NeuroSense Therapeutics Ltd. announced the completion of the safety analysis from its proof-of-concept Phase 2, randomized, double-blind, placebo-controlled study (NST-AD-001) evaluating PrimeC in Alzheimer's disease. The analysis indicated a favorable tolerability profile, with no serious adverse events or new safety signals reported. The company stated that clinical and biomarker outcome results are expected to be reported in the first quarter of 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Neurosense Therapeutics Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: IO52378) on December 22, 2025, and is solely responsible for the information contained therein.

