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Clinical Trial Summary

The objectives of this clinical study are to evaluate the safety, efficacy, and pharmacokinetics (PK) of teduglutide in Japanese participants with short bowel syndrome (SBS) who are dependent on parenteral nutrition/intravenous (PN/IV) over a 24-week treatment period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03663582
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 3
Start date July 6, 2018
Completion date August 6, 2019

See also
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