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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02500316
Other study ID # CP-4-004-extension
Secondary ID 2011-004553-60
Status Completed
Phase Phase 2
First received
Last updated
Start date February 2013
Est. completion date November 2023

Study information

Verified date February 2024
Source OPKO Health, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Protocol CP-4-004-EXT is designed as a long-term, open-label extension using single patient use, multi-dose, disposable pre-filled pen.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date November 2023
Est. primary completion date November 2023
Accepts healthy volunteers No
Gender All
Age group 3 Years to 11 Years
Eligibility 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: 1. Children with past or present intracranial tumor growth as confirmed by an MRI scan (with contrast). 2. History of radiation therapy or chemotherapy. 3. Malnourished children defined as: 1. Serum albumin below the lower limit of normal (LLN) according to the reference ranges of central laboratory; 2. Serum iron below the lower limit of normal (LLN) according to the reference ranges of central laboratory; 3. BMI < -2 Standard Deviation for age and sex; 4. Children with psychosocial dwarfism. 5. Children born small for gestational age (SGA - birth weight and/or birth length < -2 SD for gestational age). 6. Presence of anti-hGH antibodies at screening. 7. 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. 8. Patients with diabetes mellitus. 9. Patients with impaired fasting sugar (based on WHO; fasting blood sugar >110 mg/dl or 6.1 mmol/l) after repeated blood analysis. 10. 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. 11. Closed epiphyses. 12. 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)) 13. 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. 14. Major medical conditions and/or presence of contraindication to r-hGH treatment. 15. Known or suspected HIV-positive patient, or patient with advanced diseases such as AIDS or tuberculosis. 16. Drug, substance, or alcohol abuse. 17. Known hypersensitivity to the components of study medication. 18. Other causes of short stature such as coeliac disease, hypothyroidism and rickets. 19. The patient and/or the parent/legal guardian are likely to be non-compliant in respect to study conduct. 20. Participation in any other trial of an investigational agent within 30 days prior to Screening.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
MOD-4023
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).

Locations

Country Name City State
Belarus 2DKB Minsk
Greece Children's Hospital "P. A. Kyriakou" Athens
Hungary Buda Children's Hospital Budapest
Russian Federation Endocrinology Scientific Centre, Institute of Child Endocrinology Moscow
Russian Federation Russian Medical Academy of Postgraduate Education Moscow
Russian Federation SPGPMA Saint Petersburg
Russian Federation SamGMU Samara
Russian Federation SBEIHPE Ufa
Ukraine Donetsk Regional Children Clinical Hospital Donetsk
Ukraine Institute of Endocrinology Kiev
Ukraine Ukrainian Scientific Center of Endocrine Surgery Moh of Ukraine Kiev
Ukraine Odessa Regional Children'S Clinical Hospital Odessa
United States Nemours Children's Clinic Jacksonville Florida

Sponsors (1)

Lead Sponsor Collaborator
OPKO Health, Inc.

Countries where clinical trial is conducted

United States,  Belarus,  Greece,  Hungary,  Russian Federation,  Ukraine, 

Outcome

Type Measure Description Time frame Safety issue
Other IGFBP-3 levels on day 3 or 4 after MOD-4023 dosing 8 years
Primary Annual Height Velocity 8 years
Primary Delta height SDS every 12 months 8 years
Secondary Absolute IGF-I levels on day 4 after MOD-4023 dosing 8 years
Secondary IGF-I SDS on day 4 after MOD-4023 dosing 8 years
See also
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Completed NCT01947907 - Safety, PK/PD and Efficacy of ACP-001 Weekly Versus Daily hGH in Children With Growth Hormone Deficiency (GHD) Phase 2