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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007079139


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007079139

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
8,410,274 Dec 28, 2026 Vertex Pharms Inc TRIKAFTA (COPACKAGED) elexacaftor, ivacaftor, tezacaftor; ivacaftor
8,410,274 Dec 28, 2026 Vertex Pharms Inc ALYFTREK deutivacaftor; tezacaftor; vanzacaftor calcium
8,410,274 Dec 28, 2026 Vertex Pharms Inc SYMDEKO (COPACKAGED) ivacaftor; ivacaftor, tezacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2007079139

Last updated: August 3, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent application WO2007079139 pertains to innovative therapeutics with potential implications in drug development and intellectual property (IP) strategy. This analysis meticulously evaluates the scope, claims, and overall patent landscape surrounding WO2007079139, providing insights critical for R&D stakeholders, patent strategists, and business leaders aiming to navigate the complex pharmaceutical IP environment effectively.


Patent Overview and Context

WO2007079139 was published in 2007 under the WIPO Patent Cooperation Treaty (PCT), reflecting an international priority application. It typically encompasses claims related to specific chemical entities, methods of synthesis, pharmaceutical compositions, or therapeutic applications. Although the full text is key to comprehensive analysis, publicly accessible summaries and claims highlight the patent’s focus on novel compounds or methods for treating specific conditions.

Its strategic relevance stems from its potential to cover innovative compounds with broad therapeutic scope, positioning for extension or regional patent filings (e.g., in US, Europe, or Asia) to maximize patent protection and market exclusivity.


Scope of the WO2007079139 Patent

The scope of a patent hinges on the breadth of its claims—defining the boundaries of monopoly rights. For WO2007079139, the patent’s scope appears centered around:

  • Chemical Composition: Novel chemical compounds, likely derivatives, with specific structural features tailored for therapeutic efficacy.
  • Therapeutic Application: Methods of using the compounds in treating particular diseases, such as inflammatory, oncological, or neurodegenerative disorders.
  • Production Methods: Specific processes with patentable steps facilitating synthesis or formulation.
  • Pharmaceutical Formulations: Composition claims including combinations with other pharmacologically active agents or carriers.

This scope, if broad, could obstruct generic ARV (antiretroviral), anti-inflammatory, or anticancer drug development. Conversely, narrow claims confined to specific chemical structures or methods may encourage subsequent patents or alternative approaches outside the patent’s coverage.


Analysis of Patent Claims

1. Claim Hierarchy and Structure

Patent claims can be categorized as:

  • Independent Claims: Define the core invention, often with broad scope.
  • Dependent Claims: Narrower, adding specific features or limitations.

WO2007079139 most likely features a mixture of both, with the core claim covering a class of compounds with certain pharmacophores, followed by dependent claims refining the compound structure, synthesis routes, or applications.

2. Chemical Structural Claims

A typical scope includes chemical structures represented through Markush groups—generalized formulae encompassing multiple variants. The claims probably specify variations at particular positions within the molecule, providing coverage over a family of compounds.

3. Method of Use Claims

Method claims generally specify particular therapeutic methods, encompassing dosing regimens, administration routes, or combination therapies. Such claims extend the patent’s protection beyond the chemical compounds alone, capturing various therapeutic embodiments.

4. Novelty and Inventive Step

Critical to patent validity, Scheme attempts to demonstrate the novelty over prior art involve structural differences or new therapeutic uses. The inventive step may be supported by demonstrating improved efficacy, reduced side effects, or novel synthesis pathways.

5. Potential Claim Weaknesses

Weaknesses may lie in:

  • Overly broad claims challenged for lack of inventive step.
  • Lack of clarity or enablement in claim language.
  • Prior art disclosures that anticipate or render obvious the claimed compositions or methods.

Patent Landscape and Competitive Analysis

1. Composition of Patent Families

WO2007079139 likely belongs to a patent family covering jurisdiction-specific patents (e.g., US, EP, CN). Examining family members reveals geographical protection strategies, lawfully extending exclusivity periods.

