drugset / Trial / NCT03508011
A Study of IMP4297 in Patients With Advanced Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
This is a Phase I, first-in-human, open-label, dose-escalation study of IMP4297 administered orally once every day to patients with advanced solid tumors for whom standard therapy either does not exist or has proven to be ineffective or intolerable. Patients with advanced breast cancer, ovarian cancer or prostate cancer are preferred. There are two stages to this study: a dose-escalation stage and a dose-expansion stage.
Timeline
- Start
- 2017-08-23
- Primary completion
- 2020-12-16
- Completion
- 2020-12-16
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IMP4297 | Unknown | 2 mg | Oral |
| Subject | IMP4297 | Unknown | 50 mg | Oral |
| Subject | IMP4297 | Unknown | 100 mg | Oral |
| Subject | IMP4297 | Unknown | 120 mg | Oral |