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NTLA - Intellia Therapeutics Inc


IEX Last Trade
22.445
-0.555   -2.473%

Share volume: 1,395,897
Last Updated: Fri 30 Aug 2024 09:59:58 PM CEST
Research and Development in Biotechnology (except Nanobiotechnology): 0.21%

PREVIOUS CLOSE
CHG
CHG%

$23.00
-0.56
-2.41%
5D - 1M - 3M - 1Y - 3Y - 5Y - 10Y - 15Y
Fundamental analysis
18%
Profitability 25%
Dept financing 5%
Liquidity 75%
Performance 0%
Company vs Stock growth
vs
Performance
5 Days
-5.04%
1 Month
-14.58%
3 Months
1.54%
6 Months
-31.59%
1 Year
-40.89%
2 Year
-62.75%
Key data
Stock price
$22.44
P/E Ratio 
-4.48
DAY RANGE
N/A - N/A
EPS 
-$5.48
52 WEEK RANGE
$19.37 - $38.71
52 WEEK CHANGE
-$0.40
MARKET CAP 
2.279 B
YIELD 
N/A
SHARES OUTSTANDING 
101.579 M
DIVIDEND
N/A
EX-DIVIDEND DATE
N/A
NEXT EARNINGS DATE
11/11/2024
BETA 
2.13
PUBLIC FLOAT 
$0
AVERAGE 10 VOLUME 
$946,462
AVERAGE 30 VOLUME 
$1,165,790
Company detail
CEO: John Leonard
Region: US
Website: http://www.intelliatx.com/
Employees: 652
IPO year: -
Issue type: Common Stock
Market: XNAS
Industry: Research and Development in Biotechnology (except Nanobiotechnology)
Sector: Professional, Scientific, and Technical Services

intellia therapeutic’s core mission is to develop curative medicines, utilizing the promise of the crispr/cas9 gene editing technology. the development of crispr/cas9 gene editing technology opens a new frontier in biomedical research and clinical intervention. adapted from a natural cellular process, crispr/cas9 permits the editing of any gene in any organism with unprecedented simplicity and flexibility. the incredible potential of this technology for treating human genetic disease inspired a group of life science veterans to create intellia therapeutics. intellia was founded in 2014 by caribou biosciences and atlas venture, along with a consortium of scientists who have helped define the space. intellia therapeutics holds exclusive access to a broad intellectual property portfolio covering the application of crispr/cas9 technology for human therapeutic use. intellia has built an experienced team of individuals to meet the challenges of bringing crispr/cas9 therapeutics to the

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