drugset / Trial / NCT04265534

KEAPSAKE: A Study of Telaglenastat (CB-839) With Standard-of-Care Chemoimmunotherapy in 1L KEAP1/NRF2-Mutated, Nonsquamous NSCLC

NCT04265534

Phase 2 Terminated 40 enrolled Calithera Biosciences, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2, randomized, multicenter, double-blind study of the glutaminase inhibitor telaglenastat with standard-of-care pembrolizumab and chemotherapy versus placebo with standard-of-care pembrolizumab and chemotherapy for first line treatment of metastatic disease in patients with KEAP1/NRF2-mutated, stage IV, nonsquamous, non-small cell lung cancer (NSCLC). The study primary endpoints are PFS per RECIST v. 1.1 and safety. KEAP1/NRF2 mutation status (for eligibility) and STK11/LKB1 status (for stratification) will be determined by next generation sequencing. A commercial liquid biopsy (circulating tumor DNA) NGS test will be provided to study participants free of charge.

Timeline

Start
2020-07-24
Primary completion
2021-11-05
Completion
2022-02-09

Drugs

EvaluationDrugModalityDoseRoute
Subject CB-839 Unknown
Background Carboplatin Small molecule Intravenous
Background Dexamethasone Small molecule 4 mg Oral
Background Pembrolizumab Monoclonal antibody Intravenous
Background Pemetrexed Small molecule Intravenous