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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Withdrawn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
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

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

4 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    March 8, 2011
    Last Updated
    July 12, 2016
    Sponsor
    University of California, Los Angeles
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    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

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