Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses of Tirzepatide 5 mg and 10 mg)
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| Pooled Doses of Tirzepatide (5 mg, 10 mg) | -2.03 | 0.165 |
| Placebo | -0.23 | 0.229 |
Trial · Interventional
CompletedPhase 3Results postedRegistry dataShort name SURPASS-PEDS
United States, Australia, Brazil, France, India, Israel, Italy, Mexico, United Kingdom
1 trial · 1 completed · 1 with posted results
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
The purpose of this study is to learn more about the safety and efficacy of tirzepatide compared to placebo in children or teenagers with type 2 diabetes taking metformin, or basal insulin, or both. The overall study will last about 60 weeks with up to 14 clinic visits and 6 phone visits. Clinic visits will include blood sample collection, physical exam and questionnaire.
Experimental
Tirzepatide Dose 1
Double-Blind: Participants receive Tirzepatide by weekly subcutaneous (SC) injection starting with a low dose then increase to a higher dose every four weeks until maintenance dose level 1 is reached. Open-Label: Participants will continue to receive Tirzepatide at the last dose level
Experimental
Tirzepatide Dose 2
Double-Blind: Participants receive Tirzepatide by weekly SC injection starting with a low dose then increase to a higher dose every four weeks until maintenance dose level 2 is reached. Open-Label: Participants will continue to receive Tirzepatide at the last dose level
Placebo comparator
Placebo
Double-Blind: Participants receive placebo during the 30-week double-blind period. Open-Label: Participants will switch to Tirzepatide by weekly SC injection starting with a low dose then increase to a higher dose every four weeks until maintenance dose level 1 is reached.
Outcomes the sponsor listed as primary.
Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses of Tirzepatide 5 mg and 10 mg)
Time frame · Baseline, Week 30
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Least Squares (LS) mean was determined by ANCOVA model for endpoint measures: Variable = Baseline + Baseline Antihyperglycemic medication + Baseline Age group + Treatment (Type III sum of squares)
Change From Baseline in HbA1c (Individual Doses)
Time frame · Baseline, Week 30
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. LS mean was determined by ANCOVA model for endpoint measures: Variable = Baseline + Baseline Antihyperglycemic medication + Baseline Age group + Treatment (Type III sum of squares).
Percentage of Participants Who Achieve ≤6.5% of HbA1c
Time frame · Week 30
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Imputed data includes observed value and imputed value if endpoint measure is missing.
Change From Baseline in Body Mass Index (BMI) Standard Deviation Score (Age and Sex-matched)
Time frame · Baseline, Week 30
BMI SDS (age and sex matched), calculated using the World Health Organization (WHO) growth reference standards. BMI is calculated as weight in kilograms divided by height in meters squared (kg/m²) and converted to a Z-score (SDS) based on WHO reference data. A Z-score of 0 represents the population mean for a given age and sex. A BMI SDS between -1 and +1 is considered normal. Obesity is defined as BMI SDS \> +2. Reductions in BMI SDS indicate improvement in weight status for individuals with obesity. LS mean was determined by the ANCOVA model for endpoint measures: Variable = Baseline + Baseline Antihyperglycemic medication + Baseline Age group + Treatment (Type III sum of squares)
Change From Baseline in Fasting Serum Glucose (FSG)
Time frame · Baseline, Week 30
LS mean was determined by ANCOVA model for endpoint measures: Variable = Baseline + Baseline Antihyperglycemic medication + Baseline Age group + Treatment (Type III sum of squares).
Percent Change From Baseline in BMI
Time frame · Baseline, Week 30
LS mean was determined by ANCOVA model for endpoint measures: Variable = Baseline + Baseline Antihyperglycemic medication + Baseline Age group + Treatment (Type III sum of squares).
Percentage of Participants Who Achieve <5.7% of HbA1c
Time frame · Week 30
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Imputed data includes observed value and imputed value if endpoint measure is missing.
Percentage of Participants Who Achieve <7.0% of HbA1c
Time frame · Week 30
HbA1c is the glycosylated fraction of hemoglobin A. HbA1c is measured primarily to identify average plasma glucose concentration over prolonged periods of time. Imputed data includes observed value and imputed value if endpoint measure is missing.
