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Clinical Trial Summary

The purpose of the study is to evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of a single subcutaneous (SC) dose of rozanolixizumab administered to healthy participants by manual push (MP) versus (vs) syringe driver.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04828343
Study type Interventional
Source UCB Pharma
Contact
Status Completed
Phase Phase 1
Start date April 22, 2021
Completion date April 11, 2022

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