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A placebo formulation consisting of normal saline (0.9% sodium chloride) or 5% dextrose water used as an inert control in the BEYOND (Bezlotoxumab Yielded Outcomes by Addressing Personalized Needs in Clostridioides Difficile Infection) clinical trial. Conducted by the Hellenic Institute for the Study of Sepsis, this Phase 2 trial evaluated adjunctive bezlotoxumab in patients with *Clostridioides difficile* infection at high risk for unfavorable outcomes. The placebo was administered as a single intravenous infusion to match the appearance and administration of the active drug, serving as a vehicle/control rather than a therapeutic agent.
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