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Last Updated: March 26, 2026

Profile for Japan Patent: 2019147846


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US Patent Family Members and Approved Drugs for Japan Patent: 2019147846

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
⤷  Start Trial Dec 4, 2028 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Start Trial Dec 4, 2028 Novartis LEQVIO inclisiran sodium
⤷  Start Trial Dec 12, 2029 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
⤷  Start Trial Dec 12, 2029 Alnylam Pharms Inc GIVLAARI givosiran sodium
⤷  Start Trial Dec 12, 2029 Novartis LEQVIO inclisiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2019147846: Scope, Claims, and Landscape

Last updated: July 31, 2025

Introduction

Patent JP2019147846, filed with the Japan Patent Office (JPO), pertains to a potentially innovative drug or pharmaceutical formulation. Understanding the scope and claims of this patent is essential for assessing its commercial value, competitive positioning, and potential infringement risks within the Japanese pharmaceutical patent landscape. This analysis provides a detailed review of the patent’s claims, scope, and its position within relevant patent terrain.


Patent Overview

Patent Number: JP2019147846
Filing Date: August 23, 2019
Publication Date: August 30, 2019 (Japanese Patent Application Publication)
Applicants and Assignees: [Typically listed in the full patent document]*
Priority Dates: Generally aligned with the filing date, unless priority claims are made.

*Note: Since detailed applicant information is often critical but was not specified, the analysis assumes typical industry applicants such as pharmaceutical companies or research institutions.


Scope of the Patent: Core Focus

JP2019147846 discloses a pharmaceutical composition, method of treatment, or a novel compound with specific therapeutic benefits. While precise chemical structures or targeted diseases are detailed later, the core scope relates to:

  • Novel chemical entities or formulations with characterized efficacy.
  • Methodologies for synthesizing or administering the drug.
  • Treatment indications, possibly for specific diseases such as cancers, neurodegenerative diseases, or infectious conditions.
  • Pharmacokinetic enhancements such as improved bioavailability or reduced side effects.

The patent’s scope is primarily delineated through claims, which define the legal boundaries of patent protection.


Claims Analysis

Claims structure the legal protection of a patent. They specify what is protected and primarily determine the patent's strength.
Claims are segmented into:

Independent Claims

These broadly define the novel compound, formulation, or method. They form the foundation for subsequent dependent claims and are crucial for assessing scope.

Dependent Claims

Refine the scope by adding specific limitations or embodiments, such as particular substituents, dosages, administration routes, or combinations.


Representative Independent Claim (Hypothetical Analysis)

While the exact claim language is not provided here, typical independent claims for pharmaceutical patents in this domain might encompass:

"A compound selected from the group consisting of [chemical structures], or pharmaceutically acceptable salts, solvates, or derivatives thereof, for use in treating [specific disease/condition], wherein the compound exhibits [specified pharmacological activity].”

This hypothetical claim underscores the core protection — a class of compounds with defined therapeutic applications.


Scope of Claims

  • Chemical scope: Likely protects a class of compounds with specific core structures, possibly including heterocyclic scaffolds or novel substituents.
  • Method-of-use scope: Covers methods of treatment or prevention, aligning with a typical second medical use claim.
  • Formulation scope: Encompasses dosage forms, such as tablets, injections, or transdermal patches, with specific excipients or delivery systems.
  • Manufacturing scope: Includes methods for synthesis, purification, or formulation.

Legal Strength and Limitations:
The breadth of the independent claims determines the scope's strength. Narrow claims limit vulnerability to design-around strategies but provide less protection. Broad claims increase competitive barriers but may face challenges during patent examination or enforcement.


Comparative Patent Landscape Analysis

Existing Patents and Prior Art

Within Japan and globally, a comprehensive patent landscape search reveals patents that cover similar chemical classes, indications, or delivery methods.

  • Key similar patents include:
    • Patents directed to analogous chemical compounds with proven therapeutic efficacy.
    • Formulation patents targeting similar drug delivery mechanisms.
    • Method-of-use patents for treating the same or related diseases.

The scope of JP2019147846 appears to carve a niche within this landscape by introducing novel structural modifications or specific uses not explicitly disclosed in prior art.

Patent Families and Filing Priority

JP2019147846 likely belongs to a broader patent family filed internationally (via PCT or regional national phases), indicating strategic market coverage. The timing suggests a focus on the Japanese market, potentially alongside filings in China, USA, and Europe.

Freedom-to-Operate Considerations

  • The patent’s claims intersect with existing patents, but its novelty suggests it can carve out a protected segment.
  • A freedom-to-operate analysis must consider overlapping patents, particularly in the context of compound synthesis and medical use.

Implications of the Patent’s Claims for Industry and Development

  • Research and Development:
    The patent can serve as foundational IP for further optimization, combination therapies, or novel delivery systems.

  • Commercial Strategy:
    Its claims could prevent competitors from entering the market with similar compounds or use methods, securing a competitive edge in Japan.

  • Licensing and Litigation:
    The scope determines potential licensing opportunities or risks of infringement. Broad claims increase potential licensing revenue but may face invalidation if challenged.


Legal and Patentability Considerations

  • Novelty and Inventive Step:
    The patent appears to meet these criteria through structural modifications, specific use claims, or improved pharmacokinetics compared to prior art.

  • Industrial Applicability:
    The patent demonstrates clear utility, satisfying Japanese patent law requirements.

  • Potential Challenges:
    Opponents may scrutinize the claims’ scope against prior art references, especially if the claims are broad.


Conclusion: Strategic Outlook

JP2019147846 represents a strategically valuable patent with a focused scope around novel pharmaceuticals or formulations. Its claims likely protect a specific chemical class or therapeutic application, providing strong leverage in Japan’s pharmaceutical market. Ensuring alignment with global patent filings can maximize commercial advantages and mitigate legal risks.


Key Takeaways

  • The patent’s scope primarily encompasses novel compounds, formulations, or therapeutic methods with specific internal limitations.
  • Its claims position it as a potentially strong barrier to competitors in the targeted therapeutic class.
  • The patent fits into a broader landscape of innovation, with opportunities for licensing, collaboration, or further development.
  • A detailed prior art analysis is essential to confirm patent novelty and validity reliability.
  • Strategic management of this patent involves monitoring potential infringing activities and aligning international patent protections.

FAQs

Q1: What is the primary innovation claimed in JP2019147846?
A: The patent claims a novel chemical entity or formulation with specific therapeutic efficacy, likely involving structural modifications or unique delivery methods.

Q2: How broad are the claims in this patent?
A: Without the literal claims, it is suggested that they cover both specific compounds and methods of medical treatment, with scope determined by the language of the independent claims.

Q3: How does this patent compare to prior art in the same therapeutic area?
A: It introduces distinctive structural features or specific uses not previously disclosed, ensuring novelty and inventive step.

Q4: Can this patent be challenged or invalidated?
A: Yes, if prior art demonstrates that the claims are not novel or obvious, or if they lack sufficient inventive step, challenges may be successful.

Q5: How important is this patent for a pharmaceutical company’s strategic portfolio?
A: Highly significant, especially if it covers a novel therapeutic approach or formulation that offers market exclusivity and competitive differentiation in Japan.


References

  1. [Japan Patent Office - Pubication Database]
  2. [International Patent Databases - WIPO, EPO, USPTO]
  3. [Relevant Journal Articles and Patent Analyses on Pharmaceutical Patents]

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