Reyes Maribel, Lutz Justin D, Lau Audrey H, Gaggar Anuj, Grant Ethan P, Joshi Adarsh, Mackman Richard L, Ling John, Tan Susanna K, Ayithan Natarajan, Daffis Stephane, Woo Jacky, Wu Peiwen, Lam Tina, Fletcher Simon P, Kottilil Shyamasundaran, Poonia Bhawna, Gane Edward J, Mathias Anita, German Polina
Clinical Pharmacology, Gilead Sciences, Foster City, CA, USA.
Clinical Research, Gilead Sciences, Foster City, CA, USA.
Antivir Ther. 2020;25(3):171-180. doi: 10.3851/IMP3363.
Selgantolimod is a novel oral, selective Toll-like receptor 8 (TLR8) agonist in development for the treatment of chronic hepatitis B (CHB). TLR8 is an endosomal innate immune receptor and a target for treatment of viral infections. This first-in-human study investigated the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of selgantolimod in healthy volunteers.
Of 71 subjects enrolled, 59 received a single dose of selgantolimod (0.5, 1.5, 3 or 5 mg) or placebo, and 12 were evaluated for food effect. Safety, PK and PD activity by induction of cytokines, chemokines and acute phase proteins were assessed. PK/PD analyses were conducted.
Single doses of 0.5-5 mg were generally safe. No serious adverse events (AEs) or AEs leading to discontinuation were reported, and most were Grade 1 in severity. Selgantolimod displayed rapid absorption and dose-proportional PK and PD activity. Food had minimal effect on PK but resulted in diminished PD activity. In PK/PD analyses, near-saturation of induction for most evaluated biomarkers occurred at the 5-mg dose.
Single doses of up to 5 mg selgantolimod were safe and induced dose-dependent PD responses. These data support evaluation of selgantolimod in combination with other agents in future clinical studies of CHB. Australian New Zealand Clinical Trials Registration: ACTRN12616001646437.
塞尔甘托利莫德是一种新型口服选择性Toll样受体8(TLR8)激动剂,正处于治疗慢性乙型肝炎(CHB)的研发阶段。TLR8是一种内体固有免疫受体,也是治疗病毒感染的靶点。这项首次人体研究调查了塞尔甘托利莫德在健康志愿者中的安全性、耐受性、药代动力学(PK)和药效学(PD)。
在71名入组受试者中,59名接受了单剂量的塞尔甘托利莫德(0.5、1.5、3或5毫克)或安慰剂,12名受试者评估了食物影响。评估了安全性、PK以及通过诱导细胞因子、趋化因子和急性期蛋白的PD活性。进行了PK/PD分析。
0.5 - 5毫克的单剂量一般是安全的。未报告严重不良事件(AE)或导致停药的AE,大多数AE严重程度为1级。塞尔甘托利莫德显示出快速吸收以及剂量成正比的PK和PD活性。食物对PK影响极小,但导致PD活性降低。在PK/PD分析中,大多数评估生物标志物的诱导在5毫克剂量时接近饱和。
高达5毫克的塞尔甘托利莫德单剂量是安全的,并诱导剂量依赖性的PD反应。这些数据支持在未来CHB临床研究中评估塞尔甘托利莫德与其他药物联合使用。澳大利亚和新西兰临床试验注册:ACTRN12616001646437。