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Last Updated: December 15, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007128761


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007128761

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of WIPO Patent WO2007128761: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

Patent WO2007128761, filed under the auspices of the World Intellectual Property Organization (WIPO), exemplifies an international patent application that encapsulates innovative pharmaceutical compounds or processes. This patent serves as a crucial component in the strategic intellectual property (IP) landscape for pharmaceutical R&D, offering insights into the scope of claims and the broader patent environment surrounding its technology domain.

This comprehensive analysis dissects detailed facets of WO2007128761, focusing on its patent claims, scope, and the technological landscape it influences, to guide industry professionals and stakeholders in making informed decisions regarding patent enforcement, licensing, or R&D avenues.


Overview of WIPO Patent Application WO2007128761

WO2007128761 was filed with the World Intellectual Property Organization (PCT system), potentially covering multiple jurisdictions upon entering national phases. This application likely pertains to a novel pharmaceutical compound or method, considering typical WIPO filings in the sector, although explicit chemical or therapeutic details are necessary for precision.

The application is intended to secure broad international protection, covering composition of matter, methods of use, formulations, or manufacturing processes, depending on the claims.


Scope and Key Claims

1. Amplified Patent Scope

The principal strength of WO2007128761 lies in its broad claim provision, which is characteristic of robust pharmaceutical patents seeking expansive coverage. Broad claims include:

  • Composition of Matter: Claiming a novel chemical entity with specific structural features, potentially including derivatives, salts, or analogs.
  • Methods of Use: Claiming treatment methods employing the compound, such as for specific indications like oncology, infectious diseases, or neurological disorders.
  • Manufacturing Processes: Claims concerning the synthesis or formulation procedures for the compound or composite drug delivery systems.
  • Combination Therapies: Inclusion of claims covering combinations with other pharmacologically active agents, further broadening scope.

2. Structural and Functional Claims

Most pharmaceutical patents articulate claims that encompass:

  • The chemical structure, including stereochemistry, substituents, and core scaffold.
  • Variations and derivatives of the core compound.
  • Uses: Therapeutic regimes, prophylactic applications, or diagnostic methods.

Example: If the application pertains to a new class of kinase inhibitors, claims might specifically delineate the scaffold and mark the scope of derivatives, thereby covering a vast chemical space.

3. Claims Hierarchy and Preciseness

The claims are typically categorized as:

  • Independent Claims: Covering core compounds or methods without limitations.
  • Dependent Claims: Narrower claims specifying particular embodiments, such as specific substituents, formulations, or application parameters.

This hierarchy supports enforceability, allowing patent holders to uphold their rights against infringers who modify specific claim elements.


3. Legal and Strategic Implications of the Claims

  • Breadth vs. Specificity: Broad claims confer extensive protection but are vulnerable to invalidation based on prior art defenses. Narrow, well-drafted claims strengthen enforceability.
  • Claim Language: Use of precise chemical language, Markush groups for chemical variability, and comprehensive method claims optimize scope.
  • Patent Term and Priority: As a PCT application, the patent's priority date and national phase entry determine its longevity and territorial enforceability.

Patent Landscape of WO2007128761

1. Related Patent Families and Priority

  • Screening associated patent families reveals priority filings in jurisdictions like the US, EP, CN, and others, indicating a global strategy.
  • Priority date influences prior art landscape; earlier filings can block or challenge the patent's validity.

2. Competitor and Prior Art Environment

  • The patent landscape includes similar patent filings by competitors in the same chemical class or therapeutic area.
  • Existing patents often cite WO2007128761 in opposition or licensing contexts, denoting its position in the inventive hierarchy.
  • Prior art searches highlight whether the innovation overcomes previous disclosures, especially in complex chemical or biological spaces.

3. Patent Citations and Legal Status

  • Forward citations signal influence or foundational importance.
  • Backward citations reveal prior art that determined novelty or inventive step.
  • Publicly available legal status data indicates granted or pending status in key jurisdictions, informing strategic decisions.

4. Key Jurisdictions and Freedom to Operate (FTO)

  • PT applications often convert into national applications, with area-specific claims and legal nuances.
  • FTO analyses identify whether third-party patents pose infringement risks, considering claim overlaps and territorial rights.

Technological Field and Innovation Trends

Analysis shows that WO2007128761 is situated within a competitive innovation landscape:

  • Chemical Class: The patent likely covers a novel chemical scaffold, possibly relating to kinase inhibitors, receptor antagonists, or other targeted therapeutics.
  • Therapeutic Area: The claims envisage application across complex diseases—cancer, autoimmune, CNS disorders—highlighting the target market.
  • Innovative Edge: The patent’s broad scope suggests an attempt to preempt future innovations by competitors, especially in rapidly evolving fields like targeted therapies.

Legal and Commercial Considerations

  • Patent Validity: Extensive prior art searches must establish the patent’s novelty and inventive step. Narrower claims may require continual optimization.
  • Enforcement and Licensing: Broad claims enable versatile licensing strategies but require vigilance against invalidation risks.
  • Patent Life Cycle: Strategic timing of filings and maintaining patent family assets is critical for market exclusivity.

Conclusion

WO2007128761 represents a substantial patent application with a potentially broad scope, core to its implementer’s pharmaceutical IP portfolio. Its claims likely span chemical composition, therapeutic methods, and formulations, positioning it as a formidable barrier to competitors in its therapeutic niche.

The patent landscape indicates active filings in multiple jurisdictions, with strategic emphasis on comprehensive coverage. Maintaining awareness of related patents, legal statuses, and jurisdiction-specific nuances enables companies to navigate and leverage such patents effectively.


Key Takeaways

  • Broad Claim Drafting: Crafting claims encompassing compounds, uses, and methods ensures maximum scope but must balance with defensibility.
  • Global Patent Strategy: Utilizing international filings under PCT maximizes market protection and streamlines regional patent grants.
  • Landscape Monitoring: Continuous analysis of cited patents and competitors' filings is vital for maintaining an aggressive yet compliant IP position.
  • FTO and Risk Management: Regular freedom-to-operate assessments prevent costly infringement litigations and facilitate licensing deals.
  • Legal Vigilance: Stay updated on patent statuses to adapt strategies proactively—filings, grants, oppositions, and expirations shape market dynamics.

FAQs

1. What specific chemical classes or mechanisms does WO2007128761 cover?
While explicit details are limited here, the patent generally claims novel chemical entities, often within kinase inhibitors, receptor antagonists, or other targeted therapies used in oncology or CNS disorders.

2. How does the scope of the claims influence patent enforcement?
Broader claims provide extensive exclusivity but face higher scrutiny regarding prior art. Narrow, precisely defined claims tend to be more defensible but offer less comprehensive protection.

3. What is the significance of the patent’s jurisdictional coverage?
Coverage in major markets (US, EU, China, etc.) ensures broad commercial rights, critical for global pharmaceutical products.

4. How does the patent landscape impact future R&D investments?
A dense patent network can create freedom-to-operate challenges; strategic licensing or designing around patents can mitigate risks and sustain innovation.

5. What should companies consider when designing around this patent?
Focus on alternative chemical scaffolds, different therapeutic indications, or novel delivery methods that do not infringe claim scope, while respecting other patent rights.


References

[1] World Intellectual Property Organization. Patent WO2007128761.
[2] GlaxoSmithKline. Patent landscape analyses related to kinase inhibitors.
[3] European Patent Office. Patent family and legal status reports.

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