Actionable Stock Market Trading Newswire. Built for Traders, by Traders.
All news is property of their respective owners.
Read More

UPDATE: Aridis Top-Line Results Of The Phase 3 Double-blinded, Superiority Trial Of Ar-301 Primary Outcome Measures Of Safety And Tolerability Of AR-301 Were Achieved

Primary outcome measures of safety and tolerability of AR-301 were achieved. AR-301 intravenous (IV) infusion was well tolerated. Adverse Events (AEs) and Serious Adverse Events (SAEs) reported over the 28-day study period for the single IV infusion were similar across the active and placebo treatment groups, with no SAEs deemed drug-related.

ARDS