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Clinical Trial Summary

The primary purpose of this study is to evaluate the safety and tolerability of intravenous (IV) doses of IMB-101 in healthy volunteers and participants with active RA on a stable regimen of methotrexate.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06181786
Study type Interventional
Source IMBiologics Corp.
Contact Lilly Huh
Phone +82-31-8067-8191
Email junghyun.huh@imbiologics.com
Status Not yet recruiting
Phase Phase 1
Start date December 13, 2023
Completion date December 11, 2025

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