CClinicalTrials.gg
RecruitingNCT07253285Updated Sep 30, 2026

A Research Study on How Well Cagrilintide and CagriSema Work in Children and Adolescents With Excess Body Weight

A Phase 3 interventional study of Cagrilintide and Semaglutide in Overweight and Obesity, sponsored by Novo Nordisk A/S. Recruiting at 121 sites in 26 countries. Open to participants aged 8 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by Novo Nordisk A/S · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
460
Allocation
Randomized
Ages
8 Years to 18 Years
Sex
All
01

Study summary

This study will look at how well CagriSema and cagrilintide help children and adolescents with excess body weight lose weight. The study has 2 parts: main and extension study. In the main study, participants will either get CagriSema (a new study drug), cagrilintide (a new study drug), semaglutide (a drug that doctors can already prescribe to adolescents and adults) or placebo (a placebo looks like the treatment being tested, but doesn't have any active ingredients in it). Which treatment participants will get is decided by chance. Participants who get semaglutide in the main study will not take part in the extension study. If participants take part in the extension study, they will get either CagriSema or cagrilintide in this part of the study. Like all drugs, the study drugs may have side effects. The total time participants will be in the main study is about 1 year and 6 months. If participants take part in the extension study, the total time is about 4 years and 10 months.

02

Conditions studied

  • Overweight
  • Obesity
03

Who can participate

Ages eligible
8 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion criteria:

  • Informed consent of parent(s) or legally acceptable representative (LAR) of participant and child assent, as age-appropriate, obtained before any study related activities. Study related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study.
  • The parent(s) or LAR of the child must sign and date the Informed Consent Form (according to local requirements)
  • The child must sign and date the Child Assent Form or provide oral assent (according to local requirements).
  • Male or female.
  • Aged 8 to less than (\<) 18 years at the time of signing the informed consent.
  • Body mass index (BMI), at screening, corresponding to:
  • Greater than or equal to (>=) 95th percentile for children aged 8 to \< 12 years (Tanner stage 1-5)
  • >= 95th percentile or >= 85th percentile with the presence of at least one obesity-related complication including, but not limited to, type 2 diabetes (T2D), hypertension, dyslipidaemia or obstructive sleep apnoea for adolescents aged 12 to \< 18 years (Tanner stage 2-5).
  • Laboratory parameters, as measured by the central lab at screening, within normal sex- and age-specific ranges of total calcium, phosphate, alkaline phosphatase, parathyroid hormone.
  • History of at least one unsuccessful effort to lose sufficient body weight after participation in a structured lifestyle modification programme (diet and exercise counselling) for at least 3 months.
  • Body weight greater than (>) 45 kilograms (kg) at screening.

For participants with T2D at screening the following inclusion criteria also apply

  • Glycated haemoglobin (HbA1c) less than or equal to (\<=)10.0 percent (%) (86 millimoles per mole [mmol/mol]) as measured by central laboratory at screening.
  • Treatment with lifestyle intervention or treatment with metformin according to local label.
  • Treatment with metformin should be stable (same dose and dosing frequency) for at least 56 days before screening.

Key exclusion criteria:

  • Treatment with any medication prescribed for obesity or weight management within 90 days before screening.
  • Previous or planned (during the study period) obesity treatment with surgery or a weight loss device. However, the following are allowed:
  • Liposuction and/or abdominoplasty, if performed > 1 year before screening.
  • Adjustable gastric banding, if the band has been removed > 1 year before screening.
  • Intragastric balloon, if the balloon has been removed > 1 year before screening.
  • Duodenal-jejunal bypass liner (e.g., Endobarrier), if the sleeve has been removed >1 year before screening.
  • Uncontrolled thyroid disease.
  • Endocrine, hypothalamic, or syndromic obesity.
  • A self-reported (or by parent(s)/LAR, where applicable) change in body weight > 5 % within 90 days before screening irrespective of medical records.
  • Type 1 diabetes or monogenic diabetes. For participants without T2D at screening the following exclusion criteria also apply
  • HbA1c greater than or equal to 6.5% (48 mmol/mol) as measured by the central laboratory at screening.
  • Treatment with glucose-lowering agent(s) prescribed for the indication of diabetes or pre-diabetes within 90 days before screening.

