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临床试验/NCT00572156
NCT00572156终止2 期

Recombinant Human Growth Hormone (rhGH) and Recombinant Human Insulin-like Growth Factor-1 rhIGF-1) Combination Therapy in Children With Short Stature Associated With IGF-1 Deficiency: A Six-year, Randomized, Multi-center, Open-label, Parallel-group, Active Treatment Controlled, Dose Selection Trial

Ipsen1 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2007年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
Ipsen
入组人数
106
试验地点
1
主要终点
Height Velocity

研究概览

简要总结

IGF-1 (insulin-like growth factor-1) is a hormone that is normally produced in the body in response to another hormone called growth hormone. Growth Hormone is produced by a small gland at the base of the brain (the pituitary). Together IGF-1 and GH are large contributors to growth during infancy, childhood, and adolescence.

Children with IGF Deficiency are short and have an imbalance in the levels of growth hormone and IGF-1 that their body produces. Their growth hormone levels are normal or even high, but IGF-1 levels do not increase normally in response to growth hormone. As a result, they have a type of growth hormone insensitivity and an inability to grow normally.

This study is a test to see whether daily dosing with a combination of rhIGF-1 and rhGH will help children with IGFD grow taller more quickly than children treated with rhGH alone. The study medications, rhIGF-1 and rhGH, are approved by the US Food and Drug Administration (FDA) for use in some growth disorders in children, but the combination of rhIGF-1 and rhGH in children with IGF-1 deficiency (IGFD) is investigational.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Parents or legally authorized representatives must give signed informed consent before any trial-related activities
  • IGF-1 SDS of ≤ -1 for age and gender
  • Short stature, as defined by a height SDS of ≤ -2 for age and gender
  • Chronological age ≥ 5 years
  • Bone age ≤ 11 years in boys and ≤ 9 years in girls
  • GH sufficiency, defined as a maximal stimulated GH response of greater than or equal to 10 ng/mL at Visit 2 (note: upon approval of the Medical Monitor, the result of a prior GH stimulation test may satisfy this requirement).
  • Prepubertal status
  • Adequate nutrition as evidenced by a body mass index (BMI) greater than or equal to the 5th percentile for age and gender

排除标准

  • Severe Primary IGFD (defined as height and IGF-1 SDS ≤ 3, and stimulated GH response greater than or equal to 10 ng/mL)
  • Prior or current use of medications with the potential to alter growth patterns including GH, IGF-1, IGFBP-3, gonadotrophin agonists (e.g., Lupron), aromatase inhibitors, androgens and estrogens
  • Known or suspected allergy to rhGH, rhIGF-1 or a constituent of their formulations
  • Current use of medications for attention deficit disorder
  • A chronic health condition that requires anti-inflammatory steroids or daily medication unless approved by the Medical Monitor

研究组 & 干预措施

1. rhGH Alone

Active Comparator

干预措施: NutropinAq® (Somatropin [rDNA origin]) (Drug)

2. Combination Dose

Experimental

干预措施: Increlex® (Mecasermin [rDNA origin] injection) + NutropinAq® (Somatropin [rDNA origin]) (Drug)

3. Combination Dose

Experimental

干预措施: Increlex® (Mecasermin [rDNA origin] injection) + NutropinAq® (Somatropin [rDNA origin]) (Drug)

4. Combination Dose

Experimental

干预措施: Increlex® (Mecasermin [rDNA origin] injection) + NutropinAq® (Somatropin [rDNA origin]) (Drug)

结局指标

主要结局

Height Velocity

时间窗: First year of treatment

次要结局

  • Height Velocity(Second, third and fourth year)
  • Cumulative Change in Height Standard Deviation Score (SDS)(First, second, third and fourth year)
  • Predicted Adult Height (PAH)(At baseline (Day 1), year 1,2,3 and 4)
  • Changes From Baseline (Day 1) in Serum Concentrations of Insulin-Like Growth Factor Binding Protein-3 (IGFPB-3)(At Baseline (Day 1), Year 1,2,3 and 4)
  • Total Change From Baseline (Day 1) in BMI SDS(At year 1,2,3,4 and end of study (visit 23) versus baseline (day 1))
  • Skeletal Maturation(At baseline(day 1), year 1,2,3 and 4)
  • Changes From Baseline (Day 1) in Serum Concentrations of Growth Hormone (GH)(At Baseline (Day 1), Year 1,2,3 and 4)
  • Changes From Baseline (Day 1) in Serum Concentrations of Growth Hormone Binding Protein (GHBP)(At Baseline (Day 1), Year 1,2,3 and 4)
  • Changes From Baseline (Day 1) in Serum Concentrations of Insulin-Like Growth Factor Binding Protein-1 (IGFBP-1)(At Baseline (Day 1), Year 1,2,3 and 4)
  • Changes From Baseline (Day 1) in Serum Concentrations of Insulin-Like Growth Factor-1 (IGF-1)(At Baseline (Day 1), Year 1,2,3 and 4)
  • Changes From Baseline (Day 1) in Serum Concentrations of Acid-Labile Subunit (ALS)(At Baseline (Day 1), Year 1,2,3 and 4)
  • Summary of Adverse Events With Number of Occurrences(Approximately up to 4 years.)

研究者

发起方
Ipsen
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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