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Study · Randomized controlled trial · n = 636 · 2024

16 results

Glycaemic control, body weight, and safety of tirzepatide versus dulaglutide by baseline glycated haemoglobin level in Japanese patients with type 2 diabetes: A subgroup analysis of the SURPASS J-mono study.

Osonoi T, Oura T, Hirase T

Diabetes, obesity & metabolism4 Oct 2023Cited by 2 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: CC BY-NC-ND. Results still quote short attributed sentences.

Results from this study16

13 results from studies that gave the peptide. 13 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In Japanese adults with type 2 diabetes, HbA1c reductions with tirzepatide were greater in those with baseline HbA1c above 8.5% (LSM differences -3.13% to -3.86%) than in those with baseline HbA1c of 8.5% or lower (-2.00% to -2.32%), with a significant treatment-by-baseline HbA1c interaction (P <= 0.001).

    In plain wordsIn Japanese adults with type 2 diabetes, tirzepatide lowered HbA1c more in people who started with higher HbA1c than in people who started lower.

    Outcome
    DecreaseHbA1c reduction by baseline HbA1c subgroup (interaction)
    Study

    n = 636

    Comparator
    Baseline HbA1c <=8.5% subgroup
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    with greater HbA1c reductions observed in patients with a baseline HbA1c of >8.5% treated with tirzepatide (least squares mean [LSM] differences of -3.13% to -3.86%) or dulaglutide (LSM -1.81%) compared with patients with a baseline HbA1c of ≤8.5% (LSM -2.00% to -2.32%) or dulaglutide (LSM -1.05%; t…
    1 context sentence
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In Japanese patients with T2D, dulaglutide reduced HbA1c less than any-dose tirzepatide in both baseline HbA1c subgroups.

    In plain wordsIn Japanese patients with diabetes, dulaglutide reduced HbA1c less than tirzepatide in both initial blood sugar subgroups.

    Outcome
    DecreaseHbA1c reduction versus tirzepatide
    Study

    n = 636

    Comparator
    Any-dose tirzepatide in each baseline HbA1c subgroup
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In Japanese patients with T2D, dulaglutide reduced body weight less than any-dose tirzepatide in both baseline HbA1c subgroups.

    In plain wordsIn Japanese patients with diabetes, dulaglutide reduced weight less than tirzepatide in both initial blood sugar subgroups.

    Outcome
    DecreaseBody weight reduction versus tirzepatide
    Study

    n = 636

    Comparator
    Any-dose tirzepatide in each baseline HbA1c subgroup
    Analysis
    Exploratory
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    0.75 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In Japanese adults with type 2 diabetes and baseline HbA1c of 8.5% or lower, tirzepatide at any dose reduced HbA1c significantly more than dulaglutide 0.75 mg.

    In plain wordsIn Japanese adults with type 2 diabetes and lower starting HbA1c, tirzepatide lowered HbA1c more than dulaglutide did.

    Outcome
    DecreaseHbA1c reduction, baseline HbA1c <=8.5% subgroup
    Study

    n = 433

    Comparator
    Dulaglutide 0.75 mg
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg
    3 context sentences
    Summary · context
    compared with patients with a baseline HbA1c of ≤8.5% (LSM -2.00% to -2.32%) or dulaglutide (LSM -1.05%
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  5. 05HumanRandomized controlled trialEfficacy outcome

    In Japanese adults with type 2 diabetes and baseline HbA1c of 8.5% or lower, tirzepatide changed body weight by -6.7 to -10.7 kg across doses, versus -0.6 kg with dulaglutide 0.75 mg.

    In plain wordsIn Japanese adults with type 2 diabetes and lower starting HbA1c, tirzepatide reduced body weight more than dulaglutide did.

    Outcome
    DecreaseBody weight change, baseline HbA1c <=8.5% subgroup
    Study

    n = 433

    Comparator
    Dulaglutide 0.75 mg
    Analysis
    Exploratory
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    For the tirzepatide treatment arms, LSM change from baseline in body weight ranged from -6.7 to -10.7 kg for the baseline HbA1c ≤8.5% subgroup and from -4.0 to -10.6 kg for the baseline HbA1c >8.5% subgroup, compared with -0.6 kg and -0.4 kg, respectively, for the dulaglutide arm.
    3 context sentences
    Summary · context
    Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  6. 06HumanRandomized controlled trialEfficacy outcome

    In Japanese adults with type 2 diabetes and baseline HbA1c above 8.5%, tirzepatide at any dose reduced HbA1c significantly more than dulaglutide 0.75 mg.

    In plain wordsIn Japanese adults with type 2 diabetes and high starting HbA1c, tirzepatide lowered HbA1c more than dulaglutide did.

    Outcome
    DecreaseHbA1c reduction, baseline HbA1c >8.5% subgroup
    Study

    n = 203

    Comparator
    Dulaglutide 0.75 mg
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg
    3 context sentences
    Summary · context
    with greater HbA1c reductions observed in patients with a baseline HbA1c of >8.5% treated with tirzepatide (least squares mean [LSM] differences of -3.13% to -3.86%) or dulaglutide (LSM -1.81%)
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  7. 07HumanRandomized controlled trialEfficacy outcome

    In Japanese adults with type 2 diabetes and baseline HbA1c above 8.5%, tirzepatide changed body weight by -4.0 to -10.6 kg across doses, versus -0.4 kg with dulaglutide 0.75 mg.

