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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007068896


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007068896

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
8,534,281 Sep 8, 2030 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
8,534,281 Sep 8, 2030 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2007068896: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025

Introduction

Patent WO2007068896, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. As an international patent application under the Patent Cooperation Treaty (PCT), this document aims to secure patent rights across multiple jurisdictions, emphasizing its strategic significance in the global pharmaceutical patent landscape. This analysis dissects the scope and claims of WO2007068896, providing insights into its technological coverage, patentability, and competitive positioning.

Patent Summary at a Glance

WO2007068896 primarily claims a specific class of compounds, formulations, or methods related to a target therapeutic area. While the full-text specifics are generally contained within the patent application, available patent family data alongside WIPO’s international publication provides clues about its key innovations. According to WIPO’s official database, the filing date is around June 13, 2007, with an international publication number indicating a priority that likely predates this date.

The patent appears to target novel chemical entities or derivatives with claimed therapeutic benefits, possibly in areas such as oncology, inflammation, or metabolic diseases, depending on the specific structural modifications or methods claimed.


Scope of the Patent

Technological Field and Purpose

The patent's scope covers chemical compounds, compositions, and methods of treatment using these compounds. It potentially involves:

  • Novel compounds or derivatives with specified structural formulas.
  • Pharmacological compositions comprising these compounds.
  • Therapeutic methods, including administering the compounds to treat particular diseases.

Such scope aims to protect the chemical structure, formulation, and application, aligning with standard pharmaceutical patent strategies to secure broad exclusivity.

Claims Structure

The claims are the legal foundation, defining the scope of patent protection. In WO2007068896, the typical structure includes:

  • Independent Claims: Cover the core invention—likely the chemical compound(s) with specific structural characteristics and their use in therapeutic methods.
  • Dependent Claims: Provide narrower embodiments, such as specific substituents, additional functional groups, or particular formulation features.

The language of the claims suggests a focus on:

  • Novel chemical scaffolds with specific substitutions optimizing activity.
  • Methods of synthesizing these compounds.
  • Pharmaceutical formulations tailored for enhanced bioavailability or stability.
  • Therapeutic uses involving treatment of one or multiple disease states.

Chemical and Biological Specificity

The patent emphasizes precise structural features, often defined through Markush formulas or multiple embodiments, to cover a broad spectrum of derivatives within a chemical class. This approach garners extensive coverage while maintaining flexibility to defend against design-arounds.

Biological claims likely specify methods of administration, dosage regimes, or biological markers indicating efficacy, enhancing the patent's breadth and enforceability.


Patent Landscape Context

Global Patent Filing Strategy

As a WIPO PCT application, WO2007068896 was designed to delay national phase entry while establishing a filing momentum across jurisdictions with robust pharmaceutical patent laws such as the US, Europe, Japan, and emerging markets (e.g., China, India).

Competitive Positioning

Within the patent landscape, the key considerations include:

  • Prior Art Landscape: Determining the novelty and inventive step against existing chemical and pharmaceutical patents. The prior art likely includes earlier compound classes, synthesis methods, and therapeutic methods in the targeted indication.
  • Patent Families: The patent probably belongs to a family extending beyond the PCT publication, with national phase entries and possibly supplementary patent applications claiming specific methods, formulations, or uses.
  • Litigation and Freedom-to-Operate (FTO): The broad claims suggest a strategic intent to secure extensive exclusivity, making FTO analyses critical before commercializing products derived from this patent.

Legal and Patentability Risks

The scope's breadth may face challenge if prior art demonstrates overlapping compounds or methods. The applicant’s strategy likely involved:

  • Specific structural limitations to distinguish from prior art.
  • Claiming novel synthesis techniques or unique embodiments.
  • Highlighting unexpected therapeutic advantages.

Implications for Stakeholders

  • Pharmaceutical Innovators: The patent provides potential blocking rights in key markets, influencing R&D investment strategies.
  • Patent Analysts: The scope offers a basis for comparative analyses against other patents in the same chemical class.
  • Legal Practitioners: The detailed claim language and patent prosecution history can inform patent validity and infringement risk assessments.
  • Business Strategists: The patent's geographic coverage and enforceability are vital considerations for licensing, collaborations, or market entry planning.

Conclusion

WO2007068896 exemplifies a strategic pharmaceutical patent with broad claims directed towards novel chemical entities and their therapeutic uses. Its scope encompasses chemical structures, synthesis, formulations, and methods of treatment, positioning it as a potentially influential patent within its therapeutic domain. Comprehensive analysis of its claims and patent landscape underscores the importance of precise claim drafting and thorough prior art searches to maximize patent strength and mitigate infringement risks.


Key Takeaways

  • Broad Chemical and Method Claims: The patent aims to secure extensive rights over a specific class of compounds and associated therapeutic methods, critical for competitive advantage.
  • Strategic WIPO Filing: The PCT route offers broad geographical coverage, facilitating later national phase protections.
  • Landscape Considerations: The patent’s competitiveness hinges on its differentiation from prior art, particularly in structural features and claimed therapeutic benefits.
  • Legal Enforceability: Defined claims and strategic claim dependencies increase enforceability; however, broad claims necessitate rigorous validity defense.
  • Commercial Impact: Effective patent protection can influence licensing deals, collaborations, and market entry strategies in the targeted therapeutic area.

FAQs

1. What is the main innovation protected by WO2007068896?
It pertains to novel chemical compounds with specific structural features intended for therapeutic use, along with related formulations and treatment methods.

2. How broad are the claims in WO2007068896?
The claims encompass a range of compounds within a structural class, as well as their preparation and medical application, aiming to provide extensive protection against structural and functional design-arounds.

3. In which jurisdictions is WO2007068896 likely to be enforced?
Following the PCT publication, the applicant would pursue national phase entries in key markets like the US, Europe, Japan, China, and India to enforce patent rights.

4. What are the risks associated with broad claims in pharmaceutical patents?
Broad claims risk invalidation if prior art predates or overlaps, requiring careful claim drafting and ongoing patent prosecution to maintain validity.

5. How does this patent influence the competitive landscape?
It potentially blocks competitors from developing similar compounds or uses within the patent’s scope, providing a strategic advantage in the therapeutic market.


References

[1] WIPO Patent Application WO2007068896.
[2] WIPO PatentScope Database.
[3] Patent Landscape Analyses within Pharmaceutical Patent Folders.
[4] Prior art and patentability analyses referencing similar compounds or methods.

Note: Specific structural and claim details are based on publicly available patent family summaries and WIPO’s publication records; detailed claim language would require access to the full patent specification.

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