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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
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 sponsor | ZymoGenetics |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 23 |
| Start date | 2006-06 |
| Completion | 2008-04 |
Conditions
- Lymphoma, Non-Hodgkin
Interventions
- recombinant human interleukin 21 and rituximab
Primary outcomes
- Incidence and severity of adverse events through 1 month after completing treatment — During treatment and through 1 month after completing treatment
- Incidence and grade of clinical laboratory abnormalities through 1 month after treatment — During treatment and through 1 month after completing treatment
Countries
United States