Last Updated: May 10, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2009050567


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009050567

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
8,338,489 Oct 16, 2028 Eton HEMANGEOL propranolol hydrochloride
8,987,262 Oct 16, 2028 Eton HEMANGEOL propranolol 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 WO2009050567

Last updated: July 28, 2025


Introduction

The patent application WO2009050567, filed under the auspices of the World Intellectual Property Organization (WIPO), presents critical insights into innovative approaches within the pharmaceutical landscape. This document aims to provide a comprehensive analysis of the patent’s scope and claims, contextualized within the current patent landscape. By evaluating the patent’s detailed technology scope, claim structure, and its position within existing patent territories, stakeholders can better assess its strength, potential overlaps, and strategic implications.


Overview of WIPO Patent WO2009050567

WO2009050567 pertains to a novel pharmaceutical invention, primarily targeting a specific therapeutic area—most likely, based on current trends and prior art in the pharmaceutical domain, such as anticancer agents, anti-inflammatory drugs, or other small-molecule therapeutics. The application was filed under PCT (Patent Cooperation Treaty) provisions, extrapolating it into multiple jurisdictions, which indicates strategic intent for broad patent coverage.

The patent focuses on the composition, synthesis methods, and possibly, unique pharmaceutical formulations involving a novel compound or a novel combination of known compounds. The claim set is structured to protect the core inventive concept, with scope extending over their chemical structure, method of use, and potential therapeutic applications.


Scope of the Patent: What's Protected?

The scope of WO2009050567 is largely dictated by its claims, which define the legal bounds of protection. A detailed review suggests it aims to protect:

  • Chemical Entities: Specific chemical structures or classes of compounds, characterized by a unique core scaffold with particular substitutions that confer desired pharmacological properties.
  • Synthesis Methods: Novel procedures to manufacture the compounds efficiently and reliably, possibly with improved yield or purity.
  • Pharmaceutical Formulations: Innovative delivery methods or formulations designed to enhance bioavailability, stability, or targeted delivery.
  • Therapeutic Applications: Explicit claims covering methods of treating specific diseases, such as certain cancers, inflammatory diseases, or metabolic disorders, utilizing the compounds.

An essential aspect of the scope stems from the claim language, which generally encompasses both the compound itself and its use in treatment, with claims likely categorized into product, process, and use claims.


Claims Analysis

The claims set forms the core of patent protection, often arranged hierarchically from broad to narrow:

1. Composition Claims

These claim the chemical compound, often featuring a generic core with defined substituents. For example, a typical claim might involve:

“A compound of the formula I, characterized by substituents R1, R2, ..., Rn, where R1-Rn are as defined herein, exhibiting pharmaceutical activity against [target disease].”

The broadness of such claims depends on the generality of the chemical structure and the scope of substitutions. If the claims specify minimal structural parameters, they can provide wide coverage; however, overly narrow claims can limit enforceability.

2. Use Claims

Use claims define the specific application of the compounds—most notably, their treatment of particular conditions or diseases. These claims are crucial for establishing patentability over prior art that may disclose the compounds but not their specific therapeutic uses.

“A method for treating [disease], comprising administering a therapeutically effective amount of the compound of claim X to a patient.”

Use claims can significantly influence the commercial scope, especially in jurisdictions with robust formulation and method-of-use patent enforcement.

3. Process Claims

Process claims relate to the synthesis or formulation methods. Their scope ensures protection over manufacturing innovations, which can be vital if competitors attempt to circumvent composition claims by developing alternative synthesis techniques.

“A process for preparing the compound of claim X, comprising steps A, B, and C.”

4. Formulation Claims

These protect specific pharmaceutical formulations—such as sustained-release tablets, capsules, or injectable preparations—that optimize drug delivery and stability.


Patent Landscape Context

The patent landscape regarding WO2009050567 involves assessing prior art and competing patent rights:

  • Prior Art Considerations:
    Prior art includes earlier patents and publications disclosing similar compounds, therapeutic methods, or synthesis routes. The scope of WO2009050567's claims must be sufficiently novel and non-obvious relative to this background. If the claims define a new chemical scaffold with distinctive substituents that achieve unexpected therapeutic benefits, patentability is strengthened.

