Safety and Efficacy of Somatropin in Children With Growth Hormone Deficiency
Status: | Completed |
---|---|
Conditions: | Endocrine, Endocrine |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 3 - 17 |
Updated: | 3/1/2017 |
Start Date: | May 8, 2001 |
End Date: | March 5, 2003 |
Norditropin® and Norditropin® Cartridges: An Open-Label, Randomized, Comparative Safety and Efficacy Trial in Children With Growth Hormone Deficiency
This trial is conducted in the United States of America (USA). The aim of this trial is to
evaluate the safety profiles of Norditropin® (lyophilized somatropin) and Norditropin®
cartridges (liquid somatropin) in children with growth hormone deficiency.
evaluate the safety profiles of Norditropin® (lyophilized somatropin) and Norditropin®
cartridges (liquid somatropin) in children with growth hormone deficiency.
Inclusion Criteria:
- Diagnosis of short stature (height maximum 2 standard deviations of mean for age and
gender) or inadequate growth deemed secondary to growth hormone deficiency (GHD)
- Naïve to growth hormone therapy
Exclusion Criteria:
- Known or suspected allergy to the trial product or related products
- Growth retardation attributable to causes other than GHD. Growth retardation
attributable to diabetes mellitus, inborn errors of metabolism, primary bone disease,
chromosomal disorders or disease of the genitourinary, cardiopulmonary,
gastrointestinal or central nervous system; bone marrow transplantation or any
syndrome known to give short stature (examples are: Prader-Willi Syndrome,
Russell-Silver Syndrome, Turner Syndrome, Noonan Syndrome)
- Intrauterine growth retardation: birth weight below 3rd percentile, adjusted for
gestational age
- Pregnancy or the intention to become pregnant
- Breast-feeding
- Administration of other growth-altering medication
We found this trial at
18
sites
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