drugset / Trial / NCT02514447

Trilaciclib (G1T28) in Patients With Previously Treated Extensive Stage SCLC Receiving Topotecan Chemotherapy

NCT02514447 ↗

Phase 1/2 Completed 123 enrolled G1 Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This was a study to investigate the potential clinical benefit of trilaciclib (G1T28), a Cyclin Dependent Kinase (CDK) 4/6 inhibitor, in preserving the bone marrow and the immune system, in order to decrease chemotherapy-induced myelosuppression and improve anti-tumor efficacy when administered prior to topotecan in patients previously treated for extensive-stage SCLC. The study consisted of 2 parts: a limited open-label, dose-finding portion (Part 1), and a randomized double-blind portion (Part 2). Both parts included 3 study phases: Screening Phase, Treatment Phase, and Survival Follow-up Phase. The Treatment Phase began on the day of first dose with study treatment and completes at the Post-Treatment Visit.

Timeline

Start
2015-10-05
Primary completion
2018-09-28
Completion
2021-10-04

Outcome

Met primary endpoint

paper Compared with placebo, administration of trilaciclib prior to topotecan resulted in statistically significant and clinically meaningful decreases in DSN in cycle 1 PMID 33123968 ↗

paper and occurrence of SN (40.6% versus 75.9%; adjusted one-sided P = 0.016) PMID 33123968 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Topotecan Small molecule 0.75 mg/m2 Intravenous
Subject Topotecan Small molecule 1 mg/m2 Intravenous
Subject Topotecan Small molecule 1.25 mg/m2 Intravenous
Subject Topotecan Small molecule 1.5 mg/m2 Intravenous
Subject Trilaciclib Unknown 200 mg/m2 Intravenous
Subject Trilaciclib Unknown 240 mg/m2 Intravenous
Subject Trilaciclib Unknown 280 mg/m2 Intravenous