drugset / Trial / NCT02298387
A Phase 1 Study of OMP-305B83 in Subjects With Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
This is an open-label Phase 1 dose escalation and expansion study of OMP-305B83 in subjects with previously treated solid tumors. Study includes a dose escalation phase and expansion phase. Subjects will be assessed for safety, immunogenicity, pharmacokinetics, biomarkers, and efficacy.
Timeline
- Start
- 2014-12-22
- Primary completion
- 2017-05-23
- Completion
- 2017-09-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | navicixizumab | Monoclonal antibody | 0.5 mg/kg | Intravenous |
| Subject | navicixizumab | Monoclonal antibody | 1 mg/kg | Intravenous |
| Subject | navicixizumab | Monoclonal antibody | 2.5 mg/kg | Intravenous |
| Subject | navicixizumab | Monoclonal antibody | 5 mg/kg | Intravenous |
| Subject | navicixizumab | Monoclonal antibody | 10 mg/kg | Intravenous |