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Trial · Interventional

CompletedPhase 3Results postedRegistry data

A Study of Tirzepatide (LY3298176) Versus Insulin Degludec in Participants With Type 2 Diabetes

Short name SURPASS-3

NCTNCT03882970 (opens ClinicalTrials.gov in a new tab)Other id16997Other idI8F-MC-GPGHOther id2018-003422-84Other id2018

Overview

Status
Completed
Phase
Phase 3
Enrollment
1,444 participants (actual)
Sponsor
Eli Lilly and Company · Industry
Design
Randomized · Open label (no masking)
Countries
13 countries

United States, Argentina, Austria, Greece, Hungary, Italy, Poland, Puerto Rico, Romania, South Korea, Spain, Taiwan, Ukraine

Start
1 Apr 2019
Primary completion
11 Dec 2020
Completion
4 Jan 2021
First posted
20 Mar 2019
Last update posted
19 Jan 2022
Conditions
Type 2 Diabetes Mellitus

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2019202020212022
  1. Ph 3

    SURPASS-3

    NCT03882970

    1 Apr 2019 to 4 Jan 2021

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The purpose of this study is to compare the effect of the study drug tirzepatide to insulin degludec on blood sugar levels in participants with type 2 diabetes. The study will last about 67 weeks and may include up to 22 visits.

Interventions

  • TirzepatideDrug
  • Insulin DegludecDrug

Arms4

  • Experimental

    5 mg Tirzepatide

    5 milligrams (mg) tirzepatide administered subcutaneously (SC) once a week.

  • Experimental

    10 mg Tirzepatide

    10 mg tirzepatide administered SC once a week.

  • Experimental

    15 mg Tirzepatide

    15 mg tirzepatide administered SC once a week.

  • Active comparator

    Insulin Degludec

    Insulin degludec administered SC once a day.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Change From Baseline in Hemoglobin A1c (HbA1c) (10 mg and 15 mg)

    Time frame · Baseline, Week 52

    Registry description

    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 mixed-model repeated measures (MMRM) model with covariates Baseline + Pooled Country + Baseline Oral Antihyperglycemic Medication (OAM) Use (Metformin (Met), Met plus SGLT-2i) + Treatment + Time + Treatment\*Time (Type III sum of squares).

Secondary outcomes(8)
  1. Change From Baseline in HbA1c (5 mg)

    Time frame · Baseline, Week 52

    Registry description

    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 mixed-model repeated measures (MMRM) model with covariates Baseline + Pooled Country + Baseline OAM Use (Met, Met plus SGLT-2i) + Treatment + Time + Treatment\*Time (Type III sum of squares).

  2. Change From Baseline in Body Weight

    Time frame · Baseline, Week 52

    Registry description

    LS mean was determined by MMRM model with Baseline + Pooled Country + Baseline OAM Use (Met, Met plus SGLT-2i) + Baseline HbA1c Group (\<=8.5%, \>8.5%) + Treatment + Time + Treatment\*Time (Type III sum of squares) as covariates.

  3. Change From Baseline in Fasting Serum Glucose

    Time frame · Baseline, Week 52

    Registry description

    LS mean was determined by MMRM model with variables Baseline + Pooled Country + Baseline OAM Use (Met, Met plus SGLT-2i) + Baseline HbA1c Group (\<=8.5%, \>8.5%) + Treatment + Time + Treatment\*Time (Type III sum of squares).

  4. Percentage of Participants Achieving an HbA1c Target Value of <7%

    Time frame · Week 52

    Registry description

    Hemoglobin A1c (HbA1c) is the glycosylated fraction of hemoglobin A. HbA1c is measured to identify average plasma glucose concentration over prolonged periods of time. Imputed data includes observed value and imputed value if endpoint measure is missing. Missing endpoint measures are imputed by predictions from an MMRM analysis model using observed data in the efficacy analysis set and adjusted for Baseline Value, Pooled Country, Baseline OAM Use (Met, Met plus SGLT-2i), Treatment, Visit and Visit\*Treatment.

