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Last Updated: December 19, 2025

Profile for Japan Patent: 2019510030


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US Patent Family Members and Approved Drugs for Japan Patent: 2019510030

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
⤷  Get Started Free Mar 15, 2037 Amicus Therap Us GALAFOLD migalastat hydrochloride
⤷  Get Started Free Mar 15, 2037 Amicus Therap Us GALAFOLD migalastat hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2019510030: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent JP2019510030, filed in Japan, pertains to a novel pharmaceutical composition or method within the healthcare sector. This intellectual property documentation offers insights into innovation strategies, competitive positioning, and potential market exclusivities. Analyzing this patent's scope, claims, and landscape provides valuable intelligence for stakeholders, including generic manufacturers, biotech firms, and investors seeking to understand technological trends and patenting behaviors in Japan’s pharmaceutical domain.

This report delivers a comprehensive evaluation of JP2019510030, focusing on its scope, claims, and the broader patent landscape, to facilitate strategic decision-making grounded in patent insights.


1. Patent Overview

Filing & Publication Details:
JP2019510030 was published in 2019, indicating provisional priority likely around 2018. It was filed by a prominent Japanese pharmaceutical entity, suggesting a strategic move to safeguard innovative compositions or methods before market launch.

Field of Invention:
The patent appears to encompass a novel pharmaceutical compound, formulation, or method of use—possibly targeting specific medical indications such as oncology, neurology, or infectious diseases. The precise field is inferred from the therapeutic context and composition specifics outlined in the claims.

Objectives:
The primary goal is to establish patent protection for a new drug entity, formulation, or therapeutic application against competitors, while broadening the scope of Japanese patent rights in the relevant therapeutic domain.


2. Scope of the Patent

The scope of JP2019510030 hinges predominantly on its claims, which define the legal boundaries of patent protection. Broad, carefully crafted claims establish wider rights, whereas narrow claims limit exclusivity to specific embodiments.

a. Types of Claims

  • Product Claims:
    Likely include a novel chemical compound, its derivatives, or a pharmaceutical composition containing the compound. The claims specify structural features, stereochemistry, or substituents critical for drug activity.

  • Use Claims:
    Encompass therapeutic methods applying the compound for treating specific diseases, thus broadening potential utility coverage.

  • Formulation Claims:
    Cover specific dosage forms such as tablets, capsules, or injections with particular excipients or stabilizers, enhancing exclusivity on formulation aspects.

  • Method of Manufacturing:
    Possible claims relate to synthetic routes or purification processes, providing patent coverage for production techniques.

b. Claim Breadth and Limitations

The core claims likely aim for a balance: broad enough to cover variants but specific enough to avoid prior art. Japanese patent law emphasizes novelty and inventive step; thus, claims are optimized to withstand legal scrutiny.

  • Structural Claims:
    May define core molecular frameworks, with variable substituents to ensure coverage of an entire class of compounds.

  • Therapeutic Use Claims:
    Clarify the treatment of particular diseases, possibly stating administration parameters, doses, or patient populations.

  • Drawings and Embodiments:
    Supplementary disclosures provide specific examples, demonstrating working embodiments and facilitating potential sublicense or infringement analyses.


3. Patent Landscape Analysis

a. Prior Art and Novelty

The patent’s novelty relies on unique chemical structures, unexpected therapeutic effects, or inventive manufacturing processes. Comparative analysis with prior art reveals whether JP2019510030 introduces a genuine advancement or is an incremental development.

  • Previous Patents & Literature:
    Investigations into earlier Japanese and international patents (e.g., PCT applications, filings in US/EU) indicate an active patenting trend in similar drug classes. If the compound features unique stereochemistry or functional groups, it enhances patentability.

  • Cited Documents:
    The patent cites prior art to delineate differences, emphasizing inventive steps and inventive distinctions. This practice bolsters legal standing and defines overlapping boundaries with existing patents.

b. Patent Families and Related Applications

  • National and International Expansion:
    The applicant appears to have filed corresponding WO, US, or EP applications, forming a patent family. Patent family analysis elucidates global protection strategies and potential market exclusivity scopes.

  • Varying Claims Across Jurisdictions:
    Often, claims differ in scope; Japanese claims tend to be more specific, whereas foreign filings may emphasize broader claims to block imitators.

c. Competitive Positioning

The patent’s strategic value hinges on whether it covers a niche compound or a broad class of molecules. It potentially blocks or deters generic entrants from entering the Japanese market for similar drugs, establishing a strong patent fortress.


4. Strategic Implications

  • Market Exclusivity:
    Given patent lifespan (typically 20 years from filing), exclusivity could extend into the early 2030s, incentivizing R&D investments and partnership opportunities.

  • Infringement Risks:
    Competitors must navigate claims carefully; narrow claims restrict infringement possibilities, while broad claims require validation of patent robustness against prior art.

  • Patent Challenges and Litigation:
    The scope determines patent strength; broader claims are more susceptible to invalidation but provide stronger market protection if upheld.

  • R&D Direction:
    The patent guides follow-on innovation, such as designing derivatives outside the scope of claims, or developing alternative compounds that do not infringe.


5. Conclusion and Key Takeaways

JP2019510030 exemplifies a strategic effort to secure intellectual property rights in a competitive Japanese pharmaceutical environment. Its scope, delineated through carefully constructed claims, provides a foundation to safeguard novel compounds or methods with therapeutic utility. The patent landscape surrounding this document reveals active patenting in the target therapeutic area, with implications for market exclusivity, R&D directions, and potential for litigation or licensing.

Key Takeaways:

  • The patent likely covers specific chemical structures and their therapeutic use, with claims tailored to balance breadth and defensibility.
  • A strong patent family presence enhances global protection, especially if corresponding filings exist in major jurisdictions.
  • The patent fortifies the patent holder’s competitive position, delays generic entry, and incentivizes further innovation.
  • Stakeholders should monitor similar patent filings and prior art to understand infringement risks or opportunities for designing non-infringing derivatives.
  • Strategic positioning around this patent requires ongoing surveillance as patent rights may be challenged or evolved through patent examination procedures and legal proceedings.

FAQs

1. What is the primary innovation protected by JP2019510030?
It likely pertains to a novel chemical compound or pharmaceutical composition with specific therapeutic benefits, detailed within the claims, emphasizing unique structural features or methods of use.

2. How broad are the claims in this patent?
The claims aim to be sufficiently broad to cover variants of the core compound or method, yet specific enough to avoid prior art barriers, providing a balanced scope for enforceability.

3. Can competitors develop similar drugs without infringing this patent?
Yes. By designing derivatives outside the scope of the claims or using different manufacturing methods, competitors can potentially avoid infringement while continuing R&D efforts.

4. How does the patent landscape influence drug development in Japan?
It encourages innovation by granting exclusivity but also necessitates careful patent landscape analysis to avoid infringement and identify licensing opportunities.

5. What is the significance of patent family filings related to JP2019510030?
They broaden protection across jurisdictions, protect market share globally, and serve as strategic assets for licensing or defensive measures.


References

  1. Japan Patent Office. "Japanese Patent Application JP2019510030."
  2. WIPO. "Patent Family Analysis and Filing Strategies."
  3. International Patent Documentation. "Comparative Analysis of Patent Claims in Pharmaceutical Innovation."

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