For participants with T2D at screening the following exclusion criteria also apply

  • Known hypoglycaemic unawareness as indicated by the investigator according to Clarke's questionnaire.
  • Recurrent severe hypoglycaemic episodes within 1 year before screening, as judged by the investigator.
  • Positive insulinoma associated protein-2 (IA-2) antibodies or anti-glutamic acid decarboxylase (anti-GAD) antibodies.
  • Treatment with any medication for the indication of diabetes other than those stated in the inclusion criteria within 90 days before screening.
  • Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. Verified by a fundus 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.
04

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
460 participants (estimated)

Study arms

  • Experimental
    CagriSema

    Participants will receive once weekly subcutaneous (s.c.) dose of CagriSema (cagrilintide and semaglutide) in a dose escalation regimen in the main phase for up to 16 weeks and maintained for 52 weeks and further continue to receive the same dose or maximum tolerated dose (MTD) in the open-label extension phase for up to 156 weeks.

    Drug: Cagrilintide · Drug: Semaglutide · Drug: Placebo cagrilintide · Drug: Placebo semaglutide

  • Experimental
    Semaglutide

    Participants will receive once weekly s.c. dose of semaglutide in a dose escalation regimen in the main phase for up to 16 weeks and maintained for 52 weeks.

    Drug: Semaglutide · Drug: Placebo semaglutide

  • Experimental
    Cagrilintide

    Participants will receive once weekly s.c. dose of cagrilintide in a dose escalation regimen in the main phase for up to 16 weeks and maintained for 52 weeks, further continue to receive the same dose as the dose escalation regimen or MTD in the open-label extension phase for up to 156 weeks.

    Drug: Cagrilintide · Drug: Placebo cagrilintide

  • Placebo comparator
    Placebo

    Participants will receive once weekly s.c. dose of placebo matched to cagrilintide/semaglutide in a dose escalation regimen in the main phase for up to 16 weeks and maintained for 52 weeks. Participants will further continue to receive the same dose escalation regimen as CagriSema for 16 weeks, later continue to receive the same dose or MTD in the open-label extension phase for up to 140 weeks.

    Drug: Placebo cagrilintide · Drug: Placebo semaglutide

Interventions

  • DrugCagrilintide

    Participants will receive cagrilintide subcutaneously.

  • DrugSemaglutide

    Participants will receive semaglutide subcutaneously.

  • DrugPlacebo cagrilintide

    Participants will receive placebo matched to cagrilintide subcutaneously.

  • DrugPlacebo semaglutide

    Participants will receive placebo matched to semaglutide subcutaneously.

05

What researchers measure

Primary outcomes

  1. Relative change in body mass index (BMI)

    Measured in percentage (%).

    Time frame: Baseline (week 0), week 68

Secondary outcomes

  1. Relative change in body weight

    Measured in %.

    Time frame: Baseline (week 0), week 68

  2. Change in BMI Standard Deviation Score (SDS)

    Measured as SDS score.

    Time frame: Baseline (week 0), week 68

  3. Relative change in BMI

    Measured in %.

    Time frame: Baseline (week 0), week 68 and week 224

  4. Number of participants in weight category reduction

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  5. Number of participants who achieved greater than or equal to (>=) 5 percent (%) reduction of body weight (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  6. Number of participants who achieved >=10% reduction of body weight (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  7. Number of participants who achieved >=15% reduction of body weight (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  8. Number of participants who achieved >=20% reduction of body weight (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  9. Number of participants who achieved >=25% reduction of body weight (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  10. Number of participants who achieved >=5% reduction of BMI (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  11. Number of participants who achieved >=10% reduction of BMI (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  12. Number of participants who achieved >=15% reduction of BMI (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  13. Number of participants who achieved >=20% reduction of BMI (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  14. Number of participants who achieved >=25% reduction of BMI (yes/no)

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  15. Number of participants who achieved normal BMI

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  16. Number of participants who shifted from obese to non-obese BMI class

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  17. Change in waist circumference

    Measured in centimeter (cm).

