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A gel patch for replacing surgical eardrum repair with an office-based procedure

$1,479,163R44FY2019DCNIH

Tympanogen, Llc, Richmond VA

Investigators

Abstract

ABSTRACT Chronic perforations of the tympanic membrane (TM) affect over 170,000 patients in the United States annually, often stemming from ventilation tubes inserted in the TM to drain fluid from middle ear infections. Left untreated, these TM perforations can lead to significant morbidities that include recurrent ear infection, conductive and sensorineural hearing loss, mastoid bone infection, and cholesteatoma development. Currently, TM perforations are repaired with a graft applied to the TM via an invasive surgery that can take 2-4 hours to complete, cost up to $18,000 per surgery, and carry significant anesthesia-related risks for pediatric patients. A nonsurgical alternative to the existing procedure that can reduce procedure time and morbidities would be of economic benefit to patients, otolaryngologists, and payors alike. We have developed a highly regenerative gel patch, called Perf-Fix, for nonsurgical TM repair. Perf-Fix can be applied to the TM through the ear canal without incisions or abrasion of the perforation margin, then cured via blue light into a stiff scaffold through which cells can migrate. The cells degrade the gel patch as they proliferate and migrate, resulting in total replacement of Perf-Fix with regenerated TM tissue. In this proposal, we aim to perform the necessary biocompatibility testing and applicator development ahead of FDA submission. We will evaluate Perf-Fix for safety in a series of biocompatibility tests, followed by a capstone animal trial to ensure that the final, sterilized form of Perf-Fix retains its regenerative capabilities. This will be followed by the development of an applicator for Perf-Fix that is suitable for human patients, and additional mechanical testing to ensure that Perf-Fix applied with the applicator retains the same properties seen in previous bench testing. The success of this proposal will allow Tympanogen to proceed with submission of Perf-Fix to the FDA, leading to a significant medical improvement over the current standard-of-care with a major reduction in healthcare costs.

View original record on NIH RePORTER →