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Completed

NCT Number: NCT02500316

Long Term Follow up Study of Long-acting hGH (MOD-4023) in Growth Hormone Deficient Children

Protocol CP-4-004-OLE (Open Label Extension) is designed as a long-term, open-label extension using single patient use, multi-dose, disposable pre-filled pen.

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Key information

Age range

3 year–11 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

2DKB, Minsk, Belarus

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patients who completed the first year of treatment in the main study are allowed to enter the (Long Term) Open Label Extension (OLE) study.

Exclusion criteria

  • Children with past or present intracranial tumor growth as confirmed by an MRI scan (with contrast).
  • History of radiation therapy or chemotherapy.
  • Malnourished children defined as:
  • Serum albumin below the lower limit of normal (LLN) according to the reference ranges of central laboratory;
  • Serum iron below the lower limit of normal (LLN) according to the reference ranges of central laboratory;
  • BMI < -2 Standard Deviation for age and sex;
  • Children with psychosocial dwarfism.
  • Children born small for gestational age (SGA - birth weight and/or birth length < -2 SD for gestational age).
  • Presence of anti-hGH antibodies at screening.
  • Any clinically significant abnormality likely to affect growth or the ability to evaluate growth, such as, but not limited to, chronic diseases like renal insufficiency, spinal cord irradiation, etc.
  • Patients with diabetes mellitus.
  • Patients with impaired fasting sugar (based on WHO; fasting blood sugar >110 mg/dl or 6.1 mmol/l) after repeated blood analysis.
  • Chromosomal abnormalities and medical "syndromes" (Turner's syndrome, Laron syndrome, Noonan syndrome, Prader-Willi Syndrome, Russell-Silver Syndrome, short stature homeobox-containing gene (SHOX) mutations/deletions and skeletal dysplasias), with the exception of septo-optic dysplasia.
  • Closed epiphyses.
  • Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids and methylphenidate for attention deficit hyperactivity disorder (ADHD), with the exception of hormone replacement therapies (thyroxine, hydrocortisone, desmopressin (DDAVP))
  • Children requiring glucocorticoid therapy (e.g. asthma) who are taking a dose of greater than 400 µg/d of inhaled budesonide or equivalents for longer than 1 month during a calendar year.
  • Major medical conditions and/or presence of contraindication to r-hGH treatment.
  • Known or suspected HIV-positive patient, or patient with advanced diseases such as AIDS or tuberculosis.
  • Drug, substance, or alcohol abuse.
  • Known hypersensitivity to the components of study medication.
  • Other causes of short stature such as coeliac disease, hypothyroidism and rickets.
  • The patient and/or the parent/legal guardian are likely to be non-compliant in respect to study conduct.
  • Participation in any other trial of an investigational agent within 30 days prior to Screening.

Treatment and study plan

MOD-4023

Drug

Once weekly injection of long acting r-hGH (MOD-4023) provided as a solution for injection containing 20 or 50 mg/mL MOD-4023 in a single patient use, multi-dose, disposable pre-filled pen (PEN).

Primary outcomes

  1. Annualized Height Velocity

    Time frame: 8 years

    A summary of the annualized HV at the end of each year for Periods III/IV (OLE Years 1 - 4) and V (PEN Years 1 - 5).

  2. Delta Height SDS Every 12 Months

    Time frame: 8 years

    A summary of annual change in height SDS at the end of each year for Periods III/IV (OLE Years 1 - 4) and V (PEN Years 1 - 5). Height SDS (Standard Deviation Score) reflects how an individual's height compares to the average for their age and sex, calculated using Growth Analyzer and based on Switzerland 1989 (Prader) reference. A z-score of 0 indicates a height equal to the population mean, while positive scores indicate above-average heights and negative scores reflect below-average heights.

Secondary outcomes

  1. Summary of IGF-1 SDS

    Time frame: 8 years

    A summary of IGF-I SDS at the end of each year for Periods III/IV (OLE Years 1 - 4) and V (PEN Years 1 - 5). IGF-1 SDS (Standard Deviation Score) reflects how an individual's IGF-1 level compares to the average for their age and sex, based on reference values from Bidlingmaier et al. (2014, The Journal of Clinical Endocrinology & Metabolism, 99(5):1712-1721). A z-score of 0 indicates a level equal to the population mean, while positive scores indicate above-average levels and negative scores reflect below-average levels. An IGF-1 SDS below -2 suggests deficiency, whereas a score above +2 is considered elevated. In the study, when IGF-1 SDS exceeded +2, a confirmatory test was performed, and if elevation was confirmed, the dose was reduced by 15%.

Sponsors and collaborators

Lead sponsor

OPKO Health, Inc.

Industry

Registry information

Official study title

Safety and Dose Finding Study of Different MOD-4023 Dose Levels Compared to Daily R-human Growth Hormone (hGH) Therapy in Pre-pubertal Growth Hormone Deficient Children

Important dates

Study start
2014
Primary completion
2023
Study completion
2023
First posted
Jul 16, 2015
Registry last updated
Apr 9, 2025

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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