Larimar Therapeutics Inc
NASDAQ:LRMR
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Net Margin
Net Margin shows how much profit a company keeps from each dollar of sales after all expenses, including taxes and interest. It reflects the company`s overall profitability.
Net Margin shows how much profit a company keeps from each dollar of sales after all expenses, including taxes and interest. It reflects the company`s overall profitability.
Peer Comparison
| Country | Company | Market Cap |
Net Margin |
||
|---|---|---|---|---|---|
| US |
|
Larimar Therapeutics Inc
NASDAQ:LRMR
|
295.3m USD |
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|
| FR |
|
Pharnext SCA
OTC:PNEXF
|
6T USD |
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|
|
| US |
|
Abbvie Inc
NYSE:ABBV
|
385B USD |
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|
|
| US |
|
Amgen Inc
NASDAQ:AMGN
|
185.1B USD |
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|
|
| US |
|
Gilead Sciences Inc
NASDAQ:GILD
|
167.9B USD |
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|
|
| US |
|
Vertex Pharmaceuticals Inc
NASDAQ:VRTX
|
118B USD |
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|
| US |
E
|
Epizyme Inc
F:EPE
|
94.1B EUR |
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|
| US |
|
Regeneron Pharmaceuticals Inc
NASDAQ:REGN
|
78.8B USD |
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|
| AU |
|
CSL Ltd
ASX:CSL
|
87B AUD |
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|
| NL |
|
argenx SE
XBRU:ARGX
|
43.2B EUR |
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|
| US |
|
Alnylam Pharmaceuticals Inc
NASDAQ:ALNY
|
47.8B USD |
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Market Distribution
Other Profitability Ratios
Larimar Therapeutics Inc
Glance View
Larimar Therapeutics, Inc. Is a clinical-stage biopharmaceutical company, which engages in the research, development, and commercialization of novel therapeutics mitochondrial disorders and Friedreich's ataxia. The company is headquartered in Bala Cynwyd, Pennsylvania and currently employs 31 full-time employees. The company went IPO on 2014-06-19. The firm is focused on developing treatments for patients suffering from complex rare diseases using its cell penetrating peptide technology platform. The firm's protein replacement therapy platform is intended to deliver missing proteins inside the machinery of cells to treat devastating rare diseases that are ineffective or have no treatments available. Its cell penetrating peptide (CPP) technology 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. The firm's lead product candidate, CTI-1601, is a recombinant fusion protein intended to deliver human frataxin (FXN), an essential protein to the mitochondria of patients with Friedreich’s ataxia. CTI-1601 is in a Phase I clinical program.