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Study · Randomized controlled trial · n = 32 · 2020

8 results

Exenatide once weekly slows gastric emptying of solids and liquids in healthy, overweight people at steady-state concentrations.

Jones KL, Huynh LQ, Hatzinikolas S, Rigda RS, Phillips LK, Pham HT, Marathe CS, Wu T, Malbert CH, Stevens JE, Lange K, Rayner CK, Horowitz M

Diabetes, obesity & metabolism28 Jan 2020Cited by 59 (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 trialSafety outcome

    In healthy overweight participants, exenatide and placebo were well tolerated.

    In plain wordsIn healthy overweight participants, exenatide and placebo were well tolerated.

    Outcome
    Not applicableOverall tolerability
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Adverse events · Whole body
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Source sentences

    Summary
    The study treatments were well tolerated.
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  2. 02HumanRandomized controlled trialSafety outcome

    In healthy overweight participants, nausea scores were low and did not differ between exenatide and placebo.

    In plain wordsIn healthy overweight participants, nausea scores were low and did not differ between exenatide and placebo.

    Outcome
    No significant changeNausea score
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Gastrointestinal adverse events · Gastrointestinal
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Source sentences

    Summary
    Scores for nausea were consistently low, with no difference between the EXE once weekly and PBO groups.
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  3. 03HumanRandomized controlled trialEfficacy outcome

    In healthy overweight participants, exenatide slowed gastric emptying of solids compared with placebo.

    In plain wordsIn healthy overweight participants, exenatide slowed solid food leaving the stomach compared with placebo.

    Outcome
    DecreaseGastric emptying of solids
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Measurements

    P value, AUC 0-120 min
    < 0.05 P
    gastric emptying of solids

    Source sentences

    Summary
    EXE once weekly slowed gastric emptying of solids (area under the curve [AUC]0-120min : P 0-120min : P = 0.01) substantially,
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  4. 04HumanRandomized controlled trialEfficacy outcome

    In healthy overweight participants, exenatide slowed gastric emptying of liquids compared with placebo.

    In plain wordsIn healthy overweight participants, exenatide slowed liquids leaving the stomach compared with placebo.

    Outcome
    DecreaseGastric emptying of liquids
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Measurements

    P value, AUC 0-120 min
    0.01 P
    gastric emptying of liquids

    Source sentences

    Summary
    EXE once weekly slowed gastric emptying of solids (area under the curve [AUC]0-120min : P 0-120min : P = 0.01) substantially,
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  5. 05HumanRandomized controlled trialEfficacy outcome

    In healthy overweight participants, exenatide attenuated glucose absorption compared with placebo.

    In plain wordsIn healthy overweight participants, exenatide reduced glucose absorption compared with placebo.

    Outcome
    DecreaseGlucose absorption
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Glycemic control · Gastrointestinal
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Measurements

    P value, 3-OMG iAUC 0-30 min
    0.001 P
    glucose absorption

    Source sentences

    Summary
    and attenuated glucose absorption (3-OMG incremental AUC [iAUC]0-30min : P = 0.001)
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  6. 06HumanRandomized controlled trialEfficacy outcome

    In healthy overweight participants, exenatide attenuated the postprandial plasma glucose rise compared with placebo.

    In plain wordsIn healthy overweight participants, exenatide reduced the blood sugar rise after a meal compared with placebo.

    Outcome
    DecreasePostprandial glucose rise
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Measurements

    P value, glucose iAUC 0-30 min
    0.008 P
    postprandial plasma glucose

    Source sentences

    Summary
    and the postprandial rise in plasma glucose (iAUC0-30min : P = 0.008).
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  7. 07HumanRandomized controlled trialMechanism

    In healthy overweight participants, exenatide reduced plasma glucagon at 2 hours compared with placebo.

    In plain wordsIn healthy overweight participants, exenatide reduced glucagon after a meal compared with placebo.

    Outcome
    DecreasePostprandial glucagon
    Study

    n = 32

    Comparator
    Matching placebo
    Outcome group
    Glycemic control · Endocrine and hormones
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Measurements

    P value
    0.001 P
    plasma glucagon at 2 h

    Source sentences

    Summary
    Plasma glucagon at 2 h was reduced by EXE once weekly (P = 0.001).
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…
  8. 08HumanRandomized controlled trialMechanism

    In exenatide-treated participants, glucose reduction magnitude correlated inversely with the glucose drink half-emptying time.

    In plain wordsIn exenatide-treated participants, the size of the glucose reduction was inversely linked to the drink's stomach emptying time.

    Outcome
    DecreaseGlucose reduction association with gastric emptying
    Study

    n = 16

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    2 mg/wk · subcutaneous · 8 weeksAs given in this study (human).

    Measurements

    Correlation coefficient r
    −0.55 r
    glucose reduction at 30 min versus 50% emptying time of glucose drink, exenatide group
    P value
    0.03 P
    correlation

    Source sentences

    Summary
    The magnitude of the reduction in plasma glucose at t = 30 min from baseline to 8 weeks with EXE once weekly was related inversely to the 50% emptying time of the glucose drink (r = -0.55, P = 0.03).
    1 context sentence
    Summary · context
    A total of 32 healthy participants were randomized to receive either EXE once weekly (2 mg/wk subcutaneously; six men, 10 women, mean age 59.9 ± 0.9 years, mean body mass index [BMI] 29.6 ± 0.6 kg/m2 ) or matching placebo (PBO; six men, 10 women, mean age 60.6 ± 1.2 years, mean BMI 29.5 ±…

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

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