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Clinical Trial Summary

The purpose of this study is to determine the safety and tolerability of imvotamab in patients with moderate to severe rheumatoid arthritis who have failed prior therapies. Participants will be given imvotamab or placebo through a vein (i.e., intravenously). A placebo is a look-alike substance that contains no active drug


Clinical Trial Description

This is a Phase 1b, randomized, placebo-controlled, multicenter study to determine the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of imvotamab in adult participants with active RA who are refractory or intolerant to 2 previous biologic disease-modifying anti-rheumatic drugs (bDMARD) or targeted synthetic disease-modifying anti-rheumatic drugs (tsDMARD) therapies. Approximately 24 participants will be sequentially assigned to different dose escalation cohorts. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06087406
Study type Interventional
Source IGM Biosciences, Inc.
Contact Clinical Trials
Phone (877) 544-6728
Email IGM-2323-102@igmbio.com
Status Recruiting
Phase Phase 1
Start date September 13, 2023
Completion date July 2025

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