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RARE - Ultragenyx Pharmaceutical Inc.


IEX Last Trade
56.78
-0.180   -0.317%

Share volume: 754,442
Last Updated: Fri 30 Aug 2024 09:59:54 PM CEST
Research and Development in Biotechnology (except Nanobiotechnology): 0.21%

PREVIOUS CLOSE
CHG
CHG%

$56.96
-0.18
-0.32%
5D - 1M - 3M - 1Y - 3Y - 5Y - 10Y - 15Y
Fundamental analysis
8%
Profitability 0%
Dept financing 21%
Liquidity 53%
Performance 0%
Company vs Stock growth
vs
Performance
5 Days
0.05%
1 Month
27.00%
3 Months
46.91%
6 Months
7.64%
1 Year
55.31%
2 Year
15.59%
Key data
Stock price
$56.78
P/E Ratio 
-8.94
DAY RANGE
N/A - $57.79
EPS 
-$7.23
52 WEEK RANGE
$31.52 - $58.73
52 WEEK CHANGE
$0.50
MARKET CAP 
5.233 B
YIELD 
N/A
SHARES OUTSTANDING 
92.165 M
DIVIDEND
N/A
EX-DIVIDEND DATE
N/A
NEXT EARNINGS DATE
10/31/2024
BETA 
1.06
PUBLIC FLOAT 
$0
AVERAGE 10 VOLUME 
$627,817
AVERAGE 30 VOLUME 
$802,521
Company detail
CEO: Emil Kakkis
Region: US
Website: https://www.ultragenyx.com/
Employees: 1,563
IPO year: -
Issue type: Common Stock
Market: XNAS
Industry: Research and Development in Biotechnology (except Nanobiotechnology)
Sector: Professional, Scientific, and Technical Services

ultragenyx is a clinical-stage biotechnology company committed to bringing to market novel products for the treatment of rare and ultra-rare diseases, with an initial focus on serious, debilitating metabolic genetic diseases. founded in 2010, the company has rapidly built a diverse portfolio of product candidates with the potential to address diseases for which the unmet medical need is high, the biology for treatment is clear, and for which there are no approved therapies. our company is led by an experienced management team in rare disease therapeutics. recognizing that our primary responsibility is to our patients, we are working with advocacy groups to provide support and outreach to individuals and families affected by these disorders and engage them in the clinical testing process. we are also working with regulatory agencies to design and conduct high quality clinical studies that meet the requirements for approval. we are creating an improved model for successful rare disease d

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