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Clinical Trials associated with GKL-006GKL-006 注射液联合经肝动脉化疗栓塞术(TACE)对比单纯TACE 用于不可切除的肝细胞癌患者中开放、对照单次给药的安全性、耐受性和 PK/PD 的 I 期临床试验
[Translation] Phase I clinical trial of the safety, tolerability and PK/PD of GKL-006 injection combined with transarterial chemoembolization (TACE) versus TACE alone in patients with unresectable hepatocellular carcinoma
评价 GKL-006 注射液联合 TACE 在不可切除的肝细胞癌患者中单次给药的安全性和耐受性,以确定联合方案的最大耐受剂量(MTD),并评价单次给药治疗的剂量限制性毒性(DLT)。
[Translation] To evaluate the safety and tolerability of a single dose of GKL-006 injection combined with TACE in patients with unresectable hepatocellular carcinoma, to determine the maximum tolerated dose (MTD) of the combination regimen, and to evaluate the dose-limiting toxicity (DLT) of single-dose treatment.
An Open Label, Randomized, Controlled, Clinical Trial of Adoptive Autologous Invariant Natural Killer T Cells for the Treatment of Progressed Hepatocellular Carcinoma Continuing on PD-1 Inhibitor Therapy
The goal of this clinical trial is to explore the efficacy and safety of autologous iNKT cells in patients with progressed hepatocellular carcinoma (HCC) after treatment with PD-1 antibody. The main question it aims to answer are:
the efficacy of autologous iNKT cells in patients with progressed HCC after treatment with PD-1 antibody.
the safety of autologous iNKT cells in patients with progressed HCC after treatment with PD-1 antibody.
Participants will be randomized 1:1 to receive Regorafenib + PD-1 + iNKT cells (RPI group) or the treatment of Regorafenib + PD-1 (RP group).
Researchers will compare RPI group and RP group to see whether the iNKT cells can achieve a better therapeutic effect on HCC patients with PD-1 resistance.
100 Clinical Results associated with GKL-006
100 Translational Medicine associated with GKL-006
100 Patents (Medical) associated with GKL-006
100 Deals associated with GKL-006