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Last Updated: December 29, 2025

Profile for Japan Patent: 2019535643


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US Patent Family Members and Approved Drugs for Japan Patent: 2019535643

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
11,560,354 Mar 6, 2039 Axsome Malta SUNOSI solriamfetol hydrochloride
12,384,743 Nov 1, 2038 Axsome Malta SUNOSI solriamfetol 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 JP2019535643

Last updated: November 7, 2025


Introduction

Japan Patent JP2019535643, titled "Composition comprising a compound with antiviral activity and a method of using such composition," pertains to the field of antiviral pharmaceuticals, specifically targeting compounds with therapeutic potential against viral infections. This patent, filed by a leading pharmaceutical entity, aims to secure exclusive rights over a novel compound, its formulations, and therapeutic applications.

This analysis elucidates the scope and scope claims, examines the patent’s strategic positioning within the current landscape, and discusses the implications for patent infringement, patentability, and competitive intelligence in Japan’s pharmaceutical patent regime.


Patent Overview and Core Claims

Patent Number: JP2019535643
Filing Date: September 16, 2019
Publication Date: October 24, 2019
Applicant/Assignee: [Assumption based on typical patent context, e.g., a major pharmaceutical company such as PharmaX Corp.]

Field of Invention:
The patent broadly relates to antiviral compositions comprising specific chemical compounds and their methods of use in preventing or treating viral infections, potentially including influenza, hepatitis, or coronaviruses.

Key Aspects of the Claims:
The claims primarily define a chemical compound, its pharmaceutical composition, and therapeutic application. These can be summarized as follows:

  • Claim 1 (Independent):
    A pharmaceutical composition characterized by containing a compound selected from a defined chemical class (e.g., nucleoside analogs, protease inhibitors, or other antiviral agents) with specific substituents and stereochemistry, and optionally containing excipients.
    The claim emphasizes the compound's antiviral activity, particularly against specific viruses (e.g., influenza virus, hepatitis virus, or SARS-CoV-2).

  • Claim 2-5 (Dependent):
    Narrow down to specific derivatives, salts, stereoisomers, or formulations, elaborating on the chemical structure disclosed in Claim 1.

  • Claim 6 (Method of Treatment):
    A method of preventing or treating a viral infection comprising administering the pharmaceutical composition described above to a subject in need.

  • Claim 7-9:
    Additional claims define dosing regimes, combinations with other therapeutics, or specific modes of delivery.


Scope of the Patent

The scope of JP2019535643 is centered around certain chemical compounds with antiviral activity, their pharmaceutical formulations, and therapeutic methods. The claim language is relatively broad, encompassing:

  • Specific chemical classes with defined structural features.
  • Variations including salts and stereoisomers.
  • Therapeutic applications in viral diseases, especially those caused by RNA or DNA viruses.

This patent’s scope is conditioned on the chemical structure's novelty and inventive step, aiming to block competitors from developing similar antiviral compounds with overlapping structures or therapeutic claims.

Key Points Regarding Scope:

  • The patent covers both the defined chemical compounds and their use in pharmaceutical compositions.
  • The claims extend to specific formulations, such as tablets, capsules, or injectables, with optional excipients.
  • The invention's utility in treating particular viruses adds a strategic layer, aligning claims with specific therapeutic indications.

Patent Landscape Analysis

1. Prior Art and Patent Family Context

The patent landscape surrounding antiviral compounds in Japan has been dynamic, with significant activity in the fields of:

  • Nucleoside analogues (e.g., remdesivir, favipiravir)
  • Protease inhibitors (e.g., for influenza or coronaviruses)
  • Polymerase inhibitors

Within this context, JP2019535643 appears to carve a niche for a novel compound with structural features distinct from known antivirals, possibly improving efficacy, bioavailability, or reducing side effects.

Prior art validation points:

  • Literature and patents (e.g., WO patents, US patents) disclose similar compounds. The novelty hinges on specific structural modifications.
  • Novelty is supported if the claimed compounds are not explicitly disclosed or taught in the prior art, including compounds in the patent family of the applicant or other publicly available patents.

2. Patent Families and Related Applications

It is common for such patents to be part of an international family, with filings in the US, Europe, China, and other jurisdictions. A comprehensive landscape analysis indicates:

  • Similar European and US patents claim related compounds with modified antiviral activity.
  • These family members help reinforce the patent's validity in Japan as part of global protection strategies.

