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CurePompe.com

Pompe Disease research, news and information

  • IOPD
  • LOPD
    • Non-Classic Infant Onset
    • Childhood Onset
    • Juvenile Onset
    • Adult Onset
  • Treatments
    • Current Treatments
      • Enzyme Replacement Therapy (ERT)
        • Lumizyme/Myozyme (alglucosidase alfa)
      • Diet
      • Exercise
      • Therapies
        • Physical Therapy
        • Respiratory Therapy
        • Speech Therapy
        • Occupational Therapy
    • Future Treatments
      • Enzyme Replacement Therapy (ERT) – Experimental
        • Avalglucosidase alfa
        • AT-GAA (ATB200/AT2221)
      • Chaperone Therapy
        • AT-GAA (ATB200/AT2221)
      • Gene Therapy
        • ACT-101
        • AT845
        • AVR-RD-03
  • About
  • Contact Us

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    Recent Posts

    • AT845: Audentes Therapeutics Begins Recruiting Patients for new Phase 1/2 LOPD Gene Therapy Clinical Trial for Pompe Disease (FORTIS)
    • Higher dosing of alglucosidase alfa (ERT) improves outcomes in children with Pompe disease: a clinical study and review of the literature
    • Exercise training alone or in combination with high-protein diet in patients with late onset Pompe disease: results of a cross over study
    • Actus-101 Gene Therapy Promising Early Results (Phase 1/2 study of AAV2/8-LSPhGAA in Late-Onset Pompe Disease)
    • Effects of higher and more frequent dosing of alglucosidase alfa (40mg/kg/week ERT dose) and immunomodulation on long‐term clinical outcome of classic infantile Pompe patients

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