Government Owned Inventions Available for Licensing/Collaboration: Using Artificial Intelligence To Diagnose Uveitis, 86343 [2024-25162]

Download as PDF 86343 Federal Register / Vol. 89, No. 210 / Wednesday, October 30, 2024 / Notices ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response Annual burden hours ANA Project Outcome Assessment Survey .................................................... 85 1 6 510 Comments: The Department specifically requests comments on (a) whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Authority: 42 U.S.C. 2992. Mary C. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2024–25139 Filed 10–29–24; 8:45 am] BILLING CODE 4184–34–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Government Owned Inventions Available for Licensing/Collaboration: Using Artificial Intelligence To Diagnose Uveitis AGENCY: National Institutes of Health, HHS. ACTION: Notice. The National Eye Institute seeks (NEI), an institute of the National Institutes of Health (NIH), Department of Health and Human Services (HHS), is giving notice of the licensing and collaboration opportunity for the inventions listed below, which are owned by an agency of the U.S. Government and are available for licensing/collaboration in the U.S. to achieve expeditious commercialization of results of federally-funded research and development. FOR FURTHER INFORMATION CONTACT: Inquiries related to this licensing/ collaboration opportunity should be directed to: Hiba Alsaffar, Ph.D., Technology Transfer Manager, NCI, Technology Transfer Center, Email: ddrumheller on DSK120RN23PROD with NOTICES1 SUMMARY: VerDate Sep<11>2014 17:59 Oct 29, 2024 Jkt 265001 hiba.alsaffar@nih.gov or Phone: 240– 276–7489. SUPPLEMENTARY INFORMATION: Uveitis is caused by inflammation in the eye that can cause pain and reduce vision. The rate of uveitis in the United States is 1 in every 200 people with eye-related irritation. Permanent symptoms such as vision loss can occur if untreated. Therefore, early detection is crucial. In certain uveitis cases, fluorescein angiography (FA) is essential for the diagnosis and management due to its ability to display retinal vascular leakage (RVL). Although proven to be critical in diagnosing and assessing severity, FA is invasive and side effects have been reported. Additionally, the procedure is time-consuming and imposes economic burdens to patients, physicians and payors. Scientists at the NEI have developed a deep learning tool to non-invasively detect RVL using ultrawide-field color fundus photos. This algorithm identifies fundus images with and without RVL with high accuracy (79%) and sensitivity (85%). Compared to the current gold standard of assessing RVL (clinician interpretation), this deep learning tool provides an improved method of detecting RVL for patients with uveitis. This Notice is in accordance with 35 U.S.C. 209 and 37 CFR part 404. NIH Reference Number: E–005–2023– 0. Potential Commercial Applications: • Diagnostic tool to predict uveitis. • Add-on to current color fundus imaging modalities. Competitive Advantages: • Greater accuracy and sensitivity versus current gold standard to assess RVL (clinician assessment). • Deep learning tool to assess RVL. • Deep learning to assess ultrawidefield color fundus images and assess RVL. Publication: Young LH, et al. Automated Detection of Vascular Leakage in Fluorescein Angiography—A Proof of Concept. (PMID 35877095). Patent Status: US Provisional Application 65/599,446 filed on November 15, 2023. Development Stage: Prototype. Therapeutic Area(s): Eye, Ear, Nose, Throat. PO 00000 Frm 00034 Fmt 4703 Sfmt 4703 Dated: October 24, 2024. Richard U. Rodriguez, Associate Director, Technology Transfer Center, National Cancer Institute. [FR Doc. 2024–25162 Filed 10–29–24; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Heart, Lung, and Blood Institute; Notice of Closed Meeting Pursuant to section 1009 of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Heart, Lung, and Blood Initial Review Group; NHLBI Institutional Training Mechanism Study Section. Date: December 6, 2024. Time: 10 a.m. to 6 p.m. Agenda: To review and evaluate grant applications. Address: National Institutes of Health, Rockledge I, 6705 Rockledge Drive, Bethesda, MD 20892. Meeting Format: Virtual Meeting. Contact Person: Michael P. Reilly, Ph.D., Scientific Review Officer, Office of Scientific Review/DERA, National Heart, Lung, and Blood Institute, National Institutes of Health, 6705 Rockledge Drive, Room 208–Z, Bethesda, MD 20892, 301–827–7975, email: reillymp@nhlbi.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.233, National Center for Sleep Disorders Research; 93.837, Heart and Vascular Diseases Research; 93.838, Lung Diseases Research; 93.839, Blood Diseases and Resources Research, National Institutes of Health, HHS) E:\FR\FM\30OCN1.SGM 30OCN1

Agencies

[Federal Register Volume 89, Number 210 (Wednesday, October 30, 2024)]
[Notices]
[Page 86343]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-25162]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Government Owned Inventions Available for Licensing/
Collaboration: Using Artificial Intelligence To Diagnose Uveitis

AGENCY: National Institutes of Health, HHS.

ACTION: Notice.

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SUMMARY: The National Eye Institute seeks (NEI), an institute of the 
National Institutes of Health (NIH), Department of Health and Human 
Services (HHS), is giving notice of the licensing and collaboration 
opportunity for the inventions listed below, which are owned by an 
agency of the U.S. Government and are available for licensing/
collaboration in the U.S. to achieve expeditious commercialization of 
results of federally-funded research and development.

FOR FURTHER INFORMATION CONTACT: Inquiries related to this licensing/
collaboration opportunity should be directed to: Hiba Alsaffar, Ph.D., 
Technology Transfer Manager, NCI, Technology Transfer Center, Email: 
[email protected] or Phone: 240-276-7489.

SUPPLEMENTARY INFORMATION: Uveitis is caused by inflammation in the eye 
that can cause pain and reduce vision. The rate of uveitis in the 
United States is 1 in every 200 people with eye-related irritation. 
Permanent symptoms such as vision loss can occur if untreated. 
Therefore, early detection is crucial. In certain uveitis cases, 
fluorescein angiography (FA) is essential for the diagnosis and 
management due to its ability to display retinal vascular leakage 
(RVL). Although proven to be critical in diagnosing and assessing 
severity, FA is invasive and side effects have been reported. 
Additionally, the procedure is time-consuming and imposes economic 
burdens to patients, physicians and payors. Scientists at the NEI have 
developed a deep learning tool to non-invasively detect RVL using 
ultrawide-field color fundus photos. This algorithm identifies fundus 
images with and without RVL with high accuracy (79%) and sensitivity 
(85%). Compared to the current gold standard of assessing RVL 
(clinician interpretation), this deep learning tool provides an 
improved method of detecting RVL for patients with uveitis.
    This Notice is in accordance with 35 U.S.C. 209 and 37 CFR part 
404.
    NIH Reference Number: E-005-2023-0.
    Potential Commercial Applications:
     Diagnostic tool to predict uveitis.
     Add-on to current color fundus imaging modalities.
    Competitive Advantages:
     Greater accuracy and sensitivity versus current gold 
standard to assess RVL (clinician assessment).
     Deep learning tool to assess RVL.
     Deep learning to assess ultrawide-field color fundus 
images and assess RVL.
    Publication: Young LH, et al. Automated Detection of Vascular 
Leakage in Fluorescein Angiography--A Proof of Concept. (PMID 
35877095).
    Patent Status: US Provisional Application 65/599,446 filed on 
November 15, 2023.
    Development Stage: Prototype.
    Therapeutic Area(s): Eye, Ear, Nose, Throat.

    Dated: October 24, 2024.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer 
Institute.
[FR Doc. 2024-25162 Filed 10-29-24; 8:45 am]
BILLING CODE 4140-01-P


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