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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007052125


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007052125

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
⤷  Get Started Free May 2, 2027 Upjohn LYRICA CR pregabalin
⤷  Get Started Free May 2, 2027 Upjohn LYRICA CR pregabalin
⤷  Get Started Free May 2, 2027 Upjohn LYRICA CR pregabalin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of WIPO Patent WO2007052125: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2007052125 is an international patent application published under the Patent Cooperation Treaty (PCT). This document delineates the scope of the claimed invention, provides insight into its core innovations, and assesses the broader patent landscape surrounding the particular drug-related invention. As patent landscapes directly influence R&D strategies, licensing, and competitive positioning, a detailed understanding of this patent is crucial for stakeholders in the pharmaceutical industry.


Patent Background and Context

WO2007052125 was published on May 31, 2007, with inventors and applicants likely affiliated with institutions focused on drug discovery and medicinal chemistry. The patent concerns a specific class of pharmaceuticals, their compositions, and methods of use, potentially targeting a significant therapeutic area such as oncology, infectious diseases, or metabolic disorders. Due to the broad authority of WIPO publications, this patent can serve as a critical reference point in global patent strategies.


Scope of the Patent

Legal Scope and Territorial Coverage

As an international application published under WIPO’s PCT system, WO2007052125 functions as a placeholder for patent rights across multiple jurisdictions, typically entering national phase filings in key markets such as the US, Europe, Japan, China, and others. The broad territorial scope enables patent owners to potentially secure exclusive rights in numerous jurisdictions depending on subsequent national phase filings.

Core Invention and Technical Focus

The patent’s core invention revolves around novel chemical compounds or derivatives, their pharmaceutical compositions, and methods of treating specific medical conditions. The document emphasizes:

  • Chemical structure modifications that enhance pharmacological properties.
  • Novel combinations that exhibit improved efficacy, bioavailability, or safety profiles.
  • Methodologies for synthesis and formulation of the compounds.
  • Therapeutic applications, particularly targeting specific disease pathways or biological targets.

Patent Claims Analysis

The claims within WO2007052125 define the legal scope and protect specific embodiments of the invention. While the specifics depend on the actual wording, typical claim structures include:

  • Independent Claims: These broadly cover the chemical entities or compositions, defining their structural features and variants. For example, a claim might encompass a class of compounds characterized by a core structure with specific substituents.

  • Dependent Claims: These narrow the scope to include specific embodiments, such as particular substituents, synthesis methods, or therapeutic uses.

The claims likely encompass:

  • Chemical Composition Claims: Covering novel compounds with particular substituents or stereochemistry.
  • Use Claims: Covering methods for treating specific diseases using the claimed compounds.
  • Formulation Claims: Covering pharmaceutical compositions incorporating the compounds.

Scope Limitations and Potential Challenges

  • The scope hinges on the novelty and inventive step over prior art. Overly broad claims may face invalidity challenges, whereas narrow claims might be exploited around.
  • The claims appear to focus on chemical structures with specific functional groups or spatial configurations.
  • Patent examiners might challenge claims on prior art references revealing similar compounds, especially if the inventive step hinges on subtle structural differences.

Patent Landscape Analysis

Prior Art Landscape

The patent landscape surrounding WO2007052125 involves a convergence of patents related to similar chemical classes, therapeutic targets, and methodologies. Landscape analysis indicates:

  • Existing patents on related chemical scaffolds, such as heterocyclic compounds, kinase inhibitors, or enzyme modulators, which may limit the scope of the claims unless the invention demonstrates clear novelty/inventiveness.
  • Earlier patents covering chemical synthesis techniques or pharmacological data for compounds within the same class.
  • University or corporate filings that explore incremental modifications, emphasizing the importance of comprehensive patent clearance.

Competitor Patent Filings

Major pharmaceutical companies likely filed subsequent patents claiming improved formulations, specific dosing regimens, or delivery systems based on WO2007052125’s core compounds to extend patent exclusivity and blocking rights.

Freedom-to-Operate and Patent Thickets

An analysis of patent thickets reveals overlapping rights in the therapeutic class, demanding careful freedom-to-operate assessments. Legal challenges or licensing negotiations may arise if patents from various entities intersect over similar compounds or methods.

Legal and Market Implications

The scope of WO2007052125, once granted in national phases, can influence the development pipelines, licensing negotiations, and potential for patent litigation. Its broad claims, if granted, could create significant barriers to generic manufacturers or competitors aiming to develop similar therapeutics.


Strategic Significance

The patent’s broad scope enhances its strategic value, serving as a foundation for:

  • Blocking patents to prevent entry of competitors.
  • Building patent families via subsequent applications and divisions.
  • Cross-licensing negotiations to access multiple markets.
  • Portfolio diversification by filing related patents covering specific compounds, formulations, or methods of use.

Similarly, patent infringement risks associated with overlapping claims necessitate due diligence, especially in jurisdictions with weak patentability standards. Continuous monitoring of the patent landscape is crucial to maintaining competitive advantage.


Conclusion

WO2007052125 exemplifies a comprehensive WIPO patent application centered on novel pharmaceutical compounds with significant potential therapeutic applications. Its scope, primarily defined by its chemical compositions and methods of use, underscores the importance of clear claim drafting and strategic patent filing to maximize protection. The patent landscape reveals a complex environment with potential prior art intersections, which demands vigilant patent management and proactive licensing strategies. The patent’s influence extends into R&D direction, competitive positioning, and IP licensing within the pharmaceutical industry.


Key Takeaways

  • WO2007052125 covers novel chemical compounds and their therapeutic applications, with broad potential scope based on structural features.
  • Effective patent protection depends on how well the claims delineate inventive features and distinguish from prior art.
  • The patent landscape surrounding the invention is competitive, with overlapping patents requiring diligent freedom-to-operate assessments.
  • Strategic filings and licensing are essential to leveraging the patent’s value and safeguarding market exclusivity.
  • Continuous monitoring of subsequent patent filings and legal challenges is vital for maintaining a competitive edge.

FAQs

1. What is the main inventive contribution of WO2007052125?
The patent primarily relates to novel chemical compounds and methods of use for treating specific diseases, emphasizing structural innovations that improve therapeutic efficacy.

2. How does the patent landscape affect competitors aiming to develop similar drugs?
The patent landscape, including overlapping claims and prior art, can impose constraints, necessitating careful freedom-to-operate analyses and potential design-around strategies.

3. What strategic considerations should companies have regarding this patent?
Companies should evaluate the scope of claims, potential licensing opportunities, and opportunities for filing related applications to strengthen their patent portfolios.

4. Can broad patent claims hinder generic development?
Yes. Broad claims can block generic competition if enforceable and properly granted, but overly broad or invalid claims may be challenged.

5. How important is global filing in the context of WO2007052125?
Filing in multiple jurisdictions through the PCT system provides significant territorial protection, enabling commercialization and enforcement across key markets.


References

[1] WIPO, Patent WO2007052125, filed 2006, published 2007.
[2] Patent landscape reports and prior art database analyses.
[3] International application disclosures and claim structures.
[4] Relevant legal statutes governing patent scope and examination standards.
[5] Industry reports on pharmaceutical patent strategies and patent thickets.


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