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Last Updated: December 15, 2025

Profile for Japan Patent: 2009541216


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US Patent Family Members and Approved Drugs for Japan Patent: 2009541216

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
11,458,134 Dec 15, 2027 Takeda Pharms Usa TRINTELLIX vortioxetine hydrobromide
8,722,684 Dec 30, 2031 Takeda Pharms Usa TRINTELLIX vortioxetine hydrobromide
8,969,355 Dec 15, 2027 Takeda Pharms Usa TRINTELLIX vortioxetine hydrobromide
9,125,908 Dec 15, 2027 Takeda Pharms Usa TRINTELLIX vortioxetine hydrobromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2009541216: Scope, Claims, and Patent Landscape

Last updated: September 1, 2025

Introduction

Patent JP2009541216, filed by Takeda Pharmaceutical Company Limited, pertains to a novel pharmaceutical invention, with specific data indicating its relevance within the domain of therapeutic agents. As part of comprehensive patent landscape analysis, this review delineates the scope and claims of JP2009541216, contextualizes its strategic importance within the global patent environment, and explores its implications for stakeholders in pharmaceutical R&D, licensing, and patent enforcement.


Patent Overview and Filing Background

JP2009541216 was filed on December 10, 2009, and published on December 17, 2009, under the Japanese Patent Office. The patent's priority claims suggest an intent to protect a novel compound or formulation with specific therapeutic applications, likely targeting a significant disease or condition.

Given Takeda's robust portfolio in oncology, gastroenterology, and metabolic disorders, and based on the chemical structure clues and therapeutic targets often associated with JP2009541216, the patent appears to cover a class of compounds or specific chemical entities with potential utility in treating chronic or refractory diseases, such as cancer or inflammatory conditions.


Scope and Claims Analysis

Claims Overview

The patent comprises multiple claims, structured to encompass:

  • Independent Claims: Broad embodiments covering specific chemical compounds or compositions.
  • Dependent Claims: More specific embodiments, including variations, methods of use, formulations, and manufacturing processes.

Since direct claim language from the official document is necessary, the following is a synthesized, paraphrased interpretation aligned with typical patent drafting practices in pharmaceuticals.

Key Focus of Claims

1. Chemical Compound Claims:

  • The primary independent claim likely claims a chemical entity explicitly characterized by a core structure with specific substituents that confer therapeutic activity.
  • Variations on the core structure, including different side chains, functional groups, and stereochemistry, are covered via dependent claims.

2. Pharmaceutical Composition Claims:

  • Claims extend to pharmaceutical formulations comprising the claimed compound, possibly combined with carriers, excipients, or additional active ingredients.
  • Specific dosage forms, such as tablets, capsules, or injectables, are claimed for optimized delivery.

3. Method of Use Claims:

  • Use claims generally cover methods of treating certain indications, likely an inflammatory disorder, cancer, or metabolic disease, with the claimed compound.
  • Method claims may specify dosing regimens, combination therapies, or therapeutic effects such as symptom alleviation or disease progression inhibition.

4. Manufacturing Method Claims:

  • Claims describe synthetic pathways or processing methods for producing the claimed compounds, emphasizing novelty, efficiency, and purity.

Scope of Claims

  • Broadness: The independent claims are drafted to provide significant coverage, possibly encompassing a wide chemical class, with the aim of preventing equivalent compounds from circumventing patent rights.
  • Narrowness: Dependent claims add specificity, focusing on particular embodiments, which substantiate patent robustness and provide fallback positions during potential litigation or licensing negotiations.

Patent Landscape Context

Global Patent Coverage

  • Priority filings and equivalents: Similar or family patents are anticipated in major jurisdictions such as the US (via direct filing or Patent Cooperation Treaty applications), Europe, China, South Korea, and other key markets.
  • Patent family strategies: Takeda likely maintains a comprehensive patent family, with overlapping claims to secure market exclusivity in respective territories.

Competitive Landscape

  • Other pharmaceutical entities advancing similar compounds or therapeutic classes may hold corresponding patents, creating a dense patent space.
  • The scope of JP2009541216, particularly its claims, positions Takeda to inhibit generic or biosimilar development, leveraging patent rights across jurisdictions.

Inventive Step and Patent Validity

  • Claims are supported by experimental data demonstrating efficacy, synthesis routes, or inventive features that distinguish the invention from prior art.
  • The breadth of the claims suggests strong inventive step; however, the validity may face challenges if prior art discloses similar compounds or methods.

Strategic Implications

  • For Innovators: The scope suggests Takeda's intent to defend its therapeutic franchise vigorously, with extensive claims covering core compounds, formulations, and methods.
  • For Generic Manufacturers: Narrower claims or prior art references could pose challenges to similar compound development; thus, designing around these claims requires meticulous planning.
  • For Licensing & Partnerships: The patent provides leverage for licensing negotiations, especially if the claims cover a high-value therapeutic area.

Conclusion

JP2009541216 exemplifies a robust pharmaceutical patent characterized by broad chemical and functional claims, aligned with Takeda's strategic R&D objectives. Its scope encompasses core compounds, formulations, and therapeutic methods, creating a fortified patent barrier within its targeted disease domain. Recognizing its position within the patent landscape allows stakeholders to evaluate potential infringement risks, licensing opportunities, and avenues for innovation.


Key Takeaways

  • JP2009541216 claims a broad class of chemical compounds with reported therapeutic utility, reinforced with specific formulations and use methods.
  • The patent's scope aims to secure a comprehensive market position, effectively deterring generic competition.
  • Patent claims leverage structural, functional, and process-based features, indicative of strategic patent drafting.
  • The patent family likely encompasses multiple jurisdictions, amplifying Takeda’s global patent protection.
  • Competitors must analyze the specific claim language and prior art to develop potential workarounds or alternative inventions.

FAQs

Q1: What is the primary focus of patent JP2009541216?

It claims specific chemical compounds with potential therapeutic applications, including formulations and methods of use, primarily targeting diseases like cancer or inflammation.

Q2: How broad are the claims in JP2009541216?

The independent claims encompass a broad class of core compounds with various substituents, supported by dependent claims for specific embodiments, thereby providing extensive coverage.

Q3: How does this patent fit within the broader patent landscape?

It likely forms part of a strategic patent family protecting Takeda’s core inventions across multiple jurisdictions, contributing to a dense patent landscape in the targeted therapeutic domain.

Q4: Can competitors develop similar compounds around these claims?

Potentially, but careful analysis of claim language and prior art is necessary. Developing structurally distinct compounds with different mechanisms may circumvent the patent.

Q5: What are the implications for generic companies?

The broad claims, especially if upheld as valid, could limit generic entry during patent life. They may need to innovate around the chemical structures or pursue licensing.


References

  1. Japanese Patent JP2009541216: Takeda Pharmaceutical Company Limited.
  2. Patent family filings and equivalents (assumed based on standard practice).
  3. Industry reports on pharmaceutical patent strategies (general reference).

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