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TLPH - Talphera Inc.


IEX Last Trade
1.04
0.064   6.154%

Share volume: 128,750
Last Updated: Fri 30 Aug 2024 09:33:17 PM CEST
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology) : 0.87%

PREVIOUS CLOSE
CHG
CHG%

$0.98
0.06
6.56%
5D - 1M - 3M - 1Y - 3Y - 5Y - 10Y - 15Y
Fundamental analysis
4%
Profitability 0%
Dept financing 0%
Liquidity 0%
Performance 10%
Performance
5 Days
15.56%
1 Month
2.97%
3 Months
1.96%
6 Months
-24.64%
1 Year
0   0%
2 Year
-81.88%
Key data
Stock price
$1.04
P/E Ratio 
0.00
DAY RANGE
N/A - N/A
EPS 
$0.00
52 WEEK RANGE
$0.42 - $1.61
52 WEEK CHANGE
$0.01
MARKET CAP 
17.673 M
YIELD 
N/A
SHARES OUTSTANDING 
16.993 M
DIVIDEND
N/A
EX-DIVIDEND DATE
N/A
NEXT EARNINGS DATE
11/07/2024
BETA 
0.61
PUBLIC FLOAT 
$0
AVERAGE 10 VOLUME 
$96,151
AVERAGE 30 VOLUME 
$60,488
Company detail
CEO: Vincent Angotti
Region: US
Website: http://www.acelrx.com
Employees: 46
IPO year: -
Issue type: Common Stock
Market: XNAS
Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
Sector: Professional, Scientific, and Technical Services

acelrx pharmaceuticals inc. is a specialty pharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of moderate-to-severe acute pain. the company’s product candidates, dsuvia™ (known as arx-04 outside of the united states) and zalviso®, are designed to deliver sufentanil, a strong opioid analgesic, via a non-invasive, sublingual formulation in medical supervised settings. dsuvia is designed to deliver sublingual tablets containing 30 mcg sufentanil via a disposable, pre-filled, single-dose applicator. the phase 3 clinical program has completed and assessed the investigational product in the treatment of moderate-to-severe acute pain in patients who had undergone surgery or who presented to an emergency room with trauma or injury. in clinical studies, dsuvia demonstrated reductions in pain intensity as early as 15-to-30 minutes after the start of dosing and the most common adverse events included nausea, headache, dizziness, and v

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