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Randomized crossover trial will compare the pharmacokinetics and pharmacodynamics of intranasal epinephrine powder against intramuscular auto-injector and manual injection in healthy participants
Pivotal Clinical Study Poised to Start in Q3 2026
Belhaven's Investigational New Drug (IND) Application Receives FDA Authorization to Proceed
Accelerated Round Completion Positions Company for New Drug Application (NDA) Submission and Commercial Launch Partnerships
Study Confirms Nasdepi® Dose Enabling Pivotal Biocomparability Study and Commercial Manufacturing
Oversubscribed Seed Round Accelerates Nasdepi®'s Journey as the First Dry Powder Nasal, Heat-Stable Treatment for Anaphylaxis
Dry Powder Epinephrine Product Demonstrates Reliable and Consistent Delivery in Real-World Dosing Situations with a Heat-Stable Formulation