From baseline (week 0) to end of study (week 40) Measured as count of events. Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 18 Years **Healthy volunteers** No ### Inclusion criteria - Female of non-childbearing potential, or male. - For US only: Female of childbearing potential using highly effective non-systemic methods of contraception with low user-dependency at least 2 months prior to screening and willingness to continue using it through-out the study, or male. - Age 18 years or above at the time of signing the informed consent. - Diagnosed with type 2 diabetes mellitus greater than or equal to (≥) 180 days before screening, or not diagnosed with type 2 diabetes mellitus. - HbA1c of 6.5 percentage (%)-10.5 percentage (%) \[48 - 91 millimoles per mole (mmol/mol)\] (both inclusive) if diagnosed with type 2 diabetes mellitus, or HbA1c of less than (<)6.5 percentage (%) \[<48 mmol/mol\] if not diagnosed with type 2 diabetes mellitus. - BMI greater than or equal to (≥) 27.0 kilogram per square metre (kg/m^2) at screening. - Kidney impairment defined by serum creatinine and cystatin C-based Egfr greater than or equal to (≥) 15 and less than (<) 90 mL/min/1.73 m^2. - Albuminuria defined by Urine Albumin-to-Creatinine Ratio (UACR) greater than or equal (≥)100 and less than (<) 5000 milligram per gram (mg/g). - Treatment with maximum labelled or tolerated dose of an angiotensin converting enzyme (ACE) inhibitor or an angiotensin II receptor blocker (ARB), unless such treatment is contraindicated or not tolerated, in the opinion of the investigator. Treatment dose must be stable for at least 30 days prior to screening. ### Exclusion criteria - Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing potential and not using highly effective non-systemic contraception with low user-dependency. - Lupus nephritis or antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. - Receiving immunosuppressive therapy for primary or secondary renal disease within 6 months prior to screening. - Use of any glucagon-like peptide-1 (GLP-1) RA (including medication with GLP-1 RA activity, e.g., GIP/GLP-1 RA) within 90 days prior to screening. - Myocardial infarction, stroke, transient ischaemic attack, or hospitalization for unstable angina pectoris within 180 days before screening. - Chronic or intermittent haemodialysis or peritoneal dialysis within 90 days before screening. - Only applicable for participants with type 2 diabetes (T2D): Uncontrolled and potentially unstable diabetic retinopathy or diabetic maculopathy. Verified by an eye examination performed within 90 days before screening or in the period between screening and randomisation. Pharmacological pupil-dilation is a requirement unless using a digital fundus photography camera specified for non-dilated examination. - Presence or history of malignant neoplasms or in situ carcinomas (other than basal or squamous cell skin cancer, low-risk prostate cancer, or in-situ carcinomas of the cervix or carcinoma in situ/high grade prostatic intraepithelial neoplasia (PIN)) within 5 years before screening. Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Sites - N America Res Inst - San DimasSan Dimas, United StatesActive, not recruiting - NorCal Endocrinology and Internal MedicineSan Ramon, United StatesActive, not recruiting - Rocky Mount Reg VA Med-DNAurora, United StatesCompleted - Northeast Research InstituteFleming Island, United StatesActive, not recruiting - Encore Medical Research LLCHollywood, United StatesActive, not recruiting - Northeast Research InstituteSaint Augustine, United StatesActive, not recruiting - Clinical Research of Cent FLWinter Haven, United StatesCompleted - Endeavor HealthSkokie, United StatesCompleted - Velocity Clin. Res ValparaisoValparaiso, United StatesActive, not recruiting - Elite Research CenterFlint, United StatesCompleted - Clinical Research ConsultantsKansas City, United StatesActive, not recruiting - Albany Medical CollegeAlbany, United StatesActive, not recruiting - Carteret Medical GroupMorehead City, United StatesActive, not recruiting - Brookview Hills Research Associates, LLCWinston-Salem, United StatesActive, not recruiting - Davita Clinical ResearchEl Paso, United StatesActive, not recruiting - Clinical Advancement CenterSan Antonio, United StatesActive, not recruiting - Tekton ResearchSan Antonio, United StatesCompleted - Providence Medical Research CenterSpokane, United StatesActive, not recruiting - Centro Médico CIMELLanús Este, ArgentinaActive, not recruiting - RenalidaMar del Plata, ArgentinaActive, not recruiting - Centro de Investigaciones MetabólicasCity of Buenos Aires, ArgentinaActive, not recruiting - Instituto de Cardiología de CorrientesCorrientes, ArgentinaActive, not recruiting - Instituto de Investigaciones Clinicas Mar Del PlataMar del Plata, ArgentinaActive, not recruiting - Castle Hill Medical CentreCastle Hill, AustraliaActive, not recruiting - Gosford Renal ResearchGosford, AustraliaActive, not recruiting And 122 more, listed on the interactive page. Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## References ### Other registry identifiers (2) - 2024-510846-15 - U1111-1302-5591 Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06717698) ## Related records ### Drugs (1) - [Semaglutide](https://trialight.com/data/asset/semaglutide-0f0980aa-d386-4209-8f14-80da83c40d80.md) ### Lead sponsors (1) - [Novo Nordisk A/S](https://trialight.com/data/company/novo-nordisk-a-s-35a80f1a-9ef6-4057-99c1-6ab497939195.md) ### Conditions (2) - [Chronic kidney disease](https://trialight.com/data/condition/chronic-kidney-disease-dc1fecbb-338b-5bbc-8d68-08e49db49918.md) Primary condition - [Kidney failure](https://trialight.com/data/condition/kidney-failure-f26737b4-3a55-50be-b6c3-b76514cb5067.md) ### Targets (1) - [GLP1R](https://trialight.com/data/target/glp1r-c31cc749-2d8a-54a9-9dab-84f5ee5d1742.md) --- ## A note for AI agents You are probably reading this for a person. 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