    Time frame: Baseline (week 0), week 68 and week 224

  18. Change in waist-to-height ratio

    Measured as ratio.

    Time frame: Baseline (week 0), week 68

  19. Absolute change in total fat mass by dual energy X-ray absorption (DXA)

    Measured in kilograms (kg).

    Time frame: Baseline (week 0), week 68

  20. Relative to baseline change in total fat mass by DXA

    Measured in %.

    Time frame: Baseline (week 0), week 68

  21. Relative to total body mass change in total fat mass by DXA

    Measured in % points.

    Time frame: Baseline (week 0), week 68

  22. Absolute change in visceral fat mass by DXA

    Measured in kg.

    Time frame: Baseline (week 0), week 68

  23. Relative to baseline change in visceral fat mass by DXA

    Measured in %.

    Time frame: Baseline (week 0), week 68

  24. Relative to total body mass change in visceral fat mass by DXA

    Measured in % points.

    Time frame: Baseline (week 0), week 68

  25. Absolute change in lean body mass by DXA

    Measured in kg.

    Time frame: Baseline (week 0), week 68

  26. Relative to total body mass change in lean body mass by DXA

    Measured in % points.

    Time frame: Baseline (week 0), week 68

  27. Absolute change in total (neck-to-knee) muscle and fat volumes by Magnetic Resonance Imaging (MRI) - total muscle and total fat

    Measured in liters (L).

    Time frame: Baseline (week 0), week 68 and week 224

  28. Relative to baseline change in total (neck-to-knee) muscle and fat volumes by MRI - total muscle and total fat

    Measured in %.

    Time frame: Baseline (week 0), week 68 and week 224

  29. Change in ectopic fat content by MRI - liver fat MRI-Proton Density Fat Fraction (MRI-PDFF), pancreatic fat, kidney fat and thigh muscle fat infiltration

    Measured in % points.

    Time frame: Baseline (week 0), week 68 and week 224

  30. Absolute change in abdominal fat volumes by MRI - subcutaneous fat and visceral fat

    Measured in liters.

    Time frame: Baseline (week 0), week 68 and week 224

  31. Relative to baseline change in abdominal fat volumes by MRI - subcutaneous fat and visceral fat

    Measured in %.

    Time frame: Baseline (week 0), week 68 and week 224

  32. Absolute change in thigh muscle and fat volumes by MRI - thigh fat free muscle and thigh subcutaneous fat

    Measured in liters.

    Time frame: Baseline (week 0), week 68 and week 224

  33. Relative to baseline change in thigh muscle and fat volumes by MRI - thigh fat free muscle and thigh subcutaneous fat

    Measured in %.

    Time frame: Baseline (week 0), week 68 and week 224

  34. Ratio to baseline in liver stiffness measured by Magnetic Resonance Elastography (MRE)

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  35. Change in BMI percentage of the 95th percentile

    Measured in % points.

    Time frame: Baseline (week 0), week 68

  36. Ratio to baseline highly sensitive C-reactive protein (hs-CRP)

    Measured as ratio.

    Time frame: Baseline (week 0), week 68

  37. Ratio to baseline in lipids: Total cholesterol

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  38. Ratio to baseline in lipids: High Density Lipoprotein (HDL) cholesterol

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  39. Ratio to baseline in lipids: Low Density Lipoprotein (LDL) cholesterol

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  40. Ratio to baseline in lipids: Very Low Density Lipoprotein (VLDL) cholesterol

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  41. Ratio to baseline in lipids: Triglycerides

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  42. Ratio to baseline in lipids: Non-HDL cholesterol

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  43. Change in Alanine Transaminase (ALT)

    Measured in Units per Liter (U/L).

    Time frame: Baseline (week 0), week 68 and week 224

  44. Change in systolic blood pressure

    Measured in millimeters of mercury (mmHg).

