Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency
Growth Disorders, Insulin-Like Growth Factor-1 Deficiency
About this trial
This is an interventional treatment trial for Growth Disorders focused on measuring Primary IGF-1 Deficiency
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.
Sites / Locations
- Ipsen (formerly Tercica)
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
No Intervention
Experimental
Experimental
Experimental
Untreated
40 μg/kg BID (twice daily dosing)
80 μg/kg BID (twice daily dosing)
120 μg/kg BID (twice daily dosing)
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