Hereditary Orotic Aciduria
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FDA approval · 2019-12-02FDA Approved: XURIDEN — Supplemental Application (BTG International Inc)
The FDA approved a supplemental application for XURIDEN (uridine triacetate) submitted by BTG International Inc.
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CLINICAL_TRIALS trial_result · 2017-06-28Clinical Trial Update: Open-Label Study of Uridine Triacetate in Pediatric Patients With Hereditary Orotic Aciduria [Phase 3]
This open-label Phase 3 study of uridine triacetate in pediatric patients with hereditary orotic aciduria has completed and posted results.
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FDA approval · 2015-09-04FDA Approved: XURIDEN — Original Application (BTG International Inc)
The FDA approved XURIDEN (uridine triacetate) as an original New Drug Application from BTG International Inc for the treatment of hereditary…