NeuroRX says that the data submitted to the FDA is
Post# of 148116
Quote:
According to NeuroRx, across all patients and sites, RLF-100(TM) met the primary endpoint for successful recovery from respiratory failure at days 28 (P = .014) and 60 (P = .013) and also demonstrated a meaningful benefit in survival (P = < .001) after controlling for ventilation status and treatment site .
https://finance.yahoo.com/news/relief-confirm...00337.html