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A Study to Assess Growth in Children With Idiopathic Short Stature

Recruitingn/aAges 2 Years - 16 YearsAllBioMarin Pharmaceutical
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In plain words

What the trial is, and whether it could suit you

Study 111-903 will generate baseline growth data in children with ISS by collecting growth measurements and other variables of interest.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: 1. Participants must be \> 2 years old, and ≤ 14 years old (female) or ≤ 16 years old (males) at the time of signing the informed consent. 2. A height assessment corresponding to a height Z-score of ≤ -2.25 SDs in reference to the general population of the same age and sex, as calculated using the Centers for Disease Control and Prevention (CDC) growth chart (https://www.cdc.gov/growthcharts/zscore.htm). 3. Participants who have either never received hGH, or who are currently receiving hGH treatment. 4. Historic stimulation test result with serum or plasma GH level greater than 10 μg/L. 5. Parent(s) or guardian(s) are willing and able to provide written, signed informed consent. Exclusion Criteria: 1. Diagnosis of systemic disease or condition that may cause short stature, eg renal, neoplastic, pulmonary, cardiac, gastrointestinal, immunologic and metabolic disease. Children with such diagnoses can be considered for inclusion if their condition is well controlled, at the discretion of the Medical Monitor. 2. Known presence of one or more pituitary hormone deficiencies 3. Bone age advanced over chronological age by more than 3 years. 4. For hGH naïve participants, historic stimulation test result with serum or plasma GH level greater than 10 μg/L or serum IGF-1 in the normal range for age (between -1.00 SDs and +2.00 SDs). 5. For participants currently on hGH treatment, historic results before GH treatment of stimulation test with serum or plasma GH level greater than 10 μg/L or serum IGF-1 test between -1.00 SDs and +2.00 SDs. 6. Have received an investigational product (IP) or investigational medical device for any purpose within 6 months before the Screening visit. .
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What it tests

  • Not listed
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Where

38 sites
Phoenix Children's Hospital - Thomas Campus (Main)
Phoenix, United States
Children's Hospital Los Angeles
Los Angeles, United States
Harbor-UCLA Medical Center - The Lundquist Institute (Los Angeles Biomedical Research Institute (LA BioMed)
Los Angeles, United States
Children's Hospital of Orange County Main Campus - Orange
Orange, United States
Center Of Excellence in Diabetes and Endocrinology
Sacramento, United States
Rady Children's Hospital - San Diego
San Diego, United States
University of California San Francisco (UCSF)
San Francisco, United States
Connecticut Children's Medical Center
Hartford, United States

…and 30 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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