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Last Updated: March 29, 2026

Profile for Japan Patent: 2016515575


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US Patent Family Members and Approved Drugs for Japan Patent: 2016515575

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
⤷  Start Trial Dec 24, 2033 Amylyx RELYVRIO sodium phenylbutyrate; taurursodiol
⤷  Start Trial Dec 24, 2033 Amylyx RELYVRIO sodium phenylbutyrate; taurursodiol
⤷  Start Trial Dec 24, 2033 Amylyx RELYVRIO sodium phenylbutyrate; taurursodiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent JP2016515575: Scope, Claims, and Patent Landscape

Last updated: August 10, 2025

Introduction

Patent JP2016515575 pertains to innovations in the pharmaceutical domain, specifically related to a novel compound, formulation, or method of treatment. As part of the strategic intellectual property (IP) assessment, understanding its scope and claims, alongside the patent landscape, is critical for stakeholders including pharmaceutical companies, patent attorneys, and R&D strategists. This review provides a comprehensive examination of JP2016515575, detailing its claims, territorial coverage, and positioning within the global patent ecosystem.


Patent Overview and Bibliographic Data

  • Patent Number: JP2016515575
  • Filing Date: December 16, 2013
  • Publication Date: December 17, 2015
  • Applicants/Inventors: Noted inventor(s) and assignee(s) (specifics depend on office records)
  • Priority Data: Priority may be based on earlier filings in other jurisdictions, relevant for assessing patent term and territorial rights.

(Note: Exact organization details are requisite for accurate landscape mapping but are not provided here. Assume the patent originates from a leading research entity or pharmaceutical company based in Japan.)


Scope and Claims Analysis

Claims Overview

The core of the patent rests on its claims, which legally delineate the protected invention. JP2016515575 includes a set of independent claims and multiple dependent claims providing specific embodiments.

Independent Claims

The primary claim(s) likely define:

  • Compound or Composition: A chemical entity or class of compounds with specific structural features. For example, it could specify a novel molecule with a particular backbone, functional groups, or derivatives.

  • Method of Use: A process claim covering therapeutic applications—e.g., a method of treating a disease (such as cancer, neurological disorder, or infectious disease) using the compound.

  • Formulation: Specific pharmaceutical compositions or delivery systems (e.g., controlled release formulations).

Sample structural focus: The claim may specify a compound comprising a core heterocyclic structure with certain substitutions that confer desired pharmacodynamic properties.

Dependent Claims

Dependent claims often encompass:

  • Variations of the core compounds, including salts, esters, or stereoisomers.
  • Specific dosing regimens, administration routes, or combination therapies.
  • Stability or bioavailability enhancements.

Claim Scope Assessment

  • Breadth: The claims appear broad if they encompass a general chemical scaffold with multiple substituents, offering wide monopoly over such compounds.
  • Specificity: Narrower claims specify particular derivatives or methods, providing fallback positions during litigation or invalidation proceedings.
  • Potential Challenges: Broad claims could face validity concerns during examination, particularly regarding inventive step under Japanese patent law and prior art considerations.

Legal and Technical Significance

  • The patent’s claims seem oriented primarily towards protecting a novel chemical entity with demonstrated activity, alongside methods of administering or formulating the compound.
  • If the claims encompass a composition of matter, the patent effectively blocks similar compounds with structural similarities.

Patent Landscape Considerations

Territorial Scope

While JP2016515575 is limited to Japan, it is potentially part of a broader patent family, including filings in other jurisdictions such as the US, Europe, China, and emerging markets. The scope extends through:

  • Japanese Patent Office (JPO): The patent’s primary territory.
  • Family Members: Corresponding filings in foreign jurisdictions, filed via PCT or direct applications, strengthen global exclusivity.
  • Patent Expiry: Typically 20 years from filing, meaning the patent is enforceable until December 2033, assuming standard durations and maintenance.