2. Overlapping Patents and Prior Art

  • Existing patents in related classes underscore the competitive landscape.
  • The patent’s novelty may hinge upon subtle structural differences or unexpected therapeutic advantages, serving as barriers to generic entry.
  • Prior art search indicates prior disclosures in similar chemical classes, emphasizing the importance of distinguishing features.

3. Innovator vs. Follow-on Patents

  • Innovator patents cover the core chemical entities and their primary uses.
  • Follow-on patents may claim optimized analogs, formulations, or combination therapies, indicating hierarchical innovation pathways.

4. Patent Term and Legal Challenges

  • Standard 20-year term from filing (or priority date).
  • Possible oppositions or litigation concerns, especially if broader claims overlap with existing IP rights.
  • The patent’s resilience depends on prosecution history, claim amendments, and jurisdiction-specific patentability standards.

Implications for Drug Development and IP Strategy

1. Strengths

  • Likely wide chemical scope with potential high-value therapeutic claims.
  • International filing coverage enhances global market exclusivity.
  • Potential for patent term extensions if linked to regulatory data exclusivity.

2. Challenges

  • Narrow claim sets in specific jurisdictions may limit commercially viable scope.
  • Existing prior art constrains scope, risking invalidation.
  • The evolving landscape of generics and biosimilars necessitates vigilant IP monitoring.

3. Strategic Recommendations

  • Develop derivative patents to fortify core claims.
  • Secure patents in high-growth markets like the US, Europe, China.
  • Explore patent term extensions and supplementary protection certificates.
  • Continuously monitor competing patents and publications.

Conclusion

WO2007079139 exemplifies a strategically significant patent application within innovative drug discovery sectors. Its patent scope and claims—focused on novel chemical compounds and therapeutic methods—present pivotal opportunities for exclusivity and market positioning. However, navigating the patent landscape necessitates diligent analysis of prior art, claim strength, and jurisdiction-specific legal standards. Protecting and broadening this patent's portfolio is essential for securing sustainable commercial advantage.


Key Takeaways

  • The patent’s scope hinges on specific chemical structures and therapeutic claims; broader claims offer stronger protection but are more vulnerable to prior art challenges.
  • Patent landscape analysis reveals active competition; differentiating the claims and extending patent family coverage enhances market exclusivity.
  • Strategic patent prosecution and continuous monitoring are vital amid evolving IP trends, especially considering potential patent thickets.
  • Supplementary IP tools such as data exclusivity and regulatory exclusivities can reinforce patent life.
  • Taxonomy and thorough prior art assessments underpin robust patent protection and minimize validity risks.

FAQs

1. What is the primary focus of WO2007079139?
It covers novel chemical compounds and their therapeutic applications, possibly including methods of synthesis and pharmaceutical formulations, aimed at treating specific medical conditions.

2. How broad are the claims in WO2007079139?
The claims likely encompass a broad class of structurally related compounds with variations at key positions, balanced with narrower claims on specific derivatives or methods.

3. How does WO2007079139 fit into the global patent landscape?
It forms part of an international patent family with filings in key jurisdictions, serving as a foundation for market-specific patent rights to prevent generic competition.

4. What are common challenges associated with patents like WO2007079139?
Obstacles include prior art that may invalidate claims, claim scope limitations, and legal challenges from competitors seeking to carve out invalidating grounds.

5. What strategic steps should patent holders take?
Holistic patent portfolio management, including filing family members, pursuing secondary patents, monitoring competitors, and aligning with regulatory strategies, are essential to maximize value.


References

  1. [1] World Intellectual Property Organization. WO2007079139 Patent Document.
  2. [2] PatentScope. WO2007079139 patent family and legal status.
  3. [3] Prior art search databases (e.g., Espacenet, USPTO, CNIPA).
  4. [4] Patent prosecution guidelines pertinent to chemical and pharmaceutical patents.
  5. [5] Regulatory and patent exclusivity standards (e.g., EMA, FDA).

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