Charité Research Organisation, Berlin, Germany.
Kiel University Institute of Clinical Molecular Biology, Kiel, Germany.
Clin Transl Sci. 2024 May;17(5):e13832. doi: 10.1111/cts.13832.
Olamkicept selectively inhibits the cytokine interleukin-6 (IL-6) trans-signaling pathway without blocking the classic pathway and is a promising immunoregulatory therapy for inflammatory bowel disease (IBD). These first-in-human, randomized, placebo-controlled, single- (SAD) and multiple-ascending dose (MAD) trials evaluated olamkicept safety, tolerability, pharmacokinetic, and pharmacodynamic characteristics. Doses tested in the SAD trial included seven single intravenous doses (0.75, 7.5, 75, 150, 300, 600, and 750 mg) and one subcutaneous (SC) dose (60 mg) given to healthy subjects (N = 64), and three intravenous doses (75 mg, 300 mg, and 750 mg) given to patients with Crohn's disease (CD; N = 24). Doses tested in the MAD trial included multiple intravenous doses (75, 300, and 600 mg once weekly for 4 weeks) given to healthy subjects (N = 24). No severe or serious treatment-emergent adverse events (TEAEs) were recorded. The most common TEAEs were headache, nasopharyngitis, and myalgia in the SAD trial, and diarrhea, headache, and cough in the MAD trial. Infusion-related reactions occurred in one and two subjects in the SAD and MAD trial, respectively, leading to treatment discontinuation in the MAD trial. Olamkicept showed dose-independent pharmacokinetics after single and multiple administrations, and there was no major difference in systemic exposure between healthy subjects and patients with CD. Complete target engagement (inhibition of phosphorylation of signal transducer and activator of transcription-3) was achieved in blood around or above olamkicept serum concentrations of 1-5 μg/mL. Overall, these results suggest that olamkicept is safe and well-tolerated in healthy subjects and patients with CD after single intravenous/SC and multiple intravenous administrations.
奥拉米昔单抗选择性抑制细胞因子白细胞介素 6(IL-6)的转信号通路,而不阻断经典途径,是一种有前途的炎症性肠病(IBD)的免疫调节治疗方法。这些首次人体、随机、安慰剂对照、单次(SAD)和多次递增剂量(MAD)试验评估了奥拉米昔单抗的安全性、耐受性、药代动力学和药效学特征。SAD 试验中测试的剂量包括 7 种单次静脉剂量(0.75、7.5、75、150、300、600 和 750mg)和一种皮下(SC)剂量(60mg),用于健康受试者(N=64),以及 3 种静脉剂量(75mg、300mg 和 750mg)用于克罗恩病(CD)患者(N=24)。MAD 试验中测试的剂量包括多次静脉剂量(75、300 和 600mg,每周一次,连续 4 周),用于健康受试者(N=24)。未记录到严重或严重的治疗相关不良事件(TEAEs)。SAD 试验中最常见的 TEAEs 是头痛、鼻咽炎和肌痛,MAD 试验中是腹泻、头痛和咳嗽。SAD 和 MAD 试验中分别有 1 名和 2 名受试者出现输液相关反应,导致 MAD 试验中停药。奥拉米昔单抗单次和多次给药后呈现剂量依赖性药代动力学,健康受试者和 CD 患者之间的全身暴露无明显差异。在奥拉米昔单抗血清浓度为 1-5μg/ml 左右或以上时,可实现完全的靶标结合(信号转导和转录激活因子 3 的磷酸化抑制)。总的来说,这些结果表明,奥拉米昔单抗在健康受试者和 CD 患者单次静脉注射/SC 和多次静脉注射后是安全且耐受良好的。