Larimar Therapeutics, Inc. Share Price

Equities

LRMR

US5171251003

Biotechnology & Medical Research

Market Closed - Nasdaq 01:30:00 27/04/2024 am IST 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 34.26B
Net income 2024 * -79M -6.59B Net income 2025 * -144M -12.01B EV / Sales 2024 * -
Net cash position 2024 * 182M 15.19B Net cash position 2025 * 57.6M 4.8B 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 28/20/28
Chief Tech/Sci/R&D Officer - 01/18/01
Members of the board TitleAgeSince
Director/Board Member 55 28/20/28
Director/Board Member 54 28/20/28
Director/Board Member 69 03/23/03
More insiders
Date Price Change Volume
26/24/26 6.44 +1.74% 144,231
25/24/25 6.33 -2.01% 302,131
24/24/24 6.46 0.00% 222,439
23/24/23 6.46 +0.94% 243,953
22/24/22 6.4 -1.99% 238,190

Delayed Quote Nasdaq, April 27, 2024 at 01:30 am IST

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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