A Study to Assess Growth in Children With Idiopathic Short Stature

Brief Summary
Study 111-903 will generate baseline growth data in children with ISS by collecting growth measurements and other variables of interest.
Brief Title
A Study to Assess Growth in Children With Idiopathic Short Stature
Central Contacts
Central Contact Role
Contact
Central Contact Phone
18009834587
Central Contact Email
Medinfo@bmrn.com
Completion Date
Completion Date Type
Estimated
Conditions
Idiopathic Short Stature
Eligibility Criteria
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. .
Inclusion Criteria
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.

Gender
All
Gender Based
false
Healthy Volunteers
No
Last Update Submit Date
Maximum Age
16 Years
Minimum Age
2 Years
NCT Id
NCT06309979
Org Class
Industry
Org Full Name
BioMarin Pharmaceutical
Org Study Id
111-903
Overall Status
Recruiting
Primary Completion Date
Primary Completion Date Type
Estimated
Official Title
A Multicenter, Observational Study to Characterize Growth in Children With Idiopathic Short Stature
Primary Outcomes
Outcome Measure
Change in annualized growth velocity (AGV)
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Change in Height Z-score
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Change in Standing Height
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Change in BMI
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Change in BMI Z-score
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Secondary Outcomes
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Frequency of event rates of medical events of interest
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Frequency of Serious Medical Events
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Association between specific variants and growth velocity
Outcome Time Frame
Every 6 months through end of study, up to 15 years
Outcome Measure
Association between other health outcomes directly related to short stature
Start Date
Start Date Type
Actual
Status Verified Date
First Submit Date
First Submit QC Date
Study Population
The study population will include up to 600 pediatric individuals with Idiopathic Short Stature.
Std Ages
Child
Maximum Age Number (converted to Years and rounded down)
16
Minimum Age Number (converted to Years and rounded down)
2
Investigators
Investigator Type
Principal Investigator
Investigator Name
Laurie Cohen
Investigator Email
lacohen@montefiore.org