search
Back to results

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

Primary Purpose

Growth Disorders, Insulin-Like Growth Factor-1 Deficiency

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
rhIGF-1 (mecasermin, Tercica, Inc.)
Sponsored by
Ipsen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Growth Disorders focused on measuring Primary IGF-1 Deficiency

Eligibility Criteria

3 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Ipsen (formerly Tercica)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

No Intervention

Experimental

Experimental

Experimental

Arm Label

Untreated

40 μg/kg BID (twice daily dosing)

80 μg/kg BID (twice daily dosing)

120 μg/kg BID (twice daily dosing)

Arm Description

Observational Group

Injection of rhIGF-1 40 μg/kg BID. Per protocol amendment these subjects were reassigned to receive 120 μg/kg BID. Due to the dose change, the efficacy results for these subjects were analysed in a separate subanalysis. For all outcome measures, mean and standard deviations were not calculated for this arm.

Injection of rhIGF-1 80 μg/kg BID

Injection of rhIGF-1 120 μg/kg BID

Outcomes

Primary Outcome Measures

Height Velocity During the First Year - Intent to Treat (ITT)Population
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 Outcome Measures

Change From Baseline in Height Standard Deviation (SD) Score at One Year - ITT Population
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.
Changes in Bone Age From Baseline to 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.
Percent Changes From Baseline in Serum Concentrations of IGF-1 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.
Percent Changes From Baseline in Serum Concentrations of IGF-2 at One Year
Blood sample was collected for measuring the level of IGF-2 in the growth factor panel.
Percent Changes From Baseline in Serum Concentrations of Insulin-like Growth Factor Binding Protein-2 (IGFBP-2) 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.
Percent Changes From Baseline in Serum Concentrations of Insulin-like Growth Factor Binding Protein-3 (IGFBP-3) 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.
IGF Generation Test: Change of Serum IGF-1 After 7 Days Exposure to Recombinant Human Growth Hormone (rhGH)
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.
IGF Generation Test: Change of Serum IGFBP-3 After 7 Days Exposure to Recombinant Human Growth Hormone (rhGH)
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.

Full Information

First Posted
July 27, 2005
Last Updated
September 5, 2019
Sponsor
Ipsen
search

1. Study Identification

Unique Protocol Identification Number
NCT00125164
Brief Title
Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
July 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ipsen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Growth Disorders, Insulin-Like Growth Factor-1 Deficiency
Keywords
Primary IGF-1 Deficiency

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
137 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Untreated
Arm Type
No Intervention
Arm Description
Observational Group
Arm Title
40 μg/kg BID (twice daily dosing)
Arm Type
Experimental
Arm Description
Injection of rhIGF-1 40 μg/kg BID. Per protocol amendment these subjects were reassigned to receive 120 μg/kg BID. Due to the dose change, the efficacy results for these subjects were analysed in a separate subanalysis. For all outcome measures, mean and standard deviations were not calculated for this arm.
Arm Title
80 μg/kg BID (twice daily dosing)
Arm Type
Experimental
Arm Description
Injection of rhIGF-1 80 μg/kg BID
Arm Title
120 μg/kg BID (twice daily dosing)
Arm Type
Experimental
Arm Description
Injection of rhIGF-1 120 μg/kg BID
Intervention Type
Drug
Intervention Name(s)
rhIGF-1 (mecasermin, Tercica, Inc.)
Intervention Description
Twice Daily Injection
Primary Outcome Measure Information:
Title
Height Velocity During the First Year - Intent to Treat (ITT)Population
Description
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.
Time Frame
Measured at baseline and at one year
Secondary Outcome Measure Information:
Title
Change From Baseline in Height Standard Deviation (SD) Score at One Year - ITT Population
Description
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.
Time Frame
Measured at baseline and at one year
Title
Changes in Bone Age From Baseline to One Year
Description
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.
Time Frame
Measured at baseline and at one year
Title
Percent Changes From Baseline in Serum Concentrations of IGF-1 at One Year
Description
Blood sample was collected while subject is in a fasting state for measuring the level of IGF-1 in the growth factor panel.
Time Frame
Measured at baseline and at one year
Title
Percent Changes From Baseline in Serum Concentrations of IGF-2 at One Year
Description
Blood sample was collected for measuring the level of IGF-2 in the growth factor panel.
Time Frame
Measured at baseline and at one year
Title
Percent Changes From Baseline in Serum Concentrations of Insulin-like Growth Factor Binding Protein-2 (IGFBP-2) at One Year
Description
Blood sample was collected for measuring the level of insulin-like growth factor binding protein-2 (IGFBP-2) in the growth factor panel.
Time Frame
Measured at baseline and at one year
Title
Percent Changes From Baseline in Serum Concentrations of Insulin-like Growth Factor Binding Protein-3 (IGFBP-3) at One Year
Description
Blood sample was collected while subject is in a fasting state for measuring the level of IGFBP-3 in the growth factor panel.
Time Frame
Measured at baseline and at one year
Title
IGF Generation Test: Change of Serum IGF-1 After 7 Days Exposure to Recombinant Human Growth Hormone (rhGH)
Description
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.
Time Frame
Study Day 1 and Day 7
Title
IGF Generation Test: Change of Serum IGFBP-3 After 7 Days Exposure to Recombinant Human Growth Hormone (rhGH)
Description
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.
Time Frame
Study Day 1 and Day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ipsen Medical Director
Organizational Affiliation
Ipsen
Official's Role
Study Director
Facility Information:
Facility Name
Ipsen (formerly Tercica)
City
Brisbane
State/Province
California
ZIP/Postal Code
94005
Country
United States

12. IPD Sharing Statement

Learn more about this trial

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

We'll reach out to this number within 24 hrs