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RNAC - Cartesian Therapeutics Inc


IEX Last Trade
13.905
-1.005   -7.228%

Share volume: 63,678
Last Updated: Fri 30 Aug 2024 09:53:41 PM CEST
Research and Development in Biotechnology (except Nanobiotechnology): 0.21%

PREVIOUS CLOSE
CHG
CHG%

$14.91
-1.01
-6.74%
5D - 1M - 3M - 1Y - 3Y - 5Y - 10Y - 15Y
Fundamental analysis
35%
Profitability 50%
Dept financing 25%
Liquidity 60%
Performance 16%
Company vs Stock growth
vs
Performance
5 Days
1.53%
1 Month
-13.61%
3 Months
-55.60%
6 Months
-35.37%
1 Year
1,063.33%
2 Year
634.74%
Key data
Stock price
$13.90
P/E Ratio 
-1.28
DAY RANGE
N/A - N/A
EPS 
-$32.91
52 WEEK RANGE
$0.81 - $42.60
52 WEEK CHANGE
$10.35
MARKET CAP 
298.499 M
YIELD 
N/A
SHARES OUTSTANDING 
21.382 M
DIVIDEND
N/A
EX-DIVIDEND DATE
N/A
NEXT EARNINGS DATE
11/11/2024
BETA 
0.00
PUBLIC FLOAT 
$0
AVERAGE 10 VOLUME 
$57,821
AVERAGE 30 VOLUME 
$88,314
Company detail
CEO: Carsten Brunn
Region: US
Website: http://selectabio.com/
Employees: 81
IPO year: -
Issue type: Common Stock
Market: XNAS
Industry: Research and Development in Biotechnology (except Nanobiotechnology)
Sector: Professional, Scientific, and Technical Services

selecta biosciences, inc. is a clinical-stage biopharmaceutical company that is focused on unlocking the full potential of biologic therapies by mitigating unwanted immune responses. selecta plans to combine its tolerogenic synthetic vaccine particles (svp™) to a range of biologics for rare and serious diseases that require new treatment options. the company’s current proprietary pipeline includes svp-enabled enzyme, oncology and gene therapies. sel-212, the company’s lead candidate in phase 2, is being developed to treat severe gout patients and resolve their debilitating symptoms, including flares and gouty arthritis. selecta’s sel-403 product candidate, a combination therapy consisting of svp-rapamycin and lmb-100, recently entered a phase 1 trial in 2018 for the treatment of patients with malignant pleural or peritoneal mesothelioma. selecta’s proprietary gene therapy product candidates are being developed for rare inborn errors of metabolism and have the potential to enable repeat

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