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Completed

NCT Number: NCT00125164

Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency

This study is intended to determine whether twice daily weight based dosing with recombinant human insulin-like growth factor (rhIGF-1) will safely and effectively increase the growth of prepubertal children with short stature associated with low IGF-1 levels but who produce sufficient growth hormone (GH). Subjects will be randomized to either an observation arm or to active treatment.

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Key information

Age range

3 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Ipsen (formerly Tercica)

Brisbane, California, 94005, United States

About this study

Prepubertal growth failure associated with primary IGF-1 deficiency (IGFD). Primary IGFD is a term that has been used to describe patients with intrinsic cellular defects in GH action. In this protocol, primary IGFD is defined as short stature (height standard deviation score[SDS]<-2 below the mean for age and gender), low serum IGF-1 (IGF-1 SDS <-2 below the mean for age and gender), and levels of growth hormone (GH) that are normal (≥7ng/mL) after a GH stimulation test. Primary IGFD is believed to result from a lower than normal ability to produce IGF-1 when exposed to normal levels of GH, i.e., a type of GH insensitivity or GH resistance.

This trial is one year, randomized, open label, observation-controlled, parallel-dose comparison efficacy and safety study conducted in approximately 40 centers across the United States.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronological age ≥ 3 and chronological or bone age less than or equal to 11 years inclusive in girls;
  • Chronological age ≥ 3 and chronological or bone age less than or equal to 12 years inclusive for boys
  • Prepubertal
  • Height SD score of < -2
  • IGF-1 SD score of < -2

Exclusion criteria

  • Prior treatment with rhGH, rhIGF-1, or other growth-influencing medications
  • Growth failure associated with other identifiable causes (e.g., syndromes, chromosomal abnormality)
  • Chronic illness such as diabetes, cystic fibrosis, etc.

Treatment and study plan

rhIGF-1 (mecasermin, Tercica, Inc.)

Drug

Twice Daily Injection

Primary outcomes

  1. Height Velocity During the First Year - Intent to Treat (ITT)Population

    Time frame: Measured at baseline and at one year

    Height to be measured standing without shoes as the average of three measurements by the same observer using identical technique with a Harpenden or other wall mounted stadiometer. Reposition subject between each measurement.

Secondary outcomes

  1. Change From Baseline in Height Standard Deviation (SD) Score at One Year - ITT Population

    Time frame: Measured at baseline and at one year

    Height to be measured standing without shoes as the average of three measurements by the same observer using identical technique with a Harpenden or other wall mounted stadiometer. Reposition subject between each measurement. Please note that Standard Deviation (SD) Score is a term used in growth studies. The SD Score is calculated as the patient value minus the mean divided by the standard deviation. The mean and the standard deviation vary depending on the age and sex of the child.

  2. Changes in Bone Age From Baseline to One Year

    Time frame: Measured at baseline and at one year

    Plain X-rays of the left hand and wrist exposed for bone age appraisal. The films are sent to a central facility for standardized evaluation.

  3. Percent Changes From Baseline in Serum Concentrations of IGF-1 at One Year

    Time frame: Measured at baseline and at one year

    Blood sample was collected while subject is in a fasting state for measuring the level of IGF-1 in the growth factor panel.

  4. Percent Changes From Baseline in Serum Concentrations of IGF-2 at One Year

    Time frame: Measured at baseline and at one year

    Blood sample was collected for measuring the level of IGF-2 in the growth factor panel.

  5. Percent Changes From Baseline in Serum Concentrations of Insulin-like Growth Factor Binding Protein-2 (IGFBP-2) at One Year

    Time frame: Measured at baseline and at one year

    Blood sample was collected for measuring the level of insulin-like growth factor binding protein-2 (IGFBP-2) in the growth factor panel.

  6. Percent Changes From Baseline in Serum Concentrations of Insulin-like Growth Factor Binding Protein-3 (IGFBP-3) at One Year

    Time frame: Measured at baseline and at one year

    Blood sample was collected while subject is in a fasting state for measuring the level of IGFBP-3 in the growth factor panel.

  7. IGF Generation Test: Change of Serum IGF-1 After 7 Days Exposure to Recombinant Human Growth Hormone (rhGH)

    Time frame: Study Day 1 and Day 7

    Blood drawn at Study Day 1, followed by 7 days of rhGH daily dosing at 0.05 mg/kg of body weight. Additional blood draw at Study Day 7.

  8. IGF Generation Test: Change of Serum IGFBP-3 After 7 Days Exposure to Recombinant Human Growth Hormone (rhGH)

    Time frame: Study Day 1 and Day 7

    Blood drawn at Study Day 1, followed by 7 days of rhGH daily dosing at 0.05 mg/kg of body weight. Additional blood draw at Study Day 7.

Sponsors and collaborators

Lead sponsor

Ipsen

Industry

Registry information

Official study title

Recombinant Human Insulin-Like Growth Factor (rhIGF-1) Treatment of Prepubertal Children With Growth Failure Associated With Primary IGF-1 Deficiency: A Phase 3, Randomized, Open Label, Observation-Controlled, Multicenter, Parallel-Dose Comparison Trial

Important dates

Study start
2004
Primary completion
2008
Study completion
2008
First posted
Jul 29, 2005
Registry last updated
Sep 18, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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