FDA
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Ultragenyx Announces FDA Clearance of Investigational New Drug (IND) Application for UX016, a Sialic Acid Prodrug for the Treatment of GNE Myopathy
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Ultragenyx Resubmits Biologics License Application for UX111 AAV Gene Therapy to Treat Sanfilippo Syndrome Type A (MPS IIIA) to U.S. FDA
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TD Cowen Reiterates Buy Rating on Ultragenyx Pharma (RARE)
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Ultragenyx begins rolling FDA submission for GSDIa gene therapy
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Ultragenyx stock falls after FDA issues complete response letter for gene therapy
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Ultragenyx Reports First Quarter 2025 Financial Results and Corporate Update
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Ultragenyx Reports Preliminary 2024 Revenue, Financial Guidance for 2025, Pipeline Updates, and 2025 Milestones
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323,573 total articles have been posted to this entity.
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