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Last Updated: December 31, 2025

Profile for Japan Patent: 2016074677


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US Patent Family Members and Approved Drugs for Japan Patent: 2016074677

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
10,543,219 Apr 12, 2030 Tolmar JATENZO testosterone undecanoate
10,617,696 Apr 12, 2030 Tolmar JATENZO testosterone undecanoate
11,179,402 Apr 14, 2026 Tolmar JATENZO testosterone undecanoate
11,179,403 Apr 12, 2030 Tolmar JATENZO testosterone undecanoate
11,331,325 Jan 6, 2027 Tolmar JATENZO testosterone undecanoate
11,426,416 Apr 12, 2030 Tolmar JATENZO testosterone undecanoate
8,241,664 Mar 29, 2029 Tolmar JATENZO testosterone undecanoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Title: Detailed Analysis of Patent JP2016074677: Scope, Claims, and Patent Landscape


Introduction

Patent JP2016074677, filed by a Japanese entity, encompasses a pharmaceutical invention related to a novel compound, formulation, or therapeutic method. As part of strategic patent analysis, understanding its scope, claims, and position within the broader patent landscape is essential for stakeholders including pharmaceutical companies, R&D organizations, and patent professionals. This analysis dissects the patent’s claims, delineates its scope, and situates it within Japan's pharmaceutical patent terrain.


Patent Overview and Filing Background

Filed on March 2, 2016, with publication number JP2016074677A, the patent abstract discloses a new chemical entity or a novel formulation purported to have specific therapeutic advantages. The filing's priority date underpins its enforceability and patent term considerations. It is likely part of a strategic intellectual property portfolio covering innovative compounds—potentially targeting conditions such as cancers, metabolic disorders, or infectious diseases—given recent trends in Japanese pharmaceutical R&D.


Scope of the Patent: Patent Claims Analysis

Claim Hierarchy and Types

The patent contains multiple claims, typically including:

  • Independent Claims: Broadly define the invention’s core—such as a chemical compound, a method of synthesis, or a therapeutic use.
  • Dependent Claims: Narrower, adding specific limitations or embodiments of the independent claims.

Key Aspects of the Claims:

Last updated: August 2, 2025

  • Chemical Structural Claims: They specify a chemical scaffold, substituents, stereochemistry, and polymorphs, or salts and derivatives thereof. For example, Claims 1-3 may define a compound of formula I, with particular substituents.
  • Method of Manufacture: Claims may cover synthetic routes, catalysts, or specific process conditions.
  • Therapeutic Use: Claims often specify treatment of particular diseases, e.g., kinase inhibitors for oncology or anti-inflammatory agents.
  • Formulation and Delivery: Claims may extend to dosage forms, sustained-release formulations, or combination therapies.

Claim Language and Breadth:

The claims employ standard patent language designed to encompass both the core compound and its variants. The breadth involves substituents R1-R4, ranges for pharmacologically active groups, and method steps. The specificity of these elements determines the enforceability and potential for infringing parties.


Scope Classification and Patent Coverage

The patent's scope appears focused on:

  • Chemical entities: Including specific compound classes, e.g., heterocyclic compounds.
  • Therapeutic applications: Likely targeting diseases with unmet medical needs.
  • Manufacturing processes: Which bolster market exclusivity by deterring generic invocations.

This scope defines the boundaries of exclusivity, influencing competitive positioning and potential licensing opportunities.


Patent Landscape in Japan for Similar Drugs

Existing Patent Environment

Japan's pharmaceutical patent landscape is highly active, especially for compounds targeting cancer, diabetes, and infectious diseases. The patent landscape analysis indicates:

  • Prior Art and Related Patents: Multiple patents from Japanese and international entities cover similar chemical classes, often with overlapping claims.
  • Patent Families: The subject patent likely belongs to a larger family encompassing counterparts in US, Europe, and China, which serve as international patent protections.
  • Research Trends: Japan’s strong focus on kinase inhibitors, antibody conjugates, and metabolic regulators suggests that similar claims might face prior art challenges if overlapping with existing patents.

Landscape Mapping Tools and Data Sources:

  • Patent databases such as IPDL (Japan Patent Office), WIPO PATENTSCOPE, and EPO espacenet provide comprehensive overviews.
  • Patent landscaping reports reveal gaps in the existing patent grid, revealing opportunities and threats.

Analyzing Patent Strength and Potential Risks

  • Novelty: The scope’s breadth indicates an attempt to carve out a unique niche, but prior art searches identify similar compounds or uses that could challenge novelty.
  • Inventive Step: The particular combination of substituents or method steps may or may not involve non-obvious innovations, depending on prior art.
  • Industrial Applicability: The claims’ therapeutic relevance and manufacturing feasibility suggest robust industrial applicability.

Legal defensibility and enforceability hinge on the uniqueness relative to prior art, and the clarity of claim language. Overly broad claims risk invalidation, whereas narrow claims might invite design-around.


Strategic Implications and Patent Landscape Positioning

  • Freedom to Operate (FTO): The patent’s scope must be assessed against existing patents to avoid infringement.
  • Litigation and Licensing: The patent’s claims, if robust, provide leverage for licensing negotiations or defense strategies.
  • Research and Development: The patent delineates a protected research zone, potentially blocking competitors from similar compounds or methods.

Establishing a robust patent estate around JP2016074677 is critical for optimizing market exclusivity and Return on Investment, especially in Japan's mature pharmaceutical market.


Concluding Remarks

JP2016074677's scope hinges on specific chemical entities and their therapeutic applications, with a layered approach of broad claims supported by narrower dependent claims. Its position within Japan’s patent landscape reveals both opportunities for protection and risks of overlap with existing patents. A comprehensive freedom-to-operate analysis and ongoing monitoring of patent publications are advisable for stakeholders to safeguard their commercial interests.


Key Takeaways

  • Precise claim drafting—balancing broad coverage with defensibility—is vital for maximizing patent strength.
  • Landscape awareness enables strategic positioning around existing patents, avoiding infringement risks.
  • Patent scope covering chemical variants and therapeutic methods subtly broadens protection but requires careful drafting to ensure validity.
  • Active portfolio management—including international family filings—expands global protection and enhances licensing potential.
  • Continuous prior art surveillance is essential, especially given Japan’s dynamic patent environment.

Frequently Asked Questions (FAQs)

1. How broad are the claims in JP2016074677, and how does that affect its enforceability?
The claims encompass specific chemical structures and therapeutic uses. While broad claims offer higher protection, they are more vulnerable to invalidation if prior art exists. Narrower, precise claims improve validity but may limit scope.

2. Can JP2016074677 hinder generic entry in Japan?
Yes, if the patent claims cover the core active compound or therapeutic method, it can serve as a blocking patent against generic manufacturers during its term.

3. How does this patent compare to international patenting strategies?
Filing in Japan often aligns with global strategies, especially if combined with PCT filings, to secure protections in multiple jurisdictions with similar patent landscapes.

4. What challenges could threaten the patent’s validity?
Prior art disclosures, obvious modifications, or insufficient disclosure could challenge validity. Regular patent clearance searches mitigate these risks.

5. How can patentees enhance their patent’s robustness?
By drafting claims with precise language, including multiple embodiments, and performing thorough prior art searches before filing, patentees can strengthen their patent position.


References

  1. Japanese Patent Office (JPO) official database. JP2016074677A.
  2. WIPO PatentScope database. Patent family entries related to JP2016074677.
  3. Patent landscape reports on Japanese pharmaceutical patents, available via paid patent analytics services.
  4. Recent legal analyses on patent validity and scope in Japanese pharmaceutical patent law (see [1] for jurisdictional context).

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