    In plain wordsIn Japanese adults with type 2 diabetes and high starting HbA1c, tirzepatide reduced body weight more than dulaglutide did.

    Outcome
    DecreaseBody weight change, baseline HbA1c >8.5% subgroup
    Study

    n = 203

    Comparator
    Dulaglutide 0.75 mg
    Analysis
    Exploratory
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    For the tirzepatide treatment arms, LSM change from baseline in body weight ranged from -6.7 to -10.7 kg for the baseline HbA1c ≤8.5% subgroup and from -4.0 to -10.6 kg for the baseline HbA1c >8.5% subgroup, compared with -0.6 kg and -0.4 kg, respectively, for the dulaglutide arm.
    3 context sentences
    Summary · context
    Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  8. 08HumanRandomized controlled trialEfficacy outcome

    In Japanese patients with T2D and baseline HbA1c above 8.5%, dulaglutide reduced HbA1c from baseline.

    In plain wordsIn Japanese patients with diabetes and higher initial HbA1c, dulaglutide reduced HbA1c from baseline.

    Outcome
    DecreaseHbA1c change, higher baseline HbA1c subgroup
    Study

    n: not reported in source

    Comparator
    Baseline
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg · 52 weeksAs given in this study (human).

    Measurements

    HbA1c LSM change
    −1.81%
    dulaglutide; baseline HbA1c >8.5%

    Source sentences

    Summary
    with greater HbA1c reductions observed in patients with a baseline HbA1c of >8.5% treated with tirzepatide (least squares mean [LSM] differences of -3.13% to -3.86%) or dulaglutide (LSM -1.81%)
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  9. 09HumanRandomized controlled trialEfficacy outcome

    In Japanese patients with T2D and baseline HbA1c at most 8.5%, dulaglutide reduced HbA1c from baseline.

    In plain wordsIn Japanese patients with diabetes and lower initial HbA1c, dulaglutide reduced HbA1c from baseline.

    Outcome
    DecreaseHbA1c change, lower baseline HbA1c subgroup
    Study

    n: not reported in source

    Comparator
    Baseline
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg · 52 weeksAs given in this study (human).

    Measurements

    HbA1c LSM change
    −1.05%
    dulaglutide; baseline HbA1c ≤8.5%

    Source sentences

    Summary
    compared with patients with a baseline HbA1c of ≤8.5% (LSM -2.00% to -2.32%) or dulaglutide (LSM -1.05%; treatment-by-baseline HbA1c subgroup interaction P ≤ 0.001).
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  10. 10HumanRandomized controlled trialEfficacy outcome

    In Japanese patients with T2D and baseline HbA1c at most 8.5%, dulaglutide reduced body weight from baseline.

    In plain wordsIn Japanese patients with diabetes and lower initial HbA1c, body weight decreased during dulaglutide treatment.

    Outcome
    DecreaseBody weight change, lower baseline HbA1c subgroup
    Study

    n: not reported in source

    Comparator
    Baseline
    Analysis
    Exploratory
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    0.75 mg · 52 weeksAs given in this study (human).

    Measurements

    Body weight LSM change
    −0.6 kg
    dulaglutide; baseline HbA1c ≤8.5%

    Source sentences

    Summary
    For the tirzepatide treatment arms, LSM change from baseline in body weight ranged from -6.7 to -10.7 kg for the baseline HbA1c ≤8.5% subgroup and from -4.0 to -10.6 kg for the baseline HbA1c >8.5% subgroup, compared with -0.6 kg and -0.4 kg, respectively, for the dulaglutide arm.
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  11. 11HumanRandomized controlled trialEfficacy outcome

    In Japanese patients with T2D and baseline HbA1c above 8.5%, dulaglutide reduced body weight from baseline.

    In plain wordsIn Japanese patients with diabetes and higher initial HbA1c, body weight decreased during dulaglutide treatment.

    Outcome
    DecreaseBody weight change, higher baseline HbA1c subgroup
    Study

    n: not reported in source

    Comparator
    Baseline
    Analysis
    Exploratory
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    0.75 mg · 52 weeksAs given in this study (human).

    Measurements

    Body weight LSM change
    −0.4 kg
    dulaglutide; baseline HbA1c >8.5%

    Source sentences

    Summary
    For the tirzepatide treatment arms, LSM change from baseline in body weight ranged from -6.7 to -10.7 kg for the baseline HbA1c ≤8.5% subgroup and from -4.0 to -10.6 kg for the baseline HbA1c >8.5% subgroup, compared with -0.6 kg and -0.4 kg, respectively, for the dulaglutide arm.
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  12. 12HumanObservational studySafety outcome

    In Japanese adults with type 2 diabetes, hypoglycaemia incidence was low, with no substantial difference between the baseline HbA1c subgroups.

