drugset / Trial / NCT03965845

A Study of Telaglenastat (CB-839) in Combination With Palbociclib in Patients With Solid Tumors

NCT03965845

Phase 1/2 Completed 53 enrolled Calithera Biosciences, Inc
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 1b/2 study to determine the recommended phase 2 dose (RP2D), safety and tolerability, pharmacokinetics (PK) and clinical activity of the glutaminase inhibitor telaglenestat (CB-839) with the CDK4/6 Inhibitor, palbociclib in participants with advanced/metastatic solid tumors.

Timeline

Start
2019-06-25
Primary completion
2021-09-24
Completion
2021-09-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Palbociclib Small molecule 75 mg Oral
Subject Palbociclib Small molecule 100 mg Oral
Subject Palbociclib Small molecule 125 mg Oral
Subject Telaglenestat Unknown 600 mg Oral
Subject Telaglenestat Unknown 800 mg Oral