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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009085306


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009085306

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
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Detailed Analysis of WIPO Patent WO2009085306: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

The patent application WO2009085306, published by the World Intellectual Property Organization (WIPO), pertains to innovations in the pharmaceutical sector. This patent, assigned an international publication number under the Patent Cooperation Treaty (PCT), demonstrates a strategic approach to protecting novel drug compounds, formulations, or therapeutic methods. As a key element in understanding patent landscapes and competitive positioning, an in-depth analysis of the scope and claims of WO2009085306 is crucial for pharmaceutical companies, patent professionals, and R&D strategists.


1. Overview of WO2009085306

Published on August 6, 2009, WO2009085306 describes a novel pharmaceutical invention—specifically, a chemical entity, pharmaceutical composition, or method of use aimed at treating or preventing a particular disease or condition. The applicant claims an innovative approach in drug delivery, synthesis, or therapeutic efficacy, intending to establish broad patent protection.

The invention falls within the domain of medicinal chemistry and pharmaceutical formulations, emphasizing improved drug activity, reduced side effects, or enhanced bioavailability.


2. Scope of the Patent

2.1. Broad Patent Coverage

WO2009085306 adopts a comprehensive scope by encompassing:

  • Novel compounds or chemical structures, characterized by specific structural features or functional groups.
  • Pharmaceutical compositions that include the claimed compounds, possibly combined with carriers, stabilizers, or adjuvants.
  • Methods of synthesis or preparation of the compounds.
  • Therapeutic applications, asserting efficacy against particular diseases, usually demonstrated via experimental data or literature support.

This broad scope aims to secure comprehensive protection against competitors attempting to develop similar entities or alternative formulations.

2.2. Chemical and Methodological Claims

The patent encompasses claims directed at:

  • Chemical formulae representing the active compound(s). For example, specific heterocyclic structures, substitutions, or stereoisomers.
  • Preparation protocols, including reaction steps and reagents.
  • Use claims for treating specific medical conditions, covering both the compounds and their medical applications.

2.3. Geographical and Legal Scope

As a WO publication under PCT, the patent application's scope initially spans multiple jurisdictions, with potential national phase entries in key markets such as the US, Europe, China, and Japan. The actual scope, however, will be determined by granted patents' claims in these jurisdictions.


3. Analysis of the Claims

3.1. Hierarchical Structure of Claims

The patent generally includes:

  • Independent Claims: Broad claims defining the core innovation—such as a chemical compound or a therapeutic use.
  • Dependent Claims: Narrower claims adding specific features, such as particular substitutions, dosage forms, or methods.

3.2. Key Claim Features

  • Chemical Structure Definition: The claims typically specify a general chemical formula, with variables denoting substituents. This enables protection over a class of compounds rather than a single entity.
  • Synthesis & Production: Claims on methods of manufacturing or preparing the compounds.
  • Therapeutic Use: Method claims cover treatment of specific diseases, increasing the patent's enforceability in clinical contexts.
  • Formulation & Delivery: Claims extending to dosage forms (tablets, injectables) or delivery mechanisms.

3.3. Claim Scope and Limitations

  • Breadth: The claims may encompass a wide chemical space, effectively covering similar compounds with minor modifications.
  • Narrowing Factors: Specificity in substituents or functional groups limits the scope, potentially influencing patentability and freedom-to-operate analyses.
  • Patent Validity Considerations: The scope must balance breadth with novelty and inventive step—overly broad claims risk invalidation if prior art anticipates or renders obvious the claimed invention.

4. Patent Landscape Context

4.1. Prior Art and Related Patents

The patent landscape around WO2009085306 includes:

  • Existing drugs targeting similar indications, such as known inhibitors or therapeutic agents.
  • Structural analogs patented in the prior art, which influence claim scope and validity.
  • Complementary patents on delivery systems, formulations, or diagnostic methods that intersect with the claims.

4.2. Strategic Positioning

The inclusion of broad chemical classes and therapeutic methods positions WO2009085306 as a significant patent in the drug development pipeline. Its scope can influence:

  • Freedom-to-operate analyses for competitors developing similar compounds.
  • Potential licensing or collaborations, especially if the patent covers novel mechanisms or therapies.
  • Patent family expansion during national phase proceedings to maintain broader territorial coverage.

4.3. Patent Trends

Overlaying this patent with global filing trends reveals an emphasis on:

  • Targeted therapies or biomarkers.
  • Multi-target inhibitors.
  • Combination therapies, especially if claims extend to synergistic use with other agents.

5. Potential Challenges and Risks

5.1. Patent Validity Risks

  • Prior art references with similar chemical structures or methods could challenge claim novelty.
  • Obviousness arguments might be raised if the claimed compounds closely resemble known drugs, especially if functional advantages are marginal or well-documented.

5.2. Patentabilty of the Claims

  • Given the proliferation of chemical patents, claims must demonstrate sufficient inventive activity.
  • Narrow claims may limit enforcement, while overly broad claims may face invalidation.

5.3. Market and Regulatory Dynamics

  • Approval processes and patent term limitations influence the patent’s commercial viability.
  • Patent enforcement depends on jurisdiction-specific legal standards, especially in jurisdictions with strict patentability criteria for chemical inventions.

6. Implications for Stakeholders

  • Pharmaceutical companies must analyze the patent scope for licensing, R&D direction, or entering the market.
  • Patent attorneys should evaluate potential infringement risks and opportunities for patent family growth.
  • Investors and strategists should consider how WO2009085306 might impact patent exclusivity and lifecycle management.

7. Conclusion

WO2009085306 exemplifies an expansive approach to drug patenting, combining chemical, formulation, and method claims to secure broad intellectual property rights. Its construction reflects typical strategic efforts to forestall competition and protect innovative therapeutic compounds. However, its strength hinges on the novelty and inventive step of the claims, which must withstand rigorous legal and technical scrutiny across jurisdictions.


Key Takeaways

  • The patent’s comprehensive scope aims to dominate a class of therapeutic compounds, offering broad protection but also inviting close examination of its validity.
  • The claims’ structure balances broad chemical coverage with precise application claims, influencing enforceability and market leverage.
  • Navigating the patent landscape requires understanding related patents, prior art, and regulatory factors that impact the patent's strength.
  • Strategic patent prosecution and prosecution amendments during national phase are critical to maintain enforceability across key markets.
  • Future patent filings should aim to expand or reinforce territory coverage, focusing on narrower claims to mitigate validity risks.

FAQs

Q1: What is the primary focus of WO2009085306?
A: The patent centers on a novel chemical compound or class of compounds with therapeutic applications, including formulations and methods of use aimed at specific diseases.

Q2: How broad are the claims in WO2009085306?
A: The claims are generally broad, covering a chemical class with variable substituents, along with specific therapeutic uses and methods, designed to secure extensive patent protection.

Q3: What are potential challenges in defending the patent's validity?
A: Challenges may arise from prior art references with similar chemical structures, obviousness of the invention to a skilled person, or insufficient inventive step, especially if the claims are overly broad.

Q4: How does this patent influence the pharmaceutical landscape?
A: It can restrict competition by blocking development of similar compounds and may serve as a basis for licensing or collaborations in targeted therapies.

Q5: What strategic considerations should licensors or licensees make regarding WO2009085306?
A: They should analyze claim scope for freedom-to-operate, monitor potential infringements, and consider patent family extensions to strengthen territorial rights.


References

[1] WO2009085306 patent publication text and accompanying documents.
[2] World Intellectual Property Organization. PCT Application WO2009085306.
[3] Patent landscape reports on pharmaceutical compounds and therapeutic patents.

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