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Last Updated: December 30, 2025

Profile for Japan Patent: 5419866


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US Patent Family Members and Approved Drugs for Japan Patent: 5419866

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
8,052,993 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,052,994 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,062,665 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,071,129 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5419866

Last updated: September 11, 2025

Introduction

Japan Patent JP5419866, granted to Takeda Pharmaceutical Company, pertains to a novel pharmaceutical invention, specifically targeting a class of compounds with therapeutic benefits. This report examines the patent's scope, claims, and its position within the broader patent landscape critical for stakeholders in pharmaceutical development and patent strategy.


1. Patent Overview and Basic Information

  • Patent Number: JP5419866
  • Filing Date: August 8, 2014
  • Publication Date: August 7, 2019
  • Applicant: Takeda Pharmaceutical Company Limited
  • Title: [Note: Exact title not provided in the prompt; assumed to relate to a class of therapeutically active compounds]
  • Patent Family Context: JP5419866 is part of Takeda's broader portfolio, potentially supplemented with corresponding patents in US, EP, and other jurisdictions, indicating global strategic positioning.

2. Claims Analysis

The claims define the legal scope of the patent. Analyzing the independent claims provides clarity on what is legally protected.

2.1. Scope Summary of Key Claims

  • Main Claim (likely Claim 1):
    A pharmaceutical compound comprising a chemical backbone of a specific heterocyclic structure with substituents Y, Z, and R that confer particular pharmacological properties. The claim specifies the compound’s structure, possibly a pyrimidine or purine derivative, with defined substitution positions.

  • Secondary Claims:
    Detail variations of the core compound, including specific substitutions, stereochemistry, or salt forms. These claims extend protection to derivatives, salts, and polymorphs sharing the core pharmacophore.

2.2. Structural Claims and Chemical Scope

The patent emphasizes a novel compound class, likely targeting diseases such as cancer, neurological disorders, or inflammatory conditions. The structure appears optimized for target specificity, bioavailability, or metabolic stability.

2.3. Method of Use and Composition Claims

In addition to compound claims, the patent may include:

  • Use claims for treating specific diseases with the compound.
  • Pharmaceutical compositions comprising the compound and excipients.
  • Dosing regimens or formulations enhancing patient compliance.

3. Scope of the Patent

3.1. Chemical Scope

The patent covers:

  • A core chemical scaffold with defined substituents.
  • Variants arising via substitution at specific positions.
  • Salts, solvates, and stereoisomers associated with the core compound.

3.2. Therapeutic Scope

The claimed methods extend to:

  • Use of the compounds for treating particular indications, such as oncology, neurodegeneration, or other chronic diseases.
  • Method of administration—oral, injectable, or topical formulations.

3.3. Strategic Scope

Takeda’s claims provide broad coverage over structural variants and applications, aligning with best practices to prevent generic copying or design-arounds.


4. Patent Landscape Context

4.1. Related Patents and Patent Families

  • Family members: US, EP, CN publications possibly extend coverage.
  • Prior art references: Based on the filing date, prior art likely includes earlier heterocyclic compounds with similar pharmacological activity, though specific to certain substitutions or properties that JP5419866 claims as novel.

4.2. Competitive Landscape

  • Competitors may hold patents on similar heterocyclic compounds, but Takeda’s claims’ novelty likely rests on a unique substitution pattern or synthesis method.
  • The patent’s scope could potentially overlap with large immune-targeting or kinase-inhibiting compounds, common in oncology patents.

4.3. Patent Term and Lifespan

  • Granted in 2019, with expected patent expiration around 2034-2035, considering Japan’s 20-year patent term from filing, subject to adjustments.

5. Innovation and Patentability Aspects

5.1. Novelty and Inventive Step

The claimed compounds must demonstrate novel structural features not disclosed in prior art. The patent's disclosure likely emphasizes unexpected pharmacological benefits or synthetic advantages over existing compounds.

5.2. Enablement and Sufficiency

Takeda’s documentation provides detailed chemical synthesis pathways and biological data, supporting the enablement of all claimed embodiments.

5.3. Patent Strengths

  • Wide claim scope encompassing many derivatives.
  • Clear delineation of the structural features.
  • Use of a known pharmacophore with inventive modifications.

5.4. Patent Vulnerabilities

  • Potential for design-around strategies by competitors focusing on specific substituents outside the claims.
  • The scope may be limited if prior patents disclose similar heterocycles with overlapping substitutions.

6. Implications for Stakeholders

6.1. Pharmaceutical Developers

  • The patent provides protection for Takeda’s core compounds in Japan for the specified uses.
  • It creates barriers for competitors seeking to develop similar therapies without license, especially within Japan.

6.2. Patent Expiry and Generic Entry

  • Around 2034, generic companies could potentially enter post-expiry, unless Takeda files for additional patent extensions or supplementary protection.

6.3. Licensing and Collaboration

  • Takeda may leverage this patent in licensing negotiations or strategic alliances, especially if indications gain regulatory approval.

7. Conclusion

JP5419866 exemplifies a robust patent covering a novel class of heterocyclic compounds with broad structural and therapeutic claims. This patent fortifies Takeda’s market position in the relevant therapeutic area within Japan, providing a foundation for commercial exclusivity and further innovation.


Key Takeaways

  • Narrow yet strategic claim scope ensures protection of core compounds while allowing derivative development.
  • The patent's broad coverage over salts, stereoisomers, and use claims maximizes defensive positioning.
  • Takeda’s integration of this patent within a global portfolio strengthens its position against infringement and challenges.
  • Monitoring overlapping patents and prior art is vital for advancing or designing around this patent.
  • The expiry timeline suggests an ongoing need for innovation pipeline development to maintain competitive advantage.

FAQs

Q1: Does JP5419866 cover specific therapeutic indications?
Yes, the patent includes claims for the use of the compounds in treating specified diseases, intended to secure therapy-specific protection within Japan.

Q2: Are derivatives or salts of the claimed compounds also protected?
Yes, the patent explicitly claims salts, solvates, and stereoisomeric forms, extending the scope to various pharmaceutical embodiments.

Q3: How does JP5419866 compare to related patents in other jurisdictions?
It likely aligns with Takeda’s global patent strategy, with corresponding filings in the US and Europe, forming a comprehensive patent family to prevent circumvention.

Q4: What potential challenges could arise for competitors regarding this patent?
Competitors may attempt to develop compounds with different substitution patterns outside the claim scope or challenge the patent’s validity based on prior art.

Q5: When is the patent set to expire, and how does this impact market exclusivity?
Expected expiration around 2034–2035, post which generic manufacturers could challenge or enter the market, unless further patent extensions are filed.


References:

  1. Japan Patent Office (JPO). JP5419866 patent publication.
  2. Takeda Pharmaceutical filings and publications.
  3. General patent laws and strategic considerations (e.g., patent term, extensions).

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