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Clinical Trial Summary

This is a 16-week randomized controlled trial comparing a second IV weight-based induction dose at week 8 to standard 90mg subcutaneous dose at week 8, with a primary endpoint of clinical remission at week 16.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04629196
Study type Interventional
Source NYU Langone Health
Contact
Status Terminated
Phase Phase 4
Start date February 16, 2022
Completion date January 17, 2024

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