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

NCT05978401 - Safety, Tolerability, and Efficacy of GLS-012 and GLS-010 in Patients With Advanced Non-Small Cell Lung Cancer | Biotech Hunter | Biotech Hunter