Increlex Treatment of Children With Chronic Liver Disease and Short Stature
Primary Purpose
Growth Failure, Chronic Liver Disease
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Increlex
Sponsored by
About this trial
This is an interventional treatment trial for Growth Failure focused on measuring pre-pubertal children, pre-transplant, not treated with growth hormone for at least 3 months
Eligibility Criteria
Inclusion Criteria:
Pre liver transplant patients with:
- Chronic liver disease
- Short stature (< 5%)
- Low IGF-1 (<-1SDS for age)
- Chronologic age 4-18 and bone age < 14 for boys and < 12 for girls (pre-pubertal)
Exclusion Criteria:
- Status post transplant
- Evidence of malignancy
- Diabetes mellitus
- Participation in other clinical trials involving investigational products
- Treatment with growth hormone within 3 months
- Pregnancy
- Significant abnormality in clinical results
- Hypoglycemic at baseline
- Allergic to benzyl alcohol
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
All patients will be treated with IGF-1 factors
Arm Description
Patients will serve as their own control.
Outcomes
Primary Outcome Measures
Growth velocity is the primary outcome. Improved height SDS
Improved growth velocity with improved height standard deviation scores (SDS) is the primary expected result.
Secondary Outcome Measures
Improved BMI
An improved body mass index is a secondary expected result of this study.
Improved quality of life
An improved quality of life as assessed by the Pediatric Quality of Life Inventory forms is another expected result.
Full Information
NCT ID
NCT01314508
First Posted
March 8, 2011
Last Updated
July 12, 2016
Sponsor
University of California, Los Angeles
1. Study Identification
Unique Protocol Identification Number
NCT01314508
Brief Title
Increlex Treatment of Children With Chronic Liver Disease and Short Stature
Official Title
Increlex Treatment of Children With Chronic Liver Disease and Short Stature
Study Type
Interventional
2. Study Status
Record Verification Date
July 2016
Overall Recruitment Status
Withdrawn
Why Stopped
The sponsor has notified us that they are not funding the study
Study Start Date
June 2011 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
University of California, Los Angeles
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A major consequence of chronic liver disease in childhood is growth failure. This is because a chemical essential for growth called growth factor is created in the liver. Lack of response to growth hormone in people with chronic liver disease is characterized by high levels of growth hormone and low levels of growth factors. This growth hormone resistance is reflected in a variety of factors including insulin resistance and low nutritional intake. Unfortunately, growth hormone therapy has no effect for children with liver disease. In addition, failure of normal growth or malnutrition makes liver disease even worse in children, and growth hormone therapy is not likely to reverse this. A lack of proper nutrition is associated with hospitalizations and frequent complications. Poor growth is a predictor of poor outcomes after liver transplantation. Thus the management of children with liver disease remains a challenge. Children who have successful orthotopic liver transplants (OLT) show much improvement in some aspects of growth, including skin fold thickness, mid-arm circumference, and normalization of growth factor levels. However, some studies have recently reported that the growth of 15-20% of children remains poor even after a liver transplant. This can be explained by persistent abnormalities in growth factors after transplant.
Growth factor was found to be a good tool for prognosis in patients with chronic liver disease. Studies showed that patients with liver cirrhosis and growth factor levels below normal values showed lower long-term survival rates compared with patients who had above normal values. This suggests that growth factor can be a good predictor of survival and early marker of poor liver function. In this case, aggressive feeding may modestly improve growth factor levels leading to improved growth but it is unlikely that effects will be optimal. The investigators propose that growth factor administration may have a positive effect that leads to better growth which is a major predictor of good outcome. To date, no reports study the use of growth factor in children with chronic liver disease. This study proposes to examine the effect of growth factor therapy in childhood chronic liver disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Growth Failure, Chronic Liver Disease
Keywords
pre-pubertal children, pre-transplant, not treated with growth hormone for at least 3 months
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
All patients will be treated with IGF-1 factors
Arm Type
Other
Arm Description
Patients will serve as their own control.
Intervention Type
Drug
Intervention Name(s)
Increlex
Intervention Description
Increlex therapy will begin at 40 micrograms/kg/day twice a day. The dose will be escalated by 20 mcg twice a day every other week up to 100mcg/kg/week.
Primary Outcome Measure Information:
Title
Growth velocity is the primary outcome. Improved height SDS
Description
Improved growth velocity with improved height standard deviation scores (SDS) is the primary expected result.
Time Frame
One year of therapy
Secondary Outcome Measure Information:
Title
Improved BMI
Description
An improved body mass index is a secondary expected result of this study.
Time Frame
12 months
Title
Improved quality of life
Description
An improved quality of life as assessed by the Pediatric Quality of Life Inventory forms is another expected result.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pre liver transplant patients with:
Chronic liver disease
Short stature (< 5%)
Low IGF-1 (<-1SDS for age)
Chronologic age 4-18 and bone age < 14 for boys and < 12 for girls (pre-pubertal)
Exclusion Criteria:
Status post transplant
Evidence of malignancy
Diabetes mellitus
Participation in other clinical trials involving investigational products
Treatment with growth hormone within 3 months
Pregnancy
Significant abnormality in clinical results
Hypoglycemic at baseline
Allergic to benzyl alcohol
12. IPD Sharing Statement
Learn more about this trial
Increlex Treatment of Children With Chronic Liver Disease and Short Stature
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