Clinical Trial of IL - 22BP Safety, Tolerability, and Antitumor Activity in Refractory Solid Tumors.
This study aims to investigate the safety and efficacy of the IL-22BP in patients with refractory malignant solid tumors.
Male or female patients: aged ≥ 18 years old and ≤ 70 years old; [+7]
Have participated in other drug clinical trials within 4 weeks; [+11]