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LIFE - Atyr Pharma Inc


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1.9
0.050   2.632%

Share volume: 269,477
Last Updated: Tue 04 Jun 2024 10:00:00 PM CEST
Research and Development in Biotechnology (except Nanobiotechnology): 0.21%

PREVIOUS CLOSE
CHG
CHG%

$1.85
0.05
2.70%
This ticker is disabled and data are no longer maintained and up to date.
Fundamental analysis
8%
Profitability 0%
Dept financing 6%
Liquidity 75%
Performance 0%
Company vs Stock growth
vs
Performance
5 Days
2.78%
1 Month
14.91%
3 Months
-3.14%
6 Months
45.67%
1 Year
-20.26%
2 Year
-36.43%
Key data
Stock price
$1.90
P/E Ratio 
-2.37
DAY RANGE
$1.82 - $1.95
EPS 
-$0.90
52 WEEK RANGE
$1.08 - $2.45
52 WEEK CHANGE
-$0.21
MARKET CAP 
131.121 M
YIELD 
N/A
SHARES OUTSTANDING 
69.011 M
DIVIDEND
N/A
EX-DIVIDEND DATE
N/A
NEXT EARNINGS DATE
08/07/2024
BETA 
0.88
PUBLIC FLOAT 
$0
AVERAGE 10 VOLUME 
$291,943
AVERAGE 30 VOLUME 
$593,047
Company detail
CEO: Sanjay Shukla
Region: US
Website: https://www.atyrpharma.com/
Employees: 80
IPO year: -
Issue type: Common Stock
Market: XNAS
Industry: Research and Development in Biotechnology (except Nanobiotechnology)
Sector: Professional, Scientific, and Technical Services

atyr pharma (nasdaq: life) is engaged in the discovery and clinical development of innovative medicines for patients suffering from severe rare diseases using its knowledge of physiocrine biology, a newly discovered set of physiological modulators. the company's lead candidate, resolaris™, is a first-in-class intravenous protein therapeutic for the treatment of rare myopathies with an immune component. resolaris is currently in a phase 1b/2 clinical trial in adult patients with facioscapulohumeral muscular dystrophy (fshd); a phase 1b/2 trial in adult patients with limb girdle muscular dystrophy (lgmd) 2b or fshd; and a phase 1b/2 trial in patients with an early onset form of fshd. to protect this pipeline, atyr built an intellectual property estate comprising 70 issued or allowed patents and over 240 pending patent applications that are solely owned or exclusively licensed by atyr. atyr's key programs are currently focused on severe, rare diseases characterized by immune dysregulation

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