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NeuroSense Delays PrimeC New Drug Submission to March 2027
NeuroSense plans to incorporate newly generated data into its New Drug Submission to Health Canada for PrimeC, its lead investigational therapy for amyotrophic lateral sclerosis, or ALS. The NDS would be PrimeC's first marketing application in any jurisdiction, and the company believes the additional data will strengthen the application and expand the evidence available for regulatory review. The March 2027 filing target updates the previously announced December 2026 timetable, allowing the additional data to be included. Health Canada has confirmed it has no concerns with the revised timing. In the new analysis, PrimeC-treated participants demonstrated a greater reduction in NfL compared to placebo, with an even more pronounced effect observed in participants with higher baseline functionality. Additional statistical analyses are underway to further characterize these findings and support their incorporation into the planned submission to Health Canada. Following acceptance of the NDS for review, Health Canada's standard review target for an NDS is approximately 300 calendar days.
NeuroSense Files Patent for Traumatic Brain Injury Treatment
NeuroSense Therapeutics announced that it has filed a patent application with the U.S. Patent and Trademark Office covering methods of treating traumatic brain injury, or TBI, and related central nervous system injuries with the combination of ciprofloxacin and celecoxib, the active ingredients of PrimeC. The application covers the treatment of a broad range of brain injuries, from concussion and mild TBI to moderate and severe TBI, including blast-related injury, as well as their long-term consequences, such as chronic traumatic encephalopathy. If granted, the patent is expected to provide protection through 2047, subject to any extensions. Traumatic brain injury represents a major global healthcare challenge, affecting millions of people each year. TBI can result from falls, motor vehicle accidents, sports-related injuries and military-related trauma, including blast exposure. Its consequences can extend well beyond the initial event, potentially causing persistent cognitive, physical and behavioral impairment, with substantial burdens on patients, caregivers and healthcare systems.
NeuroSense Unveils Redesigned Development Plan for PrimeC
NeuroSense Therapeutics announced a redesigned development plan for PrimeC in amyotrophic lateral sclerosis, structured to reach a potential path for regulatory submission and approval faster and at materially lower cost than the Company's previously planned development path. "One of the hardest constraints in ALS is not scientific - it is that the standard development path takes longer than patients have," said Alon Ben-Noon, Co-Founder and Chief Executive Officer of NeuroSense. "We have asked a straightforward question: what is the shortest reasonable route from the data we already hold to a therapy people can actually receive? This plan is our answer. It is faster, it costs less, and it produces a stronger package - pharmacology, comparative clinical context, and a pivotal dataset - than the single-trial approach would have."
NeuroSense Targets December 2026 for New Drug Submission
NeuroSense Therapeutics announced that it is targeting December 2026 for the filing of a New Drug Submission with Health Canada for PrimeC, its lead therapeutic candidate for amyotrophic lateral sclerosis. The filing target follows the successful finalization of the Pre-NDS process with Health Canada and the associated meeting minutes. The discussions with Health Canada provided alignment regarding the content and structure of the submission. Health Canada has also indicated that it has no concerns with the company's proposed filing timeline and advised the company to target early December.
NeuroSense Files New Drug Submission for PrimeC to Treat ALS
NeuroSense Therapeutics announced it intends to proceed with the filing of a New Drug Submission, or NDS, to Health Canada for PrimeC for the treatment of amyotrophic lateral sclerosis, or ALS, following a constructive Pre-New Drug Submission meeting with the Agency. NeuroSense expects to complete and file the submission in the coming months. The recent Pre-NDS meeting was held following the generation of substantial additional evidence from the Phase 2b PARADIGM clinical program. NeuroSense presented Health Canada with a comprehensive update to its proposed NDS package, including achievement of the study's prespecified primary TDP-43 biomarker endpoint, long-term survival, external natural history analyses, and additional mechanistic and translational data generated since the Company's initial regulatory interaction. The meeting also included an expert clinical perspective from a leading Canadian ALS specialist, as well as additional supportive analyses that will form part of the planned NDS package, further strengthening the growing body of evidence supporting PrimeC's potential in ALS. NeuroSense plans to continue to work with Health Canada as it prepares the NDS filing, and looks forward to providing further updates as the submission advances.
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