Reviewed the report of the second interim analysis of RIDA by the DMC. I noted that in the press release it says:
The DMC advises the sponsor regarding the continuing safety of trial subjects and those yet to be recruited to the trial, as well as the continuing validity and scientific merit of the trial. According to the study protocol, the DMC is responsible for undertaking the two interim efficacy analyses.
Does this mean that the 3rd and final analyses is in Mercks hands and not the DMC's...
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