Aquestive Therapeutics Announces Positive Topline PK Results from its Pediatric Study and Completes the NDA Submission for Anaphylm™ (epinephrine) Sublingual Film

Core Insights - Aquestive Therapeutics announced positive topline results from its pediatric study for Anaphylm™ (epinephrine) sublingual film, indicating its potential as a treatment for severe allergic reactions in patients aged seven to seventeen [1][2] - The company has submitted the New Drug Application (NDA) for Anaphylm to the FDA, with expectations for acceptance in the second quarter of 2025 [1][6] - If approved, Anaphylm is planned to be launched in the first quarter of 2026 [2] Pediatric Study Results - The pediatric study was a multi-site, single treatment study involving thirty-two patients, demonstrating consistent pharmacokinetic (PK) profiles with previous adult studies [2] - Anaphylm was found to be safe and well-tolerated, with no serious adverse events reported [2] Product Overview - Anaphylm is a polymer matrix-based epinephrine prodrug designed for the treatment of severe allergic reactions, including anaphylaxis [3] - The product is compact, similar in size to a postage stamp, and does not require water or swallowing for administration [3] Company Background - Aquestive Therapeutics focuses on advancing medicines through innovative science and delivery technologies, with five commercialized products and collaborations with other pharmaceutical companies [4] - The company is also developing an earlier stage epinephrine prodrug topical gel for dermatological conditions [4]