drugset / Trial / NCT02635672
Phase I Dose Escalation Study for VIP152 in Patients With Advanced Cancer
Non-randomizedSequentialOpen-labelTreatment
Summary
Determine the safety, tolerability, pharmacokinetics, maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) of VIP152 (BAY 1251152) as monotherapy or in combination in patients with solid tumors and aggressive non-hodgkin's lymphoma (NHL).
Timeline
- Start
- 2016-02-10
- Primary completion
- 2024-11-11
- Completion
- 2024-11-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ENITOCICLIB | Small molecule | 5 mg | Intravenous |
| Subject | ENITOCICLIB | Small molecule | 10 mg | Intravenous |
| Subject | ENITOCICLIB | Small molecule | 15 mg | Intravenous |
| Subject | ENITOCICLIB | Small molecule | 22.5 mg | Intravenous |
| Subject | ENITOCICLIB | Small molecule | 30 mg | Intravenous |
| Background | Pembrolizumab | Monoclonal antibody | 200 mg | Intravenous |