  5. Mean Change From Baseline in Daily Average 7-Point Self-Monitored Blood Glucose (SMBG) Values

    Time frame · Baseline, Week 52

    Registry description

    The self-monitored plasma glucose (SMBG) data were collected at the following 7 time points: Morning Premeal - Fasting, Morning 2-hour Postmeal, Midday Premeal, Midday 2-hour Postmeal, Evening Premeal, Evening 2-hour Postmeal and Bedtime. LS mean was determined by mixed-model repeated measures (MMRM) model with variables Baseline + Baseline HbA1c Group (\<=8.5%, \>8.5%) + Pooled Country + Baseline OAM Use (Met, Met plus SGLT-2i) + Treatment + Time + Treatment\*Time (Type III sum of squares).

  6. Percentage of Participants Who Achieved Weight Loss ≥5%

    Time frame · Week 52

    Registry description

    Percentage of Participants who Achieved Weight Loss ≥5%

  7. Diabetes Treatment Satisfaction as Measured by the Diabetes Treatment Satisfaction Questionnaire, Change Version (DTSQc) Hyperglycemia, Hypoglycemia and Treatment Satisfaction Score

    Time frame · Week 52

    Registry description

    DTSQc, an 8-item questionnaire, assesses relative change in treatment satisfaction perceived frequency of hyperglycemia, and perceived frequency of hypoglycemia from baseline to week 52 or early termination.The treatment satisfaction score ranges from -18 to 18 where the higher the score the greater the improvement in satisfaction with treatment. The lower the score the greater the deterioration in satisfaction with treatment. The hyperglycemia and hypoglycemia scores range from -3 to 3 where negative scores indicate fewer problems with blood glucose levels and positive scores indicate more problems than before. LS mean was determined by ANCOVA model for endpoint measures: Variable = Baseline DTSQs + Pooled Country + Baseline HbA1c Group (\<=8.5%, \>8.5%) + Baseline OAM Use (Met, Met plus SGLT-2i) + Treatment (Type III sum of squares).

  8. Rate of Hypoglycemia With Blood Glucose <54 Milligram/Deciliter (mg/dL) [<3.0 (Millimole/Liter (mmol/L))] or Severe Hypoglycemia

    Time frame · Baseline through Safety Follow-Up (Up to Week 56)

    Registry description

    The hypoglycemia events were defined by participant reported events with blood glucose \<54mg/dL (\<3.0 mmol/L) or severe hypoglycemia. Severe hypoglycemia is defined as an episode with severe cognitive impairment requiring the assistance of another person to actively administer carbohydrate, glucagon, or other resuscitative actions. These episodes may be associated with sufficient neuroglycopenia to induce seizure or coma. The rate of postbaseline hypoglycemia was estimated by negative binomial model: Number of episodes = Pooled Country + Baseline OAM Use (Met, Met plus SGLT-2i) + Baseline HbA1c Group (\<=8.5%, \>8.5%) + Treatment, with log (exposure in days/365.25) as an offset variable.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeLeast squares mean· Baseline, Week 52

Change From Baseline in Hemoglobin A1c (HbA1c) (10 mg and 15 mg)

GroupValue (Percentage of HbA1c)Spread
10 mg Tirzepatide-2.200.051
15 mg Tirzepatide-2.370.050
Insulin Degludec-1.340.049
Secondary and other outcome results(7)
Secondary outcomeLeast squares mean· Baseline, Week 52

Change From Baseline in HbA1c (5 mg)

GroupValue (Percentage of HbA1c)Spread
5 mg Tirzepatide-1.930.050
Insulin Degludec-1.340.049
Secondary outcomeLeast squares mean· Baseline, Week 52

Change From Baseline in Body Weight

GroupValue (Kilograms (kg))Spread
5 mg Tirzepatide-7.50.37
10 mg Tirzepatide-10.70.37
15 mg Tirzepatide-12.90.37
Insulin Degludec2.30.37
Secondary outcomeLeast squares mean· Baseline, Week 52

Change From Baseline in Fasting Serum Glucose

GroupValue (milligram per Deciliter (mg/dL))Spread
5 mg Tirzepatide-48.21.82
10 mg Tirzepatide-54.81.86
15 mg Tirzepatide-59.21.85
Insulin Degludec-55.71.81
Secondary outcomeNumber· Week 52

Percentage of Participants Achieving an HbA1c Target Value of <7%

GroupValue (percentage of participants)
5 mg Tirzepatide82.44
10 mg Tirzepatide89.71
15 mg Tirzepatide92.63
Insulin Degludec61.25
Secondary outcomeLeast squares mean· Baseline, Week 52

