LRMR Larimar Therapeutics Inc

Larimar Therapeutics to Present at the Guggenheim 5th Annual Inflammation, Neurology & Immunology Conference

Larimar Therapeutics to Present at the Guggenheim 5th Annual Inflammation, Neurology & Immunology Conference

BALA CYNWYD, Pa., Nov. 01, 2023 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced that members of the company’s management team will participate in a fireside chat and 1x1 investor meetings at the Guggenheim 5th Annual Inflammation, Neurology & Immunology Conference, taking place in New York, NY from November 6 - 7, 2023.

Details on the fireside chat can be found below.

Date: Tuesday, November 7, 2023

Time: 1:10 – 1:40 PM ET

Webcast Link:

Following the conclusion of the fireside chat, a replay will be available for 30 days on the “” page of Larimar’s website.

About Larimar Therapeutics

Larimar Therapeutics, Inc. (Nasdaq: LRMR), is a clinical-stage biotechnology company focused on developing treatments for complex rare diseases. Larimar’s lead compound, CTI-1601, is being developed as a potential treatment for Friedreich's ataxia. Larimar also plans to use its intracellular delivery platform to design other fusion proteins to target additional rare diseases characterized by deficiencies in intracellular bioactive compounds. For more information, please visit: .

Investor Contact:                                                        

Joyce Allaire                                                                

LifeSci Advisors                                                        

                                                

(212) 915-2569

Company Contact:

Michael Celano        

Chief Financial Officer



(484) 414-2715

                                                

 



EN
01/11/2023

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 PRESS RELEASE

Larimar Therapeutics Reports First Quarter 2025 Financial Results

Larimar Therapeutics Reports First Quarter 2025 Financial Results FDA stated as part of a START pilot program meeting that it is open to considering skin FXN concentration as a reasonably likely surrogate endpoint in support of an accelerated approval BLA seeking accelerated approval planned to be submitted by year-end 2025; global Phase 3 study planned to initiate in mid-2025 Completed dosing in adolescent PK run-in study; topline 50 mg dose data from the OLE study and data from adolescent cohort planned for program update in September 2025 Strong balance sheet of $157.5 million cash, ca...

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