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Clinical Trial Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of subcutaneously administered teplizumab in adults with relatively recent onset T1DM, greater than 12 weeks and less than 52 weeks of presentation of first signs and symptoms of disease to a physician prior to randomization.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01189422
Study type Interventional
Source MacroGenics
Contact
Status Terminated
Phase Phase 1
Start date August 2010
Completion date February 2011

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