About this trial
1\) Safety and efficacy of TCR-T cells in subjects with refractory/relapsed solid tumors. 2) The activation and proliferation of TCR-T cells in the subject, and the survival time.
Eligibility criteria
Qualifiers
Voluntarily participate in clinical research; fully understand this research and sign informed consent voluntarily; be willing to follow and have the ability to complete all experimental procedures;
Male or female, aged 18 to 70 years (inclusive);
Subjects with advanced malignant solid tumors confirmed by histology or cytology;
Dose escalation phase: subjects who have no standard treatment, or who have failed or relapsed after standard treatment, or who cannot tolerate standard treatment with positive target expression;
Disqualifiers
The neutrophil count (ANC) is not lower than the lower limit of the normal value of the center;
White blood cells (WBC) are not lower than the lower limit of the normal value of the center;
Platelet count (PLT) is not lower than the lower limit of normal value in our center;
Hemoglobin (Hb) not less than 0.8*LLN (lower limit of normal);
Trial design
Treatments tested in this trial
- KSH01 injection