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依氟鸟氨酸阿尔法的安全性、药代动力学和药效学:在成人低磷酸酶血症中进行的第二代酶替代疗法的 1 期、剂量递增研究。

Safety, pharmacokinetics, and pharmacodynamics of efzimfotase alfa, a second-generation enzyme replacement therapy: phase 1, dose-escalation study in adults with hypophosphatasia.

机构信息

Program for Metabolic Bone Disorders, Vanderbilt University Medical Center, Nashville, TN 37232-8148, United States.

Development, Regulatory and Safety, Alexion, AstraZeneca Rare Disease, Boston, MA 02210, United States.

出版信息

J Bone Miner Res. 2024 Sep 26;39(10):1412-1423. doi: 10.1093/jbmr/zjae128.

Abstract

Hypophosphatasia (HPP) is a rare, inherited metabolic disease caused by deficient activity of tissue-nonspecific alkaline phosphatase (TNSALP). Efzimfotase alfa (ALXN1850) is a second-generation TNSALP enzyme replacement therapy in development for HPP. This first-in-human open-label, dose-escalating phase 1 trial evaluated efzimfotase alfa safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity. Fifteen adults (5/cohort) with HPP received efzimfotase alfa in doses of 15 mg (cohort 1), 45 mg (cohort 2), or 90 mg (cohort 3) as one intravenous (i.v.) dose followed by 3 weekly subcutaneous (s.c.) doses. The primary objective was to assess safety and tolerability. Secondary objectives included pharmacokinetics, pharmacodynamics of ALP substrates known to be biomarkers of disease (inorganic pyrophosphate [PPi] and pyridoxal 5'-phosphate [PLP]) and immunogenicity. Treatment-emergent adverse events (TEAEs) occurred in 12 (80%) participants. Eight (53%) participants had injection site reactions (ISRs), observed after 10 of 41 (24%) s.c. injections. Most ISR TEAEs were mild and resolved within 1-2 d. Peak and total exposures of efzimfotase alfa increased in a greater-than-dose proportional manner over the range of 15-90 mg after i.v. and s.c. dosing. The arithmetic mean elimination half-life was approximately 6 d; absolute bioavailability was 28.6%-36.8% over the s.c. dose range of 15-90 mg. Dose-dependent reductions in plasma concentrations of PPi and PLP relative to baseline reached nadir in the first week after i.v. dosing and were sustained for 3-4 wk after the last s.c. dose. Four (27%) participants tested positive for antidrug antibodies (ADAs), 3 of whom were ADA positive before the first dose of efzimfotase alfa. ADAs had no apparent effect on efzimfotase alfa pharmacokinetics/pharmacodynamics. No participants had neutralizing antibodies. Efzimfotase alfa demonstrated acceptable safety, tolerability, and pharmacokinetic profiles and was associated with sustained reductions in biomarkers of disease in adults with HPP, supporting further evaluation in adult and pediatric patients. Registration: ClinicalTrials.gov NCT04980248 (https://clinicaltrials.gov/study/NCT04980248).

摘要

低磷酸酯酶症(HPP)是一种罕见的遗传性代谢疾病,由组织非特异性碱性磷酸酶(TNSALP)活性缺乏引起。Efzimfotase alfa(ALXN1850)是一种正在开发的第二代 TNSALP 酶替代疗法,用于治疗 HPP。这项首次人体开放性、剂量递增的 1 期试验评估了 efzimfotase alfa 的安全性、耐受性、药代动力学、药效学和免疫原性。15 名 HPP 成年患者(每 5 名/队列)接受 15mg(队列 1)、45mg(队列 2)或 90mg(队列 3)的 efzimfotase alfa 静脉内(i.v.)单剂量,随后进行 3 周的皮下(s.c.)给药。主要目的是评估安全性和耐受性。次要目标包括药代动力学、ALP 底物的药效学,已知这些底物是疾病的生物标志物(焦磷酸(PPi)和吡哆醛 5'-磷酸(PLP))和免疫原性。治疗出现的不良事件(TEAEs)发生在 12 名(80%)参与者中。8 名(53%)参与者出现注射部位反应(ISR),在 41 次 s.c.注射中的 10 次后观察到。大多数 ISR TEAEs 为轻度,在 1-2d 内消退。静脉内和皮下给药后,efzimfotase alfa 的峰值和总暴露量以大于剂量比例的方式增加,范围为 15-90mg。算术平均消除半衰期约为 6d;在 15-90mg 的皮下剂量范围内,绝对生物利用度为 28.6%-36.8%。与基线相比,血浆中 PPi 和 PLP 浓度的剂量依赖性降低在静脉内给药后的第一周达到最低点,并在最后一次皮下给药后的 3-4 周内持续。4 名(27%)参与者检测到抗药物抗体(ADAs)阳性,其中 3 名在接受 efzimfotase alfa 首剂前就已阳性。ADAs 对 efzimfotase alfa 的药代动力学/药效学没有明显影响。没有参与者产生中和抗体。Efzimfotase alfa 表现出可接受的安全性、耐受性和药代动力学特征,并与 HPP 成年患者疾病生物标志物的持续降低相关,支持在成年和儿科患者中进一步评估。注册:ClinicalTrials.gov NCT04980248(https://clinicaltrials.gov/study/NCT04980248)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcc3/11425692/c411a1ee576a/zjae128f1.jpg

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