Wong Nancy, Bhagunde Pratik, Nyberg Joakim, Katragadda Suresh, Demissie Marek, Willemze Annemieke, Benson Craig, Macha Sreeraj
Sanofi, Cambridge, MA, USA.
Sanofi, Bridgewater, NJ, USA.
J Clin Pharmacol. 2025 Jul;65(7):860-872. doi: 10.1002/jcph.70008. Epub 2025 Mar 23.
Efanesoctocog alfa is a first-in-class high-sustained factor VIII (HSF) replacement therapy for treatment of hemophilia A. This article presents population pharmacokinetics (PopPK) of efanesoctocog alfa and repeated time-to-event (RTTE) analysis of bleeding episodes in adults/adolescents (≥12 years of age) and children (<12 years). The final PopPK dataset contained pooled data from 277 patients (4405 post-dose factor VIII [FVIII] activity records) from two Phase 1/2a studies (NCT03205163; EudraCT 2018-001535-51), and three Phase 3 studies, XTEND-1 (NCT04161495), XTEND-Kids (NCT04759131), and XTEND-ed (NCT04644575). The PopPK model developed was a linear one-compartment model including body weight effect on clearance and volume of central compartment; Asian race was identified as a statistically significant covariate on clearance. The final PopPK model adequately described the FVIII activity-time profiles in adults, adolescents, and children with once-weekly (QW) efanesoctocog alfa 50 IU/kg, consistent with experience in XTEND-1 and XTEND-Kids. Bleeding episodes in participants in XTEND-1 and XTEND-Kids were characterized by an RTTE model with a Weibull base hazard and effect of FVIII activity modeled by a power effect. The RTTE model showed the probability of being bleed-free in 1 year with efanesoctocog alfa 50 IU/kg QW regimen was >70% across all age groups, consistent with the observed clinical outcomes in the Phase 3 trials of highly effective protection from bleeding episodes in patients with severe hemophilia A, which validates the model's prediction of the long-term bleed hazard.
依费奈索托科因子α是用于治疗A型血友病的一流高持续因子VIII(HSF)替代疗法。本文介绍了依费奈索托科因子α的群体药代动力学(PopPK)以及成人/青少年(≥12岁)和儿童(<12岁)出血事件的重复事件发生时间(RTTE)分析。最终的PopPK数据集包含来自两项1/2a期研究(NCT03205163;EudraCT 2018 - 001535 - 51)以及三项3期研究XTEND - 1(NCT04161495)、XTEND - Kids(NCT04759131)和XTEND - ed(NCT04644575)的277名患者的汇总数据(4405次给药后因子VIII [FVIII]活性记录)。所建立的PopPK模型是一个线性单室模型,包括体重对清除率和中央室体积的影响;亚洲种族被确定为清除率的一个具有统计学意义的协变量。最终的PopPK模型充分描述了成人、青少年和儿童接受每周一次(QW)50 IU/kg依费奈索托科因子α治疗后的FVIII活性 - 时间曲线,这与XTEND - 1和XTEND - Kids的经验一致。XTEND - 1和XTEND - Kids参与者的出血事件采用具有威布尔基本风险的RTTE模型进行表征,FVIII活性的影响通过幂效应进行建模。RTTE模型显示,在所有年龄组中,采用每周一次50 IU/kg依费奈索托科因子α治疗方案,1年内无出血的概率>70%,这与3期试验中观察到的临床结果一致,即对重度A型血友病患者有高度有效的预防出血事件作用,从而验证了该模型对长期出血风险的预测。