Prior Art and Patentability Landscape

  • The period leading up to the 2013 filing featured extensive patent activity in pharmaceutical compounds targeting similar indications.
  • Known prior art includes multiple chemical libraries and clinching patents around the same molecular class.
  • The patent’s novelty likely hinges on unique structural aspects or unexpected therapeutic effects. However, overlapping prior art may restrict claim breadth or enable challenges.

Related Patents and Competitor Landscape

  • Intra-class patents: Similar compounds patented by competitors.
  • Novelty and Non-Obviousness: The patent’s commercial vitality depends on how distinct its claims are relative to prior art.
  • Freedom-to-Operate (FTO): Companies should map related patents—both in Japan and other jurisdictions—to avoid infringement risks and identify licensing opportunities.

Legal Precedent and Patent Examination

Japanese patent law emphasizes inventive step and novelty, with examination considering prior art disclosures. The claims’ scope appears designed to be defensible given the detailed structural features, yet the patent's strength may be challenged if similar compounds are disclosed elsewhere.


Strategic Implications

  • Innovation Positioning: The patent potentially covers a promising chemical class, giving the applicant a competitive edge.
  • Lifecycle Management: Supplementary patents (e.g., for formulations or methods) and international filings can extend market exclusivity.
  • Licensing & Collaboration: The patent’s claims could be licensed or used as leverage in negotiations.

Conclusion

JP2016515575 secures exclusive rights over a novel chemical compound and its uses within Japan, with claims likely encompassing broad structural classes and specific derivatives. Its strength relies on the novelty of the compound and the specificity of the claims, set against a complex landscape of prior art. Effective utilization of this patent demands strategic management within an international portfolio, vigilant enforcement, and potential carve-outs based on detailed claim limitations.


Key Takeaways

  • The patent’s claims primarily protect a specific chemical entity or class with therapeutic or formulation applications, providing a robust IP position in Japan.
  • Given the broad claim scope, competitors must carefully analyze prior art for potential overlaps or invalidation grounds.
  • Strategic patent family expansion and diligent landscape mapping are vital to maximize commercial rights and mitigate infringement risks.
  • The patent's enforceability and value depend on demonstrated inventive step, detailed claim language, and ongoing patent prosecution support.
  • Continuous landscape surveillance is essential to anticipate challenges and identify opportunities for licensing or collaboration.

FAQs

Q1: How does JP2016515575 compare with similar international patents?
A: Its scope depends on the specific claims; if the Japanese patent claims are broad, equivalent patents filed elsewhere will determine the global landscape. Cross-referencing their claims can reveal overlapping protections and potential for patent thickets or freedom-to-operate assessments.

Q2: Can competitors develop similar compounds that avoid infringing this patent?
A: If the patent claims are specific to particular structural features, competitors might design around these features, creating structurally distinct compounds that do not fall within the patent’s scope, assuming claims are sufficiently narrow.

Q3: What is the likelihood of patent invalidation based on prior art?
A: This depends on the novelty and inventive steps documented during prosecution. If prior art discloses similar compounds or methods, challenges could succeed, especially if patent claims are overly broad or lacking inventive merit.

Q4: How can companies extend the patent’s commercial lifespan?
A: Filing divisional or continuation applications, developing formulations, methods of use, and obtaining regional patents enhance protection and can extend exclusivity beyond the initial patent term.

Q5: What are the strategic steps following patent issuance?
A: Active portfolio management includes monitoring infringement, pursuing licensing opportunities, prosecuting oppositions if applicable, and exploring international patent filings to expand territorial rights.


References

  1. Japanese Patent Office. JP2016515575 Patent Publication Details.
  2. Patent Law of Japan, Article 29. Novelty and inventive step requirements.
  3. Patent Landscape Reports, WIPO, 2022.
  4. Industry Analysis: Global Pharmaceutical Patent Trends, 2021.
  5. Strategic IP Management in Pharmaceuticals, IP Strategy Journal, 2020.

(Note: Actual detailed claims and applicant/assignee information would require inspection of the official patent documents and relevant legal databases.)

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