NRx Pharmaceuticals NRXP has completed an analysis in the subgroup of Zyesami and placebo-treated patients previously treated with Gilead Science Inc's GILD remdesivir in the COVID-AIV trial representing approximately 70% of the study population.
- The analysis indicates a substantial improvement after Zyesami (aviptadil) treatment in patients with critical COVID-19 and Respiratory Failure over existing therapies.
- Read Next: NRx Pharma Skyrockets After BriLife COVID-19 Vaccine Data Against Delta Variant.
- The analysis identified a statistically significant 2.5 fold increased odds of being alive and free of respiratory failure at 60 days (the primary endpoint) and a statistically significant four-fold higher odds of being alive at day 60 among patients treated with aviptadil compared to those treated with placebo.
- Baseline treatment with remdesivir was prespecified as a covariate in the protocol agreed to with the FDA. Before initiation of the trial, remdesivir did not show any independent survival or recovery advantage in the subgroup.
- The FDA recently declined Emergency Use Authorization and Breakthrough Therapy Designation for Zyesami and invited a new request based on new clinical evidence.
- Price Action: NRXP shares are up 52% at $10.26 during the premarket session on the last check Monday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
Posted In:
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in