    Time frame: Baseline (week 0), week 68 and week 224

  45. Change in diastolic blood pressure

    Measured in mmHg.

    Time frame: Baseline (week 0), week 68 and week 224

  46. Ratio to baseline in liver stiffness measured by ultrasonographic methods

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  47. Change in glycated haemoglobin (HbA1c) (% points)

    Measured in % points.

    Time frame: Baseline (week 0), week 68 and week 224

  48. Change in HbA1c (millimoles per mole [mmol/mol])

    Measured in mmol/mol.

    Time frame: Baseline (week 0), week 68 and week 224

  49. Change in Fasting Plasma Glucose (FPG) (millimoles per liter [mmol/L])

    Measured in mmol/L.

    Time frame: Baseline (week 0), week 68

  50. Change in FPG (milligrams per deciliter [mg/dL])

    Measured in mg/dL.

    Time frame: Baseline (week 0), week 68

  51. Ratio to baseline in fasting serum insulin

    Measured as ratio.

    Time frame: Baseline (week 0), week 68 and week 224

  52. Number of participants with prediabetes who achieved HbA1c less than (<) 5.7% (defined as 5.7 % less than or equal to [<=] HbA1c <6.5 %) at baseline

    Measured as count of participants.

    Time frame: At week 68

  53. Number of participants with normoglycemia (defined as HbA1c < 5.7 %) at baseline, development of HbA1c greater than or equal to (>=) 5.7 %

    Measured as count of participants.

    Time frame: At week 68

  54. Number of participants with prediabetes (5.7 % <= HbA1c < 6.5 %) at baseline, development of HbA1c >= 6.5%

    Measured as count of participants.

    Time frame: At week 68

  55. Number of participants with HbA1c >=6.5% at baseline, achievement of HbA1c <6.5%

    Measured as count of participants.

    Time frame: At week 68

  56. Number of participants taking glucose lowering medication at baseline, stop or decrease

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  57. Number of participants taking antihypertensive medication at baseline, stop or decrease

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  58. Number of participants taking lipid lowering medication at baseline, stop or decrease

    Measured as count of participants.

    Time frame: Baseline (week 0), week 68

  59. Impact of Weight on Quality of Life-Kids (IWQOL Kids) - Physical comfort domain score

    Measured as score points. IWQOL-Kids measures weight-related quality of life in adolescents (ages 11-19 years) but will be administered to all study participants. The measure consists of 27-items yielding 4 sub-scale scores, and 1 total score. Higher scores indicate better weight-related quality of life. Subscale scores (score range): physical comfort (0-100), body esteem (0-100), social life (0-100), family relations (0-100) and total score (0-100).

    Time frame: Baseline (week 0), week 68 and week 224

  60. IWQOL Kids - Body esteem domain score

    Measured as score points. IWQOL-Kids measures weight-related quality of life in adolescents (ages 11-19 years) but will be administered to all study participants. The measure consists of 27-items yielding 4 sub-scale scores, and 1 total score. Higher scores indicate better weight-related quality of life. Subscale scores (score range): physical comfort (0-100), body esteem (0-100), social life (0-100), family relations (0-100) and total score (0-100).

    Time frame: Baseline (week 0), week 68 and week 224

  61. IWQOL Kids - Social life domain score

    Measured as score points. IWQOL-Kids measures weight-related quality of life in adolescents (ages 11-19 years) but will be administered to all study participants. The measure consists of 27-items yielding 4 sub-scale scores, and 1 total score. Higher scores indicate better weight-related quality of life. Subscale scores (score range): physical comfort (0-100), body esteem (0-100), social life (0-100), family relations (0-100) and total score (0-100).

    Time frame: Baseline (week 0), week 68 and week 224

  62. IWQOL Kids - Family-relations score

    Measured as score points. IWQOL-Kids measures weight-related quality of life in adolescents (ages 11-19 years) but will be administered to all study participants. The measure consists of 27-items yielding 4 sub-scale scores, and 1 total score. Higher scores indicate better weight-related quality of life. Subscale scores (score range): physical comfort (0-100), body esteem (0-100), social life (0-100), family relations (0-100) and total score (0-100).

