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Study · Randomized controlled trial · n = 30 · 2008

8 results

Effect of exenatide on 24-hour blood glucose profile compared with placebo in patients with type 2 diabetes: a randomized, double-blind, two-arm, parallel-group, placebo-controlled, 2-week study.

Schwartz SL, Ratner RE, Kim DD, Qu Y, Fechner LL, Lenox SM, Holcombe JH

Clinical therapeutics1 May 2008Cited by 37 (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: Publisher copyright. Results still quote short attributed sentences.

Results from this study8

8 results from studies that gave the peptide. 8 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide reduced 24-hour time-average glucose compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced average daily blood sugar compared with placebo.

    Outcome
    Decrease24-hour time-average glucose
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Measurements

    Time-average glucose
    7 mmol/L
    exenatide
    Time-average glucose
    8.8 mmol/L
    placebo

    Source sentences

    Summary
    After 2 weeks (study end), the 24-hour time-average glucose values were 7.0 (0.2) and 8.8 (0.3) mmol/L for exenatide-treated and placebo-administered patients, respectively (P < 0.001).
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide reduced glucose two hours after the morning meal compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced blood sugar after breakfast compared with placebo.

    Outcome
    DecreaseGlucose two hours after morning meal
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Measurements

    Post-meal glucose
    6.6 mmol/L
    exenatide, morning
    Post-meal glucose
    12 mmol/L
    placebo, morning

    Source sentences

    Summary
    The glucose values for patients treated with exenatide were lower compared with those in patients who received placebo 2 hours after the morning meal (6.6 [0.4] vs 12.0 [0.5] mmol/L; P < 0.001),
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide reduced glucose two hours after the midday meal compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced blood sugar after lunch compared with placebo.

    Outcome
    DecreaseGlucose two hours after midday meal
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Measurements

    Post-meal glucose
    8.8 mmol/L
    exenatide, midday
    Post-meal glucose
    11.8 mmol/L
    placebo, midday

    Source sentences

    Summary
    The glucose values for patients treated with exenatide were lower compared with those in patients who received placebo 2 hours after the morning meal (6.6 [0.4] vs 12.0 [0.5] mmol/L; P < 0.001), the midday meal (8.8 [0.5] vs 11.8 [0.6] mmol/L; P = 0.001), and the evening meal (6.8 [0.4] vs 11.3 [0.4…
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide reduced glucose two hours after the evening meal compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced blood sugar after dinner compared with placebo.

    Outcome
    DecreaseGlucose two hours after evening meal
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Measurements

    Post-meal glucose
    6.8 mmol/L
    exenatide, evening
    Post-meal glucose
    11.3 mmol/L
    placebo, evening

    Source sentences

    Summary
    The glucose values for patients treated with exenatide were lower compared with those in patients who received placebo 2 hours after the morning meal (6.6 [0.4] vs 12.0 [0.5] mmol/L; P < 0.001), the midday meal (8.8 [0.5] vs 11.8 [0.6] mmol/L; P = 0.001), and the evening meal (6.8 [0.4] vs 11.3 [0.4…
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  5. 05HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide shortened time above glucose 7.8 mmol/L compared with placebo.

    In plain wordsIn people with diabetes, exenatide shortened time with glucose above 7.8 mmol/L compared with placebo.

    Outcome
    DecreaseTime above glucose 7.8 mmol/L
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Measurements

    Time above threshold
    6.8 hours
    exenatide
    Time above threshold
    14.1 hours
    placebo

    Source sentences

    Summary
    The mean durations of patient exposure to glucose concentrations >7.8 and >11.1 mmol/L were significantly shorter for the exenatide group compared with the placebo group (>7.8 mmol/L: 6.8 [0.9] vs 14.1 [1.1] hours; >11.1 mmol/L: 1.0 [0.7] vs 4.7 [0.8] hours; both, P < 0.001).
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  6. 06HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide shortened time above glucose 11.1 mmol/L compared with placebo.

    In plain wordsIn people with diabetes, exenatide shortened time with glucose above 11.1 mmol/L compared with placebo.

    Outcome
    DecreaseTime above glucose 11.1 mmol/L
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Measurements

    Time above threshold
    1 hours
    exenatide
    Time above threshold
    4.7 hours
    placebo

    Source sentences

    Summary
    The mean durations of patient exposure to glucose concentrations >7.8 and >11.1 mmol/L were significantly shorter for the exenatide group compared with the placebo group (>7.8 mmol/L: 6.8 [0.9] vs 14.1 [1.1] hours; >11.1 mmol/L: 1.0 [0.7] vs 4.7 [0.8] hours; both, P < 0.001).
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  7. 07HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide reduced postprandial triglyceride excursions after the morning and evening meals compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced triglyceride rises after breakfast and dinner compared with placebo.

    Outcome
    DecreasePostprandial triglyceride excursions after morning and evening meals
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Lipids · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Source sentences

    Summary
    After 2 weeks, the postprandial triglyceride excursions after the morning and evening meals for patients treated with exenatide were significantly lower compared with those treated with placebo.
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.
  8. 08HumanRandomized controlled trialEfficacy outcome

    In patients with type 2 diabetes, exenatide had no apparent effect on free fatty acid concentrations compared with placebo.

    In plain wordsIn people with diabetes, exenatide had no apparent effect on free fatty acids compared with placebo.

    Outcome
    No significant changeFree fatty acid concentrations
    Study

    n = 30

    Comparator
    Placebo
    Outcome group
    Lipids · Metabolic and weight
    Studied dose
    5 microg BID for 1 week, then 10 microg BID for the next week · subcutaneous · 14 daysAs given in this study (human).

    Source sentences

    Summary
    There was no apparent effect on free fatty acid concentrations.
    2 context sentences
    Summary · context
    This randomized, double-blind, 2-arm, parallel-group, placebo-controlled, 2-week study was conducted in patients with type 2 diabetes with inadequate glycemic control, despite metformin with or without a TZD.
    Summary · context
    Following the baseline admission, patients were randomized to receive SC injections of either exenatide (5 microg BID for 1 week, then 10 microg BID for the next week) or placebo (volume equivalent) for 14 days.

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

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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