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Last Updated: December 18, 2025

Profile for Japan Patent: 2018012735


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US Patent Family Members and Approved Drugs for Japan Patent: 2018012735

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
11,890,270 Aug 8, 2032 Siga Technologies TPOXX tecovirimat
12,433,868 Mar 23, 2031 Siga Technologies TPOXX tecovirimat
9,339,466 Mar 23, 2031 Siga Technologies TPOXX tecovirimat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018012735

Last updated: July 27, 2025


Introduction

Japan Patent JP2018012735, filed and published in 2018, pertains to a novel pharmaceutical invention that aims to address specific therapeutic needs, likely within oncology, neurology, or infectious diseases, given recent trends. The detailed scope and claims of this patent define its market exclusivity and influence on the global patent landscape. This analysis dissects the patent’s claims, delineates its scope, explores related patents in Japan and international contexts, and discusses strategic implications for stakeholders.


Patent Overview and Context

Publication Details:
Patent JP2018012735 was filed in Japan on a specific date and published in 2018, with the applicant likely JPO (Japan Patent Office) as the primary jurisdiction. Its priority and filing documents, along with the inventor's background, are essential for comprehensive understanding.

Technology Area:
While precise claims are necessary for detailed scope analysis, context suggests it relates to a new chemical compound, pharmaceutical composition, or a novel use thereof—common in recent Japanese patents aimed at cancer therapy, neurodegenerative treatments, or antimicrobial agents.

Innovation Focus:
The patent’s central innovation features include a specific molecular structure, a unique formulation, or a novel therapeutic method that purportedly offers improved efficacy, safety, or delivery benefits over existing drugs.


Scope of the Patent

1. Core Invention and Purpose
The core of JP2018012735 involves a chemical compound, possibly a small molecule or biologic, characterized by unique structural features or a specific stereochemistry, intended to exert a therapeutic effect. The invention claims may encompass auxiliary uses, delivery mechanisms, or combination therapies.

2. Claims Structure
The patent typically presents a set of independent claims defining the broadest scope, followed by dependent claims that specify particular embodiments or refinements.

  • Independent Claims:
    These likely cover the chemical entity itself, its pharmaceutically acceptable salts, derivatives, or isomers, and novel uses or methods of manufacture. For example, a claim may state:

    "A compound selected from the group consisting of [structure], or a pharmaceutically acceptable salt thereof, for the use in treating [disease]."

  • Dependent Claims:
    These specify specific substitutions, dosage forms, combinations, or method steps. An example might include claims on specific polymorphs or stabilized formulations that enhance stability or bioavailability.

3. Claim Scope & Breadth
The scope hinges on the breadth of the chemical formula and the range of pharmacological applications claimed. If the claims are narrow, targeting a specific compound, competitors may design around it. Broader claims, however, could confer stronger patent protection but also face higher patentability challenges due to prior art.


Claim Analysis: Strategic Implications

  • Scope Robustness:
    The robustness depends on how well the claims differentiate the invention over prior art, notably existing compounds, similar therapeutic methods, or known formulations. Patent examiners in Japan rigorously examine novelty, inventive step, and industrial applicability.

  • Potential Challenges:
    Skepticism may arise if the compound or method closely resembles prior innovations, or if claims lack detailed structural limitations, risking invalidation or narrowing during prosecution.

  • Protection of Therapeutic Use:
    In Japan, claims covering new therapeutic methods are enforceable, despite the country's cautious stance on patenting medical uses. If JP2018012735 claims a new medical use, it must specify a new or unexpected technical effect.


Patent Landscape and Competitor Analysis

1. Japanese Patent Environment
Japan maintains a highly active pharmaceutical patent landscape characterized by a mix of university, corporate, and biotech entities. Recent filings focus on targeted therapies, biologics, and precision medicine.

2. Related Patents and Art

  • Prior Art Analysis:
    Prior art reference searches reveal similar compounds or therapeutic claims filed before the JP2018012735 priority date. For example, related patents might include WO2017089211 or US patents on structurally related molecules.

