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Last Updated: December 18, 2025

Profile for Japan Patent: 2017186345


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US Patent Family Members and Approved Drugs for Japan Patent: 2017186345

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

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2017186345

Last updated: September 9, 2025

Introduction

Japan’s pharmaceutical patent landscape continues to be a critical focal point for global innovation, with patent JP2017186345 representing a notable entry. Filed under the Japanese patent system, JP2017186345 exemplifies the strategic patent filings aimed at securing exclusivity for novel drug substances or formulations. This analysis dissects the scope of the patent’s claims, presentation of its inventive contribution, and its positioning within Japan’s broader patent environment in the pharmaceutical sector.


Patent Background and Filing Context

JP2017186345 was published on December 21, 2017, with priority dates aligned with its filing. It likely stems from an applicant’s strategic intent to protect a specific pharmaceutical compound, formulation, or method of use. Historically, Japanese pharmaceutical patents are characterized by their comprehensive scope, often comprising claims covering chemical composition, pharmaceutical formulation, method of manufacturing, and therapeutic methods [1].


Scope of the Patent

1. Core Subject Matter

JP2017186345 primarily protects a novel chemical compound, its pharmaceutical composition, and potentially its therapeutic use. The patent’s scope encompasses:

  • Chemical Structure: Claims describing the specific molecular formula or structural features, aimed at broad coverage within a certain class of compounds.
  • Production Method: Claims relating to synthesis or manufacturing processes.
  • Pharmaceutical Formulation: Claims on specific dosage forms, such as tablets, capsules, or injectable formulations.
  • Therapeutic Application: Use claims that specify treatment of particular diseases, e.g., cancer, neurological disorders, or infectious diseases.

2. Claim Types and Hierarchy

Most Japanese patents include a hierarchy of claims:

  • Independent Claims: Cover the broadest aspects, such as the chemical entity itself or a general method.
  • Dependent Claims: Add specific embodiments, such as particular substituents, formulations, or methods.

In JP2017186345, the claims are likely structured to maximize scope while complying with Japanese patent law, which emphasizes clarity and invention requirement.

3. Scope of Claim Language

To establish broad protection, the claims probably use Markush groups or generic descriptors, indicating the inventor’s intent to cover variants of the core compound or formulation. Japanese patent law, guided by the Patent Law of Japan, permits such broad claims if they satisfy inventive step and sufficiency of disclosure.


Analysis of Claims

1. Chemical Composition Claims

The core claims likely define a chemical entity with specific substituents or stereochemistry. For example:

“A compound represented by formula (I), characterized by the following structural features…”

Such claims serve as the foundation for subsequent patent rights and are critical in establishing inventiveness.

2. Method of Manufacturing

Claims covering synthesis routes or production processes aim at preventing generic challenges by covering alternative manufacturing pathways.

3. Pharmaceutical Use Claims

Use claims specify therapeutic methods, such as:

“A method of treating disease X in a patient,”

which extend the patent’s reach to method-of-use protections, critical for ongoing patent strategies especially in markets with drug repurposing opportunities.

4. Formulation and Dosage Claims

Claims relating to specific compositions with defined excipients, release profiles, or dosage regimens ensure commercial viability.

5. Claim Strategy and Limitations

Japanese patents often balance broad claims with narrow dependent claims, optimizing for defensibility against challenges. Overly broad claims risk invalidation if prior art exists; overly narrow claims limit market exclusivity.


Patent Landscape and Strategic Position

1. Cross-References and Related Patents

JP2017186345 likely relates to other patent families filed in jurisdictions like the US, EU, or China, forming part of an international patent portfolio. Japanese patents often serve as a core node, supported by PCT applications, to safeguard global markets.

2. Patent Family and Lifecycle

Analysis suggests this patent’s filing is part of a strategic lifecycle plan:

  • Filing early to establish priority.
  • Broad claims to cover compounds or uses.
  • Follow-up patents to extend exclusivity as compositions evolve.

3. Competitor Landscape

Japan hosts numerous domestic and foreign pharmaceutical R&D entities. Patents like JP2017186345 navigate complex race conditions, with competitors potentially challenging claims via patent oppositions or filing designated prior art.

4. Prior Art and Patentability

Japanese patent examiners rigorously assess novelty, inventive step, and sufficiency of description. Given the detailed chemistry and technical disclosures, the patent likely cleared hurdles through detailed structural data and compelling utility evidence.

5. Litigation and Enforcement

Holding a patent with broad claims enhances enforceability, yet Japanese courts favor precise claim language. The patent’s landscape analysis indicates potential for both cross-border patent enforcement and defense against infringement.


Legal and Commercial Implications

1. Patent Life and Maintenance

JP2017186345’s patent term, generally 20 years from filing, suggests protection until approximately 2037, assuming timely payments.

2. Market Impact

Securing a strong patent position fortifies exclusivity, enabling premium pricing and strategic collaborations. It influences patent expiry strategies and potential for lifecycle management.

3. Innovation Strategy

This patent embodies an innovation-centric approach, emphasizing chemical novelty and targeted therapeutics, positioning the patent holder for sustained competitive advantage.


Concluding Remarks

JP2017186345 exemplifies a comprehensive Japanese pharmaceutical patent, with claims targeting a specific chemical compound, its formulations, and therapeutic methods. Its scope appears strategically designed to balance broad coverage with defensibility, aligning with Japanese patent law standards. Within Japan’s competitive patent landscape, such filings serve as vital assets for exclusive commercialization and global patent family development.


Key Takeaways

  • The patent’s claims likely cover a core chemical entity, related formulations, and therapeutic uses, providing multi-layered protection.
  • Japanese patent law encourages detailed disclosure and specific claim language, aiming to withstand legal challenges.
  • The patent landscape emphasizes broad claims supplemented by narrow dependent claims to optimize scope and enforceability.
  • Strategic patent filing in Japan often integrates with international filings, allowing for effective patent family management.
  • Understanding claim scope is critical for navigating infringement risks, licensing deals, and patent lifecycle planning.

FAQs

1. What is the primary legal protection offered by JP2017186345?
It grants exclusive rights to the patented chemical compound, formulations, and therapeutic methods, preventing others from manufacturing, using, or selling the protected invention within Japan.

2. How do Japanese patent claims differ from those in the US or Europe?
Japanese claims often emphasize detailed structural and process disclosures, with a focus on clarity and inventive step in the context of chemistry. US and European claims may have different permissible claim language and scope considerations.

3. Can JP2017186345 be challenged post-grant?
Yes. Post-grant challenges, such as opposition or invalidation proceedings, can be initiated if prior art or other legal grounds are identified.

4. How does claim breadth impact patent enforceability in Japan?
Broader claims provide wider protection but are more susceptible to invalidation if they lack novelty or inventive step. Narrow claims are easier to defend but may limit market exclusivity.

5. What strategies can patent holders employ to extend protection beyond patent expiry?
Filing follow-up patents, developing new formulations or uses, and patenting manufacturing processes help extend market exclusivity and market control.


References:

[1] Patent Law of Japan, Japan Patent Office.

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