Alglucosidase Alfa Temporary Access Program

NCT ID: NCT00520143

Last Updated: 2014-02-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

APPROVED_FOR_MARKETING

Study Classification

EXPANDED_ACCESS

Brief Summary

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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.

Detailed Description

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Conditions

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Glycogen Storage Disease Type II (GSD-II) Pompe Disease (Late-Onset) Acid Maltase Deficiency Disease Glycogenosis 2

Interventions

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alglucosidase alfa (recombinant human acid alpha-glucosidase [rhGAA])

IV infusion: 20mg/kg qow

Intervention Type BIOLOGICAL

Other Intervention Names

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Alglucosidase alfa

Eligibility Criteria

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Inclusion Criteria

* 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.

Exclusion Criteria

* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Genzyme, a Sanofi Company

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Monitor

Role: STUDY_DIRECTOR

Genzyme, a Sanofi Company

Locations

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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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Countries

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United States

Other Identifiers

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AGLU03907

Identifier Type: -

Identifier Source: org_study_id

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