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.
- Peptide
- Apraglutide
- 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
A total of 127 adverse events was reported, which were mostly mild to moderate.
1 context sentence(design, population, supporting numbers)
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.