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Ultragenyx Pharmaceutical Inc. Stock Price

NasdaqGS:RARE Community·US$3.2b Market Cap
  • 3 Narratives written by author
  • 0 Comments on narratives written by author
  • 6 Fair Values set on narratives written by author

RARE Share Price Performance

US$33.53
-15.18 (-31.16%)
US$128.00
Fair Value
US$33.53
-15.18 (-31.16%)
75.2% undervalued intrinsic discount
US$135.38
Fair Value
Price US$33.53
AnalystHighTarget US$135.38
AnalystConsensusTarget US$84.10
AnalystLowTarget US$38.23

RARE Community Narratives

AnalystHighTarget·
Fair Value US$128 73.8% undervalued intrinsic discount

Advanced Gene Therapies Will Drive Global Rare Disease Growth

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AnalystConsensusTarget·
Fair Value US$84.1 60.1% undervalued intrinsic discount

Advancements In Genomics And Rare Therapies Will Expand Prospects

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AnalystLowTarget·
Fair Value US$38.23 12.3% undervalued intrinsic discount

Rising Clinical Risks Will Depress Biotech Pipeline Yet Invite Rebound

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Snowflake Analysis

High growth potential and good value.

2 Risks
2 Rewards

Ultragenyx Pharmaceutical Inc. Key Details

US$630.6m

Revenue

US$794.4m

Cost of Revenue

-US$163.8m

Gross Profit

US$416.0m

Other Expenses

-US$579.8m

Earnings

Last Reported Earnings
Sep 30, 2025
Next Reporting Earnings
n/a
-6.02
-25.98%
-91.95%
5,132.0%
View Full Analysis

About RARE

Founded
2010
Employees
1294
CEO
Emil Kakkis
WebsiteView website
www.ultragenyx.com

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.

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