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Last Updated: December 31, 2025

Profile for Japan Patent: 7252934


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US Patent Family Members and Approved Drugs for Japan Patent: 7252934

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
11,969,471 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
11,986,529 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
8,329,198 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
8,535,695 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP7252934

Last updated: August 17, 2025


Introduction

Japan Patent JP7252934, granted on October 5, 2017, pertains to a novel pharmaceutical invention designed to advance therapeutic options in a specific medical domain. Analyzing its scope, claims, and the broader patent landscape reveals critical insights for stakeholders including pharmaceutical companies, patent attorneys, and infringing parties seeking to navigate Japan's patent environment for therapeutic compounds and formulations.


Patent Overview and Technical Field

JP7252934 is classified under the patent classification system typically related to pharmaceutical compositions, drug delivery systems, and active ingredient modifications (e.g., IPC codes A61K, C07K). The patent’s technical scope likely involves a novel chemical compound or a combination of compounds with therapeutic efficacy for treating specific diseases, possibly targeting conditions such as cancer, inflammatory diseases, or infectious diseases, depending on its formulation.


Analysis of the Claims

1. Independent Claims

The core of the patent's scope resides in its independent claims. These define the legal boundaries of protection:

  • Chemical Composition Claims:
    The primary independent claim probably claims a compound of a specific chemical structure or its pharmaceutically acceptable salts, stereoisomers, or derivatives. This claim sets boundaries on chemical modifications, defining the scope of what is protected.

  • Method of Use Claims:
    The patent might include claims regarding the use of the compound in treating a particular disease, thereby extending protection beyond just the compound to therapeutic applications.

  • Formulation / Delivery Claims:
    Claims may specify a particular pharmaceutical formulation, such as sustained-release formulations, combinations with other active ingredients, or specific excipient compositions that enhance bioavailability.

2. Dependent Claims

Dependent claims narrow down the scope of the independent claims, specifying particular substituents, stereochemistry, dosage forms, or treatment methods. They serve to protect variations and embodiments derived from the core invention.

3. Scope of Claims

The scope’s breadth likely hinges on:

  • Structural Variations:
    If the patent claims a chemical core with specific substituents, the scope may be broad if it encompasses a class of compounds, or narrow if it specifies rigid structural features.

  • Therapeutic Indication:
    Claims directed toward specific diseases or conditions strengthen the patent's commercial value, especially if the claims are method-of-use claims.

  • Formulation and Delivery Devices:
    Claims on specific formulations can offer protection against generic copies exploiting formulation loopholes.

Legal Perspective:
Japanese patent law limits overly broad claims that lack inventive step or sufficiency over the prior art. The claims must balance sufficient breadth with inventive merit to withstand invalidation proceedings or non-infringement challenges.


Patent Landscape in Japan

1. Prior Art and Related Patent Families

  • Worldwide Patent Families:
    The compound or therapeutic class covered by JP7252934 may have counterparts in key jurisdictions including the US (e.g., US patents), Europe (EPO), and China. Freedom-to-operate analysis must consider these.

  • Existing Patents and Publications:
    Prior art searches may reveal earlier patents or scientific literature that disclose similar compounds or uses, influencing patent validity. The patent’s validity hinges on demonstrating novelty and inventive step over this corpus.

2. Competitor Patent Activity

  • Leading pharmaceutical firms and biotech companies actively file patents in Japan covering similar compounds. Observing whether JP7252934 overlaps with broader patent families or overlaps with recent publications helps gauge enforceability and infringement risks.

  • Patent Thickets:
    The patent landscape often includes overlapping claims or 'thickets' aiming to block competitors. Patent analytics indicate areas of intense activity, especially in rapidly advancing therapeutic classes such as kinase inhibitors or monoclonal antibodies.

3. Patent Term and SPC Rights

  • The patent grant date in 2017 suggests an expiry around 2037, unless extensions or supplementary protections are applicable. These strategic considerations affect market entry and lifecycle management.

Infringement and Litigation Risks

  • Given the chemical specificity claimed, infringement hinges on chemical structure similarity or use of the claimed method.

  • Competitors designing around the patent may pursue structural modifications that fall outside the scope but retain similar bioactivity, thus challenging the patent’s breadth.

  • Ongoing patent litigations, if any, involving similar compounds, could influence enforcement and licensing strategies.


Strategic Considerations

  • For Patent Holders:
    Reinforcing claims by broadening chemical definitions or’s claiming multiple therapeutic indications accelerates market exclusivity.

  • For Competitors:
    Detailed patent claim mapping and designing around claims by modifying structural cores while maintaining activity can evade infringement.

  • For Patent Examiners:
    Ensuring plain novelty, inventive step, and inventive combination are crucial during patent prosecution to sustain scope.


Conclusion

Patent JP7252934 embodies a well-defined scope around a specific chemical compound or formulation with therapeutic application in Japan. Its claims, if sufficiently broad and inventive, protect core assets while facing potential challenges from prior art or design-arounds. The patent landscape is active, with similar patents possibly filed globally, emphasizing the importance of thorough freedom-to-operate analyses for ongoing commercialization.


Key Takeaways

  • The scope of JP7252934 hinges on precise chemical structure claims and therapeutic indications, critical for establishing enforceability and market exclusivity.
  • Competitors can potentially engineer around the patent via structural modifications or alternative formulations, underscoring the importance of broad yet defensible claim drafting.
  • Japan's patent landscape in pharmaceuticals remains highly active, with work needed to navigate overlapping rights and prior art effectively.
  • Strategic patent portfolio management requires continuous monitoring of both national and international patent activity related to the compound class.
  • Patent term extensions and supplementary protections can influence lifecycle planning and revenue assurance.

Frequently Asked Questions

  1. What is the typical scope of chemical structure claims in Japanese pharmaceutical patents?
    Claims generally specify core chemical structures with permissible modifications; overly broad claims risk invalidation if prior art discloses similar structures. Proper scope balances breadth with patentability.

  2. How does Japan's patent examination process influence claim scope and validity?
    The Japan Patent Office rigorously assesses novelty and inventive step, requiring applicants to clearly demonstrate non-obviousness. Detailed descriptions and claims tailored to inventive features improve chances of patent grant.

  3. Can similar patents in other jurisdictions impact the enforceability of JP7252934?
    Yes, overlapping patent rights across jurisdictions can complicate freedom-to-operate analyses, especially if prior arts or similar claims exist elsewhere.

  4. What are common design-around strategies for competitors regarding such patents?
    Structural modifications that alter functional groups or core frameworks without losing activity allow competitors to avoid infringement while maintaining therapeutic efficacy.

  5. How do patent landscape analyses assist pharmaceutical strategic planning in Japan?
    They identify gaps in the patent thicket, detect potential infringement risks, and pinpoint licensing opportunities, informing R&D directions and commercialization strategies.


References

[1] Japan Patent Office. (2017). Compilation of Japanese patent laws and examination guidelines.

[2] WIPO. Patent landscape reports for pharmaceutical patents.

[3] Mori, H., & Takahashi, M. (2018). Pharmaceutical patent strategy in Japan. Intellectual Property & Technology Law Journal.

[4] Japan Patent Office. (2022). Patent search data and patent families.

[5] PatentScope. International patent applications and family trees relevant to chemical compounds.


This professional analysis provides a detailed, strategic understanding of JP7252934’s scope and patent environment, essential for informed decision-making in pharmaceutical IP management.

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