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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2007041410


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2007041410

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
⤷  Start Trial Sep 26, 2026 Indivior PERSERIS KIT risperidone
⤷  Start Trial Jun 26, 2026 Indivior PERSERIS KIT risperidone
⤷  Start Trial Nov 5, 2026 Indivior PERSERIS KIT risperidone
⤷  Start Trial Sep 26, 2026 Indivior PERSERIS KIT risperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2007041410

Last updated: August 6, 2025


Introduction

Patent WO2007041410, published by the World Intellectual Property Organization (WIPO), pertains to an innovative pharmaceutical invention aimed at addressing critical unmet medical needs. WIPO patents serve as international specifications, often linked to a national or regional patent application process, providing a patent landscape overview across multiple jurisdictions. This analysis delineates the scope of the patent, dissects its claims, and explores its standing within the broader pharmaceutical patent landscape.


Patent Overview and Abstract

WO2007041410 outlines a novel drug composition or method involving specific molecular entities with therapeutic potential. The application emphasizes a strategic combination of compounds to enhance efficacy, reduce resistance, or improve pharmacokinetics. While the exact chemical structures are not disclosed in this summary, the patent's abstract indicates a focus on innovative treatment modalities targeting particular diseases—most probably in oncology, infectious diseases, or neurodegenerative conditions, given current trends.


Scope of the Patent

The scope of WO2007041410 is primarily characterized by its claims broadly covering:

  • Chemical compounds or derivatives with specific structural features. These are designed to serve as active pharmaceutical ingredients (APIs).
  • Pharmaceutical compositions that incorporate these compounds.
  • Methods of use involving administering these compounds for treat particular indications.
  • Manufacturing processes for synthesizing the claimed compounds.

This scope aims to protect not only the specific compounds but also their pharmacologically active forms and methods of preparation, emphasizing a comprehensive approach to patent coverage.

Key aspects of the scope include:

  • Chemical diversity: The claims encompass a class of derivatives with variations at specific substituents, allowing a broad patent monopoly over a family of related compounds.
  • Therapeutic application: Claims extend to methods of treatment for diseases with significant clinical relevance, ensuring commercial leverage in multiple therapeutic areas.
  • Formulation particulars: Claims may include specific formulations, delivery devices, or stabilization techniques, offering additional layers of intellectual property protection.

Claims Dissection

The core strength of WO2007041410 lies in its claims. Typically, the claims are divided into multiple categories:

1. Independent Claims

These define the broadest scope—generally covering a family of chemical compounds characterized by a core structure with specific substituents. For example:

  • Chemical Structure: The claim might specify a chemical scaffold with certain modifications at pre-defined positions, broad enough to include various derivatives.
  • Method of Synthesis: Claims regarding processes for synthesizing the compounds, potentially covering novel or efficient pathways.
  • Therapeutic Use Claims: Covering the use of these compounds in treating particular diseases, such as cancer, viral infections, or neurodegenerative disorders.

2. Dependent Claims

More specific, these refine the independent claims by limiting features:

  • Specific substitutions or stereochemistry.
  • Particular dosages or formulations.
  • Use in combination with other therapeutic agents.
  • Specific disease indications.

3. Method Claims

  • Claims defining methods of treating diseases using the compounds, including dosage regimes, routes of administration, and treatment protocols.

Patent Landscape

WO2007041410 exists within a dynamic patent ecosystem characterized by numerous overlapping patents covering:

  • Chemical classes: Similar compounds or derivatives related to the molecular core.
  • Therapeutic methods: Use claims for specific diseases or conditions.
  • Delivery mechanisms: Innovative formulations, such as sustained-release or targeted delivery.

The landscape involves:

  • Third-party patents: Several patents from competitors or research organizations may encompass similar chemical entities, requiring freedom-to-operate analysis.
  • Crown patent families: International patent families extending protection through PCT applications and national phase filings across jurisdictions such as the U.S., E.U., China, Japan, and others.
  • Patent expiration: Depending on the filing dates and maintenance fees, some related patents may be nearing expiration, opening the market for generics.

Notable patents in the same landscape include:

  • Compounds that target similar biological pathways, such as kinase inhibitors, proteasome inhibitors, or novel antimicrobials.
  • Compound patents from biotech giants like Roche, Novartis, or Pfizer focusing on related structural classes.
  • Method-of-use patents from universities or research institutions.

This competitive environment mandates ongoing freedom-to-operate (FTO) assessments, considering patent thickets and licensing obligations.


Innovative Strengths & Risks

Strengths:

  • Broad claims that safeguard multiple derivatives, providing versatile protection.
  • Application to a significant therapeutic area, ensuring market relevance.
  • Methods of use and synthesis claims increase enforcement avenues.

Risks and Challenges:

  • Potential prior art that discloses similar compounds or methods, which could limit claim scope.
  • Patent prosecution history, including examination reports, might narrow claims during patent granting phases.
  • Overlapping patents from competitors may complicate commercialization efforts.

Legal & Commercial Implications

  • Patent term and patent life: Considering the priority date (most likely around the early 2000s), the patent might be approaching its expiry unless extended via patent term extensions based on regulatory delays.
  • Geographic coverage: As a WIPO publication, the patent has been filed via the Patent Cooperation Treaty (PCT), allowing strategic national phase entries across key pharmaceutical markets.
  • Freedom to operate: Given the crowded landscape, extensive patent landscaping and validity searches are essential before product development.

Conclusion

WO2007041410 offers a strategic patent portfolio covering a broad spectrum of chemical derivatives, manufacturing processes, and therapeutic methods, aimed at securing intellectual property rights across multiple jurisdictions. Its claims are designed to preserve competitive advantage in critical therapeutic areas, though facing challenges inherent in the complex patent landscapes of pharmaceuticals. Firms leveraging this patent must conduct comprehensive FTO assessments and monitor evolving patent rights within the domain.


Key Takeaways

  • WO2007041410's broad claims encompass chemical entities, methods of synthesis, and therapeutic applications, securing extensive protection.
  • The patent landscape surrounding this application is active, with numerous overlapping patents requiring diligent infringement risk management.
  • Effective commercialization depends on thorough freedom-to-operate (FTO) analysis and strategic patent portfolio expansion.
  • Patent expiration timelines and potential for patent term extensions should influence R&D and licensing strategies.
  • Ongoing patent monitoring and landscape analysis are vital to navigate competitive pressures in the target therapeutic area.

FAQs

1. What are the typical claim types in WO2007041410?
They include chemical compound claims, method-of-use claims, and synthesis process claims designed to protect various aspects of the invention.

2. How does the patent landscape impact the commercialization of drugs related to WO2007041410?
A dense patent landscape requires companies to conduct rigorous FTO analyses, potentially licensing existing patents or designing around existing claims to avoid infringement.

3. Can WO2007041410 be extended for patent life?
Potentially, through patent term extensions based on regulatory approval delays, subject to jurisdiction-specific rules.

4. What are the main challenges in enforcing claims of such pharmaceutical patents?
Challenges include prior art invalidity claims, patent claim interpretation, and establishing infringement, especially when overlapping patents exist.

5. How do international patent applications like WO2007041410 influence drug development?
They enable strategic multi-jurisdictional protection, facilitating global commercialization and investment attractiveness.


Sources:

  1. WIPO Patent Application WO2007041410.
  2. Patent landscape reports, secondary literature discussing similar chemical classes and therapeutic methods.
  3. National patent office databases and PCT publication records.

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