Notice2026-11926

Government Owned Inventions Available for License: Fluorophthalimides as Anti-Inflammatory Agents for Systemic and Neurodegenerative Disorders

Primary source

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Published
June 15, 2026

Issuing agencies

Health and Human Services DepartmentNational Institutes of Health

Abstract

The National Institute on Aging (NIA) seeks research co- development partners and/or licensees for the pre-clinical and clinical development of the compounds as anti-inflammatory therapeutics for systemic and neurodegenerative disorders.

Full Text

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<title>Federal Register, Volume 91 Issue 114 (Monday, June 15, 2026)</title>
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[Federal Register Volume 91, Number 114 (Monday, June 15, 2026)]
[Notices]
[Pages 35991-35992]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-11926]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Government Owned Inventions Available for License: 
Fluorophthalimides as Anti-Inflammatory Agents for Systemic and 
Neurodegenerative Disorders

AGENCY: National Institutes of Health, HHS.

ACTION: Notice.

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SUMMARY: The National Institute on Aging (NIA) seeks research co-
development partners and/or licensees for the pre-clinical and clinical 
development of the compounds as anti-inflammatory therapeutics for 
systemic and neurodegenerative disorders.

FOR FURTHER INFORMATION CONTACT: Inquiries related to this license 
opportunity should be directed to: Nikki Guyton, Ph.D., Unit 
Supervisor, NCI, Technology Transfer Center, Email:

[[Page 35992]]

<a href="/cdn-cgi/l/email-protection#50372529243f3e3e103e39387e373f26"><span class="__cf_email__" data-cfemail="7a1d0f030e1514143a141312541d150c">[email&#160;protected]</span></a> or Phone: 240-276-5493.

SUPPLEMENTARY INFORMATION: Numerous systemic, as well as neurological 
disorders, have a hallmark inflammatory element that can drive disease 
progression. However, the use of currently available anti-inflammatory 
agents have failed to demonstrate efficacy as potential treatment for 
systemic and neurological disorders in clinical trials.
    The immunomodulatory imide drug (IMiD) thalidomide exerts anti-
inflammatory effects through inhibition of tumor necrosis factor-alpha 
(TNF-[alpha]), which is a master regulator of the inflammatory 
response. Researchers at the National Institute on Aging (NIA) have 
synthesized novel thalidomide analogs possessing potent anti-
inflammatory actions but, importantly, hinder the cerebon binding that 
associated with the adverse teratogenic actions of classic IMiDs. This 
invention has potential to be developed as therapeutics for a variety 
of systemic and neurological disorders including inflammatory 
disorders, autoim.
    ``This Notice is in accordance with 37 CFR 404.4 Authority to grant 
licenses.''

    NIH Reference Number: E-151-2022.
    Related Technologies: E-045-2012-0; E-208-2015-0.
    Product Type: Therapeutic.
    Therapeutic Area(s): Oncology [verbar] Neurology.
    Development Stage: Pre-clinical (in vivo validation).
    Patent Information: US Nonprovisional Patent Application, US 19/
102,830, filed on February 2, 2025. Status: Pending.
    Publication: Lecca D, et al. Novel, thalidomide-like, non-cereblon 
binding drug etrafluorobornylphthalimide mitigates inflammation and 
brain injury. (PMID 36872339).
    Potential Commercial Applications:
    <bullet> Neurodegenerative diseases.
    <bullet> Inflammatory disorders.
    <bullet> Autoimmune disorders.
    <bullet> Viral infections.
    <bullet> Cancer.
    Competitive Advantages:
    <bullet> More potent anti-inflammatory properties.
    <bullet> Potentially clinically safer than classic IMiDs by lower 
risk of fetal malformations.
    <bullet> Potential to treat a wide range of significant unmet 
medical needs.

    Dated: June 10, 2026.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer 
Institute.
[FR Doc. 2026-11926 Filed 6-12-26; 8:45 am]
BILLING CODE 4167-05-P


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Indexed from Federal Register on June 15, 2026.

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