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An Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta — Meteoroid  

Osteogenesis Imperfecta Clinical Trial

Official title:
A Phase 2, Non-controlled, Open-Label, Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta

Clinical Trial Summary

The purpose of this study is to investigate the effect of BPS804 on strength/quality of bone in patients with Type I, III or IV Osteogenesis imperfecta using a special type of CT scanner. Participants will be treated for 1 year.

Clinical Trial Description

This study was previously posted by Mereo Biopharma and was transferred to Ultragenyx in February 2021. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03216486
Study type Interventional
Source Ultragenyx Pharmaceutical Inc
Contact
Status Withdrawn
Phase Phase 2
Start date October 31, 2017
Completion date November 1, 2018
View Details
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