Nasus Pharma Announces FDA Clearance to Initiate Clinical Study of NS002 in the Treatment of Anaphylaxis
Nasus Pharma announced that the FDA has cleared the initiation of a clinical study of NS002, its investigational intranasal epinephrine powder, as a needle-free alternative to EpiPen for treating anaphylaxis. The study will compare self-administration with administration by a healthcare professional, with a pivotal study planned for the fourth quarter of 2026 and topline data expected in the first quarter of 2027.
Why it matters — This FDA clearance advances NS002, a key product in Nasus Pharma's pipeline, toward pivotal clinical development for anaphylaxis treatment.