NRX Pharmaceuticals Soars 6.88% on FDA Fast Track Designation

Generated by AI AgentAinvest Pre-Market Radar
Wednesday, Aug 27, 2025 8:41 am ET1min read
Aime RobotAime Summary

- NRX Pharmaceuticals' stock rose 6.88% pre-market after FDA Fast Track designation for NRX-100, a ketamine therapy targeting depression-related suicidal ideation.

- The company expanded access to preservative-free NRX-100 and raised its success rate model to 80%, while filing a petition to remove benzethonium chloride from drug products.

- These developments aim to accelerate regulatory review, improve treatment safety, and increase patient access to ketamine-based therapies.

NRX Pharmaceuticals' stock surged 6.88% in pre-market trading on August 27, 2025, driven by significant developments in its pipeline and regulatory approvals.

NRX Pharmaceuticals received Fast Track designation from the FDA for NRX-100, a ketamine-based therapy aimed at treating suicidal ideation in patients with depression. This designation is expected to accelerate the development and review process, potentially bringing the treatment to market faster.

The company also announced an expanded access policy for NRX-100, allowing more patients to access this preservative-free ketamine treatment. This move is part of NRX Pharmaceuticals' strategy to increase the likelihood of success for NRX-100, which has seen its success rate model updated from 70% to 80%.

Additionally,

filed a Citizen Petition with the FDA seeking the removal of benzethonium chloride from certain drug products. This petition, if successful, could further enhance the safety and efficacy of NRX-100 and other treatments in development.

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