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Hereditary orotic aciduria is a unique, potentially life-threatening, genetic disorder that hinders the synthesisation of adequate amounts of uridine in the patient, and results in suffering from hematologic abnormalities, a range of developmental delays, failure to thrive, and episodes of crystalluria resulting in obstructive uropathy.
The market is being driven by the constant innovation and launches by the key industry players, such as Merck & Co., Inc. (NYSE: MRK) and Wellstat Therapeutics Corporation. In September 2016, Wellstat Therapeutics Corporation announced that the US Food and Drug Administration (FDA) approved a treatment known as uridine triacetate (Xuriden) for hereditary orotic aciduria treatment. Along with the approval of XURIDEN for the medication of HOA, the FDA has also granted the company, Wellstat Therapeutics, a Rare Pediatric Disease Priority Review Voucher. XURIDEN was made available commercially in early 2016. The rising healthcare awareness is expected to further aid the market growth in the forecast period.
Market Analysis by Drug Type, Indication, Distribution Channel, and Region:
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Merck & Co. Inc. and Wellstat Therapeutics Corporation, among others, are the key players in the global hereditary orotic aciduria treatment market. The EMR report looks into the capacity, market share, and latest developments of these major players like plant turnarounds, mergers and acquisitions, and capacity expansions.
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