This study includes two cohorts, cohort A is for non-squamous NSCLC and cohort B is for squamous NSCLC.
This study is a study of SSGJ-707 monotherapy in First-line PD-L1 Positive advanced NSCLC Patients. This study includes two cohorts, cohort A is for non-squamous NSCLC and cohort B is for squamous NSCLC. Each cohort will assess the efficacy and safety of the preset several dose levels of SSGJ-707 in advanced NSCLC Patients.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
120
bispecific antibody
The Hunan Cancer Hospital
Changsha, Hunan, China
RECRUITINGORR
Objective response rate
Time frame: 12 months
Safety and tolerability
Safety and tolerability assessed by incidence and severity of adverse events
Time frame: 12 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.