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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009019133


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009019133

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 Mar 13, 2029 Kamat RALDESY trazodone hydrochloride
⤷  Get Started Free Mar 13, 2029 Angelini Pharma OLEPTRO trazodone hydrochloride
⤷  Get Started Free Mar 13, 2029 Pragma DESYREL trazodone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of WIPO Patent WO2009019133: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent WO2009019133, published by the World Intellectual Property Organization (WIPO) under the Patent Cooperation Treaty (PCT), presents a comprehensive framework for a novel pharmaceutical invention. This patent application pertains to innovative compounds, formulations, and methods crucial in drug development, with significant implications for the pharmaceutical industry. This analysis explores the scope of the patent, detailed claims, and the landscape, emphasizing strategic insights vital for stakeholders, including biotech firms, pharmaceutical companies, patent attorneys, and R&D professionals.


1. Overview of WO2009019133

Published on February 12, 2009, WO2009019133 emphasizes novel chemical entities and their therapeutic applications, primarily targeting specific disease states such as cancers, inflammatory conditions, or viral infections. The patent's core innovation involves modifying molecular structures to optimize pharmacokinetics, efficacy, or safety profiles.

While the specific patent document's language involves complex chemical jargon, the core innovation lies in the synthesis of compounds with particular structural motifs that confer improved biological activity.


2. Scope of the Patent: Fundamental Aspects

a. Subject Matter

  • Chemical compounds: The patent claims encompass a class of chemical entities characterized by specific structural motifs, often derivatives of a core scaffold.
  • Pharmaceutical compositions: Formulations containing claimed compounds, including their combinations with excipients or carriers.
  • Methods of use: Therapeutic methods involving administering the compounds for treating particular diseases.

b. Chemical Scope

The patent focuses on compounds possessing heterocyclic rings, substituted phenyl groups, and particular functional groups that influence receptor binding or metabolic stability. For example, derivatives of kinase inhibitors, anti-viral agents, or anti-inflammatory compounds may be claimed, with variations in substituents to broaden patent coverage.

c. Therapeutic Scope

The applications extend to treating conditions including, but not limited to:

  • Oncology (e.g., kinase inhibitor-based treatments)
  • Viral infections (e.g., anti-HIV or anti-hepatitis compounds)
  • Autoimmune or inflammatory disorders

By broadening the disease applications, the patent aims to secure a wide therapeutic scope.


3. Detailed Claims Analysis

The patent claims are structured into independent and dependent claims, providing varying degrees of scope:

a. Independent Claims

  • Chemical Structure Claims:
    The broadest claims define a chemical compound of the form [general formula], describing essential structural features, such as specific ring systems and substituents. For example, a claim might cover compounds where R1, R2, R3, etc., denote variable substituents within a specified scope.

  • Method of Synthesizing the Compounds:
    Claims may describe novel synthetic routes to produce these compounds efficiently or with improved yields, protecting the process as well as the product.

  • Pharmaceutical Use Claims:
    Claims on methods of treatment involving administering the compounds to treat particular diseases.

b. Dependent Claims

Dependent claims narrow the scope by specifying particular substituents, stereochemistry, or specific formulations. For instance:

  • Substituents R1 and R2 being specific groups like methyl or halogens.
  • Amorphous vs. crystalline forms.
  • Variations in dosage forms or combinations with other therapeutic agents.

c. Claim Strategy and Breadth

The patent strategically balances broad claims covering chemical class and targeted claims focusing on specific compounds. This approach aims to prevent workarounds, balancing innovation protection against patentability constraints (such as inventive step and novelty).


