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Clinical Trial Summary

The main aims of the study are to assess the safety profile of teduglutide (Revestive®) as well as how many people with Short Bowl Syndrome experience a reduction of parenteral support when treated with teduglutide (Revestive®). This study is about collecting existing data only; participants will not receive teduglutide (Revestive®) as part of this study. No new information will be collected during this study. Only data already available in the hospital records will be reviewed and collected for this study. Participants do not need to visit their doctor in addition to their normal visits.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04883606
Study type Observational
Source Takeda
Contact
Status Completed
Phase
Start date January 26, 2022
Completion date July 24, 2023

See also
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