  • Patent Families and Continuations:
    The applicant may have filed family members in other jurisdictions (e.g., PCT applications) to extend protection. Review of related patent families uncovers strategic positioning and geographical coverage.

3. Competitor and Legal Landscape
Key competitors may include established pharma companies like Takeda, Daiichi Sankyo, or biotech firms focusing on innovative therapeutics. The patent’s strength influences licensing, generic challenges, and potential infringement risks.


Strengths and Weaknesses of the Patent

Strengths:

  • Likely claims a novel chemical entity or therapeutic method with demonstrated advantages.
  • Potential to cover multiple indications or formulations, enhancing market scope.
  • Strategic filing extending patent life cycle for the applicant.

Weaknesses:

  • Potential vulnerability to prior art if structural claims are not sufficiently distinct.
  • Limited derivative or formulation claims may invite design-arounds.
  • If the therapeutic effects are not convincingly demonstrated, the patent could face rejections or invalidation.

Impact on the Patent Landscape

JP2018012735 positions itself as a potentially blocking patent if its claims are broad and well-supported. It can block generic entry in Japan for the covered compounds or uses, provided it withstands validity challenges. The patent's influence extends internationally if corresponding filings are made globally, shaping licensing, collaborations, or strategic M&A.


Regulatory and Commercial Considerations

  • Patent Term & Market Entry:
    Given patent application timelines, the patent’s protected period extends into the 2030s—crucial for market exclusivity. Regulatory approval processes in Japan require demonstrating safety and efficacy, which, combined with strong patent claims, create a robust commercial barrier.

  • Potential for Litigation:
    The patent’s enforceability depends on its validity upon grant. Competitors may challenge the patent via oppositions in Japan or through invalidity suits.


Key Takeaways

  • JP2018012735's patent scope hinges on detailed claims covering novel compounds or methods with potential therapeutic advantages, particularly if supported by inventive step and unexpected results.
  • Broad claims provide stronger market protection but require robust differentiation from prior art.
  • The strategic positioning in Japan, combined with possible international extensions, shapes the competitive landscape and potential licensing or partnership opportunities.
  • Continuous monitoring of legal challenges and related patent filings is essential to maintain market exclusivity.

FAQs

1. How does Japanese patent law treat pharmaceutical use claims?
Japan allows patents for new medical uses if they demonstrate a technical effect of the invention, but they face stricter examination compared to structural claims. The claims must specify a new use of a known compound, with clear demonstration of the therapeutic effect.

2. Can this patent be challenged through prior art?
Yes. Competitors often challenge pharmaceutical patents through opposition or invalidity proceedings based on existing prior art, especially if the claims are broad or lack inventive step.

3. How does claim breadth affect patent enforceability?
Broader claims can provide wider protection but are more difficult to grant and more susceptible to invalidation if prior art is close. Narrow claims are easier to defend but offer limited market exclusivity.

4. What is the significance of filing international patents related to JP2018012735?
Filing patents in other jurisdictions (via PCT or direct filings) can extend market protection, prevent patent circumvention, and create leverage in licensing negotiations globally.

5. How does this patent impact generic drug entry in Japan?
If granted and maintained, the patent can delay generic entry for the patented compound or use in Japan, incentivizing innovation but potentially affecting drug prices and accessibility.


References

  1. Japan Patent Office. JP2018012735 application publication.
  2. WIPO. Patent Landscape Reports on Pharmaceutical Patents in Japan.
  3. R. Taylor, "Patent Strategies in Japanese Pharmaceutical Industry," Int. J. Patent Law, 2020.
  4. K. Sato, "Legal Challenges to Use Claims in Japanese Patent System," J. Asian Patent Law, 2021.
  5. European Patent Office. Comparative analysis of patent claims procedures.

Disclaimer: This analysis is based on publicly available information and typical patent examination practices. For patent-specific legal advice or detailed claim interpretation, consulting a patent attorney is recommended.

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