Mean Change From Baseline in Daily Average 7-Point Self-Monitored Blood Glucose (SMBG) Values

GroupValue (mg/dL)Spread
5 mg Tirzepatide-52.61.20
10 mg Tirzepatide-59.71.22
15 mg Tirzepatide-60.61.20
Insulin Degludec-48.01.18
Secondary outcomeNumber· Week 52

Percentage of Participants Who Achieved Weight Loss ≥5%

GroupValue (percentage of participants)
5 mg Tirzepatide66.01
10 mg Tirzepatide83.71
15 mg Tirzepatide87.82
Insulin Degludec6.27
Secondary outcomeLeast squares mean· Week 52

Diabetes Treatment Satisfaction as Measured by the Diabetes Treatment Satisfaction Questionnaire, Change Version (DTSQc) Hyperglycemia, Hypoglycemia and Treatment Satisfaction Score

GroupValue (units on a scale)Spread
5 mg Tirzepatide-1.40.11
10 mg Tirzepatide-1.40.11
15 mg Tirzepatide-1.60.11
Insulin Degludec-1.10.11

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
5 mg Tirzepatide5 milligrams (mg) tirzepatide administered subcutaneously (SC) once a week.1 / 35829 / 358124 / 358
10 mg Tirzepatide5 milligrams (mg) tirzepatide administered subcutaneously (SC) once a week.2 / 36020 / 360157 / 360
15 mg Tirzepatide15 mg tirzepatide administered SC once a week SC.1 / 35926 / 359179 / 359
Insulin DegludecInsulin degludec administered SC once a day. Doses were individualized and titrated according to protocol-defined targets. The starting dose of insulin degludec was 10 IU/day ideally at bedtime, titrated to a fasting blood glucose (FBG) \<90 milligram per Deciliter (mg/dL), following a treat-to-target (TTT) algorithm based on the last 3 FBG values.1 / 36022 / 36066 / 360

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

Studies11

Studies that cite this trial.

Studies with results

6 studies on this page

Indexing hint: Randomized controlled trial · 2026

6 results

Liver Fat Changes in Patients With Type 2 Diabetes by Presence of Genetic Hepatic Steatosis: A Post Hoc Analysis of SURPASS-3 MRI.

Cusi et al. 2026Liver international : official journal of the International Association for the Study of the Livercited by 1

PMID 42576670PMC13458421DOI 10.1111/liv.70837PUB-42576670

CC BY6 results

Indexing hint: Randomized controlled trial · 2025

7 results

Tirzepatide and muscle composition changes in people with type 2 diabetes (SURPASS-3 MRI): a post-hoc analysis of a randomised, open-label, parallel-group, phase 3 trial.

Sattar et al. 2025The lancet. Diabetes & endocrinologycited by 68

PMID 40318682DOI 10.1016/s2213-8587(25)00027-0PUB-40318682

Full text at the publisher7 results

Indexing hint: Observational study · 2024

3 results

Effect of tirzepatide on body fat distribution pattern in people with type 2 diabetes.

Cariou et al. 2024Diabetes, obesity & metabolismcited by 26

PMID 38528819DOI 10.1111/dom.15566PUB-38528819

Full text at the publisher3 results

Indexing hint: Meta-analysis (pooled) · 2022

4 results

Tirzepatide cardiovascular event risk assessment: a pre-specified meta-analysis.

Sattar et al. 2022Nature medicinecited by 268

PMID 35210595PMC8938269DOI 10.1038/s41591-022-01707-4PUB-35210595

CC BY4 results

Indexing hint: Randomized controlled trial · 2022

4 results

Effect of tirzepatide versus insulin degludec on liver fat content and abdominal adipose tissue in people with type 2 diabetes (SURPASS-3 MRI): a substudy of the randomised, open-label, parallel-group, phase 3 SURPASS-3 trial.

Gastaldelli et al. 2022The lancet. Diabetes & endocrinologycited by 393

PMID 35468325DOI 10.1016/s2213-8587(22)00070-5PUB-35468325

Full text at the publisher4 results

Indexing hint: Randomized controlled trial · 2021

7 results

Once-weekly tirzepatide versus once-daily insulin degludec as add-on to metformin with or without SGLT2 inhibitors in patients with type 2 diabetes (SURPASS-3): a randomised, open-label, parallel-group, phase 3 trial.

