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  2. Alglucosidase alfa - Wikipedia

    en.wikipedia.org/wiki/Alglucosidase_alfa

    Alglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD). [6] Chemically, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha ...

  3. Glycogen storage disease type II - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    In a study [23] which included the largest cohort of patients with Pompe disease treated with enzyme replacement therapy (ERT) to date findings showed that Myozyme treatment clearly prolongs ventilator-free survival and overall survival in patients with infantile-onset Pompe disease as compared to an untreated historical control population ...

  4. Avalglucosidase alfa - Wikipedia

    en.wikipedia.org/wiki/Avalglucosidase_alfa

    These trials enrolled 124 participants with late-onset Pompe disease and 22 participants with infantile-onset Pompe disease. [9] The participants were from 22 countries around the world, including the United States. [9] Avalglucosidase alfa was evaluated in four trials of 146 participants with Pompe disease. [9]

  5. Sanofi (SNY) Pompe Disease Drug Receives FDA's Approval - AOL

    www.aol.com/news/sanofi-sny-pompe-disease-drug...

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  6. SPK-3006 - Wikipedia

    en.wikipedia.org/wiki/SPK-3006

    SPK-3006 is an experimental gene therapy developed for Pompe disease by Spark Therapeutics. It is delivered via adeno-associated virus and is intended to increase alpha-glucosidase production in the liver. [1] [2]

  7. With help from Duke doctors, a rare genetic disease is ... - AOL

    www.aol.com/help-duke-doctors-rare-genetic...

    The treatment appears to be successful. One doctor said the patient, now 16 months old, looks like “any typically developing baby at this age.” With help from Duke doctors, a rare genetic ...

  8. Cipaglucosidase alfa - Wikipedia

    en.wikipedia.org/wiki/Cipaglucosidase_alfa

    Cipaglucosidase alfa, sold under the brand name Pombiliti, and used in combination with miglustat, is a medication used for the treatment of glycogen storage disease type II (Pompe disease). [4] [5] Cipaglucosidase alfa is a recombinant human acid α-glucosidase enzyme replacement therapy that provides an exogenous source of acid α-glucosidase ...

  9. Sickle cell patients share delight over approval of new treatment

    www.aol.com/sickle-cell-patients-share-delight...

    A cutting-edge gene therapy has been approved for NHS use for some patients with severe sickle cell disease. Casgevy, also known as exa-cel, was the first treatment to be licensed using gene ...

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