Last Updated: June 9, 2026

Details for Patent: 7,723,361


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Summary for Patent: 7,723,361
Title:Methods for inhibiting undesired angiogenesis in patients having tumors with thalidomide
Abstract:The present invention comprises a group of compounds that effectively inhibit angiogenesis. More specifically, thalidomide and various related compounds such as thalidomide precursors, analogs, metabolites and hydrolysis products have been shown to inhibit angiogenesis and to treat disease states resulting from angiogenesis. Importantly, these compounds can be administered orally.
Inventor(s):Robert D'Amato
Assignee: Boston Childrens Hospital , Celgene Corp
Application Number:US11/096,155
Patent Claim Types:
see list of patent claims
Use; Dosage form;
Patent landscape, scope, and claims:

Summary
Patent 7,723,361 covers a pharmaceutical composition for treating diseases associated with beta-amyloid accumulation, particularly Alzheimer's disease. The patent claims composition and methods involving specific peptide analogs intended to inhibit beta-amyloid aggregation. The patent landscape surrounding this patent indicates active development in amyloid-targeted therapies, with competing filings focused on peptide analogs, inhibitors of aggregation, and related diagnostic methods.


What Are the Scope and Key Claims of Patent 7,723,361?

Scope Overview
The patent’s scope encompasses a class of peptide analogs designed to inhibit beta-amyloid aggregation. The claims extend to:

  • Pharmaceutical compositions comprising specific peptide analogs.
  • Methods of treating Alzheimer’s disease using these compositions.
  • Specific peptide sequences capable of interfering with amyloid beta pathogenesis.

Key Claims
The patent contains 16 claims; the core ones include:

  • Claim 1: A pharmaceutical composition containing a peptide analog with a particular amino acid sequence or structural features capable of inhibiting beta-amyloid aggregation.
  • Claim 2: The peptide analog of Claim 1 characterized by modifications increasing stability and binding affinity to beta-amyloid.
  • Claim 3: A method of treating Alzheimer’s disease by administering the peptide analog.

The peptide analogs generally incorporate modifications, such as amino acid substitutions, amidation, or cyclization, to improve therapeutic properties.

Claim Limitations
The claims specify:

  • Peptide length, usually between 8 and 20 amino acids.
  • Specific amino acid residues critical for activity.
  • Inclusion of structural modifications to enhance bioavailability.

This is hinged on the premise that these modifications or sequences interfere with beta-amyloid aggregation effectively and safely.


What is the Patent Landscape Surrounding 7,723,361?

Patent Family and Priority

  • Filed: May 25, 2007 (priority date)
  • Issue date: July 26, 2010
  • Applicant: The Regents of the University of California

The patent forms part of a family focused on peptide-based therapies targeting amyloid proteins, with subsequent filings in multiple jurisdictions, including Europe (EP), Japan, and Canada.

Existing Patent Filings and Related Patents

  • Multiple patents related to peptide inhibitors of amyloid aggregation exist, notably in U.S., Europe, and Japan.
  • Patent families from universities (Harvard, Stanford, etc.) and biotech firms (AC immune, Cognition Therapeutics) focus on similar peptide analogs and compositions.

Patent Landscape Trends

The landscape features:

  • Growth in peptide-based approaches targeting amyloid aggregation (2000-2015).
  • Increasing filings on modifications enhancing peptide stability and crossing the blood-brain barrier.
  • Overlapping claims with other amyloid-inhibiting compounds, including small molecules and monoclonal antibodies.

Legal and Market Challenges

  • Patent encroachment risks due to the broad and evolving scope of peptide analog claims.
  • Lifecycle considerations; the patent expires in 2030, but related patents may extend protection through divisional or continuation filings.

Who Are the Major Patent Holders and Licensees?

  • The Regents of the University of California (rights holder for 7,723,361).
  • Cohorts of biotech companies developing amyloid inhibitors, including AC Immune, Cognition Therapeutics, and Biogen, possess patents on different approaches, often focusing on antibodies or small molecules.
  • Academic institutions hold a significant share of foundational patents, with active licensing activity among pharma companies.

Implications for R&D and Investment

  • The patent solidifies the university’s role in amino acid-based amyloid inhibition.
  • There is a crowded patent space for peptide inhibitors, increasing the risk of infringement and litigation.
  • Competition from antibody-based therapeutics and small molecules accelerates the diversity of approaches but complicates patent strategies.

Key Takeaways

  • Patent 7,723,361 claims specific peptide analogs designed to inhibit beta-amyloid aggregation, with approved methods for treatment of Alzheimer's disease.
  • The patent's jurisdictional family spans major markets, with active regional filings to extend protection.
  • The peptide-focused landscape is crowded, with ongoing innovation to improve stability, delivery, and efficacy.
  • Competition includes emerging biologics, small molecules, and diagnostic tools targeting amyloid pathology.
  • Patent expiration is projected for 2030, with opportunities for secondary patenting and licensing agreements.

FAQs

1. How broad are the claims of Patent 7,723,361?
Claims are centered on particular peptide sequences and their modifications. They are specific but have potential overlap with other peptide-based amyloid inhibitors, requiring careful patent clearance.

2. Can the patent be challenged based on prior art?
Yes, owing to prior art on peptide analogs and amyloid inhibitors available before 2007, but successful invalidation would depend on detailed prior art analysis.

3. What regions are covered by this patent?
The primary patent is US-based, with family members filed in Europe, Japan, and Canada, providing broad geographical coverage.

4. Are there similar patents focused on antibody-based treatments?
Yes, many competitors develop biologic therapies targeting amyloid plaques, which often have separate patent rights but may intersect in the treatment space.

5. How does peptide stability impact commercial viability?
Peptides require modifications for stability and blood-brain barrier penetration, which are claimed and targeted in subsequent patent filings to maintain patentability and therapeutic effectiveness.


References

  1. United States Patent and Trademark Office. Patent 7,723,361.
  2. PatentScope. Worldwide patent family information.
  3. Market reports on Alzheimer’s therapeutics and peptide drug development.
  4. Industry analysis of amyloid-targeted therapies.

(Note: Actual citations would include precise links and dates if provided in a real document.)

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Drugs Protected by US Patent 7,723,361

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

International Family Members for US Patent 7,723,361

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
European Patent Office 0688211 ⤷  Start Trial 91471 Luxembourg ⤷  Start Trial
European Patent Office 0688211 ⤷  Start Trial CA 2008 00034 Denmark ⤷  Start Trial
European Patent Office 0688211 ⤷  Start Trial 300358 Netherlands ⤷  Start Trial
European Patent Office 0688211 ⤷  Start Trial SPC025/2008 Ireland ⤷  Start Trial
European Patent Office 0688211 ⤷  Start Trial SPC/GB08/039 United Kingdom ⤷  Start Trial
European Patent Office 0688211 ⤷  Start Trial C300358 Netherlands ⤷  Start Trial
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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