Larimar Therapeutics, Inc. Share Price

Equities

LRMR

US5171251003

Biotechnology & Medical Research

Market Closed - Nasdaq 21:00:00 26/04/2024 BST 5-day change 1st Jan Change
6.44 USD +1.74% Intraday chart for Larimar Therapeutics, Inc. -1.38% +41.54%
Sales 2024 * - Sales 2025 * - Capitalization 411M 32.89B
Net income 2024 * -79M -6.32B Net income 2025 * -144M -11.53B EV / Sales 2024 * -
Net cash position 2024 * 182M 14.59B Net cash position 2025 * 57.6M 4.61B EV / Sales 2025 * -
P/E ratio 2024 *
-5.23 x
P/E ratio 2025 *
-3.07 x
Employees 42
Yield 2024 *
-
Yield 2025 *
-
Free-Float 98.66%
More Fundamentals * Assessed data
Dynamic Chart

Latest transcript on Larimar Therapeutics, Inc.

1 day+1.74%
1 week-1.38%
Current month-15.15%
1 month-11.36%
3 months+31.70%
6 months+142.11%
Current year+41.54%
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1 week
5.91
Extreme 5.91
6.88
1 month
5.91
Extreme 5.91
8.06
Current year
4.09
Extreme 4.09
13.68
1 year
2.18
Extreme 2.18
13.68
3 years
1.53
Extreme 1.53
15.49
5 years
1.53
Extreme 1.53
25.87
10 years
1.53
Extreme 1.53
25.87
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Managers TitleAgeSince
Chief Executive Officer 65 -
Director of Finance/CFO 65 27/05/20
Chief Tech/Sci/R&D Officer - 30/04/18
Members of the board TitleAgeSince
Director/Board Member 55 27/05/20
Director/Board Member 54 27/05/20
Director/Board Member 69 02/10/23
More insiders
Date Price Change Volume
26/04/24 6.44 +1.74% 144,231
25/04/24 6.33 -2.01% 302,131
24/04/24 6.46 0.00% 222,439
23/04/24 6.46 +0.94% 243,953
22/04/24 6.4 -1.99% 238,190

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

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Larimar Therapeutics, Inc. is a clinical-stage biotechnology company. The Company is focused on developing treatments for patients suffering from complex rare diseases using its novel cell penetrating peptide (CPP) technology platform. The Company’s lead product candidate, nomlabofusp, is a subcutaneously administered, recombinant fusion protein intended to deliver tissue frataxin (FXN), an essential protein, to the mitochondria of patients with Friedreich's ataxia (FA). FA is a rare, progressive, and fatal disease in which patients are unable to produce sufficient FXN due to a genetic abnormality. Its CPP platform, which enables a therapeutic molecule to cross a cell membrane in order to reach intracellular targets, has the potential to enable the treatment of other rare and orphan diseases. It intends to use its proprietary platform to target additional orphan indications characterized by deficiencies in or alterations of intracellular content or activity.
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More about the company
Sell
Consensus
Buy
Mean consensus
BUY
Number of Analysts
6
Last Close Price
6.44 USD
Average target price
19.86 USD
Spread / Average Target
+208.46%
Consensus