This New Collaboration Aims to Create Gene Therapies for Duchenne Muscular Dystrophy
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This New Collaboration Aims to Create Gene Therapies for Duchenne Muscular Dystrophy

According to CureDuchenne, two companies have began a collaboration in an effort to create new gene therapies for Duchenne muscular dystrophy (DMD). Ultragenyx and Solid Bioscience are both using their…

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ASN Kidney Week Presentation: SYNB8802 for Patients with Enteric Hyperoxaluria
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ASN Kidney Week Presentation: SYNB8802 for Patients with Enteric Hyperoxaluria

Last week, from October 22nd through the 25th, marked the American Society of Nephrology (ASN) Kidney Week. According to a press release, Synthetic Biotic medicine developer Synlogic, Inc. ("Synlogic") presented…

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Injectable XP-0863 for Acute Repetitive Seizures Given Fast Track Designation
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Injectable XP-0863 for Acute Repetitive Seizures Given Fast Track Designation

Recently, specialty pharmaceutical company Xeris Pharmaceuticals ("Xeris") announced that its injectable treatment XP-0863 received Fast Track designation for the treatment of patients with acute repetitive seizures. Xeris created this treatment…

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NTM Lung Disease Treatment ARIKAYCE Given European Marketing Authorization
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NTM Lung Disease Treatment ARIKAYCE Given European Marketing Authorization

Early on October 28, 2020, Insmed Inc. ("Insmed") announced that it received Marketing Authorization from the European Commission for ARIKAYCE. This therapy is designed for adult patients with nontuberculous mycobacterial…

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Children with Deformities Caused by X-Linked Hypophosphatemia Rickets Now Have a Chance to Live a Normal Life
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Children with Deformities Caused by X-Linked Hypophosphatemia Rickets Now Have a Chance to Live a Normal Life

  Colton’s Story Debbie Moore was 18 months old when she was diagnosed with  X-linked hypophosphatemia (XLH) a rare, deforming, and painful bone disorder. XLH causes softening of the bones…

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