[Translation] Safety, tolerability, pharmacokinetics, immunogenicity and preliminary efficacy of HC006 combined with PD-1 inhibitor in patients with advanced solid tumors: a multicenter, open-label, dose-finding and multi-cohort dose-expansion Phase Ib clinical trial 
主要目的:评估HC006 联合PD-1 抑制剂治疗晚期实体瘤患者的耐受性和安全性,确定后续 研究推荐剂量(RD)
次要目的:(1)评估HC006 联合PD-1 抑制剂治疗晚期实体瘤患者的HC006 药代动力学特征;(2) 评估HC006 联合PD-1 抑制剂治疗晚期实体瘤患者的HC006 免疫原性;(3) 评估HC006 联合PD-1 抑制剂治疗晚期实体瘤患者的有效性。
探索性目的:(1)探索治疗前肿瘤组织中CD8+免疫细胞的浸润情况,以及CCR8 和PD-L1 表达水平;若数据允许,将探索治疗后CD8+免疫细胞的浸润情况,以及CCR8 和PD-L1 表达水平;(2) 探索治疗前后血液中细胞因子水平。
 [Translation] Primary objective: To evaluate the tolerability and safety of HC006 combined with PD-1 inhibitors in patients with advanced solid tumors and determine the recommended dose (RD) for subsequent studies
Secondary objectives: (1) To evaluate the pharmacokinetic characteristics of HC006 combined with PD-1 inhibitors in patients with advanced solid tumors; (2) To evaluate the immunogenicity of HC006 combined with PD-1 inhibitors in patients with advanced solid tumors; (3) To evaluate the efficacy of HC006 combined with PD-1 inhibitors in patients with advanced solid tumors.
Exploratory objectives: (1) To explore the infiltration of CD8+ immune cells in tumor tissues before treatment, as well as the expression levels of CCR8 and PD-L1; if data permit, to explore the infiltration of CD8+ immune cells after treatment, as well as the expression levels of CCR8 and PD-L1; (2) To explore the levels of cytokines in the blood before and after treatment.