Overview

Relieving Burden of Hypophosphatasia in Adults With Functional Impairment Due to Chronic Disease

Status:
Withdrawn
Trial end date:
2022-08-01
Target enrollment:
Participant gender:
Summary
The study will evaluate safety, tolerability, efficacy, pharmacokinetics, and pharmacodynamics of 2 different doses (approved dose and lower dose) of asfotase alfa in adult participants with pediatric-onset hypophosphatasia (HPP).
Phase:
Phase 4
Details
Lead Sponsor:
Alexion Pharmaceuticals
Treatments:
Immunoglobulin G