- NeuroSense reported a net loss of USD 11 million.
- Operating loss widened to USD 11 million.
- Research and development expense climbed 8.8% to USD 6.2 million, due mainly to higher share-based pay and increased salaries and social benefits.
- FDA cleared initiation of PARAGON Phase 3 ALS trial, following Phase 2b PARADIGM data showing a 65% reduction in risk of death with more than 14-month median survival benefit.
- NeuroSense targets a pre-NDS meeting with Health Canada in May 2026, with a potential Canada filing subject to regulatory feedback.
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: 202603310920PR_NEWS_USPR_____LN23461) on March 31, 2026, and is solely responsible for the information contained therein.

