Larimar Therapeutics to Showcase Research at Key Ataxia Congress
Larimar Therapeutics Prepares for Major Ataxia Research Conference
Larimar Therapeutics, Inc. (LRMR), a biotechnology company dedicated to advancing treatments for complex rare diseases, is gearing up for an important event. The company has announced that it will present significant findings at the International Congress for Ataxia Research (ICAR), scheduled for November 12-15. This notable gathering will take place in London, U.K., bringing together experts and stakeholders in ataxia research.
Highlights of the Conference Presentations
During this prestigious conference, Larimar will showcase data from its studies on nomlabofusp, a promising therapy designed to tackle the underlying causes of Friedreich's ataxia. These presentations include critical insights from both Phase 1 and Phase 2 studies. Notably, Larimar will present three different posters, one of which will feature an accompanying oral presentation.
Key Presentation Details
The first presentation will focus on the Effect of nomlabofusp administration on tissue frataxin levels, plasma lipid profiles, and gene expression in patients with Friedreich's ataxia. Dr. Russell Clayton, Larimar's Chief Medical Officer, will lead this oral presentation on November 14. This presentation underscores the impact of nomlabofusp on essential biological markers related to the disease.
Additional Research Insights
The other two posters will delve into:
- Disease characteristics and tissue frataxin concentrations in adults participating in nomlabofusp studies
- Predicting tissue frataxin levels with long-term nomlabofusp administration in adults using modeling and simulations
Understanding Nomlabofusp and Its Impact
Nomlabofusp (CTI-1601) is an innovative recombinant fusion protein. It is engineered to deliver crucial human frataxin directly to the mitochondria, addressing the essential needs of patients with Friedreich's ataxia who struggle to produce this vital protein. The relevance of this treatment is amplified by its favorable designations from regulatory agencies, including Rare Pediatric Disease designation and Fast Track designation from the U.S. Food and Drug Administration (FDA).
Larimar Therapeutics: A Commitment to Rare Diseases
Founded to tackle the challenges posed by complex rare diseases, Larimar Therapeutics is making strides in its research and development efforts. Its flagship compound, nomlabofusp, showcases the company’s commitment to creating effective therapies for patients in need. Furthermore, with plans to harness its intracellular delivery platform, Larimar aims to develop additional fusion proteins that target other rare diseases linked to intracellular deficiencies.
Company Contacts and Further Information
For those interested in more details about the company’s research and initiatives, Larimar encourages inquiries. The Investor Contact is Joyce Allaire from LifeSci Advisors, reachable at (212) 915-2569 or via email. Additionally, Michael Celano, Chief Financial Officer, is available for corporate inquiries, offering his contact at (484) 414-2715.
Frequently Asked Questions
What is the International Congress for Ataxia Research?
The International Congress for Ataxia Research is a significant annual conference focused on research and advancements in the understanding and treatment of ataxia.
What is nomlabofusp?
Nomlabofusp is a recombinant fusion protein intended to deliver frataxin to mitochondria, targeting the treatment of Friedreich's ataxia.
Who will present at the conference?
Dr. Russell Clayton, Chief Medical Officer of Larimar Therapeutics, will present key findings during the conference.
What designations has nomlabofusp received?
Nomlabofusp has received several designations, including Rare Pediatric Disease, Fast Track, and Orphan Drug designations from the FDA.
How can I learn more about Larimar's research?
For more information about Larimar Therapeutics, you can contact their representatives or visit their official website.
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