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Study · Non-randomized trial · n = 9 · 2024

10 results

Efficacy and safety of apraglutide in short bowel syndrome with intestinal failure and colon-in-continuity: A multicenter, open-label, metabolic balance study.

Verbiest A, Hvistendahl MK, Bolognani F, Li C, Youssef NN, Huh S, Menys A, Bhatnagar G, Vanslembrouck R, Peeters R, Sartoris R, Vermeersch P and 5 more

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Wauters L, Verbeke K, Jeppesen PB, Joly F, Vanuytsel T

Clinical nutrition (Edinburgh, Scotland)16 Oct 2024Cited by 12 (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 study10

10 results from studies that gave the peptide. 10 results from people.

  1. 01HumanNon-randomized trialSafety outcome

    In adults with SBS-IF-CiC receiving apraglutide, 127 adverse events were reported, mostly mild to moderate.

    In plain wordsIn adults with short bowel syndrome receiving apraglutide, most reported adverse events were mild to moderate.

    Outcome
    Not applicableAdverse events
    Study

    n = 9

    Analysis
    Primary
    Outcome group
    Adverse events · Whole body
    Studied dose
    Dose not stated · subcutaneous · 52 weeksAs given in this study (human).

    Measurements

    Adverse events reported
    127 events
    52 weeks

    Source sentences

    Summary
    A total of 127 adverse events was reported, which were mostly mild to moderate.
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  2. 02HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC, apraglutide reduced parenteral support volume by 4702 mL/week (52%) at week 52.

    In plain wordsIn adults with short bowel syndrome, intravenous support volume decreased during apraglutide treatment.

    Outcome
    DecreaseParenteral support volume
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intensive care and hospital outcomes · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneous · 52 weeksAs given in this study (human).

    Measurements

    Change in PS volume
    −4702 mL/week
    week 52
    Relative change in PS volume
    −52%
    week 52

    Source sentences

    Summary
    PS volume decreased by -4702 mL/week (-52 %; p < 0.001) at week 52.
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  3. 03HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC receiving apraglutide, seven patients achieved at least one day off parenteral support at week 52.

    In plain wordsIn adults with short bowel syndrome receiving apraglutide, seven patients achieved at least one day without intravenous support.

    Outcome
    IncreaseAt least one day off parenteral support
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intensive care and hospital outcomes · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneous · 52 weeksAs given in this study (human).

    Measurements

    Patients with at least 1 day off PS
    7 patients
    week 52
    Patients with at least 1 day off PS
    78%
    week 52

    Source sentences

    Summary
    Seven patients (78 %) achieved ≥1 day off PS at week 52.
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  4. 04HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC, fecal output decreased by 253 g/day after apraglutide treatment.

    In plain wordsIn adults with short bowel syndrome, stool output decreased during apraglutide treatment.

    Outcome
    DecreaseFecal output
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intestinal growth and absorption · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneous · 4 weeksAs given in this study (human).

    Measurements

    Reduction in fecal output
    253 g/day
    4 weeks

    Source sentences

    Summary
    At 4 weeks, fecal output was reduced by 253 g/day (p = 0.013).
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  5. 05HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC, wet weight absorption increased by 316 g/day during apraglutide treatment.

    In plain wordsIn adults with short bowel syndrome, wet weight absorption increased during apraglutide treatment.

    Outcome
    IncreaseWet weight absorption
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intestinal growth and absorption · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneous · 48 weeksAs given in this study (human).

    Measurements

    Increase in wet weight absorption
    316 g/day
    48 weeks

    Source sentences

    Summary
    At 48 weeks, increases in wet weight absorption by 316 g/day (p = 0.039), energy absorption by 1134 kJ/day (p = 0.041) and carbohydrate absorption by 56.1 g/day (p = 0.024) were observed.
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  6. 06HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC, energy absorption increased by 1134 kJ/day during apraglutide treatment.

    In plain wordsIn adults with short bowel syndrome, energy absorption increased during apraglutide treatment.

    Outcome
    IncreaseEnergy absorption
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intestinal growth and absorption · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneous · 48 weeksAs given in this study (human).

    Measurements

    Increase in energy absorption
    1134 kJ/day
    48 weeks

    Source sentences

    Summary
    At 48 weeks, increases in wet weight absorption by 316 g/day (p = 0.039), energy absorption by 1134 kJ/day (p = 0.041) and carbohydrate absorption by 56.1 g/day (p = 0.024) were observed.
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  7. 07HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC, carbohydrate absorption increased by 56.1 g/day during apraglutide treatment.

    In plain wordsIn adults with short bowel syndrome, carbohydrate absorption increased during apraglutide treatment.

    Outcome
    IncreaseCarbohydrate absorption
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intestinal growth and absorption · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneous · 48 weeksAs given in this study (human).

    Measurements

    Increase in carbohydrate absorption
    56.1 g/day
    48 weeks

    Source sentences

    Summary
    At 48 weeks, increases in wet weight absorption by 316 g/day (p = 0.039), energy absorption by 1134 kJ/day (p = 0.041) and carbohydrate absorption by 56.1 g/day (p = 0.024) were observed.
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  8. 08HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC receiving apraglutide, small bowel length increased from 29.7 to 40.7 cm.

    In plain wordsIn adults with short bowel syndrome receiving apraglutide, small bowel length increased.

    Outcome
    IncreaseSmall bowel length
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intestinal growth and absorption · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneousAs given in this study (human).

    Measurements

    Small bowel length
    29.7 cm
    before
    Small bowel length
    40.7 cm
    after

    Source sentences

    Summary
    Moreover, small bowel length increased from 29.7 to 40.7 cm (p = 0.012), duodenal wall thickness increased by 0.8 mm (p = 0.02) and motility in the proximal colon was reduced (p = 0.031).
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  9. 09HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC receiving apraglutide, duodenal wall thickness increased by 0.8 mm.

    In plain wordsIn adults with short bowel syndrome receiving apraglutide, the duodenal wall became thicker.

    Outcome
    IncreaseDuodenal wall thickness
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Intestinal growth and absorption · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneousAs given in this study (human).

    Measurements

    Increase in duodenal wall thickness
    0.8 mm
    apraglutide

    Source sentences

    Summary
    Moreover, small bowel length increased from 29.7 to 40.7 cm (p = 0.012), duodenal wall thickness increased by 0.8 mm (p = 0.02) and motility in the proximal colon was reduced (p = 0.031).
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.
  10. 10HumanNon-randomized trialEfficacy outcome

    In adults with SBS-IF-CiC receiving apraglutide, proximal colon motility decreased.

    In plain wordsIn adults with short bowel syndrome receiving apraglutide, movement in the proximal colon decreased.

    Outcome
    DecreaseProximal colon motility
    Study

    n = 9

    Analysis
    Secondary
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    Dose not stated · subcutaneousAs given in this study (human).

    Source sentences

    Summary
    Moreover, small bowel length increased from 29.7 to 40.7 cm (p = 0.012), duodenal wall thickness increased by 0.8 mm (p = 0.02) and motility in the proximal colon was reduced (p = 0.031).
    1 context sentence
    Summary · context
    This was a 52-week phase 2 metabolic balance study (MBS) in 9 adult patients with SBS-IF-CiC receiving once-weekly subcutaneous apraglutide injections.

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

    27 Oct 2026, 18:20 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:32 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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