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Clinical Trial Summary

This study will assess the safety and preliminary efficacy of escalating doses of VAY736 in relapsed or refractory CLL patients.


Clinical Trial Description

This Phase 1, multicenter, open-label, study will investigate the safety, pharmacokinetics, pharmacodynamics, and preliminary antil-CLL activity of VAY736 in patients with relapsed/refractory CLL who have received at least two prior regimens. The study will include one arm in the dose escalation phase and two arms in the dose expansion phase. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02137889
Study type Interventional
Source Novartis
Contact
Status Terminated
Phase Phase 1
Start date July 2012
Completion date November 2012