Nasus Pharma Earnings Call Transcripts
Fiscal Year 2026
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A proprietary powder-based intranasal platform is advancing multiple acute care therapies, led by a needle-free epinephrine product that outperforms EpiPen in speed and absorption. Phase III trials begin Q4, with NDA submission planned for mid-2027, and several pipeline products are entering the clinic this year.
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Phase II results show NS002, an intranasal epinephrine powder, achieves therapeutic levels twice as fast as EpiPen, with 88% of subjects reaching threshold within 5 minutes and a favorable safety profile. The product is compact, needle-free, and may reduce the need for repeat dosing.
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A proprietary powder technology enables a needle-free epinephrine product with faster absorption and superior pharmacokinetics compared to competitors. The lead product is advancing to pivotal trials, with a robust pipeline and significant market expansion potential in the growing anaphylaxis segment.
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A proprietary powder-based intranasal technology is enabling rapid, needle-free drug delivery, with the lead epinephrine product showing superior absorption and safety versus EpiPen. The company is advancing a robust pipeline, fully funded through 2027, and is well positioned for growth as the market shifts toward needle-free solutions.