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Clinical Trial Summary

This study was to evaluate the safety and efficacy of a daily, oral dose of 10 mg RAD001 in participants with Mantle Cell Lymphoma who were refractory or intolerant to Velcade® therapy and who had received at least one prior antineoplastic agent other than Velcade®, either separately or in combination with Velcade® (see inclusion criteria). Intolerance to Velcade® therapy was determined by the study investigator based on clinical evaluations. Participants were considered refractory to Velcade® if they have documented radiological progression on or within 12 months of the last dose of Velcade® when given alone or, on or within 12 months of the last dose of the last component of a combination therapy which included Velcade®.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00702052
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date August 22, 2008
Completion date April 20, 2012