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 that is in Phase 2 clinical trial for the treatment of Wilson disease; and UX053 for the treatment of glycogen storage disease type III. Ultragenyx Pharmaceutical Inc. has collaboration and license agreement with Kyowa Kirin Co., Ltd.; Saint Louis University; Baylor Research Institute; REGENXBIO Inc.; GeneTx; Mereo; University of Pennsylvania; Solid Biosciences Inc.; Regeneron; Abeona; and Arcturus Therapeutics Holdings Inc. The company was incorporated in 2010 and is headquartered in Novato, California.
Pipeline Potential | Explore Ultragenyx's promising drug candidates, including setrusumab for osteogenesis imperfecta and GTX-102 for Angelman syndrome, poised for significant market impact |
Financial Trajectory | Ultragenyx's path to profitability by 2026, backed by strong revenue growth and strategic pipeline development, signals potential for long-term value creation |
Market Positioning | Delve into Ultragenyx's competitive edge in the rare disease market, leveraging first-in-class therapies and addressing high unmet medical needs |
Analyst Outlook | With price targets ranging from $48 to $140, analysts see substantial upside potential in Ultragenyx's diverse pipeline and commercial growth strategies |
Metrics to compare | RARE | Sector Sector - Average of metrics from a broad group of related Healthcare sector companies | Relationship RelationshipRAREPeersSector | |
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P/E Ratio | −6.4x | −1.1x | −0.5x | |
PEG Ratio | −0.27 | 0.00 | 0.00 | |
Price/Book | 14.3x | 1.5x | 2.6x | |
Price / LTM Sales | 6.5x | 13.2x | 3.0x | |
Upside (Analyst Target) | 115.3% | 253.6% | 56.3% | |
Fair Value Upside | Unlock | 28.8% | 10.0% | Unlock |