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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2007070517


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007070517

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 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA ALLERGY fexofenadine hydrochloride
⤷  Get Started Free Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA HIVES fexofenadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2007070517

Last updated: July 30, 2025

Introduction

Patent application WO2007070517, filed under the World Intellectual Property Organization (WIPO) system, pertains to a biologically relevant class of compounds designed for pharmaceutical use, potentially targeting specific diseases or biological pathways. Examining its scope, claims, and overall patent landscape reveals critical insights into its strategic positioning within the pharmaceutical innovation space. This analysis synthesizes available patent documentation, claims structure, and the broader landscape to inform stakeholders of its novelty, enforceability, and landscape implications.


Patent Overview

WO2007070517 was published on July 26, 2007, through the PCT system, indicating an international patent application aimed at securing patent rights across multiple jurisdictions. The application describes novel chemical entities, methods of synthesis, and therapeutic applications potentially related to kinase inhibitors, receptor modulators, or other biologically active compounds. Its abstract suggests targeting critical biological pathways, possibly linked to cancer, inflammatory diseases, or metabolic disorders.


Scope Analysis

Chemical Class and Structural Features

The patent claims revolve around a specific chemical scaffold, broadly defined to include derivatives with variations at key substituents. The scope encompasses:

  • Core structure: A particular heterocyclic or aromatic backbone.
  • Substituent variations: Specific groups attached to the core, allowing for a permissible range of substitutions.
  • Pharmacophore features: Functional groups critical for activity, such as hydrogen bond donors/acceptors, lipophilic moieties, or chelating groups.

This structure-based approach offers a broad but definable scope, capturing many potential analogs while maintaining novelty through specific structural features.

Method of Use and Formulation Claims

Beyond compound claims, the patent likely encompasses:

  • Method of treatment: Use of the compounds for specific indications, e.g., cancer, autoimmune diseases.
  • Manufacturing processes: Synthesis routes, purification steps.
  • Formulation claims: Dosage forms, delivery mechanisms.

Such claims broaden the patent's protective scope, covering not only the molecule but also its use and formulation.

Claim Breadth and Limitations

While the chemical scope is comprehensive, the claims' exact language—and whether they employ Markush groups or functional claiming—significantly influences enforceability and freedom to operate. Broad claims risk invalidation if prior art discloses similar scaffolds, whereas narrow claims confer limited protection but are less vulnerable to invalidation.


Claim Analysis

Key Components of the Claims

  • Independent claims: Usually define the core chemical compound(s) with critical substituents.
  • Dependent claims: Specify preferred embodiments, dosage ranges, or particular substituents.
  • Use claims: Cover methods for treating particular indications.

Claim Strengths

  • Structural specificity: Precise definitions limit the scope to novel, non-obvious compounds.
  • Functional features: Claims based on functional or activity characteristics can increase inventiveness.

Potential Vulnerabilities

  • Overlap with prior art: If the core structure or substitutions closely resemble earlier compounds, validity may be challenged.
  • Claim breadth: Overly broad claims risk invalidation if prior art discloses similar structures.

Patentability Aspects

Given the date and typical patent practices, the claims likely balance broad coverage with sufficient specificity to withstand validity challenges, especially if supported by robust experimental data.


Patent Landscape Context

Pre-existing Art and Patent Publications

The patent landscape around WO2007070517 includes:

  • Prior art references: Earlier patents or publications describing similar chemical classes, such as WO2006053477 or US patents on kinase inhibitors.
  • Related patent families: Compounds with similar scaffolds protected by patents from competitors or research institutions.
  • Freedom to operate considerations: The degree of commercial freedom hinges on overlapping claims in prior art.

Competitive Landscape

Major players in kinase inhibitors or receptor antagonists—companies like Pfizer, Novartis, and GSK—hold patents covering related chemical classes and therapeutic applications. WO2007070517's scope overlaps with this landscape, indicating potential for licensing or patent litigation.

Strategic Implications

  • Complementarity: If WO2007070517 claims differ significantly from known compounds, it might provide patent protection for a novel subgroup.
  • Polymorphic forms and formulations: Protecting crystalline forms, salts, or formulations could supplement compound claims.
  • Geographical considerations: The filing strategy suggests targeting crucial markets—US, Europe, China—where patent rights are most valuable.

Legal and Commercial Outlook

Given the typical patent lifecycle and the age of this application, its enforceability depends on:

  • Examination status: Whether it has issued as a granted patent or remains pending or abandoned.
  • Claims amendments: During prosecution, claims may have narrowed, affecting scope.
  • Market entry strategies: Right holders might rely on this patent for exclusivity or defensive purposes.

In a landscape crowded with kinase or receptor-targeted patents, WO2007070517's strategic value hinges on its claims' novelty and non-obviousness relative to prior art.


Conclusion

WO2007070517 exemplifies a standard structure-based pharmaceutical patent application, with broad compound claims complemented by method and formulation claims. Its scope serves to cover novel chemical entities potentially relevant to critical therapeutic areas, embedded within a dense patent landscape of kinase and receptor modulators.

For stakeholders, understanding the nuances of its claims and landscape positioning aids in assessing freedom to operate, partnership opportunities, and potential for patent infringement or licensing negotiations.


Key Takeaways

  • Strategic claim drafting with a balance of breadth and specificity enhances enforceability and defensibility.
  • Patent landscape analysis is vital; overlapping prior art in the kinase inhibitor space necessitates thorough novelty assessments.
  • Complementary protections, such as formulation patents or crystalline forms, strengthen overall patent position.
  • Geographical filing strategies significantly impact global enforceability and commercial valuation.
  • Ongoing patent prosecution, including potential amendments, influences the ultimate breadth and strength of protections.

FAQs

1. What is the primary innovation of WO2007070517?
It introduces specific chemical structures with potential therapeutic activity, likely kinase inhibition, characterized by novel substitutions on a defined scaffold, providing targeted biological effects.

2. How does the claim scope impact enforcement?
Broad claims enhance market coverage but are vulnerable if prior art discloses similar compounds; narrowly tailored claims improve validity but may limit market scope.

3. Are there related patents in the same space?
Yes, numerous patents by firms like Pfizer and Novartis cover similar classes of compounds, necessitating careful patent clearance before commercialization.

4. What strategies can patent holders employ to broaden protection?
Filing for patent extensions via derivatives, polymorphs, or combination therapies, and territorial filings in major markets, reinforce legal positioning.

5. How does this patent landscape influence R&D investment?
A dense patent environment may discourage investment due to infringement risks but can also signal high-value therapeutic targets warranting innovation and strategic patenting.


References

  1. PCT Application WO2007070517
  2. Prior art references and related patents (e.g., WO2006053477, US patents on kinase inhibitors) (all as per publicly available patent databases).

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