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Clinical Trial Summary

This study is designed to evaluate the safety, tolerability, pharmacokinetics and therapeutic efficacy of treatment with either VAY736 or CFZ533 in patients with SLE to enable further development of these compounds as treatment in this disease population


Clinical Trial Description

A placebo-controlled, patient and investigator blinded, randomized parallel cohort study to assess pharmacodynamics, pharmacokinetics, safety, tolerability and preliminary clinical efficacy of VAY736 and CFZ533 in patients with systemic lupus erythematosus (SLE) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03656562
Study type Interventional
Source Novartis
Contact
Status Active, not recruiting
Phase Phase 2
Start date December 19, 2018
Completion date April 24, 2026

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