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D., Fitzsimons, C
Glutathione IV drip or IV Push Injections
Identify the route and formulation
Preliminary safety reporting indicated: GI adverse event profile consistent with Phase 2 data No new safety signals identified beyond those observed in earlier trials Discontinuation rates due to adverse events were comparable to other GLP-1 class trials Full adverse event tables from TRIUMPH-4 are expected with the peer-reviewed publication
Over 18 months, participants were divided into two groups half received the active medication while the other half received placebo treatment
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