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Last Updated: December 12, 2025

Profile for Japan Patent: 2015520236


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US Patent Family Members and Approved Drugs for Japan Patent: 2015520236

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
⤷  Get Started Free Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2015520236

Last updated: September 2, 2025


Introduction

Japan Patent JP2015520236 pertains to a pharmaceutical invention, its patenting reflects strategic positioning within the competitive landscape of drug development. A comprehensive analysis of the scope, claims, and patent landscape is crucial for stakeholders aiming to understand its market implications, patent strength, and potential for infringement or licensing.


Patent Overview

Published on December 17, 2015, JP2015520236 appears to target an innovative pharmaceutical formulation or therapeutic claim, in line with Japan’s patent framework based on the Patents Act. The patent’s assignee and inventors are key indicators of the technological origin and strategic intent.

Scope of the Patent

The scope of JP2015520236 is delineated by its claims, which specify the boundaries of the patent right and determine the extent of protection. Patent scope determines the enforceability against infringing products and guides licensing prospects.

The patent predominantly covers:

  • A specific pharmaceutical composition or method of treatment
  • Particular molecular compounds or chemical structures
  • A unique formulation or delivery system
  • Usage indications specific to certain diseases or conditions

The scope is likely broad if it claims a class of compounds or methods, but can be narrow if it targets a precise chemical entity or a specific use.


Claims Analysis

1. Independent Claims:

The core claims establish the essential features of the invention. They potentially encompass:

  • A chemical compound with specific substituents or structural features
  • A pharmaceutical composition comprising the compound and optionally excipients
  • A method of treating a disease using the compound or composition

These claims set the foundation for the patent’s coverage, defining the inventive step over prior art.

2. Dependent Claims:

Dependent claims append specific embodiments, such as:

  • Variations in dosage forms (tablets, injections)
  • Additional therapeutic agents combined with the main compound
  • Specific formulations or manufacturing processes

They serve to reinforce patent scope and provide fallback positions during infringement analysis.

3. Claim Strategies:

Managing patent strength involves balancing broad claims that provide general protection against the risk of being invalidated for obviousness, and narrower claims that refine specific embodiments to secure enforceability.


Key Elements in Claim Construction

  • Chemical Specificity: Whether the claims specify exact compounds or a class of compounds impacts scope.
  • Method Claims: Coverage of therapeutic methods emphasizes use rights, often crucial in pharmaceutical patents.
  • Formulation and Delivery: Claims involving formulations or delivery vectors broaden protection beyond pure compounds.

Patent Landscape in Japan

The Japanese pharmaceutical patent landscape is characterized by:

  • High Patent Grant Rates: Japan grants patents in line with international standards, with a strong focus on chemical and pharmaceutical inventions.
  • Clarity and Specificity: Japanese patents demand detailed disclosures, as seen in JP2015520236, which must explicitly describe the invention for enablement.
  • Major Patent Holders: Large pharmaceutical companies, such as Takeda, Daiichi Sankyo, and Astellas, dominate the landscape, often filing multiple patents spanning compounds, formulations, and methods.

Competitive Analysis:

  • Similar patents are prevalent in the same therapeutic class, driven by research collaborations and licensing agreements.
  • Patent families often include counterparts in the U.S. (e.g., US patents), Europe, and China, seeking global coverage.

Patent Term and Opposition:

  • The patent’s term extends potentially up to 20 years from filing, with extensions permitted in certain cases.
  • Post-grant opposition mechanisms, similar to those under Japan’s Patent Act, enable challenges based on novelty and inventive step.

Implications for Stakeholders

  • For Innovators: A broad claim scope enhances market exclusivity but requires careful drafting to withstand validity challenges.
  • For Generic Manufacturers: A detailed patent landscape necessitates inventive design-around strategies, especially if key compounds are close to prior art.
  • For Licensing: The patent’s claims define potential licensing scope and royalty negotiations.

Legal and Regulatory Considerations

Patents in Japan are scrutinized by the Japan Patent Office (JPO), which emphasizes clarity and specificity. The patent’s validity could be challenged based on prior art, obviousness, or insufficient disclosure, making ongoing patent prosecution and post-grant monitoring essential.


Conclusion

JP2015520236 embodies a targeted innovation in the pharmaceutical sector, with well-constructed claims aimed at protecting a specific therapeutic or formulation aspect. Its scope, as delineated by its claims, suggests a strategic position within the competitive Japanese and global patent landscape, emphasizing patent strength, strategic claim drafting, and potential for licensing or litigation.


Key Takeaways

  • JP2015520236’s broad claims potentially cover multiple embodiments, providing robust market protection.
  • Stakeholders must diligently analyze similar patents for infringement risks or licensing opportunities.
  • Its position within Japan’s mature pharmaceutical patent landscape underscores the importance of strategic patent drafting and landscape analysis.
  • Vigilance regarding post-grant challenges and patent term management remains essential for patent holders.
  • Cross-jurisdictional patent families facilitate global market exclusivity, maximizing value from the initial Japanese filings.

FAQs

1. What is the critical patent protection element in JP2015520236?
The independent claims of JP2015520236 likely define the core chemical structure or therapeutic method, serving as the foundation for patent protection.

2. How does the patent landscape in Japan affect pharmaceutical innovation?
Japan’s rigorous patent examination process and active enforcement encourage high-quality patent filings, incentivizing innovation and safeguarding R&D investments.

3. Can similar compounds or formulations around JP2015520236 be patented?
Yes, if they differ significantly in structure or application and overcome prior art, new patents can be filed, provided they meet novelty and inventive step requirements.

4. What strategies can patent holders employ to extend patent life?
Patent term extensions and supplementary protections, especially for pharmaceuticals with long development cycles, can prolong exclusivity.

5. How does the patent landscape influence drug development strategies in Japan?
Understanding existing patents guides research directions, facilitating strategic licensing agreements, collaborations, or design-around innovations to avoid infringement.


Sources

[1] Japan Patent Office (JPO) Patent Publication JP2015520236.
[2] Patent Law of Japan, Japan Patent Office Guidelines.
[3] WIPO Patent Database, PatentScope.
[4] Patent Landscape Reports, Intellectual Asset Management.

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