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SB1DC018255

Project Grant

Overview

Grant Description
Clinical study to enable commercialization of nonsurgical gel patch for eardrum repair - 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 that fits the existing clinical workflow for myringoplasty. 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 will conduct a human study in both adult and pediatric patients to evaluate the efficacy of PERF-FIX. This human study is the last milestone before submission of PERF-FIX to FDA for clearance as a Class II medical device. During the study, patients will be evaluated for: perforation closure rate, application time, time to closure, changes in hearing scores, safety of device through adverse events and failure rates.

The endpoints for this study include: TM closure rate at 3 weeks and 3 months, incidence of adverse events, procedural success, and functional hearing results. The data from this study will be compiled in a final report that will be included in the De Novo submission to FDA.

This SBIR project concludes with submission of the De Novo application. The success of this proposal will supply the necessary data to market PERF-FIX successfully after product launch, leading to a significant medical improvement over the current standard-of-care with a major reduction in healthcare costs.
Awardee
Funding Goals
TO INVESTIGATE SOLUTIONS TO PROBLEMS DIRECTLY RELEVANT TO INDIVIDUALS WITH DEAFNESS OR DISORDERS OF HUMAN COMMUNICATION IN THE AREAS OF HEARING, BALANCE, SMELL, TASTE, VOICE, SPEECH, AND LANGUAGE. THE NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS (NIDCD) SUPPORTS RESEARCH AND RESEARCH TRAINING, INCLUDING INVESTIGATION INTO THE ETIOLOGY, PATHOLOGY, DETECTION, TREATMENT, AND PREVENTION OF DISORDERS OF HEARING AND OTHER COMMUNICATION PROCESSES, PRIMARILY THROUGH THE SUPPORT OF BASIC AND APPLIED RESEARCH IN ANATOMY, AUDIOLOGY, BIOCHEMISTRY, BIOENGINEERING, EPIDEMIOLOGY, GENETICS, IMMUNOLOGY, MICROBIOLOGY, MOLECULAR BIOLOGY, THE NEUROSCIENCES, OTOLARYNGOLOGY, PSYCHOLOGY, PHARMACOLOGY, PHYSIOLOGY, PSYCHOPHYSICS, SPEECH-LANGUAGE PATHOLOGY, AND OTHER SCIENTIFIC DISCIPLINES. THE NIDCD SUPPORTS: (1) RESEARCH INTO THE EVALUATION OF TECHNIQUES AND DEVICES USED IN DIAGNOSIS, TREATMENT, REHABILITATION, AND PREVENTION OF DISORDERS OF HEARING AND OTHER COMMUNICATION PROCESSES, (2) RESEARCH INTO PREVENTION AND EARLY DETECTION AND DIAGNOSIS OF HEARING LOSS AND SPEECH, VOICE, AND LANGUAGE DISORDERS AND RESEARCH INTO PREVENTING THE EFFECTS OF SUCH DISORDERS BY MEANS OF APPROPRIATE REFERRAL AND REHABILITATION, (3) RESEARCH INTO THE DETECTION, TREATMENT, AND PREVENTION OF DISORDERS OF HEARING AND OTHER COMMUNICATION PROCESSES IN THE ELDERLY POPULATION AND ITS REHABILITATION TO ENSURE CONTINUED EFFECTIVE COMMUNICATION SKILLS, AND (4) RESEARCH TO EXPAND KNOWLEDGE OF THE EFFECTS OF ENVIRONMENTAL AGENTS THAT INFLUENCE HEARING OR OTHER COMMUNICATION PROCESSES. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO ENCOURAGE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Place of Performance
Virginia United States
Geographic Scope
State-Wide
Analysis Notes
Amendment Since initial award the End Date has been extended from 07/31/24 to 11/30/25.
Tympanogen was awarded Clinical Study Nonsurgical Gel Patch Eardrum Repair Project Grant SB1DC018255 worth $3,235,980 from National Institute on Deafness and Other Communication Disorders in August 2019 with work to be completed primarily in Virginia United States. The grant has a duration of 6 years 3 months and was awarded through assistance program 93.173 Research Related to Deafness and Communication Disorders. The Project Grant was awarded through grant opportunity SBIR/STTR Commercialization Readiness Pilot (CRP) Program Technical Assistance and Late Stage Development (SB1 Clinical Trial Required).

SBIR Details

Research Type
SBIR Phase II
Title
Clinical study to enable commercialization of nonsurgical gel patch for eardrum repair
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 that fits the existing clinical workflow for myringoplasty. 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 will conduct a human study in both adult and pediatric patients to evaluate the efficacy of Perf-Fix. This human study is the last milestone before submission of Perf- Fix to FDA for clearance as a class II medical device. During the study, patients will be evaluated for: perforation closure rate, application time, time to closure, changes in hearing scores, safety of device through adverse events and failure rates. The endpoints for this study include: TM closure rate at 3 weeks and 3 months, incidence of adverse events, procedural success, and functional hearing results. The data from this study will be compiled in a final report that will be included in the de novo submission to FDA. This SBIR project concludes with submission of the de novo application. The success of this proposal will supply the necessary data to market Perf-Fix successfully after product launch, leading to a significant medical improvement over the current standard-of-care with a major reduction in healthcare costs.
Topic Code
NIDCD
Solicitation Number
PAR20-130

Status
(Ongoing)

Last Modified 4/4/25

Period of Performance
8/25/19
Start Date
11/30/25
End Date
96.0% Complete

Funding Split
$3.2M
Federal Obligation
$0.0
Non-Federal Obligation
$3.2M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to SB1DC018255

Transaction History

Modifications to SB1DC018255

Additional Detail

Award ID FAIN
SB1DC018255
SAI Number
SB1DC018255-3744705081
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75N300 NIH National Institute on Deafness and Other Communication Disorders
Funding Office
75N300 NIH National Institute on Deafness and Other Communication Disorders
Awardee UEI
W8RKQ5AJK6G6
Awardee CAGE
72LC5
Performance District
VA-90
Senators
Mark Warner
Timothy Kaine

Budget Funding

Federal Account Budget Subfunction Object Class Total Percentage
National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Health and Human Services (075-0890) Health research and training Grants, subsidies, and contributions (41.0) $3,235,980 100%
Modified: 4/4/25