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Additionally, improvements in itch and disease severity were observed as early as two weeks after the first dose and continued throughout active treatment, which is important for these children and their families. The FDA evaluated the Dupixent application under Priority Review, which is reserved for medicines that represent potentially significant improvements in efficacy or safety in treating serious conditions

We want to modernize the strategy with the most up-to-date research to give schools the best opportunity to support the health of student-athletes." Concussion safety protocol checklist The committee also approved revisions to a variety of concussion resources, including the Concussion Safety Protocol Checklist, the Concussion Safety Protocol Template and the Concussion Fact Sheets