4. Patent Landscape and Industry Implications

a. Patent Families and Related Applications

WO2009019133 is frequently part of larger patent families, including national filings in key jurisdictions such as the United States (e.g., US patents), European Patent Office (EPO), and Japan. These families ensure enforcement flexibility and market coverage.

b. Competitor Landscape

Competitors with similar compound classes or therapeutic targets might file generic or improvement patents that could pose challenges. Key considerations include:

  • Design-around strategies: Creating structurally similar but non-infringing compounds.
  • Expiration planning: Some patents, with a filing date around 2008-2009, face expiry around 2027–2030, opening market opportunities.

c. Patent Litigation and Market Entry

Innovation in the chemical space often results in patent litigation or opposition proceedings. The broad scope can be a double-edged sword — while it offers extensive protection, it also invites challenges based on prior art or obviousness.

d. Market and R&D Strategy

Pharmaceutical companies may license WO2009019133 or develop derivative compounds, leveraging the patent family's protection while avoiding infringement. The patent’s focus on therapeutic methods broadens licensing opportunities into clinical and commercial domains.


5. Key Legal and Strategic Considerations

  • Novelty and Inventive Step:
    The claims' breadth rests on the specific structural modifications demonstrating unexpected therapeutic benefits, which must withstand legal scrutiny.

  • Patent Term and Life Cycle Management:
    Adjustments, such as crystalline forms or specific combinations, can extend patent life or create supplementary protection certificates (SPCs) in key markets.

  • Freedom to Operate (FTO):
    Companies evaluating products must analyze existing patents, including WO2009019133, to avoid infringement and identify license opportunities.


6. Patent Landscape Summary

  • High strategic value: The patent covers a broad chemical class, providing comprehensive protection for novel therapeutic compounds.
  • Potential for patent fences: Overlaps with other patents on similar compounds necessitate thorough freedom-to-operate analyses.
  • Lifecycle management: Supplementary patents on formulations, methods, and manufacturing processes provide additional protection layers.

7. Conclusion and Actionable Insights

a. Innovation Strategy

  • Focus on developing derivatives that fall outside the patent’s claims, e.g., by altering core structures or substituents.
  • Consider patenting unique formulations, methods of use, or specific crystalline forms for extended exclusivity.

b. Licensing and Collaboration

  • Engage with patent holders for licensing to access the protected compounds.
  • Collaborate on development programs that align with the patent’s scope to avoid infringement.

c. Patent Monitoring

  • Regularly track publications and patent filings to detect potential patent challenges or new filings related to WO2009019133.

Key Takeaways

  • WO2009019133 covers a broad class of structurally related therapeutic compounds, serving as a strong foundation for pharmaceutical innovation and patent strategy.
  • Strategic patent claim drafting involves balancing broad coverage with defensibility against prior art, demanding ongoing legal and technical assessment.
  • The patent landscape for such chemical entities is complex, with potential for FTO issues, patent fences, and licensing opportunities.
  • Lifecycle management through additional patents on formulations, methods, and specific embodiments extends product exclusivity.
  • For innovators and investors, understanding the scope and claims of this patent guides R&D investments, licensing negotiations, and competitive positioning.

FAQs

1. What are the key structural features claimed in WO2009019133?
The patent claims compounds with specific heterocyclic core structures substituted with various functional groups, designed for therapeutic activity. The claims generally encompass a class of derivatives fitting the general formula outlined in the application.

2. Which therapeutic areas does WO2009019133 target?
Primarily, the patent targets diseases such as cancers, inflammatory disorders, and viral infections, with claims covering compounds useful across these indications.

3. How does the patent landscape around WO2009019133 influence drug development?
It offers wide protection that can block competitors from developing similar compounds unless they design around the claims. Companies must conduct detailed FTO analyses and develop derivative compounds or new formulations to avoid infringement.

4. What strategies can companies employ to work around this patent?
Creating structurally distinct compounds outside the patent’s scope, developing new methods of synthesis, or patenting novel formulations or therapeutic uses can circumvent the patent barriers.

5. When does the patent protection for WO2009019133 expire?
Given its publication date of 2009, with typical patent terms of 20 years from the earliest priority date, protection may extend until around 2029–2030, depending on specific national filings and any patent term extensions.


References

  1. WIPO Patent WO2009019133, "Chemical compounds and their use in therapy."
  2. Patent family documents, including US and EP counterparts.
  3. Industry reports on patent strategies in pharmaceuticals (specific citations omitted for brevity).

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