NCT00520143

Brief Summary

Pompe disease (also known as glycogen storage disease Type II) is caused by a deficiency of a critical enzyme in the body called acid alpha-glucosidase (GAA). Normally, GAA is used by the body's cells to break down glycogen (a stored form of sugar) within specialized structures called lysosomes. In patients with Pompe disease, an excessive amount of glycogen accumulates and is stored in various tissues, especially heart and skeletal muscle, which prevents their normal function. The objective of this expanded access study is to provide patients with Pompe disease in the United States (US), access to alglucosidase alfa produced from a scaled up manufacturing process for a limited time until production at this scale is approved for commercial use by the Food and Drug Administration.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

74 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 21, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 23, 2007

Completed
Last Updated

February 6, 2014

Status Verified

February 1, 2014

First QC Date

August 21, 2007

Last Update Submit

February 4, 2014

Conditions

Keywords

GSD-II, Pompe Disease, Glycogen Storage Disease II

Interventions

IV infusion: 20mg/kg qow

Also known as: Alglucosidase alfa

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • The patient or patient's legal guardian must provide signed, informed consent prior to performing any study-related procedures.
  • The patient must reside in the US.
  • The patient must have a confirmed diagnosis of Pompe disease defined as documented acid alpha-glucosidase (GAA) enzyme deficiency from any tissue source and/or GAA gene mutations.
  • The patient must have/had documented clinical signs and symptoms of Pompe disease.
  • The patient must have/had prior treatment with alglucosidase alfa produced at commercial scale OR be naive to enzyme replacement therapy (ERT) for the treatment of Pompe disease and meet at least 1 of the following criteria: require a wheelchair OR require some respiratory assistance for any number of hours (including night time) through non-invasive ventilation.
  • The patient must be capable of complying with the required program schedule of assessments.

You may not qualify if:

  • Females who are pregnant or lactating
  • The patient has a clinical condition unrelated to Pompe disease that would interfere with program assessments.
  • The patient is currently enrolled in any clinical studies.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (74)

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Sheffield, Alabama, United States

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Anchorage, Alaska, United States

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Phoenix, Arizona, United States

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Prescott, Arizona, United States

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Scottsdale, Arizona, United States

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Tucson, Arizona, United States

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Bakersfield, California, United States

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Beverly Hills, California, United States

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Loma Linda, California, United States

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Los Angeles, California, United States

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Sacramento, California, United States

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San Diego, California, United States

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Stanford, California, United States

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Aurora, Colorado, United States

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Washington D.C., District of Columbia, United States

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Bradenton, Florida, United States

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Coral Springs, Florida, United States

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Daytona Beach, Florida, United States

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Gainsville, Florida, United States

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St. Petersburg, Florida, United States

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Decatur, Georgia, United States

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Boise, Idaho, United States

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Chicago, Illinois, United States

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Evansville, Indiana, United States

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Iowa City, Iowa, United States

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Kansas City, Kansas, United States

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Louisville, Kentucky, United States

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New Orleans, Louisiana, United States

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Shreveport, Louisiana, United States

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Augusta, Maine, United States

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Baltimore, Maryland, United States

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Boston, Massachusetts, United States

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Springfield, Massachusetts, United States

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Detroit, Michigan, United States

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Grand Rapids, Michigan, United States

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Lake Orion, Michigan, United States

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Rochester Hills, Michigan, United States

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Saint Joseph, Michigan, United States

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Minneapolis, Minnesota, United States

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Missoula, Montana, United States

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Omaha, Nebraska, United States

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Midland Park, New Jersey, United States

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Albuquerque, New Mexico, United States

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Albany, New York, United States

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Corning, New York, United States

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Manhasset, New York, United States

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New York, New York, United States

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Asheville, North Carolina, United States

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Durham, North Carolina, United States

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Jacksonville, North Carolina, United States

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Cincinnati, Ohio, United States

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Cleveland, Ohio, United States

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Greenville, Ohio, United States

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Toledo, Ohio, United States

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Oklahoma City, Oklahoma, United States

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Tulsa, Oklahoma, United States

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Portland, Oregon, United States

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Philadelphia, Pennsylvania, United States

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Pittsburgh, Pennsylvania, United States

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Greenville, South Carolina, United States

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West Colombia, South Carolina, United States

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Houston, Texas, United States

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San Antonio, Texas, United States

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Waco, Texas, United States

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Salt Lake City, Utah, United States

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Charlottesville, Virginia, United States

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Chesapeake, Virginia, United States

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Newport News, Virginia, United States

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Richmond, Virginia, United States

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Winchester, Virginia, United States

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Pullman, Washington, United States

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Seattle, Washington, United States

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Morgantown, West Virginia, United States

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Green Bay, Wisconsin, United States

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MeSH Terms

Conditions

Glycogen Storage Disease Type II

Interventions

GAA protein, human

Condition Hierarchy (Ancestors)

Lysosomal Storage Diseases, Nervous SystemBrain Diseases, Metabolic, InbornBrain Diseases, MetabolicBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMetabolism, Inborn ErrorsGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesGlycogen Storage DiseaseCarbohydrate Metabolism, Inborn ErrorsLysosomal Storage DiseasesMetabolic DiseasesNutritional and Metabolic Diseases

Study Officials

  • Medical Monitor

    Genzyme, a Sanofi Company

    STUDY DIRECTOR

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 21, 2007

First Posted

August 23, 2007

Last Updated

February 6, 2014

Record last verified: 2014-02

Locations