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Clinical Trial Summary

The purpose of the study is to evaluate the safety and efficacy of GLASSIA as an add-on biopharmacotherapy to standard-of-care steroid treatment as the first-line treatment in participants with acute GvHD with lower GI involvement.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02956122
Study type Interventional
Source Takeda
Contact
Status Terminated
Phase Phase 2/Phase 3
Start date April 26, 2017
Completion date May 3, 2018

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