Synermore Biologics Co. Ltd, Taipei City, Taiwan.
Rabies Laboratory, Kansas State Veterinary Diagnostic Laboratory, Kansas State University, Manhattan, Kansas, USA.
Clin Pharmacol Drug Dev. 2021 Jul;10(7):807-817. doi: 10.1002/cpdd.917. Epub 2021 Jan 25.
SYN023 is a mixture of 2 humanized monoclonal antirabies antibodies (CTB011, CTB012). Two first-in-human studies evaluated ascending intramuscular (IM) injected doses (Study SYN023-001; N = 15) and IM vs subcutaneous (SC) administration (Study SYN023-003; N = 35) in healthy adults. In both studies, end points were safety, pharmacokinetics (PK), pharmacodynamics/rabies virus neutralizing activity (RVNA), and immunogenicity (anti-SYN023 antibodies). Adverse events were mild and infrequent at all doses tested by IM injection (0.3 mg/kg, 1.0 mg/kg, 2.0 mg/kg), or by SC injection (0.3 mg/kg). There were no apparent trends in adverse event frequency or nature with increased dose or with administration route. Serum PK of SYN023 component antibodies appeared comparable to each other at each dose tested and when administered IM versus SC with serum exposure doubling over the second week after administration. At the lowest dose tested (0.3 mg/kg) by either IM or SC injection, RVNA levels exceeded the concentration generally accepted as protective against rabies (≥0.5 IU/mL) by day 1 after administration. Supra-inhibitory levels persisted >42 days. RVNA increased with higher doses. Anti-CTB011 and anti-CTB012 antibodies occurred with no apparent effect on PK or safety. These data support the potential use of SYN023 in antirabies postexposure prophylaxis.
SYN023 是由 2 种人源化单克隆抗狂犬病抗体(CTB011、CTB012)组成的混合物。两项首次人体研究评估了递增肌内(IM)注射剂量(研究 SYN023-001;N=15)和 IM 与皮下(SC)给药(研究 SYN023-003;N=35)在健康成年人中的情况。在这两项研究中,终点是安全性、药代动力学(PK)、药效学/狂犬病病毒中和活性(RVNA)和免疫原性(抗 SYN023 抗体)。通过 IM 注射(0.3mg/kg、1.0mg/kg、2.0mg/kg)或 SC 注射(0.3mg/kg),所有测试剂量均观察到轻度和不频繁的不良事件。随着剂量增加或给药途径改变,不良事件的频率或性质没有明显的趋势。SYN023 成分抗体的血清 PK 似乎在每个测试剂量下彼此相似,并且在 IM 与 SC 给药时相似,给药后第 2 周血清暴露增加一倍。在通过 IM 或 SC 注射测试的最低剂量(0.3mg/kg)下,RVNA 水平在给药后第 1 天即超过了通常被认为可预防狂犬病的浓度(≥0.5IU/mL)。超抑制水平持续>42 天。RVNA 随剂量增加而增加。抗 CTB011 和抗 CTB012 抗体的出现并未对 PK 或安全性产生明显影响。这些数据支持 SYN023 在狂犬病暴露后预防中的潜在用途。