Notice2026-07770

Government-Owned Inventions; Availability for Licensing

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
April 22, 2026

Issuing agencies

Health and Human Services DepartmentNational Institutes of Health

Abstract

The National Institute of Allergy and Infectious Diseases (NIAID), an institute of the National Institutes of Health (NIH), Department of Health and Human Services (HHS), is giving notice of the invention listed below, which is owned by an agency of the U.S. Government and is available for licensing to achieve expeditious commercialization of results of federally funded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies and may also be available for licensing.

Full Text

<html>
<head>
<title>Federal Register, Volume 91 Issue 77 (Wednesday, April 22, 2026)</title>
</head>
<body><pre>
[Federal Register Volume 91, Number 77 (Wednesday, April 22, 2026)]
[Notices]
[Page 21509]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-07770]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Government-Owned Inventions; Availability for Licensing

AGENCY: National Institutes of Health, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The National Institute of Allergy and Infectious Diseases 
(NIAID), an institute of the National Institutes of Health (NIH), 
Department of Health and Human Services (HHS), is giving notice of the 
invention listed below, which is owned by an agency of the U.S. 
Government and is available for licensing to achieve expeditious 
commercialization of results of federally funded research and 
development. Foreign patent applications are filed on selected 
inventions to extend market coverage for companies and may also be 
available for licensing.

FOR FURTHER INFORMATION CONTACT: Inquiries related to this licensing 
opportunity should be directed to: Brian Bailey at 240-669-5128, or 
<a href="/cdn-cgi/l/email-protection#660404070f0a031f260b070f0a48080f0e48010910"><span class="__cf_email__" data-cfemail="1f7d7d7e76737a665f727e76733171767731787069">[email&#160;protected]</span></a>. Licensing information may be obtained by 
communicating with the Technology Transfer and Intellectual Property 
Office, National Institute of Allergy and Infectious Diseases, 5601 
Fishers Lane, Rockville, MD 20852: tel. 301-496-2644. A signed 
Confidential Disclosure Agreement will be required to receive copies of 
unpublished information related to the invention.

SUPPLEMENTARY INFORMATION: Technology description follows:

Neutralizing Antibodies Against West Nile Virus

    Description of Technology:
    West Nile virus (WNV) is a mosquito-borne virus that can cause 
severe disease affecting the brain and nervous system, especially in 
older adults and people with weakened immune systems. There is no 
approved human vaccine or specific antiviral treatment for WNV.
    Researchers at NIAID's Vaccine Research Center (VRC), together with 
collaborators at Sheba Medical Center and the Israeli Ministry of 
Health, have identified and characterized seven new fully human 
monoclonal antibodies that bind to the WNV envelope (E) protein--the 
main surface protein the virus uses to enter cells. In laboratory 
studies, these antibodies (AIS-196, AIS-204, AIS-259, AIS-260, AIS-261, 
AIS-262, and AIS-265) strongly blocked WNV infection, and several also 
showed protective effects in a mouse model.
    The invention includes the antibody sequences and tools needed to 
produce them, supporting development of full-length antibody therapies 
or smaller antibody fragments. These antibodies could help prevent WNV 
disease in people at higher risk or treat infection early, either 
individually or in combination. Modified versions are also included 
that may extend how long the antibodies remain active in the body or 
adjust how they interact with the immune system. The antibodies may 
also be useful in laboratory tests for WNV diagnosis, surveillance, and 
research.
    This technology is available for licensing for commercial 
development in accordance with 35 U.S.C. 209 and 37 CFR part 404, as 
well as for further development and evaluation under a research 
collaboration.
    Potential Commercial Applications:
    <bullet> Prevention or treatment antibodies for WNV, especially for 
people at higher risk of severe disease or after a known exposure.
    <bullet> Fully human antibodies that strongly neutralize virus 
infection by targeting its key surface E protein.
    <bullet> Flexible formats for different uses, including full-length 
antibodies or antibody fragments, and the option to use a single 
antibody or a combination (``cocktail'').
    <bullet> Engineered versions designed to last longer in the body 
and tune immune functions for safety and performance.
    <bullet> High-quality antibodies for WNV testing and surveillance, 
supporting laboratory detection, public health monitoring, and 
research.
    <bullet> Neutralizing antibodies as components of delivery systems 
for prophylactic or therapeutic applications.
    Competitive Advantages:
    <bullet> An antibody-based approach for WNV prevention or 
treatment, given the lack of an approved human vaccine, specific 
antiviral treatment, or licensed antibody therapy.
    <bullet> Strong virus-neutralizing activity.
    <bullet> Fully human antibodies, which are less likely to cause 
anti-drug immune responses than non-human or humanized antibodies.
    <bullet> Engineered versions that may last longer in the body and 
tune immune activity to improve safety and effectiveness.
    <bullet> High-quality antibodies that support WNV prevention or 
treatment and can also be used in diagnostic tests, public health 
surveillance, and research.
    Development Stage:
    <bullet> Pre-Clinical
    Inventors: Dr. Theodore Pierson, Dr. Kimberly Dowd, and Dr. Daniel 
Douek, all of NIAID; Dr. Dror Harats, Dr. Yael Ottolenghi, and Dr. Gili 
Regev-Yochay, all of Sheba Impact Ltd.; Dr. Yaniv Lustig, of Sheba 
Impact Ltd. and Ministry of Health, State of Israel.
    Intellectual Property: HHS Reference No. E-021-2026-0. Provisional 
Patent Application No. 63/991,485, filed on February 26, 2026.
    Licensing Contact: To license this technology, please contact Brian 
Bailey at 240-669-5128, or <a href="/cdn-cgi/l/email-protection#f49696959d98918db499959d98da9a9d9cda939b82"><span class="__cf_email__" data-cfemail="056767646c69607c4568646c692b6b6c6d2b626a73">[email&#160;protected]</span></a>, and reference E-021-
2026-0.
    Collaborative Research Opportunity: The National Institute of 
Allergy and Infectious Diseases is seeking statements of capability or 
interest from parties interested in collaborative research to further 
develop, evaluate, or commercialize this technology. For collaboration 
opportunities, please contact Brian Bailey at 240-669-5128, or 
<a href="/cdn-cgi/l/email-protection#6a08080b03060f132a070b030644040302440d051c"><span class="__cf_email__" data-cfemail="bedcdcdfd7d2dbc7fed3dfd7d290d0d7d690d9d1c8">[email&#160;protected]</span></a>.

    Dated: April 17, 2026.
Surekha Vathyam,
Director, Technology Transfer and Intellectual Property Office, 
National Institute of Allergy and Infectious Diseases.
[FR Doc. 2026-07770 Filed 4-21-26; 8:45 am]
BILLING CODE 4167-05-P


</pre><script data-cfasync="false" src="/cdn-cgi/scripts/5c5dd728/cloudflare-static/email-decode.min.js"></script></body>
</html>
Indexed from Federal Register on April 22, 2026.

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.