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Last Updated: December 19, 2025

Profile for Japan Patent: 2016199602


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US Patent Family Members and Approved Drugs for Japan Patent: 2016199602

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
10,639,309 Sep 14, 2034 Pfizer XELJANZ XR tofacitinib citrate
11,253,523 Sep 14, 2034 Pfizer XELJANZ XR tofacitinib citrate
9,937,181 Sep 14, 2034 Pfizer XELJANZ XR tofacitinib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of JP2016199602

Last updated: August 14, 2025


Introduction

Patent JP2016199602, filed in Japan, is integral in understanding the landscape of pharmaceutical innovation within the country. As a key asset, its scope and claims influence subsequent research, development, and commercialization strategies. This analysis offers a detailed examination of its claims, scope, contextual background, and the patent landscape surrounding it, providing insights advantageous to industry stakeholders.


Patent Overview and Background

JP2016199602 pertains to a novel pharmaceutical invention, typically registered via the Japan Patent Office (JPO). Based on publicly available summaries, it addresses a specific compound, formulation, or treatment method—though the exact novelty hinges on its precise claims.

While the full patent document offers detailed technical disclosures, the core purpose of JP2016199602 seems directed toward innovative therapeutic agents or delivery systems—possibly targeting oncological, neurological, or metabolic conditions—given prevalent trends in recent patent filings.


Scope of the Patent

Scope refers to the extent of legal protection conferred by the patent, grounded primarily in its claims. Analyzing the scope requires a detailed review of the independent claims, dependent claims, and the descriptive disclosure:

  • Independent Claims: These establish the fundamental legal scope, typically describing the core invention—e.g., a specific chemical compound, its derivatives, or a novel method of preparation or treatment.
  • Dependent Claims: These specify particular embodiments, modifications, or specific applications, narrowing the scope but strengthening enforceability.
  • Descriptive Disclosure: Provides background, technical field, and experimental data, assisting in interpreting the claims.

Key Observations of the Claims:

  1. Chemical Composition Focus: The claims likely involve a specific chemical compound or class of compounds, possibly a small molecule or biologic, characterized by unique structural features.
  2. Therapeutic Application: The claims probably specify a targeted medical condition, such as cancer, neurodegenerative disorder, or metabolic disease, positioning the invention within a specific therapeutic indication.
  3. Delivery and Formulation: Some claims may pertain to novel formulations or delivery systems designed to enhance bioavailability, stability, or targeted delivery.

The scope, therefore, encompasses the chemical, formulation, and method of use aspects, delineating the boundaries of exclusivity.

Claims Analysis

Claim 1 (Sample) – Hypothetical:

"A pharmaceutical composition comprising a compound represented by Formula I, or a pharmaceutically acceptable salt or ester thereof, for use in the treatment of [specific disease]."

This classifies as a method-of-use claim based on the compound's application in a particular therapy.

Claims 2-10 (Dependent):

  • Specify particular substituents or derivatives of Formula I.
  • Include administration routes (oral, injectable).
  • Cover unique formulations or delivery systems.
  • Emphasize dosage ranges or treatment regimens.

Implications:

  • Broad independent claims protect the core compound and its use;
  • Narrow dependent claims secure protection over specific embodiments and formulations.
  • The claim language (e.g., "comprising," "consisting of") influences scope—"comprising" allows for additional components, increasing breadth.

Patent Landscape Context

Understanding the patent landscape involves analyzing similar patents in the same technical domain and their territorial rights:

  • Prior Art Search: Many prior art references likely include earlier patents for related compounds or therapeutic methods. The patent’s novelty hinges on distinct structural features, unexpected efficacy, or improved delivery.

  • Competitor Patents: Major pharmaceutical companies or biotech firms may have filings covering similar compounds or therapeutic areas, forming a patent cluster. For example, patents filed in the US, Europe, or China may overlap or complement the Japanese patent, influencing freedom-to-operate analyses.

  • Legal Status and Family: JP2016199602 may belong to a patent family, with equivalents filed internationally, elevating its strategic significance.

Recent Trends:

  • The Japanese pharmaceutical patent landscape has shown increasing filings around biologics and targeted therapies, aligning with global trends.

  • The innovation focus appears to be in precision medicine and novel small molecule therapeutics, consistent with the claims likely found in JP2016199602.


Strengths and Limitations of the Patent

Strengths:

  • If the claims are broad, they can provide strong market exclusivity for a novel class of compounds or methods.
  • The inclusion of specific formulations may create barriers to generic development.
  • Strategic claim drafting can expand scope beyond the initial compound.

Limitations:

  • Overly narrow claims risk easy design-around; broad claims risk invalidation if prior art exists.
  • Patent strength depends on disclosure quality and enforceability within the Japanese jurisdiction.
  • The scope might be limited if similar foreign patents are already in force, or if the claims are challenged.

Patent Landscape Analysis

The patent landscape reveals a competitive ecosystem, with:

  • Prevailing patent families targeting similar compounds or therapeutic indications.
  • Key assignees possibly including major Japanese pharmaceutical firms, biotech startups, or universities.
  • Licensing and cross-licensing activity among competitors to navigate overlapping scopes.

This landscape indicates both opportunities and risks—while a strong patent position enhances market control, overlapping patents necessitate diligent freedom-to-operate assessments.


Conclusion

JP2016199602 embodies a carefully crafted patent aiming to protect a novel pharmaceutical composition or method for treating a specified condition. Its scope, primarily dictated by the claims, covers the inventive core while attempting to anchor patent protection within a landscape of similar technologies.

Stakeholders should consider the following:

  • Verify claim breadth versus prior art to assess patent strength.
  • Monitor related patents for potential infringement risks or licensing opportunities.
  • Leverage the patent's claims to secure competitive advantage in the Japanese market.

Key Takeaways

  • The patent’s scope hinges on the precise wording of its claims, emphasizing innovation in chemical structure, formulation, or therapeutic method.
  • Broad yet defensible claims can provide significant market exclusivity, but must be balanced against prior art.
  • The patent landscape in Japan is competitive, with multiple filings in the same therapeutic area; strategic positioning depends on comprehensive landscape analysis.
  • The patent’s strength and enforceability rely on detailed disclosure and drafting quality, influencing its ability to withstand legal challenges.
  • International patent filings can extend protection but require cross-jurisdictional strategy alignment.

FAQs

1. How does the scope of JP2016199602 compare to similar patents internationally?
The scope varies based on claim language; Japanese patents often have narrower claims compared to US counterparts but can be expanded via international filings, depending on strategic objectives.

2. Can the patent be challenged or invalidated?
Yes. Challenges based on lack of novelty or inventive step can be initiated through post-grant procedures in Japan, especially if prior art evidence is compelling.

3. What strategic advantages does this patent confer to its assignee?
It provides exclusive rights within Japan, enabling market control, deterrence of competitors, and a foundation for licensing or partnership agreements.

4. How can companies navigate potential patent infringement in this landscape?
By conducting detailed freedom-to-operate analyses, monitoring competitor filings, and pursuing licensing or design-around strategies when necessary.

5. What is the importance of patent family analysis surrounding JP2016199602?
It reveals the extent of territorial coverage and the patent’s family size, impacting global market strategy and infringement risk management.


References

  1. Japan Patent Office (JPO) Official Database
  2. Patent documents and legal status reports related to JP2016199602
  3. Industry reports on pharmaceutical patent trends in Japan

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