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QED Therapeutics develops targeted therapies for rare genetic skeletal disorders. Its lead program, infigratinib, an oral FGFR inhibitor, has received FDA Breakthrough Therapy Designation for achondroplasia and is being evaluated in ongoing clinical studies. The company focuses on addressing the underlying genetic causes of conditions like achondroplasia and hypochondroplasia by targeting FGFR3 overactivity. Infigratinib remains investigational and not yet approved by regulatory authorities.
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