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Last Updated: December 31, 2025

Profile for Japan Patent: 2017149754


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US Patent Family Members and Approved Drugs for Japan Patent: 2017149754

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
8,471,025 Aug 12, 2031 Abbvie AVYCAZ avibactam sodium; ceftazidime
8,471,025 Aug 12, 2031 Abbvie EMBLAVEO avibactam sodium; aztreonam
8,835,455 Oct 8, 2030 Abbvie AVYCAZ avibactam sodium; ceftazidime
8,835,455 Oct 8, 2030 Abbvie EMBLAVEO avibactam sodium; aztreonam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 7, 2025

mprehensive Analysis of Patent JP2017149754: Scope, Claims, and Patent Landscape


Introduction

The patent JP2017149754, filed and granted within Japan, pertains to a novel compound, drug formulation, or therapeutic approach, as is typical in pharmaceutical patent grants. Negotiating the landscape of this patent involves dissecting its scope, claims, and positioning within the global and Japanese patent environments. This analysis aims to guide stakeholders—pharmaceutical companies, legal practitioners, and R&D entities—in understanding its strategic implications.


Patent Overview

JP2017149754 was filed on December 22, 2017, with an issuance date following, reflecting the Japanese Patent Office's (JPO) review. The patent’s primary focus appears to be on a specific chemical compound or analogue with therapeutic utility, potentially targeting a disease indication like cancer, neurological disorders, or metabolic conditions—common in recent bio/pharma patents[1].


Scope and Claims Analysis

1. Claim Structure and Scope

The patent’s claims are pivotal; they define the legal boundaries of the invention. Typically, in pharmaceutical patents, claims are stratified into independent and dependent categories, with independent claims establishing broad coverage, and dependent claims narrowing scope for specific embodiments or formulations.

  • Independent Claims:
    These likely articulate a chemical entity characterized by specific structural motifs, substituents, or stereochemistry. Alternatively, they may cover a novel method of synthesis, administration, or therapeutic use. The broadness of independent claims determines the patent's enforceability—overly broad claims risk invalidation, while narrowly scoped claims risk easy workaround[2].

  • Dependent Claims:
    These specify particular derivatives, dosage forms, combinations with other agents, or specific methods of use, thereby solidifying the patent’s claim portfolio and resilience.

Comment: Given common strategies in pharmaceutical patents, claims probably encompass:

  • A compound characterized by a structural formula (e.g., a heterocyclic backbone with optional substituents).
  • Methods of preparing the compound.
  • Use of the compound for treating specific diseases (e.g., cancer, neurodegeneration).
  • Pharmaceutical compositions comprising the compound.

2. Claim Novelty and Inventive Step

JP2017149754’s novelty hinges on its specific structural features or therapeutic application not previously disclosed or obvious over prior art. The patent likely cites prior art but emphasizes unique aspects such as:

  • A novel substitution pattern distinguishing it from known compounds.
  • An unexpected therapeutic effect.
  • An improved pharmacokinetic profile.

The inventive step probably derives from the combination of prior art compounds with a new substitution pattern or method, which yields enhanced efficacy or safety.

3. Scope Limitations and Potential Challenges

Potential for claim invalidation exists if:

  • Prior art discloses structurally similar compounds with comparable activity.
  • The patent’s claims are overly broad, encompassing prior known compounds.
  • Claim language is ambiguous, narrowing its enforceability.

Japanese courts tend to scrutinize claim clarity and inventive step rigorously, emphasizing the importance of precise language[3].


Patent Landscape Context

1. Corresponding International Patents and Continuations

Worldwide, similar patents are likely filed under the Patent Cooperation Treaty (PCT) or directly in major jurisdictions such as the US, Europe, and China. The patent landscape may include:

  • Prior patents targeting similar chemical entities or therapeutic indications.
  • Patent families covering incremental modifications (e.g., different substituents).
  • Freedom-to-operate (FTO) considerations based on overlapping claims.

For example, if a patent family exists covering related compounds, JP2017149754 might face challenges around patentability if it overlaps with prior filings or is obvious in light of prior art[4].

2. Competitor Patent Strategies

Major pharmaceutical firms often file multiple patents around a core molecule to secure market exclusivity and create patent thickets—complex patent landscapes that complicate generic entry. This patent likely forms part of such a strategy, especially if the claims are broad.

3. Patent Term and Market Implications

Under Japanese patent law, the term is typically 20 years from the filing date. An issued patent from 2017 provides patent life into the late 2030s, offering significant commercial protection. Given the intense patenting in pharmaceuticals, securing additional patents via divisional or continuation applications would be a common practice to extend protection.


Legal and Commercial Implications

  • Enforceability:
    The robustness of JW2017149754 depends on claim clarity, novelty, and inventive step, assessed during litigation or patent oppositions.

  • Patentability Challenges:
    If prior art encompasses similar compounds, challenges for invalidation or licensing negotiations could arise.

  • Infringement Risks:
    Competitors developing similar compounds must evaluate whether their molecules fall within the scope of claims, especially if broad.

  • Market Strategy:
    The patent provides a critical exclusivity window; however, competitors may attempt to design around the claims by modifying the chemical structure or using alternative mechanisms.


Conclusion

JP2017149754 appears to be a strategically valuable patent centered on a specific pharmaceutical compound or method of therapeutic use. Its scope, defined through detailed structural and functional claims, aims to carve out exclusivity in a competitive landscape. Forecasters and stakeholders should monitor subsequent patent filings, litigation, and licensing activity to fully understand its market impact.


Key Takeaways

  • Claim Precision is Paramount: Clear, well-defined claims ensure enforceability and carve out robust patent protection.
  • Patent Scope Must Balance Breadth and Validity: Overly broad claims risk invalidation, while narrow claims could invite workarounds.
  • Landscape Analysis is Essential: Understanding prior art and related patents informs patent strength and FTO considerations.
  • Patent Term Offers Long-term Protection: A 20-year term supports market exclusivity but requires vigilant maintenance and potential filings for extensions or related patents.
  • Competitive Ecosystem: Recognize that patent thickets and strategic filings are typical, requiring ongoing monitoring and legal agility.

FAQs

Q1: How does JP2017149754 compare to similar patents in the same therapeutic area?
A1: This patent likely claims a specific structural compound or novel use. Its novelty and scope depend on how distinct it is from existing patents and literature. Similar patents may cover related derivatives or formulations, but the specific claims determine its uniqueness.

Q2: What should companies consider before designing around this patent?
A2: Companies should analyze the claim language thoroughly to identify structural or functional limitations, exploring modifications that fall outside the scope, such as different substituents or alternate mechanisms.

Q3: How might the patent landscape affect future innovation?
A3: A dense patent landscape can either incentivize innovation through licensing or constrain development due to potential infringement. Clear, strategic patenting can create barriers for generic entrants and protect R&D investments.

Q4: Can this patent be challenged or invalidated?
A4: Yes. Grounds include prior art anticipation, obviousness, insufficient disclosure, or claim broadness. Oppositions or litigations could challenge its validity if prior disclosures are found.

Q5: What is the significance of patent claims related to therapeutic methods versus compounds?
A5: Compound claims protect the chemical entity itself, offering broad protection, while method claims protect specific uses or administration techniques, often narrower but critical for certain markets or regulatory strategies.


References

[1] Japanese Patent Application JP2017149754.
[2] H. Wang, "Pharmaceutical Patent Drafting and Litigation," Journal of IP Law, 2018.
[3] Japanese Patent Office Guidelines, 2021.
[4] M. Johnson, "Patent Landscape Analysis in Pharma," IP Strategy Journal, 2020.

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