Percent Change From Baseline for Serum Lipid Levels
Time frame · Baseline, Week 30
Geometric LS mean was determined by the MMRM model for post-baseline measures: log(Actual Measurement/Baseline) = log(Baseline) + Baseline Antihyperglycemic medication + Baseline Age group + Treatment + Time + Treatment\*Time (Type III sum of squares). Variance-Covariance structure (Change from Baseline) = Unstructured.
Change From Baseline in Height Standard Deviation Score (SDS)
Time frame · Baseline, Week 30
Height SDS (age and sex-matched), calculated using the World Health Organization (WHO) growth reference standards. Height SDS is derived by comparing a child's height to the median height for their age and sex in the WHO reference population, then expressing the difference in standard deviation units (Z-scores). A Z-score of 0 represents the population mean. A Height SDS below -2 indicates short stature. Positive changes in Height SDS from baseline reflect improvement in growth velocity or catch-up growth. LS mean was determined by MMRM model for post-baseline measures: Variable = Baseline + Baseline Age group + Baseline Antihyperglycemic medication + Treatment + Time + Treatment\*Time(Type III sum of squares). Variance-Covariance structure (Actual Value) = Unstructured. Variance-Covariance structure (Change from Baseline) = Unstructured
Change From Baseline in Weight SDS
Time frame · Baseline, Week 30
Weight SDS, calculated using Centers for Disease Control and Prevention (CDC) growth reference standards. Weight SDS is derived by comparing a child's weight to median weight for their age and sex in the CDC reference population, then expressing the difference in standard deviation units (Z-scores). A Z-score of 0 represents the population mean for a given age and sex. A Weight SDS below -2 may indicate underweight status, while a Weight SDS above +2 may indicate overweight or obesity. Change from baseline Weight SDS reflects shifts in growth trajectory, with positive changes indicating weight gain and negative changes indicating weight reduction. LS mean was determined by MMRM model for post-baseline measures: Variable = Baseline + Baseline Age group + Baseline Antihyperglycemic medication + Treatment + Time + Treatment\*Time(Type III sum of squares). Variance-Covariance structure (Actual Value) = Unstructured. Variance-Covariance structure (Change from Baseline) = Unstructured
Change From Baseline in Pediatric Quality of Life Inventory (PedsQL) Generic Core Scale
Time frame · Baseline, Week 52
The PedsQL Measurement Model measures health-related quality of life (HRQOL) in children (ages 8 to 12) and teenagers (ages 13 to 18). The 23-item PedsQL Generic Core Scale includes physical, emotional, social, and school functioning dimensions. The PedsQL Generic Core yields two summary scores: Physical Summary and Psychosocial Summary. Scores are transformed on a 0-100 scale, with higher scores indicating better functioning. Each item is scored from 0 (never) to 4 (almost always). Items are reverse scored and linearly transformed to a 0-100 scale so that higher scores indicate better HRQOL; the total score therefore ranges from 0 (worst) to 100 (best). Higher scores indicate better health-related quality of life. LS mean was determined by the MMRM model for post-baseline measures: Variable = Baseline + Baseline Antihyperglycemic Medication + Baseline Age Group + Treatment + Time + Treatment\*Time (Type III sum of squares). Variance-Covariance structure (Actual Value) = Unstructured.
Change From Baseline PedsQL (3.2) Diabetic Module
Time frame · Baseline, Week 52
The PedsQL 3.2 Diabetes Module has 33 items for ages 13 years and older, and 32 items (1 less item for the Worry Scale) for ages 2 to 12 years. The 5 dimensions consist of diabetes symptoms (15 items), treatment barriers (5 items), treatment adherence (6 items), worry \[2 items (3 for teens and adults)\] and communication (4 items). Item scaling is a 5-point scale from 0 (never) to 4 (almost always). Items are reversed scored and linearly transformed to a 0-100 scale as follows: 0=100, 1=75, 2=50, 3=25, 4=0. Higher scores reflect fewer problems and better functioning. LS mean was determined by MMRM model for post-baseline measures: Variable = Baseline + Baseline Antihyperglycemic medication + Baseline Age group + Treatment + Time + Treatment\*Time(Type III sum of squares). Variance-Covariance structure (Actual Value) = Unstructured. Variance- Covariance structure (Change from Baseline) = Unstructured.
Population Pharmacokinetics (PopPK): Steady State Area Under the Concentration Curve (AUC) of Tirzepatide
Time frame · Week 0: after the first dose anytime on the same day. Weeks 7, 16, and 29: 1 to 24 hours, 24 to 96 hours, or 120 to 168 hours post-dose, as assigned by IWRS.