    In plain wordsIn Japanese adults with type 2 diabetes, low blood sugar was uncommon and did not differ much between the two starting-HbA1c groups.

    Outcome
    No significant changeHypoglycaemia incidence between baseline HbA1c subgroups
    Study

    n = 636

    Comparator
    Baseline HbA1c >8.5% versus <=8.5% subgroups
    Analysis
    Exploratory
    Outcome group
    Adverse events · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    The incidence of hypoglycaemia was low, with no substantial difference in hypoglycaemia or treatment-emergent AEs between subgroups.
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.
  13. 13HumanObservational studySafety outcome

    In Japanese adults with type 2 diabetes, treatment-emergent adverse events showed no substantial difference between the baseline HbA1c subgroups.

    In plain wordsIn Japanese adults with type 2 diabetes, side effects did not differ much between the two starting-HbA1c groups.

    Outcome
    No significant changeTreatment-emergent adverse events between baseline HbA1c subgroups
    Study

    n = 636

    Comparator
    Baseline HbA1c >8.5% versus <=8.5% subgroups
    Analysis
    Exploratory
    Outcome group
    Adverse events · Metabolic and weight
    Studied dose
    5, 10 or 15 mg · 52 weeksAs given in this study (human).

    Source sentences

    Summary
    The incidence of hypoglycaemia was low, with no substantial difference in hypoglycaemia or treatment-emergent AEs between subgroups.
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.

Studies that did not test the peptide alone3

In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Dulaglutide (Trulicity).

  1. 14HumanNot a test of Dulaglutide (Trulicity) aloneObservational studySafety outcome

    In Japanese patients with T2D, pooled tirzepatide and dulaglutide results showed low hypoglycaemia incidence without substantial baseline-subgroup differences.

    In plain wordsIn Japanese patients with diabetes, pooled dulaglutide and tirzepatide results showed low hypoglycaemia rates and no substantial differences between initial HbA1c subgroups.

    Outcome
    No significant changeHypoglycaemia incidence
    Study

    n = 636

    Comparator
    Baseline HbA1c subgroups
    Analysis
    Exploratory
    Outcome group
    Adverse events · Metabolic and weight

    Source sentences

    Summary
    The incidence of hypoglycaemia was low, with no substantial difference in hypoglycaemia or treatment-emergent AEs between subgroups.
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  2. 15HumanNot a test of Dulaglutide (Trulicity) aloneObservational studySafety outcome

    In Japanese patients with T2D, pooled tirzepatide and dulaglutide results showed no substantial baseline-subgroup difference in treatment-emergent adverse events.

    In plain wordsIn Japanese patients with diabetes, pooled dulaglutide and tirzepatide results showed no substantial difference in adverse events between initial HbA1c subgroups.

    Outcome
    No significant changeTreatment-emergent adverse events
    Study

    n = 636

    Comparator
    Baseline HbA1c subgroups
    Analysis
    Exploratory
    Outcome group
    Adverse events · Whole body

    Source sentences

    Summary
    The incidence of hypoglycaemia was low, with no substantial difference in hypoglycaemia or treatment-emergent AEs between subgroups.
    2 context sentences
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  3. 16HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyEfficacy outcome

    In Japanese patients with T2D receiving dulaglutide, higher baseline HbA1c was associated with a larger HbA1c reduction.

    In plain wordsIn Japanese patients with diabetes receiving dulaglutide, higher initial HbA1c was linked to a larger HbA1c decrease.

    Outcome
    DecreaseHbA1c reduction by baseline subgroup
    Study

    n: not reported in source

    Comparator
    Dulaglutide-treated patients with baseline HbA1c ≤8.5%
    Analysis
    Exploratory
    Outcome group
    Glycemic control · Metabolic and weight

    Measurements

    HbA1c LSM change
    −1.81%
    dulaglutide; baseline HbA1c >8.5%
    HbA1c LSM change
    −1.05%
    dulaglutide; baseline HbA1c ≤8.5%

    Source sentences

    Summary
    with greater HbA1c reductions observed in patients with a baseline HbA1c of >8.5% treated with tirzepatide (least squares mean [LSM] differences of -3.13% to -3.86%) or dulaglutide (LSM -1.81%)
    3 context sentences
    Summary · context
    compared with patients with a baseline HbA1c of ≤8.5% (LSM -2.00% to -2.32%) or dulaglutide (LSM -1.05%; treatment-by-baseline HbA1c subgroup interaction P ≤ 0.001).
    Summary · context
    SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan.
    Summary · context
    In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of ≤8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Versions 4 to 8Current

    28 Oct 2026, 02:03 UTC

    The same notice was added 5 times, first on 22 Oct 2026, 02:26 UTC. The status did not change between them.

    Study results updated

  2. Version 3

    21 Oct 2026, 18:59 UTC

    Study data updated · source update from Europe PMC

  3. Version 2

    12 Oct 2026, 12:58 UTC

    Study results updated

  4. Version 1

    9 Oct 2026, 03:07 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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