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Spots Global Cancer Trial Database for A Study of Sapanisertib in Relapsed/Refractory NFE2L2-Mutated and Wild-Type Squamous Non-Small Cell Lung Cancer

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Trial Identification

Brief Title: A Study of Sapanisertib in Relapsed/Refractory NFE2L2-Mutated and Wild-Type Squamous Non-Small Cell Lung Cancer

Official Title: A Randomized, Open-Label Phase 2 Study of the TORC 1/2 Inhibitor Sapanisertib in Relapsed/Refractory NFE2L2 (NRF2)-Mutated and Wild-Type (WT) Squamous Non-Small Cell Lung Cancer (sqNSCLC)

Study ID: NCT05275673

Interventions

sapanisertib

Study Description

Brief Summary: This is a multicenter, randomized, open-label Phase 2 study of sapanisertib in biomarker-defined populations of sqNSCLC. Patients with NFE2L2 (the name for gene encoding the protein called NRF2)-mutated or wild-type sqNSCLC should have disease that has progressed on or after at least two prior systemic therapies for metastatic disease including platinum-doublet chemotherapy and a programmed cell death 1 ligand 1 (PD-L1) inhibitor. The study will evaluate sapanisertib monotherapy in patients with relapsed/refractory sqNSCLC as two separate groups: Group A: NFE2L2-mutated sqNSCLC and Group B: NFE2L2-WT sqNSCLC.

Detailed Description: NFE2L2 mutation status for all patients will be identified using local or central next generation sequencing (NGS) testing on archival or fresh tissue or circulating tumor deoxyribonucleic acid (ctDNA), the results of which must be reviewed and approved by the Sponsor prior to enrollment. Each group will be randomized 1:1 to one of two doses/schedules of sapanisertib. Approximately 30 NFE2L2-mutant and 20 NFE2L2-wild type patients will be enrolled. Patients will be treated with sapanisertib until disease progression per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1), unacceptable toxicity, withdrawal of consent, or death.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UC Davis Comprehensive Cancer Center, Davis, California, United States

Providence Medical Group Santa Rosa - Cancer Center, Santa Rosa, California, United States

Florida Cancer Specialists, Fort Myers, Florida, United States

Ocala Oncology Center, Ocala, Florida, United States

Florida Cancer Specialists, Tallahassee, Florida, United States

Norton Cancer Institute, Downtown, Louisville, Kentucky, United States

Karmanos Cancer Institute, Detroit, Michigan, United States

Washington University - Patient Care Coordinator Center, Saint Louis, Missouri, United States

Memorial Sloan Kettering Cancer Center - Thoracic, New York, New York, United States

Zangmeister Cancer Center, Columbus, Ohio, United States

Providence Cancer Institute Franz Clinic, Portland, Oregon, United States

UPMC Cancer Pavilion, Pittsburgh, Pennsylvania, United States

Tennessee Oncology, Nashville, Tennessee, United States

Virginia Cancer Specialist, PC, Fairfax, Virginia, United States

Contact Details

Name: Bradley J Sumrow, MD

Affiliation: Calithera Biosciences, Inc

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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