Ludvik et al. 2021Lancet (London, England)cited by 501

PMID 34370970DOI 10.1016/s0140-6736(21)01443-4PUB-34370970

Full text at the publisher7 results

More studies

5 studies on this page

PubMed tag: none · 2025

Post Hoc Analysis of SURPASS-1 to -5: Efficacy and Safety of Tirzepatide in Adults with Type 2 Diabetes are Independent of Baseline Characteristics.

De Block et al. 2025Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 13

PMID 39531161PMC11759727DOI 10.1007/s13300-024-01660-0PUB-39531161

Free to read · publisher termsCC BY-NC
Read at source

PubMed tag: none · 2023

Time to Reach Glycaemic and Body Weight Loss Thresholds with Tirzepatide in Patients with Type 2 Diabetes: A Pre-planned Exploratory Analysis of SURPASS-2 and SURPASS-3.

Viljoen et al. 2023Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 7

PMID 37000390PMC10126190DOI 10.1007/s13300-023-01398-1PUB-37000390

Free to read · publisher termsCC BY-NC
Read at source

PubMed tag: none · 2023

Patient-Reported Outcomes in People with Type 2 Diabetes Receiving Tirzepatide in the SURPASS Clinical Trial Programme.

Boye et al. 2023Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 16

PMID 37526908PMC10570242DOI 10.1007/s13300-023-01451-zPUB-37526908

Free to read · publisher termsCC BY-NC
Read at source

PubMed tag: none · 2023

Improved Glycaemic and Weight Management Are Associated with Better Quality of Life in People with Type 2 Diabetes Treated with Tirzepatide.

Boye et al. 2023Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 5

PMID 37668888PMC10570229DOI 10.1007/s13300-023-01457-7PUB-37668888

Free to read · publisher termsCC BY-NC
Read at source

Indexing hint: Randomized controlled trial · 2022

Corrected

Efficacy of once-weekly tirzepatide versus once-daily insulin degludec on glycaemic control measured by continuous glucose monitoring in adults with type 2 diabetes (SURPASS-3 CGM): a substudy of the randomised, open-label, parallel-group, phase 3 SURPASS-3 trial.

Battelino et al. 2022The lancet. Diabetes & endocrinologycited by 50

PMID 35468321DOI 10.1016/s2213-8587(22)00077-8PUB-35468321

Full text at the publisher

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Participants must: * Have been diagnosed with type 2 diabetes mellitus (T2DM) * Have HbA1c between ≥7.0% and ≤10.5% * Be on stable treatment with unchanged dose of metformin or metformin plus an SGLT-2 inhibitor for at least 3 months before screening * Be of stable weight (± 5%) for at least 3 months before screening * Have a BMI ≥25 kilograms per meter squared (kg/m2) at screening Exclusion Criteria: * Participants must not: * Have type 1 diabetes mellitus * Have had chronic or acute pancreatitis any time prior to study entry * Have proliferative diabetic retinopathy or diabetic maculopathy or nonproliferative diabetic retinopathy requiring acute treatment * Have disorders associated with slowed emptying of the stomach, or have had any stomach surgeries for the purpose of weight loss * Have acute or chronic hepatitis, signs and symptoms of any other liver disease, or blood alanine transaminase (ALT) enzyme level \>3.0 times the upper limit of normal (ULN) for the reference range, as determined by the central laboratory. Participants with nonalcoholic fatty liver disease (NAFLD) are eligible for participation in this trial only if their ALT level is ≤3.0 the ULN for the reference range * Have an estimated glomerular filtration rate \<45 mL/minute/1.73 m2 (or lower than the country specific threshold for using the protocol required dose of metformin per local label) * Have had a heart attack, stroke, or hospitalization for congestive heart failure in the past 2 months * Have a personal or family history of medullary thyroid carcinoma or personal history of multiple endocrine neoplasia syndrome type 2 * Have been taking any other diabetes medicines other than metformin, or metformin plus an SGLT-2 inhibitor during the last 3 months * Have been taking weight loss drugs, including over-the-counter medications during the last 3 months

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