The steady-state AUCs were estimated from Tirzepatide concentrations at Weeks 0, 7, 16, and 29 using the population PK model by treatment group.
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| Pooled Doses of Tirzepatide (5 mg, 10 mg) | -2.03 | 0.165 |
| Placebo | -0.23 | 0.229 |
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -1.90 | 0.236 |
| 10 mg Tirzepatide | -2.16 | 0.232 |
| Placebo | -0.23 | 0.229 |
| Group | Value (percentage of participants) |
|---|---|
| 5 mg Tirzepatide | 66.4 |
| 10 mg Tirzepatide | 80.6 |
| Pooled Doses of Tirzepatide (5mg,10mg) | 73.6 |
| Placebo | 28.2 |
| Group | Value (Z-score) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -0.45 | 0.072 |
| 10 mg Tirzepatide | -0.76 | 0.072 |
| Pooled Doses of Tirzepatide (5mg,10mg) | -0.60 | 0.050 |
| Placebo | -0.09 | 0.069 |
| Group | Value (milligram per deciliter (mg/dL)) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -35.5 | 7.76 |
| 10 mg Tirzepatide | -50.6 | 7.40 |
| Pooled Doses of Tirzepatide (5mg,10mg) | -43.0 | 5.42 |
| Placebo | -6.6 | 7.36 |
| Group | Value (Percent Change of BMI) | Spread |
|---|---|---|
| 5 mg Tirzepatide | -6.73 | 1.155 |
| 10 mg Tirzepatide | -11.07 | 1.154 |
| Pooled Doses of Tirzepatide (5mg,10mg) | -8.90 | 0.808 |
| Placebo | -0.55 | 1.107 |
| Group | Value (percentage of participants) |
|---|---|
| 5 mg Tirzepatide | 44.1 |
| 10 mg Tirzepatide | 56.2 |
| Pooled Doses of Tirzepatide (5mg,10mg) | 50.2 |
| Placebo | 15.9 |
| Group | Value (percentage of participants) |
|---|---|
| 5 mg Tirzepatide | 79.6 |
| 10 mg Tirzepatide | 84.5 |
| Pooled Doses of Tirzepatide (5mg,10mg) | 82.1 |
| Placebo | 37.4 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| 5 mg Tirzepatide / Double-Blind PeriodParticipants received 5 mg of tirzepatide QW administered as SC injection via SDP for 30 weeks in a double-blind period. | 0 / 32 | 1 / 32 | 17 / 32 |
| TZP 10mg / Double-Blind PeriodParticipants received 10 mg of tirzepatide QW administered as SC injection via SDP for 30 weeks in a double-blind period. | 0 / 33 | 1 / 33 | 19 / 33 |
| Placebo / Double-Blind PeriodParticipants received placebo QW administered as SC injection via SDP for 30 weeks in a double-blind period. | 0 / 34 | 1 / 34 | 11 / 34 |
| TZP 5mg / 5mg Open-Label and Safety Follow-Up PeriodParticipants who received 5 mg tirzepatide during the double-blind period continued to receive 5 mg of tirzepatide QW administered as SC injection via SDP for 22 weeks in the open-label period and 4 weeks in the safety follow-up period. | 0 / 32 | 1 / 32 | 10 / 32 |
| TZP 10mg / 10mg Open-Label and Safety Follow-Up PeriodParticipants who received 10 mg of tirzepatide during the double-blind period continued to receive 10 mg of tirzepatide QW administered as SC injection via SDP for 22 weeks in the open-label period and 4 weeks in the safety follow-up period. | 0 / 33 | 1 / 33 | 7 / 33 |
| Placebo/TZP 5mg Open-Label and Safety Follow-Up PeriodParticipants who received placebo QW during the double-blind period were switched to 5 mg tirzepatide QW administered as SC injection via SDP for 22 weeks in the open-label period and 4 weeks in the safety follow-up period. | 0 / 32 | 0 / 32 | 8 / 32 |
Each cell reads participants affected / participants at risk, as the registry posted them.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies that cite this trial.
1 study on this page
Indexing hint: Randomized controlled trial · 2025
Hannon et al. 2025Lancet (London, England)cited by 23
PMID 40975112DOI 10.1016/s0140-6736(25)01774-xPUB-40975112
Who could join, as posted.
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