| Date | Title | Description |
| 24.03.2025 | Larimar Therapeutics Provides Nomlabofusp Development Update and Reports Fourth Quarter and Full Year 2024 Financial Results | FDA stated in written correspondence for 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
FDA recommended measuring skin FXN ... |
| 11.03.2024 | Larimar Therapeutics Announces the Dosing of the First Patient in Long-term Open Label Extension Study for Nomlabofusp in Patients with Friedreich’s Ataxia | Study will inform on long-term safety profile and tissue frataxin levels OLE initiated with 25 mg daily subcutaneous injections of nomlabofusp Frataxin data and safety data from the OLE study are intended to help support a potential Biologi... |
| 11.03.2024 | Larimar Therapeutics Announces the Dosing of the First Patient in Long-term Open Label Extension Study for Nomlabofusp in Patients with Friedreich’s Ataxia | - |
| 06.03.2024 | Larimar Therapeutics to Present at the Leerink Partners Global Biopharma Conference | - |
| 11.08.2022 | Larimar Therapeutics Provides Updates on CTI-1601 Clinical Program Following a Type C Meeting with the U.S. Food and Drug Administration and Reports Second Quarter 2022 Operating and Financial Results | Larimar plans to submit a complete response to CTI-1601’s clinical hold in the third quarter of 2022
In conjunction with the complete response, Larimar is proposing a Phase 2, four-week dose exploration study in Friedreich’s ataxia (FA) pat... |
| 19.05.2022 | Larimar Therapeutics Announces Upcoming Poster Presentations at the 4th Pan American Parkinson’s Disease and Movement Disorders Congress | BALA CYNWYD, Pa., May 19, 2022 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced that data from the ... |
| 12.05.2022 | Larimar Therapeutics Reports First Quarter 2022 Operating and Financial Results | - CTI-1601 Type C Meeting to discuss clinical hold has been granted by the U.S. Food and Drug Administration and is scheduled for early in the third quarter of 2022
- Cash at March 31, 2022 of $62.6 million provides projected cash runway in... |
| 25.03.2022 | Larimar Therapeutics Reports Fourth Quarter and Full Year 2021 Operating and Financial Results | BALA CYNWYD, Pa., March 25, 2022 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today reported its full year 2021... |
| 15.02.2022 | Larimar Therapeutics : Provides Update on CTI-1601 Clinical Program - Form 8-K | Larimar Therapeutics Provides Update on CTI-1601 Clinical Program
Bala Cynwyd, PA, February 14, 2022 - Larimar Therapeutics, Inc. ("Larimar") (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments ... |
| 15.02.2022 | Larimar Therapeutics Provides Update on CTI-1601 Clinical Program | BALA CYNWYD, Pa., Feb. 14, 2022 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced that it has receiv... |
| 12.11.2021 | Larimar Therapeutics Reports Third Quarter 2021 Operating and Financial Results | BALA CYNWYD, Pa., Nov. 12, 2021 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today reported its third quarter a... |
| 12.11.2021 | Larimar Therapeutics Reports Third Quarter 2021 Operating and Financial Results - Form 8-K | Larimar Therapeutics Reports Third Quarter 2021 Operating and Financial Results
Bala Cynwyd, PA, November 12, 2021 - Larimar Therapeutics, Inc. ("Larimar") (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developi... |
| 12.11.2021 | Larimar Therapeutics Reports Third Quarter 2021 Operating and Financial Results | BALA CYNWYD, Pa., Nov. 12, 2021 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today reported its third quarter a... |
| 19.08.2021 | Larimar Therapeutics : Announces Upcoming Oral Presentation at the World Orphan Drug Congress | BALA CYNWYD, Pa., Aug. 19, 2021 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced that David Bettoun... |
| 12.08.2021 | Larimar Therapeutics : Reports Second Quarter 2021 Operating and Financial Results (Form 8-K) | Larimar Therapeutics Reports Second Quarter 2021 Operating and Financial Results
- Reported positive proof-of-concept and dose response data from Phase 1 program evaluating CTI-1601 in patients with Friedreich's ataxia (FA)
- Subcutaneous i... |
| 12.08.2021 | Larimar Therapeutics Reports Second Quarter 2021 Operating and Financial Results | - Reported positive proof-of-concept and dose response data from Phase 1 program evaluating CTI-1601 in patients with Friedreich’s ataxia (FA)
- Subcutaneous injections of CTI-1601 at doses of 50 mg or 100 mg resulted in frataxin levels in ... |
| 26.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics : Reports FDA Clinical Hold on CTI-1601 and Termination of Recently Announced Private Placement Financing (Form 8-K) | Larimar Therapeutics Reports FDA Clinical Hold on CTI-1601 and Termination of Recently Announced Private Placement Financing
Bala Cynwyd, PA, May 25, 2021 - Larimar Therapeutics, Inc. ('Larimar') (Nasdaq: LRMR), a clinical-stage biotechnolo... |
| 26.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics Reports FDA Clinical Hold on CTI-1601 and Termination of Recently Announced Private Placement Financing | BALA CYNWYD, Pa., May 25, 2021 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for Friedreich’s ataxia (FA) and other complex rare diseases, ... |
| 21.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics : Receives European Medicines Agency Priority Medicines (PRIME) Designation for CTI-1601 in Friedreich's Ataxia (Form 8-K) | Larimar Therapeutics Receives European Medicines Agency Priority Medicines (PRIME) Designation for CTI-1601 in Friedreich's Ataxia
Bala Cynwyd, PA, May 20, 2021 - Larimar Therapeutics, Inc. ('Larimar') (Nasdaq: LRMR), a clinical-stage biote... |
| 21.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics Announces $95 Million Private Placement Financing | BALA CYNWYD, Pa., May 21, 2021 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for Friedreich’s ataxia (FA) and other complex rare diseases, ... |
| 20.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics Receives European Medicines Agency Priority Medicines (PRIME) Designation for CTI-1601 in Friedreich's Ataxia | BALA CYNWYD, Pa., May 20, 2021 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (“Larimar”) (Nasdaq: LRMR), a clinical-stage biotechnology company focused on developing treatments for Friedreich’s ataxia (FA) and other complex rare diseases, ... |
| 12.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics : Topline data from placebo-controlled Phase 1 program in Friedreich's ataxia patients to be announced tomorrow, May 11, 2021- Management to discuss du... | - Topline data from placebo-controlled Phase 1 program in Friedreich's ataxia patients to be announced tomorrow, May 11, 2021- Management to discuss during webcast and conference call at 8 a.m. ET
- Cash and investments of $81.4 million as ... |
| 11.05.2021 | LARIMAR THERAPEUTICS, INC.
Larimar Therapeutics Reports Positive Topline Phase 1 Clinical Trial Data Showing Dose-Dependent Increases in Frataxin Levels in Patients with Friedreich's Ataxia | Data demonstrate proof-of-concept by showing that daily subcutaneous injections of CTI-1601 for up to 13 days resulted in dose-dependent increases in frataxin levels from baseline compared to placebo in all evaluated tissues
Data show that ... |
| 04.03.2021 | Larimar Therapeutics Reports Fourth Quarter and Full Year 2020 Operating and Financial Results | Reported preliminary Phase 1 findings from a Single Ascending Dose (SAD) trial that suggest single subcutaneous injections of CTI-1601 were well tolerated at doses up to 100 mg in Friedreich's ataxia (FA) patients
Placebo-controlled Phase 1... |