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临床试验/NCT01205152
NCT01205152已完成2 期

Extension Study of ENB-0040 (Human Recombinant Tissue-Nonspecific Alkaline Phosphatase Fusion Protein) in Severely Affected Infants and Young Children With Hypophosphatasia (HPP)

Alexion Pharmaceuticals, Inc.15 个研究点 分布在 3 个国家目标入组 10 人开始时间: 2009年4月最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
10
试验地点
15
主要终点
Long-term Tolerability of Subcutaneous (SC) Asfotase Alfa

研究概览

简要总结

This clinical trial studied the long term safety and efficacy of asfotase alfa in infants and young children with infantile onset HPP who completed study ENB-002-08 (NCT00744042).

Partial funding for this study was provided by the Office of Orphan Product Development (OOPD).

详细描述

Asfotase Alfa was formerly referred to as ENB-0040

Hypophosphatasia (HPP) is a life-threatening, genetic, and ultra-rare metabolic disease characterized by defective bone mineralization and impaired phosphate and calcium regulation that can lead to progressive damage to multiple vital organs, including destruction and deformity of bones, profound muscle weakness, seizures, impaired renal function, and respiratory failure. There are limited data available on the natural course of this disease over time, particularly in patients with the juvenile-onset form.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
24 Weeks 至 42 Months(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

asfotase alfa

Experimental

An initial single intravenous (IV) infusion of 2 mg/kg asfotase alfa, followed by subcutaneous (SC) injections of 1 mg/kg asfotase alfa 3 times per week

干预措施: asfotase alfa (Biological)

结局指标

主要结局

Long-term Tolerability of Subcutaneous (SC) Asfotase Alfa

时间窗: 84 months

Outcome measure is the number of patients with 1 or more treatment-emergent adverse event. The time period is from Baseline in the ENB-003-08 study to the end of the ENB-003-08 study.

Long-term Efficacy of Asfotase Alfa in Treating Rickets in Infants and Young Children With Hypophosphatasia (HPP).

时间窗: Up to 90 Months

Outcome measure is the evaluation of radiographic change in rickets severity using a qualitative Radiographic Global Impression of Change (RGI-C) Scale. Skeletal radiographs obtained at the patient's last assessment were compared with skeletal radiographs obtained before initiation of treatment (Baseline in Study ENB-002-08 \[NCT00744042\]). The RGI-C is a 7-point rating scale that ranges from -3 (indicative of severe worsening of HPP-associated rickets) to +3 (indicative of complete or near complete healing of HPP-associated rickets). The time period is pre-dose (Baseline from ENB-002-08 study) to the last assessment for each patient in the ENB-003-08 study, which represents up to 90 months of exposure for the combined studies.

次要结局

  • Long-term Pharmacodynamics (PD) of SC Asfotase Alfa: Plasma Inorganic Pyrophosphate (PPi) Levels(Up to 90 Months)
  • Long-term Pharmacodynamics (PD) of SC Asfotase Alfa: Pyridoxal-5-phosphate (PLP) Levels(Up to 90 Months)
  • Effect of SC Asfotase Alfa on Growth: Weight Z-scores(Up to 90 Months)
  • Effect of SC Asfotase Alfa on Growth: Height/Length Z-scores(Up to 90 Months)
  • Effect of SC Asfotase Alfa on Respiratory Function(Up to 90 Months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (15)

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