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Effect of Oral Galactose on Focal Segmental Glomerulosclerosis (FSGS) Permeability Factor

Primary Purpose

Focal Segmental Glomerulosclerosis

Status
Terminated
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Galactose
Sponsored by
Northwell Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Focal Segmental Glomerulosclerosis focused on measuring FSGS, Permeability factor, Galactose, Primary FSGS, resistant to immunosuppressive medication

Eligibility Criteria

2 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary FSGS
  • Resistance to steroids and another immunosuppressive medication

Exclusion Criteria:

  • Secondary FSGS

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    1

    Arm Description

    Galactose

    Outcomes

    Primary Outcome Measures

    Reduction in FSGS permeability factor

    Secondary Outcome Measures

    Full Information

    First Posted
    December 31, 2008
    Last Updated
    September 8, 2015
    Sponsor
    Northwell Health
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00816478
    Brief Title
    Effect of Oral Galactose on Focal Segmental Glomerulosclerosis (FSGS) Permeability Factor
    Official Title
    Effect of Galactose on Permeability Factor in Patients With Focal Segmental Glomerulosclerosis (FSGS)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2015
    Overall Recruitment Status
    Terminated
    Why Stopped
    Study closed by Institutional Review Board
    Study Start Date
    December 2008 (undefined)
    Primary Completion Date
    December 2009 (Actual)
    Study Completion Date
    December 2009 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Northwell Health

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study is a proof-of-concept clinical study designed to test the hypothesis that oral administration of galactose can lower the level of a circulating factor that increases glomerular permeability to albumin in patients with resistant FSGS.
    Detailed Description
    Patients with resistant FSGS have persistent proteinuria and a high risk of progression to end stage kidney disease (ESKD). A circulating factor that increases glomerular permeability to albumin (Palb) has been detected in over 50% of these patients. While the molecular identity of the factor has not been fully established, in vitro studies and limited clinical experience suggest that galactose can reduce the level of the FSGS permeability factor. This study is a pilot study to determine if oral administration of galactose can lower the circulating level of the FSGS permeability factor. Two groups of patients with biopsy proven primary FSGS who are resistant to steroids and one other immunosuppressive agents will be studied: l. FSGS, pre-ESKD 2. FSGS, with ESKD on renal replacement therapy The only eligibility factor is presence of the FSGS permeability factor. Five patients will be included in each group. The experimental intervention is administration of galactose, orally, 0.2 g/kg body weight/dose twice daily. the duration of treatment will be 28 days,. Patients will be seen on days 0, 14, and 28 of treatment. They will be seen at week 8, 16 and 24 after discontinuation of the galactose. Physical examination and routine laboratory tests (SMAC, CBC, urine protein:creatinine ratio in an early morning sample) will be done at each visit. The FSGS permeability factor will be assayed at days 0 and 28 of treatment and 6 months after discontinuation of the galactose. The permeability factor will be tested in the laboratory of Virginia Savin MD (Medical college of Wisconsin) using previously described methods. All other treatments will be unchanged during the 28 day oral galactose Treatment Period. The study will be analyzed based on the number of patients in whom the FSGS permeability factor is lowered to normal levels.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Focal Segmental Glomerulosclerosis
    Keywords
    FSGS, Permeability factor, Galactose, Primary FSGS, resistant to immunosuppressive medication

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    15 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Experimental
    Arm Description
    Galactose
    Intervention Type
    Drug
    Intervention Name(s)
    Galactose
    Intervention Description
    Oral galactose, 0.2 g/kg/dose twice daily for 28 days
    Primary Outcome Measure Information:
    Title
    Reduction in FSGS permeability factor
    Time Frame
    28 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    2 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Primary FSGS Resistance to steroids and another immunosuppressive medication Exclusion Criteria: Secondary FSGS
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Howard Trachtman, MD
    Organizational Affiliation
    Schneider Children's Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    15384010
    Citation
    Trachtman H, Greenbaum LA, McCarthy ET, Sharma M, Gauthier BG, Frank R, Warady B, Savin VJ. Glomerular permeability activity: prevalence and prognostic value in pediatric patients with idiopathic nephrotic syndrome. Am J Kidney Dis. 2004 Oct;44(4):604-10.
    Results Reference
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    Effect of Oral Galactose on Focal Segmental Glomerulosclerosis (FSGS) Permeability Factor

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