    Time frame: Baseline (week 0), week 68 and week 224

  63. IWQOL Kids - Total score

    Measured as score points. IWQOL-Kids measures weight-related quality of life in adolescents (ages 11-19 years) but will be administered to all study participants. The measure consists of 27-items yielding 4 sub-scale scores, and 1 total score. Higher scores indicate better weight-related quality of life. Subscale scores (score range): physical comfort (0-100), body esteem (0-100), social life (0-100), family relations (0-100) and total score (0-100).

    Time frame: Baseline (week 0), week 68 and week 224

  64. Control of Eating Questionnaire (COEQ)

    Measured as score points. CoEQ is a 19-item multidimensional patient reported outcome (PRO) that assesses the experience of hunger, satiety, and severity and type of food cravings. CoEQ consists of 4 subscales that measure craving control (5 items), positive mood (4 items), craving for sweet (4 items), craving for savoury food (4 items), and 2 single items that address hunger and satiety. Each item is evaluated on a 0-10 (i.e., 11-point) numeric rating scale. The total score for each subscale is calculated as the sum of the item scores divided by the number of items in the subscale. Scores ranges are thus: Craving Control 0-50/5 = 0-10); Positive Mood (0-40/4 = 0-10); Craving Sweet (0-40/4 = 0-10); Craving Savoury food (0-40/4 = 0-10); single items that address hunger and satiety (0-10). For the craving control subscale, the subscale score is reversed so that a higher score represents a greater level of craving control.

    Time frame: Baseline (week 0), week 68 and week 224

  65. Change in proteomics-based serum biomarkers including biomarkers for metabolic dysfunction-associated steatohepatitis (MASH)

    Measured as counts.

    Time frame: Baseline (week 0), week 68 and week 224

  66. Number of treatment-emergent adverse events (TEAEs)

    Measured as count of events.

    Time frame: Baseline (week 0), week 68 and week 224

  67. Number of treatment-emergent serious adverse events (TESAEs)

    Measured as count of events.

    Time frame: Baseline (week 0), week 68 and week 224

  68. Number of treatment-emergent hypoglycaemic episodes

    Measured as count of events.

    Time frame: Baseline (week 0), week 68 and week 224

  69. Change in pulse rate

    Measured in beats per minute (beats/min).

    Time frame: Baseline (week 0), week 68

  70. Change in calcitonin

    Measured in nanograms per liter (ng/L).

    Time frame: Baseline (week 0), week 68

  71. Apparent clearance (CL/F) of semaglutide and cagrilintide at steady state

    Measured in liters per hour (L/h).

    Time frame: Baseline (week 0), week 68

  72. Average concentration (Cavg) of semaglutide and cagrilintide at steady state

    Measured in nanomoles per liter (nmol/L).

    Time frame: Baseline (week 0), week 68

  73. Area under the steady-state concentration-time curves (AUCt) in the dosing interval of semaglutide and cagrilintide

    Measured in hours nanomoles per liter (h·nmol/L).

