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The authors described the methods, stating that: Participants were randomly assigned 1:1, using a central interactive web response system, to receive once-weekly subcutaneous injections of semaglutide 1mg or visually identical placebo, in addition to the maximum labelled or tolerated dose of a RAAS blocking agent (unless contraindicated or not tolerated). They also stated that they permitted the use of SGLT2i, and that randomisation was stratified by use at baseline