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ATYR - Atyr Pharma Inc


IEX Last Trade
1.87
-0.020   -1.070%

Share volume: 98,715
Last Updated: Fri 30 Aug 2024 09:59:59 PM CEST
Research and Development in Biotechnology (except Nanobiotechnology): 0.21%

PREVIOUS CLOSE
CHG
CHG%

$1.89
-0.02
-1.06%
5D - 1M - 3M - 1Y - 3Y - 5Y - 10Y - 15Y
Fundamental analysis
4%
Profitability 0%
Dept financing 0%
Liquidity 0%
Performance 10%
Performance
5 Days
-1.06%
1 Month
-5.56%
3 Months
6.25%
6 Months
-1.58%
1 Year
5.65%
2 Year
-45.00%
Key data
Stock price
$1.87
P/E Ratio 
-2.45
DAY RANGE
$1.85 - N/A
EPS 
-$0.91
52 WEEK RANGE
$1.08 - $2.50
52 WEEK CHANGE
$0.10
MARKET CAP 
141.739 M
YIELD 
N/A
SHARES OUTSTANDING 
75.796 M
DIVIDEND
N/A
EX-DIVIDEND DATE
N/A
NEXT EARNINGS DATE
11/07/2024
BETA 
0.87
PUBLIC FLOAT 
$0
AVERAGE 10 VOLUME 
$156,579
AVERAGE 30 VOLUME 
$298,540
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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