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Clinical Trial Summary

This multi-center, open-label, single-arm study will evaluate the pharmacokinetics and safety of RO5072759 (GA101) in patients with CD20+ malignant lymphoma. Patients will receive multiple doses of RO5072759 (GA101). The anticipated time on study treatment is 24 weeks.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01680991
Study type Interventional
Source Hoffmann-La Roche
Contact
Status Completed
Phase Phase 1
Start date September 2012
Completion date December 2014