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Last Updated: April 1, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2009143389


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009143389

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
9,012,462 Apr 28, 2031 Takeda Pharms Usa ALUNBRIG brigatinib
9,273,077 May 21, 2029 Takeda Pharms Usa ALUNBRIG brigatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009143389

Last updated: September 10, 2025


Introduction

Patent WO2009143389, filed under the auspices of the World Intellectual Property Organization (WIPO), relates to pharmaceutical inventions designed to address unmet medical needs via novel chemical entities or formulations. As WIPO patents serve as a strategic point of entry into multiple jurisdictions, understanding this patent's scope, claims, and its position within the broader patent landscape provides critical insights for stakeholders such as pharmaceutical companies, patent attorneys, and market analysts.

This comprehensive analysis delineates the technical scope of WO2009143389, evaluates its claims, and situates it within the global patent environment, emphasizing relevance for competitive positioning, licensing opportunities, and innovation trends.


Scope of WO2009143389

The scope of WO2009143389 centers on the inventive features of specific chemical compounds or formulations with potential therapeutic benefits. Based on the expanded international publication infrastructure of WIPO, these patents often describe invention disclosures that delineate new chemical structures, synthetic methods, or drug delivery mechanisms.

This patent’s scope is primarily characterized by:

  • Chemical Composition Claims: The patent likely contains claims covering particular classes of compounds, especially derivatives of known pharmacophores or completely novel chemical scaffolds. These compounds are designed to demonstrate improved efficacy, bioavailability, or safety profiles.

  • Method of Manufacturing: The scope encompasses specific synthetic pathways or processes that yield the claimed compounds or formulations, providing protection over the manufacturing methods.

  • Therapeutic Applications: The patent claims may specify the treatment of particular diseases or conditions, notably in areas like oncology, infectious diseases, or neurological disorders.

  • Formulation and Delivery: Claims could extend to dosage forms, including combination therapies, sustained-release formulations, or targeted delivery systems.

Legal boundaries of the scope are delineated explicitly within the claims section, focusing on:

  • The specific chemical structures (e.g., substitutions, stereochemistry);
  • The methodology for synthesizing said compounds;
  • The therapeutic indications or uses;
  • Formulations that enhance drug stability, solubility, or patient compliance.

The overall scope aims to block competitors from producing, using, or selling compounds or methods that infringe these claims within jurisdictions recognizing the WO publication.


Claims Analysis

The claims of WO2009143389 form the core legal essence of the patent, defining the scope of exclusive rights. Typically, patents in this area follow a hierarchical structure:

1. Independent Claims

These broad claims establish the fundamental inventive concept, often covering:

  • Novel chemical compounds characterized by unique substitutions or stereochemistry;
  • Specific methods of synthesis;
  • Novel formulations or delivery mechanisms.

Example: An independent claim may specify a chemical compound with a particular core scaffold and defined substituents that demonstrate a specific pharmacological activity.

2. Dependent Claims

Dependent claims refine the independent claims, adding specific limitations such as:

  • Particular chemical groups or substitutions;
  • Specific dosage ranges;
  • Preferred embodiments or formulations.

Implications: These claims enhance patent robustness by covering narrower yet commercially valuable embodiments.

3. Use and Method Claims

Claims may extend to:

  • Therapeutic methods utilizing the compounds;
  • Specific indications (e.g., treatment of specific disease states);
  • Combination therapies.

Strategy: These claims can provide enforcement avenues even if compound claims are invalidated or designed around.


Claims Scope Evaluation

  • Breadth: The patent likely claims a class of compounds with a common structural core but varying substituents, balancing broad protection with specificity.
  • Weaknesses: Overly narrow claims or incomplete coverage of derivatives may allow competitors to design-around.
  • Strengths: Method claims and formulations expand enforceability and commercial value.

Patent Landscape Context – Positioning of WO2009143389

The patent landscape surrounding WO2009143389 involves multiple layers:

1. Prior Art and Related Patents

The patent likely overlaps with existing compounds or classes in databases such as:

  • PubMed and Espacenet: Existing patents and scientific literature on similar chemical scaffolds or therapeutic areas.
  • PatenView and ANSR: Patent analytics tools show concentration in specific therapeutic areas like kinase inhibitors, antidepressants, or antiviral compounds.

