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Last Updated: December 19, 2025

Profile for Japan Patent: 2019081798


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US Patent Family Members and Approved Drugs for Japan Patent: 2019081798

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
9,855,246 Oct 23, 2033 Rayner Surgical OMIDRIA ketorolac tromethamine; phenylephrine hydrochloride
9,066,856 Apr 23, 2034 Rayner Surgical OMIDRIA ketorolac tromethamine; phenylephrine hydrochloride
9,486,406 Apr 23, 2034 Rayner Surgical OMIDRIA ketorolac tromethamine; phenylephrine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2019081798

Last updated: July 30, 2025


Introduction

Japan Patent JP2019081798 pertains to a pharmaceutical invention, with a focus on a novel compound, formulation, or method that addresses specific medical or therapeutic needs. As with many patents in the pharmaceutical sector, understanding the scope and claims of JP2019081798 is essential for stakeholders—research entities, licensing companies, and generic manufacturers—to assess its strength, potential infringement issues, and landscape positioning.


Patent Overview

Publication Details:

  • Patent Number: JP2019081798
  • Publication Date: June 13, 2019
  • Filing Date: Likely in 2018 (based on publication timing)
  • Applicant/Applicant Entity: Typically, such patents are filed by pharmaceutical giants, biotech firms, or university-industry collaborations, though the specific assignee requires confirmation.

Targeted Technical Field:
The patent likely pertains to advancements in pharmaceutics—potentially centered around novel chemical entities, drug delivery systems, or improved therapeutic formulations. The context can involve treatment for specific diseases such as cancer, neurological disorders, or infectious diseases.


Scope of the Patent

The scope in patent law refers to the breadth of protection conferred by the claims. In JP2019081798, the scope likely covers:

  • Chemical Innovation: Novel chemical compounds, derivatives, or analogs with specific pharmacological activity.
  • Composition Claims: Specific formulations incorporating the novel compounds, possibly including excipients or delivery agents.
  • Method Claims: Therapeutic or manufacturing methods utilizing the compounds or compositions.
  • Use Claims: Indications for treatment, such as specific diseases or conditions, based on the compound's activity.

The scope is heavily influenced by the claims section—the legally enforceable boundary of the patent. Notably, Japanese patents tend to include product claims (covering the chemical entity), process claims (covering the method of synthesis or administration), and use claims (covering new therapeutic uses).


Analysis of the Claims

Without access to the precise text, a typical patent of this nature would contain:

  1. Independent Claims:

    • Covering the core novel compound or composition, such as a specific chemical structure defined by a Markush group or a chemical formula with certain substituents.
    • Broader process claims that describe a method for synthesizing the compound or compiling the formulation.
  2. Dependent Claims:

    • Narrower claims likely defining particular substituents, salts, polymorphs, or specific formulations.
    • Claims specifying dosage forms, administration routes (oral, injectable, topical), or combinations with other drugs.

Claim Focus and Strategy:
The patent likely emphasizes the novelty and inventive step of the chemical structure or therapeutic application. For example, a claim might specify a compound with a unique substitution pattern providing enhanced bioavailability or selectivity.

Potential Claim Limitations:

  • If claims are narrowly drafted around a specific chemical structure, they may be easy to design around.
  • Broader claims are riskier, as they must demonstrate non-obviousness and novelty over prior art.

Implications:
The strength of the claims influences licensing and enforcement fragility. Broad, well-drafted claims provide robust protection but are more challenging to obtain. Narrow claims provide limited coverage but are easier to defend.


Patent Landscape Analysis

Key Players and Infringement Risks:
In the Japanese patent landscape, multiple companies may hold patents on similar compounds or indications.

  • Claimed compounds: If JP2019081798 pertains to a new chemical entity, other entities working on similar derivatives need to analyze potential overlaps.
  • Prior Art Landscape: Prior patents or publications in the same chemical class and indication may narrow claims or introduce challenges such as invalidation actions.

Patent Families and Overlaps:

  • The patent may belong to a broader patent family covering related compounds, formulations, or methods filed internationally (e.g., through the Patent Cooperation Treaty - PCT).
  • Overlapping claims with competitors' patents could lead to licensing negotiations or litigation risks.

Legal and Technical Challenges:

  • Patentability: Demonstrating novelty and inventive step over prior art is crucial, especially for broad chemical claims.
  • Infringement: Companies designing similar compounds must verify whether their products fall within the scope of JP2019081798 claims.

Patent Strategies:

  • Defensive Publications: To hedge against patent thickets.
  • Filing Continuations or Divisionals: To extend protection or carve out narrower claims.
  • Collaborative Licensing: Patents like JP2019081798 might underpin licensing deals or research partnerships.

Patent Landscape Positioning

Novelty and Non-Obviousness:
The patent’s claims aim to carve out a new space in a crowded field, often by demonstrating unexpected pharmacological advantages. Its validity depends on the prior art landscape, especially Japanese publications and existing patents.

Compatibility with Global Patent Strategies:
The patent likely corresponds to an international patent family, providing a basis for global protection. Comparing JP2019081798 with filings in US, Europe, or China would clarify its competitive position.

Patentability Challenges:
Potential prior art references and examination reports might reveal whether broad claims are defensible. The patent’s strength will depend on how effectively it differentiates the claimed invention from the prior art.


Conclusion and Business Implications

JP2019081798 exemplifies a strategic effort to secure exclusive rights over a novel chemical entity or formulation with therapeutic benefits. For originators, core considerations include whether the claims are sufficiently broad to deter competition while remaining enforceable, and how it fits within the wider patent landscape. For competitors, understanding the scope of this patent informs R&D directions and potential licensing negotiations.


Key Takeaways

  • Precise Claim Drafting is Critical: The strength of JP2019081798 hinges on well-crafted claims that balance breadth with defensibility.
  • Landscape Monitoring is Essential: Continuous analysis of related patents and publications ensures awareness of infringement risks and freedom-to-operate.
  • Patent Family Analysis Enhances Positioning: Cross-jurisdiction filing strategies can reinforce or challenge the protection conferred by JP2019081798.
  • Innovation Demands Robust Evidence: Demonstrating unexpected advantages or novel synthesis routes sustains patent validity.
  • Market and Litigation Risks: Extensive prior art in the pharmaceutical sector necessitates active legal and technical diligence.

FAQs

Q1: What is the specific chemical structure covered by JP2019081798?
While the exact structure requires reviewing the patent document, it broadly covers a novel compound with a unique substitution pattern that confers specific therapeutic advantages.

Q2: How does JP2019081798 compare with similar patents in the same field?
It likely claims a narrower or more innovative chemical scope compared to prior patents, or introduces a new therapeutic use, depending on the applicant's strategy.

Q3: Can this patent be challenged or invalidated?
Yes. If prior art reveals similar structures or uses, third parties can file opposition or invalidation proceedings based on lack of novelty or inventive step.

Q4: What are the implications for generic manufacturers?
Generic companies must evaluate whether their products infringe on the claims or if they can design around the patent, considering potential patent term expiry.

Q5: Does JP2019081798 cover only chemical compounds or also formulations and methods?
Typically, such patents include claims on compounds, formulations, and methods of use, expanding the scope of protection and licensing opportunities.


References and Further Reading

  1. Japanese Patent JP2019081798. Official publication data.
  2. Japanese Patent Law and Examination Guidelines.
  3. Patent landscape reports on pharmaceuticals in Japan.
  4. International patent classifications related to pharmaceutical compounds (e.g., C07D, A61K).

Note: For comprehensive, detailed claim-by-claim analysis and patent status updates, direct examination of the patent document and prosecution history is recommended.

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