152
Participants
Start Date
August 10, 2023
Primary Completion Date
April 1, 2025
Study Completion Date
April 1, 2026
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.
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.
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.
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.
Shang Hai Pulmonary Hospital, Shanghai
Guangzhou Gloria Biosciences Co., Ltd.
INDUSTRY