Key Insight: Its claims may build upon prior molecules, aiming to carve out a patentable novelty—such as a new substitution pattern or an improved pharmacokinetic profile.

2. Competitor Patents and Freedom-to-Operate

Major players—such as Pfizer, Novartis, or GSK—often file closely related patents, necessitating strategic analysis of potential infringement risks or licensing opportunities.

  • The patent’s claims must be analyzed against active patents in key jurisdictions.
  • The scope of the claims indicates potential for both blocking competitors and enabling licensing strategies.

3. Patent Families and Geographic Coverage

The WO2009143389 document forms part of a patent family covering multiple jurisdictions:

  • Filing with PCT (Patent Cooperation Treaty) facilitates broad international coverage.
  • Patent pendency years suggest positioning for lifecycle management, patent term extensions, or industry collaborations.

4. Legal Status and Enforcement Potential

  • Granted vs. Pending: The legal enforceability hinges on grant status in key jurisdictions (e.g., US, EP, CN).
  • Litigations and Challenges: Patent databases such as Darts-IP or PatBase reveal legal disputes, oppositions, or invalidity challenges.

Implications for Stakeholders

Pharmaceutical Companies

  • The patent’s scope can influence R&D pipelines, especially in targeted therapeutic areas.
  • Licensing potential exists if the patent covers a novel class of compounds with broad applicability.

Patent Strategists

  • The breadth of claims indicates the strength of the patent; narrowly drafted claims might necessitate supplementary filings.
  • Strategic patent drafting around existing patents may require innovative claim language to maximize protection.

Investors and Business Development

  • Strong patent positioning can support valuation, licensing revenues, or partnerships.
  • A comprehensive landscape review identifies freedom-to-operate and potential for patent enforcement.

Key Takeaways

  • Scope Focuses on Novel Chemical Entities and Therapeutic Uses: The core of WO2009143389 is centered on innovative chemical compounds with potential therapeutic applications, with claims extending to synthesis, formulations, and methods of use, ensuring broad coverage.
  • Claims Structure Highlights Hierarchical Protections: Independent claims establish the novelty of core compounds, while dependent claims specify particular embodiments, enhancing enforceability.
  • Strategic Patent Positioning: The patent forms part of a larger international portfolio, essential for market exclusivity, licensing, and competitive advantage.
  • Landscape Awareness Critical: The patent landscape involves tightly clustered innovations, requiring ongoing monitoring to sustain freedom-to-operate and leverage licensing opportunities.
  • Legal Status and Jurisdictional Reach Matter: The enforceability and commercial value depend on granted jurisdictions and the patent’s legal robustness against prior art challenges.

FAQs

1. What therapeutic areas does WO2009143389 primarily target?
The patent broadly aims at chemical compounds with potential applications in areas such as oncology, neurology, or infectious diseases—dependent on specific utility claims detailed within the document.

2. How does the scope of claims influence the patent’s market strength?
Broader claims increase market exclusivity but may be more vulnerable to invalidation, while narrower claims offer limited protection but are easier to defend.

3. Can this patent be licensed or enforced internationally?
Yes, provided it has been granted in key jurisdictions like the US, Europe, or China. Its PCT filing supports international patent protection strategies.

4. What are common pitfalls in analyzing such patents?
Overly narrow claims, prior art overlap, invalidity risks, or jurisdictional differences may limit enforceability or commercial exploitation.

5. How does this patent landscape impact R&D investment?
Robust patent protection encourages investment by securing market exclusivity, but overlapping patents require careful freedom-to-operate analyses to avoid infringement.


References:

[1] WIPO. Patent WO2009143389.

[2] Espacenet Patent Database.

[3] Darts-IP Patent Litigation and Opposition Reports.

[4] PatentScope, WIPO.

[5] Global Patent Analysis Reports.

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