drugset / Trial / NCT03134638

A Study of SY-1365 in Adult Patients With Advanced Solid Tumors

NCT03134638

Phase 1 Terminated 107 enrolled Syros Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject SY-1365 Unknown Intravenous
Background Carboplatin Small molecule
Background Fulvestrant Small molecule 500 mg Intramuscular