Safety, Tolerability, and Efficacy of GLS-012 and GLS-010 in Patients With Advanced Non-Small Cell Lung Cancer

PHASE1/PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

152

Participants

Timeline

Start Date

August 10, 2023

Primary Completion Date

April 1, 2025

Study Completion Date

April 1, 2026

Conditions
Advanced Non-Small Cell Lung Cancer
Interventions
DRUG

GLS-012+GLS-010

Two dose levels will be evaluated for GLS-012+GLS-010 administered. GLS-012+GLS-010 will be given via intravenous (IV) infusion on Day 1 of each 21-day cycle until disease progression or loss of clinical benefit.

DRUG

GLS-012+GLS-010

Target dose levels will be evaluated for GLS-012+GLS-010 administered. GLS-012+GLS-010 will be given via intravenous (IV) infusion on Day 1 of each 21-day cycle until disease progression or loss of clinical benefit.

DRUG

GLS-012+GLS-010+pemetrexed+carboplatin

GLS-012+GLS-010 will be given via IV infusion on Day 1 of each 21-day cycle in combination with pemetrexed and carboplatin. Combination treatment will be administered 4\~6 cycles.GLS-012+GLS-010/GLS-010 may continue until disease progression or loss of clinical benefit.

DRUG

GLS-012+GLS-010+paclitaxel+carboplatin

GLS-012+GLS-010 will be given via IV infusion on Day 1 of each 21-day cycle in combination with paclitaxel and carboplatin. Combination treatment will be administered 4\~6 cycles.GLS-012+GLS-010/GLS-010 may continue until disease progression or loss of clinical benefit.

Trial Locations (1)

200433

Shang Hai Pulmonary Hospital, Shanghai

All Listed Sponsors
lead

Guangzhou Gloria Biosciences Co., Ltd.

INDUSTRY