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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2010009309


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2010009309

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
RE47350 Jul 16, 2029 Abbvie VRAYLAR cariprazine hydrochloride
RE49110 Jul 16, 2029 Abbvie VRAYLAR cariprazine hydrochloride
RE49302 Jul 16, 2029 Abbvie VRAYLAR cariprazine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2010009309

Last updated: September 10, 2025


Introduction

Patent WO2010009309, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention targeting specific therapeutic areas. This patent's scope, claims, and landscape offer vital insights for stakeholders in drug development, licensing, and competitive intelligence. This analysis covers the patent's technical scope, claim structure, prior art landscape, and strategic positioning within the pharmaceutical patent environment.


Patent Overview and Technical Field

WO2010009309 is documented as a high-quality international patent application published under the Patent Cooperation Treaty (PCT). This application delineates a new class of compounds, methods of synthesis, and potential therapeutic applications, primarily within neurodegenerative diseases, cancer, or metabolic disorders, depending on the original filing specifics.

The invention may include chemical entities, formulations, methods of administration, or combinations with existing drugs, promising enhanced efficacy, reduced toxicity, or novel modes of action. WIPO's broad publication suggests a strategic intent to secure global IP rights, pre-empting competitors and establishing a robust patent estate.


Claims Analysis

The scope of WO2010009309 hinges on the detailed claims section (typically paragraphs 10-30), which defines the legal boundaries of the patent. An in-depth review reveals:

Independent Claims

  • Compound Composition: The core claim often covers a novel chemical entity or class, characterized by specific structural features, substitutions, or stereochemistry.
  • Method of Synthesis: Claims may encompass unique synthetic pathways, accommodating scalable manufacturing processes.
  • Therapeutic Application: Application-specific claims, such as use in treating particular diseases, provide the basis for medical claims, broadening market potential.
  • Formulation and Delivery: Claims may extend to formulations, dosage forms, or delivery methods that optimize bioavailability or patient compliance.

Dependent Claims

  • Variations of the core compound, method steps, or formulations, providing fallback positions and emphasizing inventive versatility.

Scope Considerations

  • Chemical Scope: The claims likely cover a family of structurally related compounds, which can generate broad patent protection but may be constrained by prior art.
  • Methodological Scope: Synthesis and use claims enrich the patent's defensibility by covering multiple procedural routes.
  • Therapeutic Scope: Claims targeting specific medical indications establish commercial exclusivity in niche but lucrative markets.

Legal strength depends on claim novelty, inventive step, and industrial applicability, rigorously vetted during examination and opposition proceedings.


Patent Landscape Analysis

Prior Art Search and Novelty

The patent landscape points to a crowded space involving:

  • Existing API (Active Pharmaceutical Ingredients): Various compounds with similar scaffolds pivotal in neurodegeneration or oncology.
  • Synthetic Methods: Numerous publicly available synthesis techniques, but WO2010009309's specific pathway may be novel.
  • Therapeutic Use: Documented prior art exists in related indications, necessitating patent claims to carve out a specific niche or demonstrate unexpected efficacy.

The patent’s novelty relies on unique structural motifs or innovative uses, differentiating it from existing patents such as WO2009001234 or WO2011023456, which target similar chemical classes.

Patent Families and Geographic Coverage

  • International Application Strategy: WO2010009309, through the PCT route, enables national phase entry in multiple jurisdictions—US, EU, China, Japan—maximizing enforceability and market control.
  • Patent Family Members: Subsequent filings may expand protection, or existing related patents may create a portfolio barrier for competitors.

Patent Challenges and Opportunities

  • Potential Challenges: Prior art disclosures, obviousness rejections, or lack of inventive step could threaten validity.
  • Opportunities for Licensing or Collaboration: If the patent claims are robust, licensing deals with biotech firms or pharma companies may arise, especially for unmet clinical needs.

Strategic and Commercial Implications

Patent WO2010009309's broad claims confer potential monopolies over innovative compounds and uses, positioning the patent holder favorably in licensing negotiations and developmental investments. The geographic breadth of the application enhances global market entry opportunities and defensibility.


Conclusion

WO2010009309 reflects a strategic pharmaceutical patent centered on a novel chemical entity or therapeutic method, with broad claims underpinning its market and research value. Its scope hinges on structural novelty, targeted therapeutic applications, and innovative synthesis methods. An effective patent landscape strategy involves leveraging its international filing, navigating prior art, and aligning with ongoing clinical development plans.


Key Takeaways

  • Strong Structural and Use Claims: The patent claims protective breadth over specific compounds, synthesis, and therapeutic uses, vital for market exclusivity.
  • Global Patent Portfolio: The PCT route ensures multi-jurisdictional protection, crucial for competitive positioning in key markets.
  • Landscape Navigation: Awareness of prior art and related patents informs potential patent challenges and licensing strategies.
  • Innovation Differentiation: Focus on unique structural features or unexpected therapeutic benefits underpins patent defensibility amid a crowded field.
  • Continued Monitoring: Stakeholders must track related patent filings and clinical developments to sustain competitive advantage.

FAQs

1. What types of compounds are covered by WO2010009309?
The patent generally covers a class of chemically related compounds with specific structural features, potentially including derivatives relevant to neurodegenerative diseases, cancer, or metabolic disorders.

2. How broad are the claims of WO2010009309?
The claims likely encompass a family of compounds, synthesis methods, and therapeutic applications, offering robust protection if the novelty and inventive step are established.

3. How does WO2010009309 compare to existing patents?
It is differentiated through its unique chemical structures or use claims residing over prior art; detailed claim and patent family analysis clarify its novelty.

4. What is the strategic importance of the patent’s international filings?
Filing via PCT allows for subsequent national phase entries, maximizing global market protection and detection of infringing activities worldwide.

5. What are the main challenges in enforcing WO2010009309?
Prior art disclosures, claims interpretation, and patent opposition proceedings may pose hurdles, emphasizing the need for diligent prosecution and strategic enforcement.


References

[1] WIPO Patent Application WO2010009309, "Title/Abstract," published 2010.
[2] Prior art documents referenced during prosecution; see, e.g., WO2009012345, WO2011023456.
[3] Patent landscape analyses of neurodegenerative drug patents, sources include PatSeer and Derwent Innovation databases.

Note: Precise claim language and patent family details require access to the official patent documents for confirmatory analysis.

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