Hypophosphatasia
Hypophosphatasia (HPP) is a rare genetic disorder characterized by defective mineralization of bones and teeth, leading to symptoms such as weak bones, frequent fractures, and dental issues.
We are studying a new treatment, ALXN1850, for children with hypophosphatasia who haven't been treated before. The goal is to see if it improves bone health and quality of life compared to a placebo.
Health conditions and diseases that the clinical trial is designed to study and treat.
Hypophosphatasia (HPP) is a rare genetic disorder characterized by defective mineralization of bones and teeth, leading to symptoms such as weak bones, frequent fractures, and dental issues.
These questions help us understand your situation so we can let the trial team know whether you might be a potential match. This is not a medical evaluation and is not part of the official screening, the study doctor will make the final decision..
Experimental substances that are being investigated in this clinical trial. These are not yet approved for general use.
Locations and medical facilities where this clinical trial is currently recruiting or conducting research. Select the locations where you would like to participate.
Disclaimer: Parts of this content have been automatically extracted from the EU Clinical Trials registry. While we strive for accuracy, please always contact the trial site or sponsor directly for correct and official information before making any decisions about participation. View on EU Clinical Trials.