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A Phase I Study of Recombinant Human Interleukin-18 (SB-485232) in Combination With Ofatumumab After Autologous Peripheral Blood Stem Cell Transplantation for Lymphoma
The purpose of this study is to test the safety of rhIL-18 combined with ofatumumab to see what effects (good and bad) it has on subjects and their non-Hodgkin's lymphoma.
Details
| Lead sponsor | Michael John Robertson |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 9 |
| Start date | 2013-02 |
| Completion | 2017-08-03 |
Conditions
- Non-Hodgkin's Lymphoma
Interventions
- Ofatumumab combined with SB-485232
Primary outcomes
- To evaluate the the number of subjects with adverse events who receive SB-485232 when given in combination with ofatumumab — 8 weeks
Adverse events will be graded using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.0 which uses a scale of 1 (mild) to 5 (caused death).
Countries
United States