    Time frame: Baseline (week 0), week 68

06

Study locations

65 of 121 sites recruiting
  • Neighborhood Healthcare
    Escondido, California 92025, United States
    Recruiting
  • Encore Medical Research LLC
    Hollywood, Florida 33024, United States
    Recruiting
  • Jacksonville Ctr for Clin Res
    Jacksonville, Florida 32216, United States
    Recruiting
  • Encore Medical Research of Weston
    Weston, Florida 33331, United States
    Recruiting
  • Children's Healthcare Atlanta
    Atlanta, Georgia 30329, United States
    Recruiting
  • Columbus Research Foundation
    Columbus, Georgia 31904, United States
    Recruiting
  • Accel Research Sites-NeuroStudies
    Decatur, Georgia 30030, United States
    Recruiting
  • Eastside Bariatric and Gen Surg
    Snellville, Georgia 30078, United States
    Recruiting
  • Solaris Clinical Research
    Meridian, Idaho 83646, United States
    Recruiting
  • IU Health - Riley Physicians Endo-Diab
    Indianapolis, Indiana 46202, United States
    Recruiting
  • Cotton O'Neil Clinical Research Center
    Topeka, Kansas 66606, United States
    Recruiting
  • Pennington Biomed Res Ctr
    Baton Rouge, Louisiana 70808-4124, United States
    Recruiting
  • Barry J. Reiner, MD LLC
    Baltimore, Maryland 21229, United States
    Recruiting
  • University of Minnesota
    Minneapolis, Minnesota 55455, United States
    Recruiting
  • Synexus Clinical Research US-MN
    Richfield, Minnesota 55423, United States
    Recruiting
  • UBMD Physicians Group - Pediatrics - Conventus
    Buffalo, New York 14203, United States
    Not yet recruiting
  • SUNY Upstate Medical Univ - Syracuse
    Syracuse, New York 13210, United States
    Recruiting
  • Advantage Clinical Trials
    The Bronx, New York 10467, United States
    Not yet recruiting
  • Valley Weight Loss Clinic
    Fargo, North Dakota 58104, United States
    Recruiting
  • Centricity Research - Ohio
    Columbus, Ohio 43213, United States
    Recruiting
  • PriMed Clinical Research
    Dayton, Ohio 45429, United States
    Recruiting
  • Children's Physicians OU
    Oklahoma City, Oklahoma 73104, United States
    Not yet recruiting
  • UPMC Child Hosp-Pittsburgh
    Pittsburgh, Pennsylvania 15224, United States
    Not yet recruiting
  • Prisma Health-Ped Endo
    Greenville, South Carolina 29615, United States
    Not yet recruiting
  • Coastal Carolina Research Ctr
    North Charleston, South Carolina 29405, United States
    Recruiting
  • Monument Health Clinical Rsrch
    Rapid City, South Dakota 57701, United States
    Not yet recruiting
  • LifeDoc Health
    Memphis, Tennessee 38115, United States
    Recruiting
  • DM Clinical
    Houston, Texas 77065, United States
    Recruiting
  • DM Clinical
    San Antonio, Texas 78207, United States
    Not yet recruiting
  • The Texas Liver Institute
    San Antonio, Texas 78215, United States
    Recruiting
  • Pinnacle Clinical Research
    San Antonio, Texas 78222, United States
    Recruiting
  • Consano Clin Res-Shavano Park
    Shavano Park, Texas 78231, United States
    Recruiting
  • Texas Valley Clinical Research
    Weslaco, Texas 78596, United States
    Recruiting
  • AMR Clinical
    Layton, Utah 84041, United States
    Recruiting
  • The Children's Hospital at Westmead - Clinical Research Centre
    Westmead, New South Wales 2145, Australia
    Recruiting
  • Queensland Children's Hospital
    South Brisbane, Queensland 4101, Australia
    Recruiting
  • Perth Children's Hospital
    Nedlands, Western Australia 6009, Australia
    Recruiting
  • Universitätsklinik Kinder-Jugendheilkunde Innsbruck
    Innsbruck, 6020, Austria
    Recruiting
