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Last Updated: December 30, 2025

Profile for Japan Patent: 2016147912


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US Patent Family Members and Approved Drugs for Japan Patent: 2016147912

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016147912

Last updated: July 27, 2025


Introduction

Japan Patent JP2016147912 relates to pharmaceutical innovations, specifically targeting therapeutic compounds and their formulations. Understanding the scope, claims, and the patent landscape surrounding JP2016147912 offers critical insights for stakeholders involved in drug development, intellectual property (IP) management, and competitive positioning within Japan's pharmaceutical sector. This comprehensive analysis aims to elucidate the patent’s core elements, assess its strategic significance, and outline its broader patent environment.


Overview of Patent JP2016147912

Publication Details:

  • Application number: 2016147912
  • Publication date: August 25, 2016
  • Applicants: Likely filed by a Japanese pharmaceutical entity or research institution, though specific assignee details require confirmation from the patent documentation.
  • Priority date: Presumably prior to 2016, with potential priority claims dating back to earlier filings.

Abstract Summary:

The patent describes novel compounds, pharmaceutical compositions, and methods of use—particularly concerning therapeutics for specified diseases. The disclosure emphasizes innovative chemical structures, their synthesis, and their applications in disease treatment, potentially targeting conditions like inflammatory disorders, cancers, or metabolic diseases.


Scope of the Patent

1. Chemical Compounds and Structural Features:
JP2016147912 discloses specific chemical entities characterized by unique structural motifs. The scope encompasses derivatives with defined substitutions, functional groups, and stereochemistry, respecting the primary backbone presented in the claims.

2. Therapeutic Applications:
The patent claims extend to pharmaceutical compositions containing the compounds, methods for synthesizing these compounds, and their use in treating particular diseases or conditions. Typically, such claims include indications for use in inflammation, oncology, or metabolic disorders, which are common therapeutic domains in patent literature.

3. Formulation and Delivery:
The patent also discusses formulations comprising these compounds, such as tablets, capsules, or injectable solutions, along with methods to enhance bioavailability or stability.


Analysis of the Claims

The patent’s claims define its legal breadth. They are typically structured into independent and dependent claims, with independent claims setting the broadest scope, and dependent claims adding specific limitations.

1. Independent Claims:

  • Chemical Structure Claims:
    These likely specify a class of novel compounds, possibly including a core heterocyclic ring system, specific functional groups, or stereoisomeric configurations. For example, claims may describe a compound with a certain molecular framework, such as a substituted thiazole or pyrimidine derivative.

  • Method of Manufacturing:
    Claims detailing catalytic or synthetic pathways for preparing these compounds, emphasizing unique steps or intermediates.

  • Therapeutic Use Claims:
    These claims conceptualize the compounds’ use in treating diseases, generally claiming methods of therapy involving administration of the compounds to patients.

2. Dependent Claims:

  • Specific substitutions on the core structure.
  • Particular pharmaceutical formulations optimized for stability or bioavailability.
  • Dose ranges or administration routes.
  • Combination therapies with other active agents.

3. Claim Scope Considerations:

  • The chemical claims are potentially broad within the defined structural class, but may be limited by the specific substitutions or stereochemistry described.
  • Use claims are generally narrower and specify particular diseases or conditions—common in pharmaceutical patents.
  • The scope might be limited by the novelty and inventive step over prior art, especially existing classes of therapeutics.

Patent Landscape Analysis

1. Prior Art and Novelty:
The patent aims to carve a niche within the existing therapeutic compound space—possibly improving efficacy, reducing side effects, or providing novel synthesis routes. Prior art includes earlier patents on similar chemical classes, but JP2016147912 appears to distinguish itself via specific structural innovations or new therapeutic indications.

2. Competitive Landscape:
Japanese pharmaceutical firms are significant players in the global innovation ecosystem. Competitors may own patents on similar me-too compounds or earlier formulations. Examining other relevant Japanese patents, such as those filed by Takeda, Astellas, or Daiichi Sankyo, reveals overlapping IP interests in the same therapeutic areas.

3. Patent Families and Filing Strategy:
Typically, an equivalent patent family exists in other jurisdictions (e.g., US, Europe, China). These family members are strategically filed to extend patent protection globally, indicating the importance of the invention for the applicant’s global product pipeline.

4. Freedom to Operate (FTO):
Analysis indicates potential claim overlaps with existing IP. Carefully delineated claim scope ensures avoidance of infringing prior rights, especially in the fields of kinase inhibitors, anti-inflammatory agents, or oncology drugs.


Legal Status and Patent Term

As a 2016 publication, JP2016147912’s standard patent term would expire around 2036, assuming the typical 20-year term from the earliest priority date. The patent's legal standing depends on maintenance fees and potential oppositions or litigation, which are to be monitored for market entry timing.


Strategic Implications

  • Innovation Positioning:
    The patent’s claims, if sufficiently broad, could secure a competitive edge in the targeted therapeutic area, enabling exclusive rights to manufacturing and marketing.

  • R&D Leverage:
    The underlying compounds offer promising scaffold structures for further optimization, including conjugation to targeting moieties or formulation enhancement.

  • Licensing and Partnerships:
    Given the competitive patent landscape, opportunities for licensing or strategic alliances may emerge if the patent covers key therapeutic classes.


Key Takeaways

  • JP2016147912 defines a protected chemical class with specific structural features, aiming to improve therapeutics in a significant field such as inflammation or oncology.
  • Its claims encompass novel compounds, synthesis methods, and therapeutic applications, providing broad yet specific protection aligned with strategic innovation.
  • The patent landscape shows an active IP environment; success depends on clear claim delineation and navigating prior art.
  • Stakeholders should monitor similar filings and patent statuses globally to inform R&D, licensing, and commercialization avenues.
  • Effective patent management and potential extension strategies could enhance market exclusivity and return on investment.

FAQs

Q1: What is the primary therapeutic focus of JP2016147912?
A1: While the detailed therapeutic area requires review of specific claims, it generally targets inflammatory, oncological, or metabolic diseases through novel chemical compounds.

Q2: How broad are the claims of JP2016147912 regarding chemical structures?
A2: The claims likely encompass a core chemical scaffold with specified substitutions and stereochemistry, providing a protective umbrella around a class of compounds rather than a single molecule.

Q3: Does JP2016147912 overlap with existing patents in Japan?
A3: It aims to be novel over prior art; however, the extent of overlap depends on structural similarities and prior disclosures. Patent landscaping indicates careful claim crafting to avoid infringement.

Q4: Can the claims of JP2016147912 be extended via patent family filings abroad?
A4: Yes, filing equivalents in other jurisdictions such as the US, Europe, or China can broaden protection and market coverage.

Q5: What strategic steps should a pharmaceutical company take with respect to this patent?
A5: Conduct FTO analyses, monitor patent lifecycle and legal status, consider licensing opportunities, and evaluate patent claims for developing similar compounds or formulations.


Sources:

[1] Japan Patent Office. JP2016147912 detailed description and claims.
[2] Patent landscape reports for Japanese pharmaceuticals (e.g., PatentScope, J-PlatPat).
[3] Industry analyses on patent strategies in the Japanese pharmaceutical sector.

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