Targeting bone diseases.

Help us learn more about what it’s like to live with HPP.
> Click here to participate in a survey

Stay Informed

Receive the latest news and updates on hypophosphatasia.
I am a:
Privacy & Confidentiality Policy
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.