OTO-104: a sustained-release dexamethasone hydrogel for the treatment of otic disorders

• Published in: Otology & neurotology Vol. 32; no. 1; p. 171
• Main Authors: Piu, Fabrice, Wang, Xiaobo, Fernandez, Rayne, Dellamary, Luis, Harrop, Anne, Ye, Qiang, Sweet, Jenifer, Tapp, Rachel, Dolan, David F, Altschuler, Richard A, Lichter, Jay, LeBel, Carl
• Format: Journal Article
• Language: English
• Published: United States 01.01.2011
• Subjects: Animals; Delayed-Action Preparations; Dexamethasone - administration & dosage; Dexamethasone - analysis; Dexamethasone - pharmacokinetics; Ear, Inner - chemistry; Guinea Pigs; Hydrogels - administration & dosage; Hydrogels - analysis; Hydrogels - pharmacokinetics; Injections; Perilymph - chemistry; Sheep
• ISSN: 1537-4505
• DOI: 10.1097/MAO.0b013e3182009d29

To investigate whether OTO-104, a poloxamer-based hydrogel containing micronized dexamethasone for intratympanic delivery, can provide long-lasting inner ear exposure and be well tolerated. OTO-104 was administered intratympanically to guinea pigs and sheep, and its pharmacokinetic and toxicity profiles were examined. After a single intratympanic injection of OTO-104 (from 0.6% to 20%, w/w), significant and prolonged exposure to dexamethasone in the inner ear was observed. Increasing the concentration of OTO-104 resulted in higher perilymph drug levels as well as a more prolonged duration of exposure. At the highest dose, therapeutic perilymph levels of dexamethasone could be sustained over 3 months in guinea pigs and more than 1 month in sheep. A toxicologic evaluation was conducted, including assessments of middle and inner ear function and physiology, as well as appraisal of local and systemic toxicity. A small and transient shift in hearing threshold was observed, most probably conductive in nature. No significant histologic changes in middle or inner ear tissues were noted. Although macroscopically mild erythema/inflammation was documented in a subset of guinea pigs treated with 20% OTO-104, the nature and the severity of these changes were not different between the poloxamer vehicle, saline, and 20% OTO-104 groups. No evidence of acute dermal toxicity, delayed hypersensitivity, or systemic adverse effects was found. OTO-104 is a novel proprietary therapeutic delivery system that can achieve prolonged, sustained release of dexamethasone within the inner ear fluids. The administration of this clinical candidate formulation via intratympanic injection is expected to be well tolerated both locally and systemically.