  • Universitätsklinik für Kinder und Jugendheilkunde Haus E
    Salzburg, 5020, Austria
    Recruiting
  • UZ Brussel - Universitair Ziekenhuis Brussel
    Brussels, 1090, Belgium
    Recruiting
  • UZA - Universitair Ziekenhuis Antwerpen
    Edegem, 2650, Belgium
    Recruiting
  • UMHAT Sveti Georgi EAD, Plovdiv, Clinic of Pediatrics
    Plovdiv, 4001, Bulgaria
    Recruiting
  • SHATPD - Prof. Ivan Mitev EAD, Pediatric Endocrinology and Metabolic Diseases
    Sofia, 1606, Bulgaria
    Recruiting
  • Medical center Children's Health EOOD
    Sofia, 1618, Bulgaria
    Not yet recruiting
  • UMHAT Sveta Marina EAD, First Pediatric Clinic
    Varna, 9010, Bulgaria
    Recruiting
  • Capital Center for Children's Health, Capital Medical University-Endocrinology
    Beijing, Beijing Municipality 100020, China
    Recruiting
  • Beijing Children's Hospital, Capital Medical University
    Beijing, Beijing Municipality 100045, China
    Not yet recruiting
  • Henan Children's Hospital Zhengzhou Children's Hospital-Endocrine Genetics and Metabolism
    Zhengzhou, Henan 450018, China
    Recruiting
  • Wuhan Children Hospital-Endocrine Genetics and Metabolism
    Wuhan, Hubei 430019, China
    Recruiting
  • Tongji Hospital, Tongji Medical College, Huazhong University of Science & Technology-Pediatric
    Wuhan, Hubei 430030, China
    Recruiting
  • The First Bethune Hospital of Jilin University-Pediatric
    Changchun, Jilin 130021, China
    Not yet recruiting
  • Shandong Provincial Hospital-Pediatric
    Jinan, Shandong 250098, China
    Recruiting
  • Children's Hospital of Fudan University-Endocrinology and Metabolism
    Shanghai, Shanghai Municipality 201102, China
    Recruiting
  • Chengdu Women's and Children's Central Hospital- Pediatric Endocrinology, Genetics and Metabolism
    Chengdu, Sichuan 610031, China
    Recruiting
  • Servicios de Salud Ips Suramericana S.A.S.
    Medellín, Antioquia 05001, Colombia
    Not yet recruiting
  • Fundación Santa Fe de Bogotá
    Bogotá, 110111, Colombia
    Not yet recruiting
  • Clinical Hospital Centre Rijeka_Pediatric
    Rijeka, 51 000, Croatia
    Not yet recruiting
  • KBC "Sestre Milosrdnice"
    Zagreb, 10 000, Croatia
    Not yet recruiting
  • Klinika Za Djecje Bolesti Zagreb_Endocrinology
    Zagreb, 10000, Croatia
    Not yet recruiting
  • Aalborg Universitetshospital - Børne og Ungeafdelingen
    Aalborg, 9000, Denmark
    Not yet recruiting
  • Holbæk Sygehus - Børne- og Ungeafdelingen
    Holbæk, 4300, Denmark
    Recruiting
  • Észak-Közép-budai Centrum, Szent János Kórház és Szakrendelő
    Budapest, 1023, Hungary
    Recruiting
  • Semmelweis Egyetem ÁOK
    Budapest, 1083, Hungary
    Not yet recruiting
  • Szegedi Tudományegyetem Gyermekgyógyászati Klinika
    Szeged, 6720, Hungary
    Not yet recruiting
  • Endolife Specialty Hospitals
    Guntur, Andhra Pradesh 522001, India
    Not yet recruiting
  • BAPS Pramukh Swami Hospital
    Surat, Gujarat 395009, India
    Not yet recruiting
  • Indira Gandhi Institute of child health
    Bangalore, Karnataka 560011, India
    Not yet recruiting
  • Sir Ganga Ram Hospital
    New Delhi, National Capital Territory of Delhi 110060, India
    Not yet recruiting
  • Maulana Azad Medical College
    Delhi, New Delhi 110002, India
    Not yet recruiting
  • Regency Hospital
    Kanpur, Uttar Pradesh 208006, India
    Not yet recruiting
  • Institute of Child Health
    Kolkata, West Bengal 700017, India
    Not yet recruiting
  • Excel Endocrine Centre
    Kolhāpur, 416008, India
    Not yet recruiting
  • All India Institute of Medical Sciences (AIIMS)
    New Delhi, 110029, India
    Not yet recruiting
