drugset / Trial / NCT02252263
A Phase I Open Label Study of the Safety and Tolerability of Elotuzumab (BMS-901608) Administered in Combination With Either Lirilumab (BMS-986015) or Urelumab (BMS-663513) in Subjects With Multiple Myeloma
RandomizedParallel-groupOpen-labelTreatment
Summary
To assess the safety and tolerability, characterize the dose limiting toxicities (DLTs) and identify the maximally tolerated dose (MTD) of Elotuzumab administered in combination with either Lirilumab or Urelumab in subjects with multiple myeloma.
Timeline
- Start
- 2014-12-09
- Primary completion
- 2017-10-10
- Completion
- 2017-10-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Elotuzumab | Monoclonal antibody | — | Intravenous |
| Subject | Lirilumab | Monoclonal antibody | — | Intravenous |
| Subject | Urelumab | Monoclonal antibody | — | Intravenous |