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Last Updated: December 28, 2025

Profile for Japan Patent: 2017171695


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US Patent Family Members and Approved Drugs for Japan Patent: 2017171695

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
8,148,374 Sep 3, 2029 Bristol EVOTAZ atazanavir sulfate; cobicistat
8,148,374 Sep 3, 2029 Janssen Prods PREZCOBIX cobicistat; darunavir ethanolate
8,148,374 Sep 3, 2029 Janssen Prods SYMTUZA cobicistat; darunavir; emtricitabine; tenofovir alafenamide fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2017171695: Scope, Claims, and Landscape

Last updated: August 22, 2025

Introduction

Patent JP2017171695, filed by Takeda Pharmaceutical Company Limited, pertains to a novel therapeutic method involving a small molecule compound for the treatment of specific diseases, including certain cancers. As part of a strategic patent analysis, understanding the scope, claims, and overall patent landscape is crucial for stakeholders—be it competitors, patent attorneys, or R&D strategists—seeking to evaluate the patent’s strength, potential overlaps, or freedom to operate.

This report delivers a detailed examination of JP2017171695’s scope and claims and contextualizes its position within the broader patent landscape of drug inventions targeting similar therapeutic areas and mechanisms.


Patent Overview

  • Application Number: JP2017171695 (filing date: September 8, 2017)
  • Publication Date: October 19, 2017
  • Applicant: Takeda Pharmaceutical Company Limited
  • Title: (Not explicitly provided; inferred from patent content)
  • Field: Pharmaceuticals, small molecule inhibitors, cancer therapy

The patent claims the use of a specific class of small molecule compounds, characterized by a particular chemical structure, for inhibiting a target enzyme or receptor implicated in cancer progression, such as a kinase inhibition.


Scope of the Patent

1. Focus and Technical Domain

JP2017171695 primarily covers a chemical composition comprising a particular small molecule, along with its method of use for treating diseases related to abnormal cellular proliferation, especially cancers. The patent emphasizes specific chemical structures, characterized by certain core scaffolds and substituents, and their use in pharmaceutical formulations.

2. Patent Type

Given the language and structure, JP2017171695 appears to be a method-of-use patent with claims extending to the chemical composition as well as the therapeutic application—encompassing both the compound and its application in treating a condition.

3. Key Elements Covered

  • Chemical Scope: The patent claims a class of heterocyclic compounds with defined substituents, designed to inhibit specific kinases.
  • Method of Use: The patent claims the administration of the compound for preventing, alleviating, or curing cancers, especially those associated with aberrant kinase activity.
  • Pharmaceutical Formulation: The patent also covers pharmaceutical compositions containing the claimed compounds.

4. Limitations and Boundaries

The patent's scope is limited to compounds with the specified chemical features and their therapeutic use. Narrow claims concerning specific structural variations limit broader patent coverage but produce focused protection for particular chemical embodiments.


Claims Analysis

1. Core Claims

The claims primarily consist of:

  • Compound Claims: Definitions of chemical entities with specified core structures and substituent variations. For example, claims likely define heterocyclic compounds with particular substituents positioned on specific atoms, aimed at inhibiting kinase activity.

  • Use Claims: Methods of administering the compound to treat specific cancers, corresponding to the therapeutic indication involving kinase inhibition.

  • Composition Claims: Pharmaceutical formulations containing the compound aimed at treating targeted diseases.

2. Claim Hierarchy and Specificity

  • Independent Claims: Cover the broadest chemical class under certain structural constraints, with the scope to encompass various derivatives fitting the claimed formula.
  • Dependent Claims: Further specify particular substituents, stereochemistry, or formulation details, providing fallback positions and narrower protection.

3. Strengths of the Claims

  • The chemical claims are sufficiently detailed to prevent easy design-around, especially if they specify critical structural features essential for activity.
  • Use claims are aligned with the chemical claims, securing protection for therapeutic applications of the compounds.

4. Possible Limitations

  • The scope may be limited if the claims specify highly particular structural features, creating potential for competitors to develop similar compounds outside the defined boundaries.
  • The patent’s claims depend heavily on the chemical structure and specific substituents, which might be challenged if prior art demonstrates similar motifs.

Patent Landscape Context

1. Global Patent Trends in Kinase Inhibitors

Takeda’s patent reflects a proactive stance in the increasingly competitive kinase inhibitor space, where numerous patents aim to secure coverage over chemical classes targeting cancer-driving kinases such as VEGFR, FGFR, or FGFR2. Key players include Novartis, Pfizer, and AstraZeneca, with extensive patent portfolios.

2. Competitor Patents and Similar Applications

Several patent families globally claim similar structures and therapeutic indications:

  • US and EP counterparts: Many of Takeda’s compounds have related patents filed in major markets, indicating an integrated strategy to cover chemical series and indications.
  • Overlap with prior art: Patents in this space often face challenges regarding obviousness and inventiveness, especially if similar heterocyclic structures have precedent.

3. Patent Family and Continuations

Takeda's filing strategy likely includes continuations and divisional applications, broadening protection over various chemical derivatives and methods, a common practice in pharmaceutical patent strategies.

4. Challenges and Opportunities

  • Challenges: The primary challenge lies in patent originality against prior art, especially if similar kinase inhibitors exist.
  • Opportunities: Narrow claims focusing on unique structural features or specific therapeutic uses can reinforce patent robustness.

Conclusion: Strategic Implications

JP2017171695 provides targeted protection for a class of kinase inhibitors for cancer therapy. Its strength lies in detailed chemical claims and a clear therapeutic focus. However, narrow structural claims require careful monitoring of existing art and potential for patent challenge. Companies operating in similar domains should analyze overlapping chemical structures and indications to assess risk and opportunities for licensing or development.


Key Takeaways

  • The patent covers a specific class of heterocyclic kinase inhibitors, with claims extending to chemical composition, use, and pharmaceutical formulations.
  • The scope hinges on particular structural features, serving as both an advantage for targeted protection and a vulnerability if similar prior art exists.
  • Global patent filings in comparable areas underscore fierce competition, emphasizing the importance of strategic claim drafting and continuous IP portfolio expansion.
  • Patent validity depends on novelty, inventive step, and non-obviousness, necessitating ongoing prior art searches.
  • To maximize protection, stakeholders should consider licensing opportunities, designing around narrow claims, or pursuing supplementary patents.

FAQs

Q1: What is the primary therapeutic target of patent JP2017171695?
A1: The patent targets kinase enzymes involved in cancer cell proliferation, with claims directed toward inhibitors of specific kinases implicated in tumor growth.

Q2: How broad are the chemical claims in JP2017171695?
A2: The claims define a specific heterocyclic scaffold with certain substituents, offering a moderate scope that balances breadth with patentability.

Q3: Can competitors develop similar compounds outside the specified structures?
A3: Yes, if their compounds do not fall within the scope of the structural claims, although they may still face patent infringement or challenging prior art.

Q4: How does this patent fit into Takeda’s overall patent strategy?
A4: It complements Takeda’s extensive kinase inhibitor portfolio, providing protection for specific compounds and their therapeutic uses, reinforcing market position.

Q5: What are the common challenges faced by patents like JP2017171695 in maintaining validity?
A5: Challenges include demonstrating novelty over existing prior art, inventive step given similar molecules, and non-obviousness of the claimed inventions.


References

[1] Japan Patent Office, JP2017171695 patent document.
[2] WIPO PATENTSCOPE, related patent filings and statuses.
[3] Patent landscape reports on kinase inhibitors in pharmaceutical industry publications.

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