Clinical Trial of Growth Hormone in MPS I, II, and VI

Phase 2

Terminated

Conditions: Mucopolysaccharidosis VI
Mucopolysaccharidosis I
Mucopolysaccharidosis II

Lead Sponsor: Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center

Brief Summary: The purpose of this study is to determine whether growth hormone is a safe and effective treatment for short stature in children with Mucopolysaccharidosis type I, II, and VI.

Detailed Description: Although children with MPS I, II, and VI who are treated with Hematopoietic Cell Transplantation (HCT) and/or enzyme replacement therapy (ERT) are living into adulthood with good cognitive development, their quality of life is significantly impacted by their skeletal abnormalities (i.e., kyphosis, scoliosis, and genu valgum), contractures, and severe short stature. Here at the University of Minnesota we have seen some promising clinical outcomes in children with MPS IH whom we have treated with human growth hormone (hGH). There are currently no reports in the literature of the impact of treating children with MPS and short stature, with hGH on their growth velocity or characteristic skeletal abnormalities. This study will advance the care of these children by providing data in this yet unexplored area of pediatric medicine with the goal of improving the quality of life for these children by improving height, mobility, and neuropsychological functioning.

This is a Phase II/III randomized, single-center, 12 month clinical trial of growth hormone in male and female participants with MPS I, II, or VI, followed by 12 months open label. Participants with height ≤ -2 SDS for age and gender will be randomized for the first 12 months 1:1 to treatment or no treatment. At the conclusion of the 12 months, all subjects will be offered an additional 12 months of treatment.

Recruitment & Eligibility

Inclusion Criteria

A parent or legally authorized representative must provide written informed consent and comply with study assessments for the full duration of the study.
Chronologic age ≥ 5 years and bone age ≤12 years
Diagnosis of MPS I, II, or VI
Height ≤ -2 SDS for age and gender
Ability to travel to study center for evaluations.
Ability of the participant to cooperate with study procedures, to notify a guardian of symptoms, and provide assent for participation in the study.

Exclusion Criteria

History of treatment with hGH
Untreated pituitary deficiency
Pregnancy (positive urine pregnancy test) prior to enrollment in the study
Participation in another simultaneous medical intervention trial
Patients with closed epiphysis
Active neoplasm
Orthopedic procedure of the femur within the last 6 months.
Known or suspected allergy to trial product or related products.
Structural lesion on brain MRI resulting in brain compression
Any other social or medical condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated or be detrimental to the study.
Obstructive sleep apnea without BiPAP or tonsillectomy/adenoidectomy treatment.
CNS shunt.
Abnormal cardiac function based on echocardiogram within 6 months prior to enrollment :
Ejection fraction less than 50%
Left ventricular chamber size greater than or less than 2 standard deviations of normal for body surface area
Left ventricular wall thickness greater than or less than 2 standard deviations of normal for body surface area
More than mild to moderate aortic insufficiency with abdominal aortic run-off
More than mild to moderate mitral insufficiency with pulmonary hypertension
Abnormal pulmonary function based on pulmonary function tests within 6 months prior to enrollment:
abnormal FVC < 80% of predicted for age, gender, and height
abnormal FEV1 < 80% predicted for age, gender, and height
abnormal FEV1/FVC
abnormal oxygen saturation