Lumizyme approved for Pompe disease - ONA

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Lumizyme approved for Pompe disease - ONA

oncologynurseadvisor.com

Genzyme announced the FDA approval of Lumizyme (alglucosidase alfa), a lysosomal glycogen-specific enzyme, for the treatment of patients 8 years of age with late (non-infantile) onset Pompe disease (acid -glucosidase (GAA) deficiency) who do not have evidence of cardiac hypertrophy

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Tags: Heart, Disease and Condition, FDA, Genzyme, disease

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Most Recently Shared on May 25, 2010 at 8:42 pm By:

Physician's Weekly Article - Treatment Approved for Late-Onset Pompe Disease

physweeklyarchives.com — “Physician's Weekly, your source for medical news, information on new drugs and devices, clinical updates, CME accreditation for radiology, emergency medicine, pediatrics, mammography, and anesthesia .View full resource at physweeklyarchives.com

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Most Recently Shared on August 26, 2010 at 9:29 pm By:

PriMed_Alerts Pri-Med Medical Education

Treatment Approved for Late-Onset Pompe Disease - The FDA has approved alglucosidase alfa (Lumizyme, Genzyme Corp.) ... http://ow.ly/18JYcf

2 years ago...

UF administers Lumizyme for late-onset Pompe disease

news-medical.net — “The first commercially available treatment in the United States for patients with late-onset Pompe disease was administered Wednesday, June 16, at the University of Florida.View full resource at news-medical.net

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Most Recently Shared on June 18, 2010 at 7:45 am By:

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UF administers Lumizyme for late-onset Pompe disease: The first commercially available treatment in the United Sta... http://bit.ly/bU5ITz

2 years ago...

Lumizyme Approved for Non-Infantile Pompe Disease --Doctors Lounge

doctorslounge.com — “Lumizyme Approved for Non-Infantile Pompe Disease --Doctors LoungeView full resource at doctorslounge.com

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Most Recently Shared on May 29, 2010 at 4:24 am By:

Lung_Breathing Lungs and Breathing OW Health

Lumizyme Approved for Non-Infantile Pompe Disease: A rare genetic disorder http://bit.ly/bDe1si

2 years ago...

FDA Approves Lumizyme for Late-Onset Pompe Disease

drugs.com — “Lumizyme (alglucosidase alfa) is used to treat Pompe disease. Includes Lumizyme side effects, interactions and indications.View full resource at drugs.com

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Most Recently Shared on May 28, 2010 at 8:31 am By:

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FDA Approves Lumizyme for Late-Onset Pompe Disease - http://bit.ly/avpJ9U

2 years ago...

FDA approves drug for late-onset Pompe disease - Related Stories - AAP SmartBrief

smartbrief.com — “The FDA granted marketing approval for Genzyme's drug Lumizyme for patients age 8 and older with non-infantile Pompe disease. The agency said Lumizyme will be sold with a boxed warning on its label about potential adverse effects, including severe allergic reaction and anaphylaxis. <a href='/servletView full resource at smartbrief.com

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Most Recently Shared on May 27, 2010 at 4:23 am By:

New treatment approved for children with late-onset Pompe's disease

pediatricsupersite.com — “The FDA has approved alglucosidase alfa for children aged 8 years and older who have late-onset Pompe’s disease, a rare genetic disorderView full resource at pediatricsupersite.com

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Most Recently Shared on May 26, 2010 at 8:09 pm By:

PedSuperSite Pediatric SuperSite Health Site

New treatment approved for children with late-onset Pompe’s disease: http://ow.ly/1Qkif

2 years ago...

Lumizyme receives FDA approval for patients with late-onset Pompe disease

news-medical.net — “The U.S. Food and Drug Administration approved Lumizyme (alglucosidase alfa) for patients ages 8 years and older with late-onset (non-infantile) Pompe disease, a rare genetic disorder.View full resource at news-medical.net

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Most Recently Shared on May 26, 2010 at 9:19 am By:

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Stroke News: Lumizyme receives FDA approval for patients with late-onset Pompe disease: The U.S. Food and Drug A... http://twurl.nl/18htwo

2 years ago...

Lumizyme approved for Pompe disease - MPR

empr.com — “Genzyme announced the FDA approval of Lumizyme (alglucosidase alfa), a lysosomal glycogen-specific enzyme, for the treatment of patients 8 years of age with late (non-infantile) onset Pompe disease (acid -glucosidase (GAA) deficiency) who do not have evidence of cardiac hypertrophyView full resource at empr.com

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Most Recently Shared on May 25, 2010 at 5:44 pm By:

eMPR MPR Medical Publisher

Lumizyme approved for Pompe disease: Genzyme announced the FDA approval of Lumizyme (alglucosidase alfa), a lysoso... http://bit.ly/c4DNLj

2 years ago...

Lumizyme approved for Pompe disease - MPR

empr.com — “Genzyme announced the FDA approval of Lumizyme (alglucosidase alfa), a lysosomal glycogen-specific enzyme, for the treatment of patients 8 years of age with late (non-infantile) onset Pompe disease (acid -glucosidase (GAA) deficiency) who do not have evidence of cardiac hypertrophyView full resource at empr.com

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Most Recently Shared on May 25, 2010 at 5:40 pm By:

eMPR MPR Medical Publisher

MPR News: Lumizyme approved for Pompe disease: Genzyme announced the FDA approval of Lumizyme (alglucosidase alfa)... http://bit.ly/d9RDQi

2 years ago...

FDA Approves New Treatment for Late-Onset Pompe Disease | Earth Times News

earthtimes.org — “FDA Approves New Treatment for Late-Onset Pompe Disease | Earth Times NewsView full resource at earthtimes.org

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Most Recently Shared on May 25, 2010 at 2:59 pm By:

JohnCFierce John Carroll Health Communicator

RT @adamfeuerstein: $GENZ -- FDA approved lumizyme for pompe disease. This is surprisingly early. >> PR: http://bit.ly/avDG4N

2 years ago...

UPDATE 2-Genzyme's Pompe drug rejected--new production woes | Reuters

reuters.com — “* FDA rejects Genzyme's Pompe disease drug * Cites deficiencies at manufacturing plant in Boston * Shares up as shipping still on track (Updates with details from company conference call) By ToniView full resource at reuters.com

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Most Recently Shared on November 16, 2009 at 5:29 pm By:

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Genzyme says FDA declines to approve Pompe disease drug - Reuters http://ow.ly/1623UI

2 years ago...

FDA approves ZyStor Therapeutics' ZC-701 for Phase I human safety trial

news-medical.net — “ZyStor Therapeutics, Inc., a biotechnology company developing a new class of targeted protein therapeutics for the treatment of Lysosomal Storage Diseases using the Company's proprietary Glycosylation Independent Lysosomal Targeting technology, today announced that it has received clearance from the U. S. Food and Drug Administration to proceed into a clinical trial for its first drug candidate, ZC-701, an enzyme replacement therapy for the treatment of Pompe disease.View full resource at news-medical.net

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Most Recently Shared on October 15, 2009 at 1:01 am By:

Genetics_News News-Medical.Net Health News

Genetics News: FDA approves ZyStor Therapeutics' ZC-701 for Phase I human safety trial: ZyStor Th.. http://buzzup.com/ffcp

3 years ago...

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