Larimar Therapeutics, Inc. Stock

Equities

LRMR

US5171251003

Biotechnology & Medical Research

Market Closed - Nasdaq 04:00:00 2024-05-16 pm EDT 5-day change 1st Jan Change
7.43 USD -5.59% Intraday chart for Larimar Therapeutics, Inc. -5.47% +63.30%
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Sales 2024 * - Sales 2025 * - Capitalization 502M
Net income 2024 * -77M Net income 2025 * -138M EV / Sales 2024 * -
Net cash position 2024 * 185M Net cash position 2025 * 59.3M EV / Sales 2025 * -
P/E ratio 2024 *
-5.73 x
P/E ratio 2025 *
-3.66 x
Employees 42
Yield 2024 *
-
Yield 2025 *
-
Free-Float 98.55%
More Fundamentals * Assessed data
Dynamic Chart

Latest transcript on Larimar Therapeutics, Inc.

1 day-5.59%
1 week-6.19%
Current month+7.84%
1 month+1.78%
3 months-44.05%
6 months+153.58%
Current year+63.30%
More quotes
1 week
7.04
Extreme 7.04
8.11
1 month
5.91
Extreme 5.91
8.33
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
More quotes
Managers TitleAgeSince
Chief Executive Officer 65 -
Director of Finance/CFO 65 20-05-27
Chief Tech/Sci/R&D Officer - 18-04-30
Members of the board TitleAgeSince
Director/Board Member 55 20-05-27
Director/Board Member 54 20-05-27
Director/Board Member 69 23-10-02
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Date Price Change Volume
24-05-16 7.43 -5.59% 465,555
24-05-15 7.87 -0.13% 165,636
24-05-14 7.88 +7.65% 328,292
24-05-13 7.32 +2.81% 213,961
24-05-10 7.12 -9.41% 362,529

Delayed Quote Nasdaq, May 16, 2024 at 04:00 pm EDT

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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
7.43 USD
Average target price
20.19 USD
Spread / Average Target
+171.69%
Consensus
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