Study of Recombinant Interleukin 21 in Combination With Rituxan for Non-Hodgkin's Lymphoma
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- ZymoGenetics
- Study ID
- NCT00347971
- Phase
- PHASE1
- Status
- Completed
Conditions
- Lymphoma, Non-Hodgkin
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- recombinant human interleukin 21 and rituximab — DRUGrIL-21 (30, 100, 150 ug/kg) IV rituximab (375 mg/m2) IV
Study Details
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).
Key Dates
- Start date
- Jun 30, 2006
- Status verified
- Sep 2008
- Primary completion
- Apr 30, 2008
- Completion
- Apr 30, 2008
Study Design
- Enrollment
- 23 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Primary Outcome Measure
Incidence and severity of adverse events through 1 month after completing treatment [ Time Frame: During treatment and through 1 month after completing treatment ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, Los Angeles | Los Angeles | California | 90095 | - |
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