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Phase 1, Open-Label, Dose-Escalation Study to Assess the Safety and Pharmacokinetics of Recombinant Interleukin 21 (rIL-21) Administered in Combination With Rituxan (Rituximab) in Subjects With B-Cell Non Hodgkin's Lymphoma

NCT00347971 Phase 1 COMPLETED

The purpose of the study is to evaluate whether recombinant IL-21 used in combination with rituximab is safe for patients with non-Hodgkin's lymphoma (NHL).

Details

Lead sponsorZymoGenetics
PhasePhase 1
StatusCOMPLETED
Enrolment23
Start date2006-06
Completion2008-04

Conditions

Interventions

Primary outcomes

Countries

United States