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NCT Number: NCT06309979

A Study to Assess Growth in Children With Idiopathic Short Stature

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

Recruiting

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Key information

Age range

2 year–16 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Phoenix Children's Hospital - Thomas Campus (Main), Phoenix, Arizona, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must be > 2 years old, and ≤ 14 years old (female) or ≤ 16 years old (males) at the time of signing the informed consent.
  • 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).
  • Participants who have either never received hGH, or who are currently receiving hGH treatment.
  • Historic stimulation test result with serum or plasma GH level greater than 10 μg/L.
  • Parent(s) or guardian(s) are willing and able to provide written, signed informed consent.

Exclusion criteria

  • 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.
  • Known presence of one or more pituitary hormone deficiencies
  • Bone age advanced over chronological age by more than 3 years.
  • 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).
  • 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.
  • Have received an investigational product (IP) or investigational medical device for any purpose within 6 months before the Screening visit. .

Treatment and study plan

Primary outcomes

  1. Change in annualized growth velocity (AGV)

    Time frame: Every 6 months through end of study, up to 15 years

  2. Change in Height Z-score

    Time frame: Every 6 months through end of study, up to 15 years

  3. Change in Standing Height

    Time frame: Every 6 months through end of study, up to 15 years

  4. Change in BMI

    Time frame: Every 6 months through end of study, up to 15 years

  5. Change in BMI Z-score

    Time frame: Every 6 months through end of study, up to 15 years

Secondary outcomes

  1. Frequency of event rates of medical events of interest

    Time frame: Every 6 months through end of study, up to 15 years

  2. Frequency of Serious Medical Events

    Time frame: Every 6 months through end of study, up to 15 years

  3. Association between specific variants and growth velocity

    Time frame: Every 6 months through end of study, up to 15 years

  4. Association between other health outcomes directly related to short stature

    Time frame: Every 6 months through end of study, up to 15 years

Study contacts

Contact information is provided by the study sponsor or research team.

Trial Specialist

CONTACT

[email protected]

18009834587

Sponsors and collaborators

Lead sponsor

BioMarin Pharmaceutical

Industry

Registry information

Official study title

A Multicenter, Observational Study to Characterize Growth in Children With Idiopathic Short Stature

Important dates

Study start
2024
Primary completion
2040
Study completion
2040
First posted
Mar 13, 2024
Registry last updated
Jun 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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