drugset / Trial / NCT00830869
A Phase 1 Study of IXAZOMIB in Adult Patients With Advanced Nonhematologic Malignancies
Non-randomizedSingle-groupOpen-labelTreatment
Summary
This is an open-label, multicenter, phase 1, dose escalation study of IXAZOMIB. The primary purpose of this study is to determine the safety profile, establish the maximum tolerated dose, and inform the phase 2 dose of IXAZOMIB administered intravenously in participants with nonhematologic malignancies.
Timeline
- Start
- 2009-03-02
- Primary completion
- 2012-04-20
- Completion
- 2012-04-20
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ixazomib | Unknown | 0.125 mg/m2 | Intravenous |
| Subject | Ixazomib | Unknown | 0.25 mg/m2 | Intravenous |
| Subject | Ixazomib | Unknown | 0.5 mg/m2 | Intravenous |
| Subject | Ixazomib | Unknown | 1 mg/m2 | Intravenous |
| Subject | Ixazomib | Unknown | 1.33 mg/m2 | Intravenous |
| Subject | Ixazomib | Unknown | 1.76 mg/m2 | Intravenous |
| Subject | Ixazomib | Unknown | 2.34 mg/m2 | Intravenous |
Indications
No indication recorded.