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Study · Randomized controlled trial · 2022

9 results

Insulin-glucagon-like peptide-1 receptor agonist relay and glucagon-like peptide-1 receptor agonist first regimens in individuals with type 2 diabetes: A randomized, open-label trial study.

Takeshita Y, Kita Y, Tanaka T, Goto H, Nakano Y, Teramura C, Enyama Y, Takamura T

Journal of diabetes investigation8 Feb 2022Cited by 4 (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. Results still quote short attributed sentences.

Results from this study9

2 results from studies that gave the peptide. 2 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In adults with poorly controlled type 2 diabetes, liraglutide given first lowered fasting plasma glucose significantly by week 24.

    In plain wordsIn adults with poorly controlled type 2 diabetes, liraglutide lowered fasting blood glucose by week 24.

    Outcome
    DecreaseFasting plasma glucose change by week 24 (liraglutide first group)
    Study

    n: not reported in source

    Analysis
    Primary
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.9 mg · subcutaneous · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    The levels of fasting plasma glucose and HbA1c significantly decreased in the Insulin-GLP-1 RA relay group (P < 0.001) and GLP-1 RA first group (P < 0.001) by week 24
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…
  2. 02HumanRandomized controlled trialEfficacy outcome

    In adults with poorly controlled type 2 diabetes, liraglutide given first lowered HbA1c significantly by week 24.

    In plain wordsIn adults with poorly controlled type 2 diabetes, liraglutide lowered HbA1c by week 24.

    Outcome
    DecreaseHbA1c change by week 24 (liraglutide first group)
    Study

    n: not reported in source

    Analysis
    Primary
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.9 mg · subcutaneous · 24 weeksAs given in this study (human).

    Source sentences

    Summary
    The levels of fasting plasma glucose and HbA1c significantly decreased in the Insulin-GLP-1 RA relay group (P < 0.001) and GLP-1 RA first group (P < 0.001) by week 24
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

Studies that did not test the peptide alone7

In this study, Liraglutide 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 Liraglutide.

  1. 03HumanNot a test of Liraglutide aloneRandomized controlled trialEfficacy outcome

    In adults with poorly controlled type 2 diabetes, a relay of degludec then liraglutide lowered fasting plasma glucose significantly by week 24.

    In plain wordsIn adults with poorly controlled type 2 diabetes, insulin followed by liraglutide lowered fasting blood glucose by week 24.

    Outcome
    DecreaseFasting plasma glucose change by week 24 (insulin-then-liraglutide relay group)
    Study

    n: not reported in source

    Analysis
    Primary
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    The levels of fasting plasma glucose and HbA1c significantly decreased in the Insulin-GLP-1 RA relay group (P < 0.001)
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

  2. 04HumanNot a test of Liraglutide aloneRandomized controlled trialEfficacy outcome

    In adults with poorly controlled type 2 diabetes, a relay of degludec then liraglutide lowered HbA1c significantly by week 24.

    In plain wordsIn adults with poorly controlled type 2 diabetes, insulin followed by liraglutide lowered HbA1c by week 24.

    Outcome
    DecreaseHbA1c change by week 24 (insulin-then-liraglutide relay group)
    Study

    n: not reported in source

    Analysis
    Primary
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    The levels of fasting plasma glucose and HbA1c significantly decreased in the Insulin-GLP-1 RA relay group (P < 0.001)
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

  3. 05HumanNot a test of Liraglutide aloneRandomized controlled trialEfficacy outcome

    In adults with poorly controlled type 2 diabetes, fasting plasma glucose did not differ between the insulin-then-liraglutide relay group and the liraglutide-first group at week 24.

    In plain wordsIn adults with poorly controlled type 2 diabetes, fasting glucose did not differ between insulin-then-liraglutide and liraglutide-first groups.

    Outcome
    No significant changeFasting plasma glucose, relay versus liraglutide first, week 24
    Study

    n: not reported in source

    Comparator
    Liraglutide first group
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    although no intergroup differences were observed.
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

  4. 06HumanNot a test of Liraglutide aloneRandomized controlled trialEfficacy outcome

    In adults with poorly controlled type 2 diabetes, HbA1c did not differ between the insulin-then-liraglutide relay group and the liraglutide-first group at week 24.

    In plain wordsIn adults with poorly controlled type 2 diabetes, HbA1c did not differ between insulin-then-liraglutide and liraglutide-first groups.

    Outcome
    No significant changeHbA1c, relay versus liraglutide first, week 24
    Study

    n: not reported in source

    Comparator
    Liraglutide first group
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    although no intergroup differences were observed.
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

  5. 07HumanNot a test of Liraglutide aloneRandomized controlled trialEfficacy outcome

    In participants in the lowest C-peptide quartile, the HbA1c reduction tended to be larger with the insulin-then-liraglutide relay than with liraglutide first, without reaching significance (P = 0.072).

    In plain wordsIn people with the lowest C-peptide, HbA1c fell somewhat more with insulin then liraglutide than with liraglutide first, but this was not statistically significant.

    Outcome
    No significant changeHbA1c reduction in the lowest C-peptide quartile, relay versus liraglutide first
    Study

    n: not reported in source

    Comparator
    Liraglutide first group
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    The reduction of HbA1c in the Insulin-GLP-1 RA relay group tended to be larger than that in the GLP-1 RA first group in the lowest CPR (C-peptide immunoreactivity) quartile (P = 0.072).
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

  6. 08HumanNot a test of Liraglutide aloneRandomized controlled trialSafety outcome

    In adults with poorly controlled type 2 diabetes, adverse events in the trial, which covered insulin and liraglutide regimens, were mostly gastrointestinal problems.

    In plain wordsIn adults with poorly controlled type 2 diabetes, most side effects in the trial were stomach and gut problems.

    Outcome
    Not applicableGastrointestinal adverse events
    Study

    n: not reported in source

    Outcome group
    Gastrointestinal adverse events · Gastrointestinal

    Source sentences

    Summary
    The adverse events consisted of gastrointestinal problems, followed by hypoglycemia.
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

  7. 09HumanNot a test of Liraglutide aloneRandomized controlled trialSafety outcome

    In adults with poorly controlled type 2 diabetes, hypoglycemia was the next most common adverse event type in the trial, which covered insulin and liraglutide regimens.

    In plain wordsIn adults with poorly controlled type 2 diabetes, low blood sugar was the second most common side effect in the trial.

    Outcome
    Not applicableHypoglycemia
    Study

    n: not reported in source

    Outcome group
    Adverse events · Metabolic and weight

    Source sentences

    Summary
    The adverse events consisted of gastrointestinal problems, followed by hypoglycemia.
    1 context sentence
    Summary · context
    In an open-label, parallel trial, participants with poorly controlled type 2 diabetes were recruited and randomized to receive once-daily insulin therapy, degludec (Insulin-GLP-1 RA relay group, mean 16.8 ± 11.4 IU/day), for 12 weeks and then liraglutide for 12 weeks or subcutaneous injections of GL…

    In this study, Liraglutide 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 Liraglutide.

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. Version 2Current

    12 Oct 2026, 11:11 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:05 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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