(MENAFN - Investor Brand Network) Clene (NASDAQ: CLNN)
received FDA guidance on leveraging data from its ongoing expanded access programs ("EAPs") to support an accelerated approval application for CNM-Au8, its treatment for ALS. The FDA recommended using neurofilament light chain ("NfL") biomarker analyses to substantiate the drug's efficacy. Clene plans to submit additional data in mid-2025, alongside commencing the Phase 3 RESTORE-ALS trial. Clinical findings presented at an FDA meeting highlighted CNM-Au8's significant survival benefits and benign safety profile, underscoring its potential as a transformative ALS therapy. Clene remains committed to addressing the urgent unmet needs of ALS patients.

To view the full press release, visit

About Clene Inc.

Clene (along with its subsidiaries,"Clene") and its wholly owned subsidiary Clene Nanomedicine Inc., is a late clinical-stage biopharmaceutical company focused on improving mitochondrial health and protecting neuronal function to treat neurodegenerative diseases, including amyotrophic lateral sclerosis, Parkinson's disease and multiple sclerosis. CNM-Au8(R) is an investigational first-in-class therapy that improves central nervous system cells' survival and function via a mechanism that targets mitochondrial function and the NAD pathway while reducing oxidative stress. CNM-Au8(R) is a federally registered trademark of Clene Nanomedicine, Inc. The company is based in Salt Lake City, Utah, with R&D and manufacturing operations in Maryland. For more information, please visit
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The latest news and updates relating to CLNN are available in the company's newsroom at

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