CTTQ
Status and phase
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About
This study is an open, single-center, multi-cohort phase Ib exploratory study, and 50 subjects are planned to be enrolled to observe the objective response rate of each subject. The safety evaluation of this study adopts common terminology criteria for adverse events version (CTCAE) 5.0 to evaluate the adverse events of drugs. Efficacy was evaluated using response evaluation criteria in solid tumors version (RECIST) 1.1 for immune-based therapeutics criteria.
Enrollment
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Inclusion criteria
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Primary purpose
Allocation
Interventional model
Masking
50 participants in 1 patient group
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Central trial contact
Jun Guo, Doctor; SiMing Li, Doctor
Data sourced from clinicaltrials.gov
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