Ridgreback biotherapeutics recently reported molnu
Post# of 72440
https://www.merck.com/news/ridgeback-biothera...nupiravir/
IPIX trial describes the interim report being a safety report. So I doubt any reporting of efficacy or secondary endpoints will be reported.
" After an interim analysis safety review, by an independent Data Monitoring Committee (DMC), dosing may be extended to 5 days."
https://clinicaltrials.gov/ct2/show/NCT04784897
Nice review of Covid19 DMC responsibilities and reporting :
https://www.sciencedirect.com/science/article...329#bb0180
GLTA Farrell