跳至主要内容
临床试验/EUCTR2004-002991-40-Outside-EU/EEA
EUCTR2004-002991-40-Outside-EU/EEA进行中(未招募)不适用

Evolution of Growth Rate in Children Suffering From aDisease Associated With Growth Retardation and Treated byGenotonorm. A Pilot Study

Pfizer Inc0 个研究点目标入组 46 人开始时间: 2015年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Pfizer Inc
入组人数
46

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. For GH treatment issue bone age should be less than (<) 13 years for a boy and < 11 years for a girl.2. Naïve child: with measured height should be < 2.5 SD for chronological age (CA).
  • Child currently treated by GH should have annual growth rate greater than equal to (>=) +1 SD and measured height <-2.5 SD for CA at the time GH was started.
  • 3. Documented disease or pathological conditions known to be associated with growth
  • retardation and/or an adult height < -2 SD.
  • 4. Children with the same pathological condition or disease.
  • 5. Genotonorm treatment can be initiated by a physician according to the French SCP. that is to say a physician working in a hospital pediatric department or in a hospital endocrinology and metabolic disease department and, who is a pediatrician and/or a pediatric endocrinologist
  • 6. The child benefits of the French social security cover.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 46
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Idiopathic short stature.
  • 2. Pathological condition or disease for which GH treatment is already approved in France.
  • 3. Glucose intolerance on an oral glucose tolerance test dated less than 3 months or diabetes mellitus.
  • 4. Syndrome known to be associated with an increased risk of cancer example. family history of adenomatous polyposis.
  • 5. Participation in any other studies involving investigational or marketed products, concomitantly or within 30 days prior to entry in the study.
  • 6. Unable and/or unlikely to comprehend and/or follow GH treatment and/or the
  • 7. A previous history of intolerance or hypersensitivity to the study drug, or to drugs with similar chemical structures.
  • 8. Subjects who are known or are suspected allergic to the preservative metacresol.
  • 9. Pharmacological treatment with steroids for 1 year or more.

研究者

发起方
Pfizer Inc

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