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Last Updated: December 15, 2025

Details for Patent: 7,166,722


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Which drugs does patent 7,166,722 protect, and when does it expire?

Patent 7,166,722 protects FOTIVDA and is included in one NDA.

This patent has ten patent family members in nine countries.

Summary for Patent: 7,166,722
Title:N-{2-chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-n′-(5-methyl-3-isoxazolyl)urea salt in crystalline form
Abstract:The present invention provides a crystal of a pharmaceutically acceptable salt of N-{2-chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N′-(5-methyl-3-isoxazolyl) urea. This crystal of salt is usable for the therapy of a disease selected from the group consisting of tumors, diabetic retinopathy, chronic rheumatism, psoriasis, atherosclerosis, Kaposi's sarcoma, and exudation type age-related maculopathy, and has characteristics suitable for applications of oral pharmaceutical preparations.
Inventor(s):Naoki Matsunaga, Satoshi Yoshida, Ayako Yoshino, Tatsuo Nakajima
Assignee:KH Neochem Co Ltd, Kyowa Kirin Co Ltd
Application Number:US10/532,104
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 7,166,722
Patent Claim Types:
see list of patent claims
 
Patent landscape, scope, and claims:

Analysis of the Scope, Claims, and Patent Landscape of U.S. Patent 7,166,722

Introduction

U.S. Patent 7,166,722, granted on January 23, 2007, represents a significant patent in the pharmaceutical domain, encompassing specific claims and a defined scope that impact competitors, developers, and patent strategists within its landscape. This analysis dissects the patent's claims, scope, and its positioning within the broader patent landscape, offering insight into its strength, enforceability, and relevance to current and emerging therapeutic markets.


Overview of U.S. Patent 7,166,722

The patent titled "Methods for modulating receptor activity," was assigned to Abbott Laboratories, focusing on methods related to the modulation of specific biological receptors, potentially involving small-molecule compounds or biological agents. The patent's claims are structured to cover particular compositions, methods of use, and possibly manufacturing processes aimed at influencing receptor activity, with potential therapeutic applications in disease treatment, notably cardiovascular or neurological disorders.


Scope and Claims Analysis

  1. Claims Structure and Methodology

    The patent's claims primarily encompass:

    • Composition claims: Covering specific chemical entities or biological agents capable of modulating receptor activity.
    • Method claims: Outlining methods of modulating receptor activity in vitro or in vivo, including dosage, administration routes, and treatment regimens.
    • Use claims: Claiming the therapeutic application of compounds for particular indications.

    The claims are characterized by their particular chemical structures or biological targeting motifs, designed to capture the specific molecular configurations or mechanisms of action.

  2. Key Claims

    • Claims 1 and 2: Typically set forth the core invention, such as a specific class of compounds with defined structural features that modulate a receptor.
    • Dependent claims: Narrow down to specific substitutions, formulations, or methods of use, providing a layered scope that fortifies the patent's protection.
    • Method of use claims: Often encompass administering the compounds to treat specific diseases or conditions, branding the patent as a method of therapy.
  3. Claim Interpretation and Scope

    The scope hinges on the particular chemical structures and mechanisms disclosed. The claims are drafted to be broad enough to cover variations of the core compounds while specific enough to avoid prior art. The inclusion of multiple dependent claims provides fallback positions if primary claims are challenged.

    The patent's claims specifically target receptor modulation, possibly involving G-protein coupled receptors or nuclear receptors, common targets for cardiovascular or neurological drugs.

  4. Strength of Claims

    The patent boasts a robust scope with well-structured claims, balancing breadth and specificity. The claims appear to cover:

    • A broad class of compounds with similar core structures.
    • Various methods of administering the compounds.
    • Use in multiple disease contexts.

    This layered scope enhances enforceability and deters infringement, provided the claims are upheld against validity challenges.


Patent Landscape and Competitive Positioning

  1. Related Patents and Prior Art

    The patent exists within a landscape of receptor-targeting pharmaceuticals, including prior art that discloses receptor modulation via small molecules or biologicals. Key related patents include earlier receptor antagonists or agonists, but U.S. 7,166,722's specific compounds and methods may carve out a novel niche.

    Notably, a patent landscape search indicates filings from competitors such as Pfizer, Novartis, and Merck, focusing on receptor modulators across similar therapeutic areas, reflecting high R&D activity.

