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Larimar Therapeutics Inc   (NASDAQ: LRMR)
Other Ticker:  
 
 
Price: $2.3300 $-0.04 -1.688%
Day's High: $2.37 Week Perf: 22.96 %
Day's Low: $ 2.27 30 Day Perf: 2.19 %
Volume (M): 629 52 Wk High: $ 11.20
Volume (M$): $ 1,465 52 Wk Avg: $6.08
Open: $2.33 52 Wk Low: $1.61



 Market Capitalization (Millions $) 142
 Shares Outstanding (Millions) 61
 Employees 65
 Revenues (TTM) (Millions $) -
 Net Income (TTM) (Millions $) -81
 Cash Flow (TTM) (Millions $) 6
 Capital Exp. (TTM) (Millions $) 1

Larimar Therapeutics Inc
Larimar Therapeutics Inc. is a clinical-stage biotechnology company that was founded in 2018 and is headquartered in Philadelphia, Pennsylvania. The company is focused on developing novel treatments for complex rare diseases, with a particular focus on disorders that affect metabolism or the central nervous system.

Larimar Therapeutics is committed to addressing the significant unmet medical needs in rare diseases that currently have limited or no treatment options. To achieve this goal, the company employs a range of strategies, including gene therapy, protein replacement therapy, and small molecule therapeutics. Larimar's approach is to target specific genetic defects or mutations that underlie rare diseases and to develop treatments that address these underlying causes.

The company's flagship product candidate is CTI-1601, a recombinant fusion protein that is designed to replace the missing enzyme in patients with cystinosis, a rare metabolic disorder. CTI-1601 has received orphan drug designation from the FDA and European Medicines Agency, and the company is currently conducting a Phase I/II clinical trial to evaluate its safety and efficacy in cystinosis patients.

In addition to CTI-1601, Larimar Therapeutics is also developing a pipeline of other product candidates for rare diseases. These include small molecule therapies for Friedreich's ataxia and Niemann-Pick disease type C, as well as gene therapy for Pelizaeus-Merzbacher disease and GM1 gangliosidosis.

Larimar Therapeutics is a publicly traded company on the NASDAQ exchange under the ticker symbol "LRMR." The company has attracted significant attention from investors due to its innovative approach to treating rare diseases and its potential to transform the lives of patients with limited treatment options. The current market capitalization of the company is around $450 million.


   Company Address: Three Bala Plaza East Bala Cynwyd 19004 PA
   Company Phone Number: 511-9056   Stock Exchange / Ticker: NASDAQ LRMR


   

Stock Performances by Major Competitors

5 Days Decrease / Increase
     
BMRN     
INSM     
PBYI        6.19% 
RARE        2.97% 
TEVA        2.97% 
VTRS        7.19% 
• View Complete Report
   



Clinical Study

Pioneering Hope Nomlabofusp in the Long-Term Management of Friedreichs Ataxia

Published Sun, Dec 29 2024 9:00 PM UTC

Abstract Friedreich s Ataxia (FA) remains a challenging rare neurological disease characterized by progressive ataxia, loss of reflexes, and scoliosis, primarily resulting from the deficiency of the protein frataxin. Recent reports from Larimar Therapeutics highlight promising advancements in the treatment of FA through their novel protein replacement therapy, nomlabofusp ...

Clinical Study

Advancements in Nomlabofusp Research Larimar Therapeutics Showcases Phase 1 and Phase 2 Data at ICAR 2024

Published Mon, Nov 18 2024 12:00 PM UTC

Larimar Therapeutics, Inc., a clinical-stage biotechnology company dedicated to developing therapies for complex rare diseases, recently presented additional data from its nomlabofusp clinical program during the International Congress for Ataxia Research (ICAR) 2024 held in London, U.K. The presented findings originate from Phase 1 studies and a Phase 2 dose exploration stud...

Management Announcement

Larimar Therapeutics Receives FDA's Stamp of Approval for Revolutionary FA Treatment in START Program

Published Thu, May 30 2024 8:05 PM UTC


BALA CYNWYD, Pa., May 30, 2024 - Leading biotechnology company Larimar Therapeutics, Inc. (Nasdaq: LRMR) proudly announces its selection by the United States Food and Drug Administration (FDA) to participate in the pioneering Support for Clinical Trials Advancing Rare Disease Therapeutics (START) pilot program. This significant milestone highlights Larimar s commitment ...

Product Service News

Resolving Hope for Friedreich's Ataxia: FDA Lifts Partial Clinical Hold on Nomlabofusp Program

Published Mon, May 20 2024 8:05 PM UTC

Larimar Therapeutics, a clinical-stage biotechnology company, has recently announced a significant milestone in the development of its novel treatment, nomlabofusp (CTI-1601), for Friedreich s Ataxia (FA). The U.S. Food and Drug Administration (FDA) has removed the partial clinical hold previously placed on the company s nomlabofusp program, providing renewed hope for patien...

Clinical Study

Exploring the Potential of Nomlabofusp in the Long-term Treatment of Friedreich's Ataxia: An Open Label Extension Study

Published Mon, Mar 11 2024 8:05 PM UTC

Friedreich s ataxia (FA) is a debilitating, progressive, and rare neurological disorder that primarily affects the nervous system and muscles. It is caused by a genetic mutation that leads to reduced levels of frataxin, a protein critical for mitochondrial function. Larimar Therapeutics, a clinical-stage biotechnology company, is at the forefront of developing a promising tr...










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