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NeuroSense Skyrockets on FDA Clearance for ALS Drug Study

By Sam Boughedda

Investing.com -- Neurosense Therapeutics Ltd (NASDAQ:NRSN), a company developing treatments for severe neurodegenerative diseases, rocketed over 290% higher Monday after announcing it has received clearance from the Food and Drug Administration to initiate a pharmacokinetic study of PrimeC.

PrimeC is a drug designed to target key components of amyotrophic lateral sclerosis (ALS) and potentially inhibit the progression. PrimeC is comprised of two FDA-approved drugs: ciprofloxacin and celecoxib.

The drug was previously granted Orphan Drug Designation by the FDA and the European Medicines Agency.

NeuroSense completed a Phase 2a clinical study that met safety and efficacy endpoints, including reducing functional and respiratory deterioration.

The company now plans to initiate a Phase 2b multinational study in the second quarter.

"Data from our Phase IIa clinical study confirmed that PrimeC is a novel therapy with the potential to help people with ALS and address a $3 billion market in need of a more effective treatment," said NeuroSense CEO Alon Ben-Noon.

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