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Larimar Therapeutics Announces FDA has Removed Partial Clinical Hold for Nomlabofusp Program in Friedreich's Ataxia

Larimar Therapeutics Announces FDA has Removed Partial Clinical Hold for Nomlabofusp Program in Friedreich's Ataxia
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Larimar Therapeutics Announces FDA has Removed Partial Clinical Hold for Nomlabofusp Program in Friedreich's Ataxia Seite 1

20.05.2024 - Food and Drug Administration (FDA) removed partial clinical hold following review of Phase 2 dose exploration study data Ongoing open label extension (OLE) study initially evaluating 25 mg; Larimar plans to dose escalate to 50 mg following further . Seite 1 ....

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Larimar Therapeutics Reports First Quarter 2024 Operating and Financial Results

Larimar Therapeutics Reports First Quarter 2024 Operating and Financial Results
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Larimar Therapeutics Announces the Dosing of the First Patient in Long-term Open Label Extension Study for Nomlabofusp in Patients with Friedreich's Ataxia

Larimar Therapeutics Announces the Dosing of the First Patient in Long-term Open Label Extension Study for Nomlabofusp in Patients with Friedreich's Ataxia
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Larimar Therapeutics Reports Third Quarter 2023 Operating and Financial Results

Larimar Therapeutics Reports Third Quarter 2023 Operating and Financial Results
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