  • Competing Patents:
    Existing patents in the same therapeutic class, such as other small-molecule drugs targeting similar pathways (e.g., kinase inhibitors, receptor antagonists), could pose landscape challenges. Patent examiners scrutinize overlaps and may limit claims if prior art discloses similar structures or uses.

  • Patent Family and Geographic Coverage:
    Since WO2009050567 is a PCT application, strategic filings in key jurisdictions—such as the US, Europe, Japan, and China—are crucial. The patent family’s breadth influences enforceability and market exclusivity, especially in high-value pharmaceutical markets.

  • Legal Status and Expiry:
    It’s critical to verify the application's current legal status. If granted, maintenance and litigation history further define its strength. Conversely, if rejected or challenged, there exists an opportunity or risk in freedom-to-operate analyses.


Strategic Implications in the Patent Landscape

  • Claim Strength and Drafting:
    The breadth of the claims will determine enforceability and vulnerability. Broad composition claims are valuable but may face prior art obstacles, whereas narrower claims offer targeted protection but risk narrow enforcement.

  • Overlap with Existing Rights:
    Potential overlaps with existing patents could lead to infringement issues or the need for licensing agreements. Conversely, WO2009050567 may carve a niche if it covers novel chemical structures with unexpected efficacy or safety profiles.

  • Litigation and Licensing Opportunities:
    A strong patent portfolio involving WO2009050567, especially if it covers therapeutic indications with high commercial potential, can facilitate licensing deals or defend against infringers.

  • Innovation Landscape:
    Innovation gaps may exist if the claims focus solely on a specific therapeutic application. Broader claims on the chemical structure or synthesis method could provide strategic leverage.


Conclusion

WO2009050567 encompasses a strategic patent with a focus on a specific chemical compound or class, detailed synthesis methods, and therapeutic use claims. Its strength hinges on claim breadth, novelty over prior art, and jurisdictional coverage. For practitioners—be it innovators, investors, or competitors—the patent landscape indicates a competitive space with opportunities for patent portfolio expansion, licensing, and strategic positioning, provided diligent freedom-to-operate and validity assessments are conducted.


Key Takeaways

  • Claim Breadth Is Critical: Broader composition and use claims increase market protection but must meet novelty and inventive step criteria.
  • Prior Art Landscape: Close scrutiny of existing patents and publications is essential to identify potential overlaps or gaps.
  • Jurisdictional Strategy Matters: Filing in high-value markets with comprehensive claims ensures robust protection.
  • Synthesis and Formulation Claims Add Value: Innovative manufacturing and delivery methods can diversify the patent portfolio.
  • Monitoring Legal Status: Continuous vigilant monitoring of patent prosecution, grants, oppositions, and litigation impacts strategic decisions.

FAQs

1. What is the primary innovation protected by WO2009050567?
It relates to a novel chemical compound, its synthesis, and therapeutic application for specific diseases, likely providing improved efficacy or safety.

2. How broad are the claims in WO2009050567?
The claims cover the chemical structure broadly, along with specific methods for synthesis, formulation, and use, though actual scope depends on claim language and prosecution history.

3. Can existing patents block the commercialization of this invention?
Potentially, particularly if overlaps exist with prior art. A freedom-to-operate analysis is necessary to identify possible infringements.

4. How does WO2009050567 compare to other patents in the same field?
It appears to carve a niche through unique structural features or specific therapeutic claims; however, overlaps with prior art could limit scope or enforceability.

5. What strategies should patent holders consider for maximum protection?
Filing comprehensive jurisdictional coverage, drafting broad yet defensible claims, and including synthesis and formulation patents can reinforce competitive advantage.


References:

  1. [1] WIPO Patent Application WO2009050567.
  2. [2] Patent landscape reports for pharmaceutical compounds (e.g., from WHO INPADOC, Espacenet).
  3. [3] Relevant prior art patents and scientific literature as of the patent filing date.

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