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Safety and Efficacy of Intravenous Immune Globulin in Treating Spinocerebellar Ataxia

Primary Purpose

Spinocerebellar Ataxia

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
IVIG
Sponsored by
University of South Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinocerebellar Ataxia

Eligibility Criteria

10 Years - 50 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Outpatients with SCA diagnosed by a movement disorder specialist.
  2. Age 10 years to 80 years.
  3. Able to ambulate with or without assistance for 30 feet.
  4. Women of child-bearing potential must use a reliable method of contraception and must provide a negative pregnancy test at entry into the study.
  5. Serum creatine kinase, complete metabolic panel, complete blood count, liver function tests, renal function tests, platelets and EKG do not reveal clinically significant abnormalities (results obtained from primary care physician and dated within the past 6 months or obtained at screening visit).
  6. Stable doses of all medications for 30 days prior to study entry and for the duration of the study.
  7. Stable doses of all antidepressants and vitamins (including internet purchased idebenone) for 30 days prior to study entry and for the duration of the study. Throughout the study, all possible efforts should be made to maintain stable doses of all other medications.
  8. Subject permission (informed consent).

Exclusion Criteria:

  1. Any unstable illness that in the investigator's opinion precludes participation in this study.
  2. Use of any investigational product within the past 30 days.
  3. Presence of clinically significant cardiac disease (as determined by the investigator based on EKG and echocardiogram results within the past 6 months). Specifically, an ejection fraction <40%, or a prolonged QT interval (>50% of cycle duration) will be excluded. If the investigator notes clinically significant abnormalities on the EKG or echocardiogram, the subject will be eligible IF they provide clearance from a cardiologist.
  4. Presence of diabetes (as determined by blood glucose labs within the past 6 months).
  5. Dementia or other psychiatric illness that prevents the subject from giving informed consent (MMSE less than 25).
  6. Legal incapacity or limited legal capacity.
  7. Presence of severe renal disease (estimated creatinine clearance <50 mL/min) or hepatic disease (AST or ALT>2x times normal) (as evidenced by labs reported within the past 6 months).
  8. Clinically significantly abnormal WBC, hemoglobin or platelet count (as evidenced by labs reported within the past 6 months).
  9. IgA deficiency (evidenced by screening lab evaluations)

Sites / Locations

  • University of South Florida

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

IVIG

Arm Description

Intravenous Immune Globulin

Outcomes

Primary Outcome Measures

Scale for the Assessment and Rating of Ataxia

Secondary Outcome Measures

Timed 25 foot walk
Clinical Global impression
Biodex Balance SD
Gait Rite Mat
Berg balance scale
Complete Metabolic Panel
Complete Blood Count

Full Information

First Posted
April 20, 2011
Last Updated
July 19, 2013
Sponsor
University of South Florida
Collaborators
Baxter Healthcare Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01350440
Brief Title
Safety and Efficacy of Intravenous Immune Globulin in Treating Spinocerebellar Ataxia
Official Title
Safety and Efficacy of Intravenous Immune Globulin in Treating Spinocerebellar Ataxia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of South Florida
Collaborators
Baxter Healthcare Corporation

4. Oversight

5. Study Description

Brief Summary
This is a preliminary study to determine the safety and efficacy of intravenous immune globulin in treating Spinocerebellar Ataxia. The investigators aim to assess changes in clinical measures of disease severity before and after treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinocerebellar Ataxia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
IVIG
Arm Type
Experimental
Arm Description
Intravenous Immune Globulin
Intervention Type
Biological
Intervention Name(s)
IVIG
Intervention Description
Intravenous Immune Globulin
Primary Outcome Measure Information:
Title
Scale for the Assessment and Rating of Ataxia
Time Frame
participants will be followed for approximately 4 months
Secondary Outcome Measure Information:
Title
Timed 25 foot walk
Time Frame
participants will be followed for approximately 4 months
Title
Clinical Global impression
Time Frame
participants will be followed for approximately 4 months
Title
Biodex Balance SD
Time Frame
participants will be followed for approximately 4 months
Title
Gait Rite Mat
Time Frame
participants will be followed for approximately 4 months
Title
Berg balance scale
Time Frame
participants will be followed for approximately 4 months
Title
Complete Metabolic Panel
Time Frame
participants will be followed for approximately 4 months
Title
Complete Blood Count
Time Frame
participants will be followed for approximately 4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Outpatients with SCA diagnosed by a movement disorder specialist. Age 10 years to 80 years. Able to ambulate with or without assistance for 30 feet. Women of child-bearing potential must use a reliable method of contraception and must provide a negative pregnancy test at entry into the study. Serum creatine kinase, complete metabolic panel, complete blood count, liver function tests, renal function tests, platelets and EKG do not reveal clinically significant abnormalities (results obtained from primary care physician and dated within the past 6 months or obtained at screening visit). Stable doses of all medications for 30 days prior to study entry and for the duration of the study. Stable doses of all antidepressants and vitamins (including internet purchased idebenone) for 30 days prior to study entry and for the duration of the study. Throughout the study, all possible efforts should be made to maintain stable doses of all other medications. Subject permission (informed consent). Exclusion Criteria: Any unstable illness that in the investigator's opinion precludes participation in this study. Use of any investigational product within the past 30 days. Presence of clinically significant cardiac disease (as determined by the investigator based on EKG and echocardiogram results within the past 6 months). Specifically, an ejection fraction <40%, or a prolonged QT interval (>50% of cycle duration) will be excluded. If the investigator notes clinically significant abnormalities on the EKG or echocardiogram, the subject will be eligible IF they provide clearance from a cardiologist. Presence of diabetes (as determined by blood glucose labs within the past 6 months). Dementia or other psychiatric illness that prevents the subject from giving informed consent (MMSE less than 25). Legal incapacity or limited legal capacity. Presence of severe renal disease (estimated creatinine clearance <50 mL/min) or hepatic disease (AST or ALT>2x times normal) (as evidenced by labs reported within the past 6 months). Clinically significantly abnormal WBC, hemoglobin or platelet count (as evidenced by labs reported within the past 6 months). IgA deficiency (evidenced by screening lab evaluations)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Theresa Zesiewicz, MD
Organizational Affiliation
University of South Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Safety and Efficacy of Intravenous Immune Globulin in Treating Spinocerebellar Ataxia

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