
Nasus Pharma Reports Positive Interim Phase 2 Results for Intranasal Epinephrine NS002

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Nasus Pharma Ltd. reported positive interim results from its Phase 2 study of NS002, an intranasal epinephrine formulation for anaphylaxis treatment. The data indicated faster absorption and higher peak concentrations compared to the EpiPen®, with 91% of participants reaching the plasma threshold at 5 minutes. NS002 was well-tolerated with no serious adverse events. Full results are expected by Q1 2026, with a pivotal study planned for Q4 2026.
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