Targeting bone diseases.

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Enobia’s clinical abstract submitted to ESPE was awarded the Henning Anderson Prize for best clinical abstract at the upcoming European Pediatric Endocrine Society, Sept 22-25, Prague. Data will be presented in the plenary session, September 24, 10:15am, Prague Czech Republic

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Enobia develops therapies to treat serious genetic bone disorders for which there are no approved treatments. Our lead product, ENB-0040 (human recombinant tissue non-specific alkaline phosphatase), is a subcutaneous bone-targeted A medical treatment that replaces an enzyme in patients who either lack or have a deficient form of the particular enzyme.enzyme replacement therapy for A rare, inherited, and sometimes fatal metabolic bone disease characterized by poor bone mineralization and profound skeletal defects.hypophosphatasia and is currently in Phase 2 clinical studies.

A rare, inherited, and sometimes fatal metabolic bone disease characterized by poor bone mineralization and profound skeletal defects.Hypophosphatasia is a rare genetic skeletal dysplasia characterized by skeletal hypomineralization. Symptoms include failure to thrive, respiratory insufficiency, rickets, myopathy and seizures in infants; rickets, myopathy, poor growth, non-traumatic fractures and early loss of primary teeth in children; and osteomalacia or “soft bones”, frequent non-traumatic fractures, bone pain and early permanent tooth loss in adults. 

 

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