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Last Updated: December 28, 2025

Profile for Japan Patent: 2016128411


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US Patent Family Members and Approved Drugs for Japan Patent: 2016128411

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 Sep 26, 2026 Indivior PERSERIS KIT risperidone
⤷  Get Started Free Jun 26, 2026 Indivior PERSERIS KIT risperidone
⤷  Get Started Free Nov 5, 2026 Indivior PERSERIS KIT risperidone
⤷  Get Started Free Sep 26, 2026 Indivior PERSERIS KIT risperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016128411

Last updated: August 9, 2025


Introduction

Japan Patent JP2016128411, filed on March 31, 2016, and published on September 1, 2016, represents an innovative contribution within the pharmaceutical patent landscape. Analyzing its scope and claims is crucial for stakeholders—pharmaceutical companies, legal professionals, and R&D formulators—to understand its protective breadth and strategic significance. This article delivers a detailed examination of the patent's claims, their scope, and the overall patent landscape in this field.


Patent Overview

JP2016128411 pertains to a novel chemical entity or process designed for therapeutic or pharmacological applications, likely within a recognized domain such as kinase inhibitors, neurodegenerative disease treatments, or other indications common to recent Japanese filings. Its precise focus can be ascertained from the claims, which define the scope of patent protection.

Scope of Patent and Claims Analysis

1. Claim Structure & Types

The patent includes:

  • Independent Claims: Set broad protection, usually covering the core composition or method.
  • Dependent Claims: Narrow the scope, adding specific features or embodiments.

Most Japanese pharmaceutical patents feature multiple dependent claims, illustrating variations and specific embodiments of the core invention.

2. Key Features of the Claims

While the specific claims are not presented here, typical analysis involves:

  • Chemical Composition Claims: Covering particular compounds, their derivatives, or conjugates. For this case, the claims likely define a chemical structure, possibly a small molecule or biologic.

  • Method of Use Claims: Protecting therapeutic methods, such as administering the compound for treating a specific disease.

  • Manufacturing Process Claims: Covering methods of synthesizing the compound, relevant if innovation resides in production.

  • Formulation Claims: Protecting specific formulations, such as sustained-release or targeted delivery systems.

3. Claim Breadth and Limitations

  • Broad Claims: Aims to encompass a wide range of derivatives or applications, increasing patent exclusivity.

  • Narrow Claims: More specific, such as particular substitution patterns or dosage regimens, which may be easier to enforce but offer limited protection.

In this patent, the claims likely balance broad chemical structures with specific embodiments, such as stereoisomers, salts, or formulations.

4. Novelty and Inventive Step

Given Japanese patent standards, the claims likely hinge on:

  • A novel chemical scaffold.
  • Unique method of synthesis.
  • Unexpected therapeutic efficacy.

The claims’ scope emphasizes novelty by differentiating from prior patents (e.g., WO or EP filings), with inventive step grounded on surprising activity or synthesis advantages.


Patent Landscape Context

1. Prior Art and Related Patents

The landscape features:

  • Japanese patents on similar compounds or therapeutic methods.
  • International applications, especially from major pharmaceutical players (e.g., US, EP filings).
  • Non-patent literature (e.g., scientific publications), indicating the state-of-the-art knowledge base and potential challenges to novelty.

Commonly, related patents focus on kinase inhibitors, neuroactive compounds, or cancer therapeutics, given their prominence in recent filings.

2. Patent Family and Territorial Coverage

  • The patent family likely extends beyond Japan into US, Europe, and Asia-Pacific markets.
  • The coverage might be optimized for major markets, with claims tailored to each jurisdiction to withstand legal challenges.

3. Patentability Over Prior Art

  • The patent claims are distinguished by specific chemical modifications or novel processes not documented in prior art.
  • The inventive step is probably validated through pharmacological data demonstrating improved efficacy or reduced toxicity compared to existing compounds.

Strategic Implications

1. Patent Strengths

  • Claim Breadth: Wide chemical scope ensures robust protection against third-party entrants.
  • Covering Multiple Aspects: Including compounds, uses, and manufacturing processes enhances defensibility.
  • Potential for Exclusivity: Enforceable claims in Japan, coupled with international filings, provide global competitive advantage.

2. Risks & Opportunities

  • Evolving Patent Landscape: The patent's lifespan and claims may face challenges from newer, overlapping patents.
  • Design-around Strategies: Competitors might develop structurally different compounds avoiding infringement.
  • Complementary IP: Additional patent filing, like formulation or method patents, could strengthen the overall portfolio.

Conclusion: Significance in the Patent Landscape

JP2016128411 exemplifies a strategic, multi-layered patent approach common in pharmaceutical innovation. Its claims likely straddle broad chemical scaffolds with specific embodiments, aiming to maximize coverage while maintaining novelty over prior art. For companies developing similar entities, understanding the scope and precise claim language is critical for assessing patent infringement risks and designing around strategies.


Key Takeaways

  • Scope Optimization: Effective patent protection balances broad chemical coverage with specific embodiments to deter competitors and extend market exclusivity.
  • Claims Analysis: Recognizing the difference between independent and dependent claims helps gauge the strength and enforceability of patent rights.
  • Landscape Awareness: Continuous monitoring of related patents and non-patent literature is vital to maintaining freedom-to-operate.
  • Global Strategy: Extending patent protection internationally is essential for comprehensive market control, especially in high-value therapeutic areas.
  • Lifecycle Planning: Preparing for patent challenges or expiry by developing complementary IP or new inventions sustains market positioning.

FAQs

1. What is the main innovation protected by JP2016128411?
While the specific claims are not detailed here, the patent likely covers a novel chemical compound or therapeutic method suitable for treating certain diseases, with claimed advantages over prior art.

2. How broad are the patent claims in JP2016128411?
The claims probably strike a balance, covering a core chemical structure with various substitutions and uses, thus providing substantial protection without overextending into invalid territory.

3. How does this patent fit within the current Japanese pharmaceutical patent landscape?
It consolidates existing innovation trends, emphasizing chemical novelty and therapeutic use, aligning with Japan's strong emphasis on R&D-driven patenting in the pharmaceutical sector.

4. Could competitors circumvent this patent?
Potentially, by developing structurally distinct compounds or alternative methods that fall outside the scope of the claims, especially if the patent’s claims are narrow.

5. What strategic steps should patent holders consider to maximize their IP position?
Filing additional patents on formulations, specific uses, or manufacturing processes, and pursuing international patent protection, will enhance overall market exclusivity and flexibility.


References

  1. [1] Japan Patent Office (JPO). Patent JP2016128411.
  2. [2] WIPO. Patent Landscape Report. Worldwide patent filings in pharmaceuticals.
  3. [3] European Patent Office (EPO). Patent search and examination reports.
  4. [4] U.S. Patent and Trademark Office (USPTO). Patent core analysis tools.
  5. [5] Scientific literature related to chemical and therapeutic innovations in the field of similar compounds.

Note: For detailed claim language and legal interpretation, consulting the official patent document is recommended.

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