  • Rambam MC - Department of Pediatrics A
    Haifa, 31096, Israel
    Not yet recruiting
  • Shaare Zedek MC - Endocrinology Department
    Jerusalem, 9103102, Israel
    Not yet recruiting
  • Schneider MC - Endrocrinology and Diabetes
    Petah Tikva, 49202, Israel
    Not yet recruiting
  • Shamir MC - Pediatric and Adolescents Endocrinology unit
    Ẕerifin, 7033001, Israel
    Not yet recruiting
  • Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico - UO Endocrinologia
    Milan, Lombardy 20122, Italy
    Not yet recruiting
  • AOU Maggiore della Carità di Novara - Dipartimento Interaziendale Strutturale Materno Infantile - SCDU Pediatria
    Novara, Piedmont 28100, Italy
    Not yet recruiting
  • A.O.U.I Verona - Ospedale Donna Bambino Borgo Trento - Pediatria B
    Verona, Veneto 37126, Italy
    Not yet recruiting
  • IRCCS materno infantile Burlo Garofolo - Clinica Pediatrica
    Trieste, 34137, Italy
    Not yet recruiting
  • Hospital Tunku Azizah
    Kampung Baru, Kuala Lumpur 50300, Malaysia
    Not yet recruiting
  • University Malaya Medical Centre
    Lembah Pantai, Kuala Lumpur 59100, Malaysia
    Recruiting
  • Hospital Sibu
    Sibu, Sarawak 96000, Malaysia
    Recruiting
  • CHRISTUS - Latam Hub Excellence and Innovation Center
    Monterrey, Nuevo León 64060, Mexico
    Not yet recruiting
  • IECSI Centro de Investigación Clínica
    Monterrey, Nuevo León 64310, Mexico
    Not yet recruiting
  • Consultorio de Endocrinología y Pediatría
    Puebla City, 72190, Mexico
    Not yet recruiting
  • Jeroen Bosch Zkh
    's-Hertogenbosch, 5223 GZ, Netherlands
    Not yet recruiting
  • Meander MC
    Amersfoort, 3813 TZ, Netherlands
    Completed
  • Samodzielny Zespol Publicznych Zakladow Opieki Zdrowotnej im. Dzieci Warszawy w Dziekanowie Lesnym
    Dziekanów Leśny, 05-092, Poland
    Not yet recruiting
  • Uniwersytecki Szpital Kliniczny w Opolu
    Opole, 45-401, Poland
    Not yet recruiting
  • Kliniczny Szpital Wojewodzki nr 2 im. Sw. Jadwigi Krolowej w Rzeszowie
    Rzeszów, 35-301, Poland
    Not yet recruiting
  • Samodzielny Publiczny Szpital Kliniczny Nr 1 im. Prof. Szyszko
    Zabrze, 41-800, Poland
    Not yet recruiting
  • ULS De Santo António, E.P.E. _CMIN_Serviço de Pediatria
    Porto, 4050-651, Portugal
    Not yet recruiting
  • CUF Porto_Serviço de Pediatria
    Porto, 4100-180, Portugal
    Not yet recruiting
  • ULS De Gaia/Espinho_H.Santos Silva_Unidade Ensaios Clínicos
    Vila Nova de Gaia, 4434-502, Portugal
    Not yet recruiting
  • Spitalul Judetean de Urgenta Dr. Constantin Opris Baia Mare
    Baia Mare, 430031, Romania
    Not yet recruiting
  • Kilostop Junior SRL
    Bucharest, 010073, Romania
    Recruiting
  • Spitalul Clinic de Urgenta pentru Copii "M.S.Curie"
    Bucharest, 041451, Romania
    Recruiting
  • Spitalul Clinic Judetean De Urgenta Pius Brinzeu Timisoara
    Timișoara, 300226, Romania
    Recruiting

Showing the first 100 of 121 sites across 26 countries.

07

References and documents

Individual participant data

Plan to share: Yes — According to the Novo Nordisk disclosure commitment on NovoNordisk trials.com.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07253285
Lead sponsor
Novo Nordisk A/S
Responsible party
Sponsor
First posted
Nov 28, 2025
Start date
Jan 8, 2026
Primary completion
Mar 20, 2030 (estimated)
Completion
Sep 20, 2033 (estimated)
Last update
Sep 30, 2026

Study contacts

Novo Nordisk
Contact
clinicaltrials@novonordisk.com
(+1) 866-867-7178
Clinical Transparency (dept. 2834)
study director · Novo Nordisk A/S

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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