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HIV/HBV Treatment Using CD8-Targeting Fusion Proteins

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Summary

USPTO published patent application US20260098090A1 on April 9, 2026, disclosing fusion proteins for treating chronic viral infections including HIV and HBV. The application describes methods using CD8-targeting fusion proteins comprising antibodies specific to CD8b or CD8ab antigens combined with cytokines, chemokines, or growth factors. Inventors are Kelly Dare Moynihan, Yik Andy Yeung, and Ivana Djuretic, with filing date September 28, 2023.

What changed

USPTO published application US20260098090A1 on April 9, 2026, covering fusion proteins and methods for treating chronic viral infections such as HIV and HBV. The application claims fusion proteins combining CD8-targeting antibody moieties with cytokines, chemokines, or growth factors. The application was filed September 28, 2023, and is pending examination.

This publication establishes a priority date and discloses claimed subject matter that may eventually become granted patent rights. Pharmaceutical manufacturers, biotech companies, and researchers developing immunotherapies or antivirals for HIV or HBV should monitor this application's prosecution. Patent applications do not currently restrict others from developing similar products, but if granted, the patent could impose exclusivity on the claimed fusion protein compositions and treatment methods.

What to do next

  1. Monitor for updates on patent examination status

Archived snapshot

Apr 12, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

FUSIONS WITH CD8 ANTIGEN BINDING MOLECULES FOR TREATING CHRONIC VIRAL INFECTION

Application US20260098090A1 Kind: A1 Apr 09, 2026

Inventors

Kelly Dare MOYNIHAN, Yik Andy YEUNG, Ivana DJURETIC

Abstract

Provided herein are methods of treating chronic viral infection (e.g., hepatitis B virus (HBV) and/or human immunodeficiency virus (HIV) infection) comprising administering to an individual in need thereof an effective amount of a fusion protein that comprises: (a) a first moiety comprising an antibody or antigen-binding fragment thereof that specifically binds human CD8b and/or human CD8ab with at least 10-fold higher affinity than its binding to human CD8a and/or human CD8aa; and (b) a second moiety comprising a cytokine, chemokine, or growth factor.

CPC Classifications

C07K 16/2815 A61K 45/06 A61P 31/20 C07K 14/55 C07K 2317/24 C07K 2317/31 C07K 2317/522 C07K 2317/524 C07K 2317/526 C07K 2317/53 C07K 2317/565 C07K 2317/569 C07K 2317/622 C07K 2317/92 C07K 2319/30

Filing Date

2023-09-28

Application No.

19114281

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Last updated

Classification

Agency
USPTO
Published
April 9th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260098090A1

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers Clinical investigators
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent applications Biotechnology research Drug development
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare Public Health

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