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临床试验/NCT02233322
NCT02233322已完成不适用

Iron Therapy for Autosomal Dominant Hypophosphatemic Rickets: A Pilot

Indiana University2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2014年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
8
试验地点
2
主要终点
Does increasing serum iron concentrations above 100 mcg/dl in patients with ADHR result in a decrease in intact FGF23.

研究概览

简要总结

The purpose of the study is to gain a better understanding of the effect of iron on fibroblast growth factor 23 (FGF23) in the inherited disorder, autosomal dominant hypophosphatemic rickets (ADHR). ADHR is an inherited disorder in which the body makes too much FGF 23 and causes low blood phosphorus levels and bone problems such as rickets (bowed legs in children) or bone pain and weakness in adults. This study is to test whether or not giving iron helps correct the high FGF23 and there by correcting the phosphate problem.

详细描述

Iron will be provided in an open label treatment to all enrolled subjects. Iron levels will be monitored in blood and doses adjusted with the target of getting the iron levels to or a little above 100 mcg/dl.

The study will look to see if there is a decrease of FGF23 level. It will also look at how long does it take to decrease the level of FGF 23 and how long it takes for the serum and urine phosphate to normalize.

研究设计

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

入排标准

年龄范围
25 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • FGF Mutation in either Arginine 176 or arginine 179
  • able and willing to provide consent or have a parent that is able/willing to consent, if a minor
  • either serum iron <50mcg/dl (regardless of phosphate or intact FGF23 concentration); or iron between 500 and 100mcg/dl with serum phosphorus value below 3.0mg/dl for adults or less than or equal to 0.5 mg/dl the lower limit of normal for age in children and intact FGF23 about 30pg/ml
  • age >2 years
  • May be receiving treatment with phosphate and calcitriol, but must be willing to undergo dose adjustments by the investigators if iron resolves the phosphate wasting defect.

排除标准

  • malignancy within the last 5 years, except treated squamous or basal cell skin carcinoma
  • terminal illness/hospice.
  • severe end-organ disease, e.g. cardiovascular, pulmonary, etc, which may limit ability to complete study.
  • estimated GFR <45ml/min/1.73m2, calculated using MDRD formula for adults or modified Schwartz equation for children
  • pregnancy or plan on becoming pregnant

结局指标

主要结局

Does increasing serum iron concentrations above 100 mcg/dl in patients with ADHR result in a decrease in intact FGF23.

时间窗: FGF23 will be measured at 1, 2, 3, 6, 9, and 12 months

Perform a pilot study in ADHR patients with low serum iron concentrations (defined below) to determine if increasing serum iron concentrations above 100 mcg/dl results in a decrease in intact FGF23 (primary endpoint) and C-terminal FGF23 concentrations by at least 20% and normalizes serum phosphorus and TMP/GFR (tubular maximum phosphate reabsorption/ glomerular filtration rate) within 6 months of attaining goal iron concentrations.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Econs

Professor of Endocrinology and Metabolism

Indiana University

研究点 (2)

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