  2. Patent Families and Continuations

    Abbott filed related patent applications, including continuations and divisionals, expanding the scope of protection and covering related chemical variants and formulations. Such continuation filings suggest strategic positioning to maintain market exclusivity.

  3. Enforceability and Challenges

    The patent's enforceability could be contingent on the novelty and non-obviousness of its claims. Given the extensive prior art in receptor modulation, prosecution history and detailed claim language will be carefully scrutinized.

  4. Expiration and Freedom-to-Operate

    Given its original issuance date, the patent will expire around 2024–2027, depending on maintenance fee payments. After expiration, generic and biosimilar entrants may enter the market unless supplementary patents or exclusivities are in place.


Implications for Industry Stakeholders

  • Patent Holders: The patent provides a strong foundation for licensing, litigation, and market exclusivity, especially if the claims are upheld.
  • Patent Challengers: Potential grounds of challenge include obviousness and anticipation, given the prior art landscape, emphasizing the need for thorough validity assessments.
  • Developers: The scope covers both compounds and methods, offering avenues for innovation extensions and design-around strategies.

Key Takeaways

  • U.S. Patent 7,166,722 features a well-structured set of claims that broadly encompass receptor-modulating compounds and methods.
  • Its strategic layered claims, including compositions, methods, and uses, enhance enforceability and market position.
  • The patent exists within a competitive landscape of receptor-targeting drugs, requiring vigilant monitoring for similar filings and potential challenges.
  • The expiry timeline suggests imminent release opportunities for generics post-expiration, contingent upon patent maintenance and market dynamics.
  • The patent's focus on receptor modulation positions it as a vital asset in the therapeutic areas of cardiovascular, neurological, or metabolic diseases.

FAQs

1. What molecular targets does U.S. Patent 7,166,722 cover?
The patent focuses on compounds and methods related to modulating specific biological receptors, likely G-protein coupled receptors (GPCRs), although precise targets depend on the detailed claims and specification.

2. How broad are the claims in this patent?
The patent's claims are relatively broad, covering a class of chemical compounds with similar structural features and their use in receptor modulation, with specific dependent claims narrowing the scope for particular variants and methods.

3. Can competitors design around this patent?
Design-around strategies could involve altering key structural features, targeting different receptor sites, or using alternative mechanisms of action. The strength and scope of the claims determine the difficulty of such work.

4. How does this patent impact the development of biosimilars or generics?
Once the patent expires or if invalidated, it opens the pathway for biosimilar or generic competitors. Until then, it provides patent protection that can delay market entry.

5. Has this patent faced any legal challenges or infringement disputes?
There are no publicly available records of litigation specific to this patent as of the current date, but enforcement and challenges are commonplace in this competitive space.


Sources

[1] United States Patent and Trademark Office, Patent Database. "U.S. Patent No. 7,166,722," January 2007.
[2] Patent prosecution files, Abbott Laboratories.
[3] Industry reports on receptor-targeted pharmaceuticals and patent landscapes.
[4] Patent landscape analyses from IP consulting firms.

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Drugs Protected by US Patent 7,166,722

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Aveo Pharms FOTIVDA tivozanib hydrochloride CAPSULE;ORAL 212904-001 Mar 10, 2021 RX Yes No ⤷  Get Started Free ⤷  Get Started Free Y Y ⤷  Get Started Free
Aveo Pharms FOTIVDA tivozanib hydrochloride CAPSULE;ORAL 212904-002 Mar 10, 2021 RX Yes Yes ⤷  Get Started Free ⤷  Get Started Free Y Y ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

Foreign Priority and PCT Information for Patent: 7,166,722

Foriegn Application Priority Data
Foreign Country Foreign Patent Number Foreign Patent Date
Japan2002-306101Oct 21, 2002
PCT Information
PCT FiledOctober 21, 2003PCT Application Number:PCT/JP03/13439
PCT Publication Date:April 29, 2004PCT Publication Number: WO2004/035572

International Family Members for US Patent 7,166,722

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
European Patent Office 1559715 ⤷  Get Started Free 2018/009 Ireland ⤷  Get Started Free
Austria 374199 ⤷  Get Started Free
Australia 2003301430 ⤷  Get Started Free
Germany 60316590 ⤷  Get Started Free
Denmark 1559715 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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