Notice2026-06283

Prospective Grant of an Exclusive Patent License: Pigment Epithelium-Derived Factor (PEDF) Peptides and Use for Treating Retinal Degeneration

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 1, 2026

Issuing agencies

Health and Human Services DepartmentNational Institutes of Health

Abstract

The National Eye Institute, an institute of the National Institutes of Health, United States Department of Health and Human Services, is contemplating the grant of an Exclusive Patent License to practice the inventions embodied in the patent applications listed in the SUPPLEMENTARY INFORMATION section of this notice to Perpetual Biosciences, Inc., a company located in New York, NY.

Full Text

<html>
<head>
<title>Federal Register, Volume 91 Issue 62 (Wednesday, April 1, 2026)</title>
</head>
<body><pre>
[Federal Register Volume 91, Number 62 (Wednesday, April 1, 2026)]
[Notices]
[Pages 16205-16206]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-06283]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Prospective Grant of an Exclusive Patent License: Pigment 
Epithelium-Derived Factor (PEDF) Peptides and Use for Treating Retinal 
Degeneration

AGENCY: National Institutes of Health, HHS.

ACTION: Notice.

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

[[Page 16206]]

SUMMARY: The National Eye Institute, an institute of the National 
Institutes of Health, United States Department of Health and Human 
Services, is contemplating the grant of an Exclusive Patent License to 
practice the inventions embodied in the patent applications listed in 
the SUPPLEMENTARY INFORMATION section of this notice to Perpetual 
Biosciences, Inc., a company located in New York, NY.

DATES: Only written comments and/or applications for a license which 
are received by the National Cancer Institute's Technology Transfer 
Center, representing the National Eye Institute, on or before April 16, 
2026 will be considered.

ADDRESSES: Requests for copies of the patent application, inquiries, 
and comments relating to the contemplated an Exclusive Patent License 
should be directed to: Geoffrey E. Ravilious, Ph.D., NCI Technology 
Transfer Center, Telephone: 240-276-6391; Email: 
<a href="/cdn-cgi/l/email-protection#7116141e17170314085f031007181d181e0402311f18195f161e07"><span class="__cf_email__" data-cfemail="d5b2b0bab3b3a7b0acfba7b4a3bcb9bcbaa0a695bbbcbdfbb2baa3">[email&#160;protected]</span></a>.

SUPPLEMENTARY INFORMATION:

Intellectual Property

    1. United States Provisional Patent Application No. 63/430,251 
filed December 5, 2022, entitled ``PIGMENT EPITHELIUM-DERIVED FACTOR 
PEPTIDES AND USE FOR TREATING RETINAL DEGENERATION'' [HHS Reference No. 
E-028-2023-0-US-01];
    2. International Patent Application PCT/US2024/064947 filed March 
24, 2023, entitled ``PIGMENT EPITHELIUM-DERIVED FACTOR PEPTIDES AND USE 
FOR TREATING RETINAL DEGENERATION'' [HHS Reference No. E-028-2023-0-
PCT-01]; and
    3. Australian Patent No. 2023390868 issued June 5, 2025, entitled 
``PIGMENT EPITHELIUM-DERIVED FACTOR PEPTIDES AND USE FOR TREATING 
RETINAL DEGENERATION'' [HHS Reference No. E-028-2023-0-AU-01];
    4. Canadian Patent Application No. 3,275,801 effective filing date 
of June 3, 2025, entitled ``PIGMENT EPITHELIUM-DERIVED FACTOR PEPTIDES 
AND USE FOR TREATING RETINAL DEGENERATION'' [HHS Reference No. E-028-
2023-0-CA-01];
    5. European Patent Application No. 23720018.3 filed July 1, 2025, 
entitled ``PIGMENT EPITHELIUM-DERIVED FACTOR PEPTIDES AND USE FOR 
TREATING RETINAL DEGENERATION'' [HHS Reference No. E-028-2023-0-EP-01];
    6. Japanese Patent Application No. 2025-555099 effective filing 
date of June 4, 20125, entitled ``PIGMENT EPITHELIUM-DERIVED FACTOR 
PEPTIDES AND USE FOR TREATING RETINAL DEGENERATION'' [HHS Reference No. 
E-028-2023-0-JP-01];
    7. United States Patent No. 19/135,668, entitled ``PIGMENT 
EPITHELIUM-DERIVED FACTOR PEPTIDES AND USE FOR TREATING RETINAL 
DEGENERATION'' [HHS Reference No. E-028-2023-0-US-02].
    8. United States Provisional Patent Application No. 63/604,026 
filed November 29, 2023, entitled ``MODIFIED PIGMENT EPITHELIUM-DERIVED 
FACTOR PEPTIDES AND METHODS OF USE'' [HHS Reference No. E-028-2023-0-
US-01]; and
    9. PCT Patent Application No. PCT/US2024/057784 filed November 27, 
2024, entitled ``MODIFIED PIGMENT EPITHELIUM-DERIVED FACTOR PEPTIDES 
AND METHODS OF USE'' [HHS Reference No. E-028-2023-0-PCT-01];
    10. any and all other U.S. and ex-U.S. patents and patent 
applications claiming priority to any one of the foregoing, now or in 
the future.
    The patent rights in these inventions have been assigned to the 
Government of the United States of America.
    The prospective exclusive license territory may be worldwide and 
the field of use may be limited to the following:
    ``Peptide therapeutics for human ophthalmological diseases that may 
include but not be limited to retinitis pigmentosa, glaucoma, or age-
related macular degeneration.''
    This technology describes chemically synthesized peptide fragments 
derived from PEDF, a naturally occurring neurotrophic factor that is 
produced by retinal pigment epithelia. The biological roles of PEDF 
suggest that peptide fragments of PEDF have the potential to treat 
multiple diseases that fall within the Field of Use. Efforts to utilize 
native PEDF for therapeutic effect, as well as many invasive gene 
therapy approaches, have had minimal effect on outcomes for patients 
with ophthalmic diseases that result from neurodegeneration or retinal 
cell death. The subject invention potentially addresses the limited 
efficacy of approved therapeutic treatments for ophthalmic diseases 
that result from neurodegenerative pathologies and/or retinal cell 
death.
    This Notice is made in accordance with 35 U.S.C. 209 and 37 CFR 
part 404. The prospective exclusive license will be royalty bearing, 
and the prospective exclusive license may be granted unless within 
fifteen (15) days from the date of this published notice, the National 
Eye Institute, receives written evidence and argument that establishes 
that the grant of the license would not be consistent with the 
requirements of 35 U.S.C. 209 and 37 CFR part 404.
    Complete applications for a license that are timely filed in 
response to this notice will be treated as objections to the grant of 
the contemplated exclusive patent license. In response to this Notice, 
the public may file comments or objections. Comments and objections, 
other than those in the form of a license application, will not be 
treated confidentially, and may be made publicly available.
    License applications submitted in response to this Notice will be 
presumed to contain business confidential information and any release 
of information in these license applications will be made only as 
required and upon a request under the Freedom of Information Act, 5 
U.S.C. 552.

     Dated: March 30, 2026.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer 
Institute.
[FR Doc. 2026-06283 Filed 3-31-26; 8:45 am]
BILLING CODE 4140-01-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 1, 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.