Ultragenyx Pharmaceutical Inc. Stock Price
- 4 Narratives written by author
- 0 Comments on narratives written by author
- 18 Fair Values set on narratives written by author
RARE Community Narratives
Advancements In Genomics And Rare Therapies Will Expand Prospects
burns cash despite four approved drugs, trapped by structural inefficiencies and gene-therapy scaling hurdles that thin safety margins.
Advanced Gene Therapies Will Drive Global Rare Disease Growth
burns cash despite four approved drugs, trapped by structural inefficiencies and gene-therapy scaling hurdles that thin safety margins.
View narrativeAdvancements In Genomics And Rare Therapies Will Expand Prospects
View narrativeAdvanced Gene Therapies Will Drive Global Rare Disease Growth
View narrativeRising Clinical Risks Will Depress Biotech Pipeline Yet Invite Rebound
View narrativeTrending Discussion
No trending discussion available.
Recently Updated Narratives
burns cash despite four approved drugs, trapped by structural inefficiencies and gene-therapy scaling hurdles that thin safety margins.
RARE: Genglycos And UX111 Commercial Execution Will Support 2027 Profitability
RARE: Genglycos Approval And Angelman Phase 3 Data Will Drive Repricing
Snowflake Analysis
Ultragenyx Pharmaceutical Inc. Key Details
- -5.96
- -20.78%
- -81.73%
- -423.2%
About RARE
- Founded
- 2010
- Employees
- 1371
- CEO
- Website
View website
Ultragenyx Pharmaceutical Inc., a biopharmaceutical company, focuses on the identification, acquisition, development, and commercialization of novel products for the treatment of rare and ultra-rare genetic diseases in North America, Latin America, Europe, the Middle East, Africa, and the Asia-Pacific. Its biologic products include Crysvita (burosumab), an antibody targeting fibroblast growth factor 23 for the treatment of X-linked hypophosphatemia, as well as tumor-induced osteomalacia; Mepsevii, an enzyme replacement therapy for the treatment of children and adults with Mucopolysaccharidosis VII; Dojolvi for the treatment of long-chain fatty acid oxidation disorders; and Evkeeza (evinacumab) for the treatment of homozygous familial hypercholesterolemia. The company’s products candidates that are in Phase 3 clinical trials include UX143, a human monoclonal antibody for the treatment of osteogenesis imperfecta; UX111, an AAV9 gene therapy product candidate for the treatment of patients with Sanfilippo syndrome type A, or MPS IIIA, a rare lysosomal storage disease; DTX401, an adeno-associated virus 8 (AAV8) gene therapy clinical candidate for the treatment of patients with glycogen storage disease type Ia; DTX301, an AAV8 gene therapy for the treatment of patients with ornithine transcarbamylase; and GTX-102, an antisense oligonucleotide for the treatment of Angelman syndrome. It also develops UX701, an adeno-associated AAV9 gene therapy which is in Phase 2 clinical trial for the treatment of Wilson liver disease. The company has collaboration and license agreement with Kyowa Kirin Co., Ltd.; Saint Louis University; Baylor Research Institute; REGENXBIO Inc.; GeneTx; Mereo; University of Pennsylvania; Regeneron; and Abeona. Ultragenyx Pharmaceutical Inc. was incorporated in 2010 and is headquartered in Novato, California.