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Clinical Trial Summary

This study was designed to evaluate the safety, tolerability, pharmacodynamics (PD) of DS-1211b, and pharmacokinetics (PK) in individuals with Pseudoxanthoma elasticum (PXE). PXE is a rare disease that is associated with significant risks of visual impairments and comorbidity from peripheral and cardiovascular diseases, and adversely impacts the quality of life in afflicted individuals.


Clinical Trial Description

DS-1211b, a potent small-molecule inhibitor of tissue-nonspecific alkaline phosphatase, is being developed for the treatment ectopic calcification diseases such as PXE. This study will assess DS-1211b (low-, middle-, and high-dose tablets) administered once daily for 12 weeks in individuals with PXE. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05569252
Study type Interventional
Source Daiichi Sankyo, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date October 20, 2022
Completion date April 2024

See also
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