drugset / Trial / NCT02432326
A Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
This is an open label, multi-center, phase 1 study of BBI608 and BBI503 administered orally in combination to patients with advanced solid tumors. The primary goal is to determine the safety, tolerability, and recommended phase II dose (RP2D) of the combination regimen.
Timeline
- Start
- 2015-04
- Primary completion
- 2019-12
- Completion
- 2020-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | AMCASERTIB | Small molecule | 100 mg | Oral |
| Subject | AMCASERTIB | Small molecule | 200 mg | Oral |
| Subject | Napabucasin | Small molecule | 80 mg | Oral |
| Subject | Napabucasin | Small molecule | 160 mg | Oral |
| Subject | Napabucasin | Small molecule | 240 mg | Oral |
| Subject | Napabucasin | Small molecule | 480 mg | Oral |