drugset / Trial / NCT03134638
A Study of SY-1365 in Adult Patients With Advanced Solid Tumors
Non-randomizedParallel-groupOpen-labelTreatment
Summary
This study consists of two parts. Part 1 is a dose-escalation/safety evaluation to provisionally identify a dose and regimen of SY-1365 for further evaluation in Part 2. Following the identification of a recommended dose and regimen from Part 1, the study entered Part 2 to further evaluate safety and the antitumor activity of SY-1365 in patients with select solid tumors, and to confirm target engagement and downstream pathway impact in patients with any solid tumor histology.
Timeline
- Start
- 2017-05-12
- Primary completion
- 2020-05-15
- Completion
- 2020-06-24
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SY-1365 | Unknown | — | Intravenous |
| Background | Carboplatin | Small molecule | — | — |
| Background | Fulvestrant | Small molecule | 500 mg | Intramuscular |