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This placebo gel is an inactive control used in Phase 3 clinical trials conducted by the Naval Aeromedical Research Unit, Dayton (NAMRU-D) in collaboration with Defender Pharmaceuticals. It was specifically utilized in a randomized, double-blind study to evaluate the efficacy and safety of DPI-386 (an intranasal scopolamine gel) for the prevention and treatment of motion sickness among personnel on ocean-going vessels. The placebo gel is formulated to be physically indistinguishable from the active DPI-386 gel but contains no active pharmaceutical ingredient, serving to establish a baseline for comparing the therapeutic effects of scopolamine.
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