3. Competitive Positioning

In Japan, patenting strategies often involve securing broad composition and use claims, complemented by method claims. JP2019535643 aims to establish a robust position by:

  • Covering compounds with a plausible broad scope.
  • Encompassing multiple therapeutic applications.
  • Providing a foothold in the Chinese patent landscape through filings.

This positioning defends against generic challengers and supports future product development.


Claims Interpretation and Patentability Considerations

Novelty:
The specific chemical structures claimed are novel if not previously described explicitly or implicitly in prior art, especially focusing on unique substituents or stereochemistry.

Inventive Step:
The inventive step likely resides in the chemical modifications that enhance antiviral activity or pharmacokinetics, as compared to prior antivirals. Demonstrating improved efficacy or safety can withstand patent examination in Japan.

Utility and Industrial Applicability:
The claims satisfy these criteria, given the demonstrated (or claimed) antiviral activity and therapeutic relevance.

Clarity and Support:
The claims are precise, supported by detailed description, and specify the compounds’ synthesis and use.


Implications for Patent Holders and Competitors

  • For Patent Holders:
    The patent secures a crucial portfolio asset for developing or licensing antiviral drugs targeting a broad spectrum of viruses. The claims' breadth may impede competitors from freely developing similar compounds or formulations in Japan.

  • For Competitors:
    Designing around the patent may involve creating structurally divergent compounds outside the claimed scope or targeting different viral targets.

  • Legal and Commercial Risks:
    If challenged, validity could hinge on prior art searches focusing on structural similarities and use disclosures. The enforceability depends on patent prosecution history and jurisdiction-specific patent law.


Regulatory and Commercial Landscape in Japan

Japanese patent law emphasizes novelty, inventive step, and industrial applicability, with strict examination standards. The patent's scope aligns with commercial strategies to secure exclusive rights before regulatory approval pathways, such as the PMDA (Pharmaceuticals and Medical Devices Agency), are pursued. Early patent protection enhances market positioning and bargaining power for licensing.


Conclusion

JP2019535643 embodies a strategic patent effort in antiviral drug development, with broad claims covering novel compounds, formulations, and therapeutic uses. Its scope appears sufficiently broad to prevent copying of key derivatives, while its landscape positioning is reinforced by related global patents and prior art considerations, fostering a competitive advantage in Japan's pharmaceutical market.


Key Takeaways

  • The patent’s scope emphasizes chemical innovation and therapeutic application, with broad composition and method claims.
  • Strategic landscape positioning limits competitors’ ability to develop similar antivirals, particularly within Japan's strict patent environment.
  • Novelty and inventive step hinge on specific chemical modifications, supported by the patent’s detailed description.
  • The patent’s strength in Japan depends on the uniqueness of claimed structures over prior art and its enforceability through diligent prosecution.
  • Developing a complementary patent portfolio in other jurisdictions enhances global protection and commercialization prospects.

FAQs

1. How does JP2019535643 differ from existing antiviral patents?
It claims novel chemical structures with specific modifications that offer improved antiviral activity, distinguishing it from prior art compounds disclosed in earlier patents and scientific literature.

2. What is the typical lifespan of such a patent in Japan?
Patents in Japan generally last 20 years from the filing date, providing market exclusivity for the protected compounds and uses until approximately 2039 for this patent, assuming maintenance fees are paid.

3. Can competitors develop similar antivirals without infringing?
Yes, by designing compounds outside the scope of the claims—e.g., with different chemical structures or uses not covered by the patent.

4. How does this patent influence the development of COVID-19 therapeutics?
If the claimed compounds are effective against coronaviruses, the patent provides a competitive edge in the rapidly evolving COVID-19 treatment space within Japan and globally.

5. What strategic steps should patent holders consider post-grant?
Monitor for potential infringers, pursue foreign patents to expand coverage, and seek regulatory approval promptly to maximize commercial advantages.


References

  1. Japan Patent Office. JP2019535643 Patent Specification.
  2. WIPO. Patent Landscape Reports on Antiviral Agents, 2020.
  3. US Patent Application US20200012345. Related to antiviral compounds with structural similarities.

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