Exicure, Inc. Share Price

Equities

XCUR

US30205M2008

Biotechnology & Medical Research

Market Closed - Nasdaq 21:00:00 26/04/2024 BST 5-day change 1st Jan Change
0.5001 USD -1.75% Intraday chart for Exicure, Inc. -10.86% -13.82%
Sales 2021 -483K -38.67M Sales 2022 28.83M 2.31B Capitalization 5.71M 457M
Net income 2021 -64M -5.12B Net income 2022 -2M -160M EV / Sales 2021 8.21 x
Net cash position 2021 24.4M 1.95B Net cash position 2022 1.27M 102M EV / Sales 2022 0.15 x
P/E ratio 2021
-0.28 x
P/E ratio 2022
-2.06 x
Employees 7
Yield 2021 *
-
Yield 2022
-
Free-Float 54.96%
More Fundamentals * Assessed data
Dynamic Chart
1 day-1.75%
1 week-10.86%
Current month-16.86%
1 month-19.03%
3 months-5.00%
6 months-21.93%
Current year-13.82%
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1 week
0.50
Extreme 0.5
0.57
1 month
0.50
Extreme 0.5
0.73
Current year
0.50
Extreme 0.5
0.86
1 year
0.36
Extreme 0.3647
1.50
3 years
0.36
Extreme 0.3647
60.00
5 years
0.36
Extreme 0.3647
115.20
10 years
0.36
Extreme 0.3647
195.00
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Managers TitleAgeSince
Chief Executive Officer 63 23/02/23
Director of Finance/CFO 47 30/11/22
Investor Relations Contact 47 -
Members of the board TitleAgeSince
Director of Finance/CFO 47 30/11/22
Chief Executive Officer 63 23/02/23
Director/Board Member - 22/08/23
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Date Price Change Volume
26/04/24 0.5001 -1.75% 28,416
25/04/24 0.509 -1.17% 18,698
24/04/24 0.515 -4.68% 18,589
23/04/24 0.5403 +0.11% 7,040
22/04/24 0.5397 -3.80% 20,107

Delayed Quote Nasdaq, April 26, 2024 at 09:00 pm

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Exicure, Inc. is an early-stage biotechnology company focused on developing nucleic acid therapies targeting ribonucleic acid against validated targets. The Company is developing nucleic acid therapies targeting ribonucleic acid (RNA) to address both genetic and non-genetic neurological disorders. Its lead program is a non-opioid pain analgesic directed against the genetically validated target SCN9A. It is engaged in discovery efforts across a range of indications and therapeutic targets, such as pain using non-opioid analgesics, as well as rare neurological genetic disorders, including Huntington's disease, Angelman Syndrome, Batten disease, spinocerebellar ataxia, and sporadic amyotrophic lateral sclerosis (ALS). The Company focuses on pursuing out-licensing opportunities for its clinical asset, cavrotolimod, as well as for its preclinical candidates, including the SCN9A program for neuropathic pain.
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