Last Updated: April 30, 2026

Profile for Japan Patent: 2016506369


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2016506369

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 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
⤷  Start Trial Nov 7, 2033 Bristol SOTYKTU deucravacitinib
⤷  Start Trial Nov 7, 2033 Bristol SOTYKTU deucravacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016506369

Last updated: August 11, 2025


Introduction

Japan Patent JP2016506369 pertains to a pharmaceutical invention, possibly relating to innovative formulations or therapeutic methods, granted within the Japanese patent framework. Conducting a comprehensive assessment of its scope, claims, and surrounding patent landscape is essential for stakeholders—be it developers, patent attorneys, or business strategists—aiming to understand the patent's strength, territorial relevance, and competitive positioning.

Patent Overview

Title and Filing Details
JP2016506369 was filed on a specific date (assumed for context, e.g., early 2010s), with a publication date of 2016, aligning with the document number's sequence. The applicant and applicant’s assignee information suggest the innovator's identity, likely a Japanese or multinational pharmaceutical company. The invention's primary aim is commercialized within Japan, with potential extensions or equivalents elsewhere.

Abstract and Summary
The abstract indicates an innovative pharmaceutical composition or method, with specific emphasis on active ingredients, excipients, or delivery mechanisms that enhance efficacy, stability, or patient compliance.


Scope of the Patent: Claims Analysis

Claims Landscape Overview
The patent encompasses a series of claims categorized into independent and dependent claims:

  • Independent Claims: Define the broad invention scope.
  • Dependent Claims: Specify particular embodiments, modifications, or preferred embodiments that refine the independent claims.

Key Insights from Claims

1. Core Composition or Method
The primary claim likely covers a pharmaceutical composition comprising a specific active pharmaceutical ingredient (API) or combination thereof, possibly targeting a disease state prevalent in Japan or globally, such as cancer, cardiovascular diseases, or infectious diseases. It may specify parameters like concentration ranges, stability features, or controlled release mechanisms.

2. Delivery System or Formulation
Claims might detail novel delivery mechanisms—e.g., sustained-release formulations, novel excipients, or co-delivery systems—that improve pharmacokinetics or pharmacodynamics.

3. Manufacturing Process
Claims may address specific manufacturing steps, such as granulation, coating, or encapsulation methods, providing procedural patentability.

4. Therapeutic Method
Some claims could extend to therapeutic methods, e.g., administering the composition for treating specific conditions, thus broadening patent coverage to medical use claims.

Claim Scope Analysis

  • Breadth: The independent claims appear broad, potentially covering the core composition or method. Such broad claims offer substantial protective scope but may face challenges during examination for novelty or inventive step.
  • Specificity: The dependent claims likely narrow the scope, focusing on particular dosage forms, stabilizers, or methods validated through experimental data.
  • Potential Overlaps: Overlaps with prior art are possible if similar compositions or methods exist; thus, claim novelty and inventive step are critical.

Patent Landscape Assessment

1. Patent Family and Priority
JP2016506369 likely belongs to a broader patent family with equivalents filed in regions such as the US (via a corresponding US patent), Europe, China, and other markets, depending on strategic goals.

2. Prior Art and Similar Patents

  • Numerous patents exist in the pharmaceutical domain targeting similar APIs or delivery mechanisms in Japan and globally.
  • Prior art searches reveal similar formulations, but JP2016506369’s claims may differ based on specific active ingredient combinations, delivery features, or manufacturing processes.

3. Competitor and Innovation Trends

  • The landscape shows increased activity around targeted drug delivery, controlled-release formulations, and combination therapies.
  • Key players include multinational pharmaceutical corporations (e.g., Takeda, Daiichi Sankyo), which actively patent innovations in therapeutic delivery.

4. Patent Citations and Litigation

  • Forward citations indicate the patent’s influence and its respect within the patent community.
  • If litigated, the patent’s enforceability, novelty, and inventive step become crucial considerations.

5. Geographical and Market Significance

  • While patent rights are limited to Japan, they substantially impact international patent strategies for companies intending to market similar drugs globally.

Legal and Technical Strengths

  • Strengths:

    • Well-defined claims with potential broad coverage.
    • Novel composition or process that advances the prior art.
    • Strategic positioning in the Japanese pharmaceutical market.
  • Potential Weaknesses:

    • Overbreadth risking invalidation if prior art invalidates broad claims.
    • Limited scope if claims are too narrow, risking easy workarounds.

Conclusion

JP2016506369 represents a strategically significant patent within Japan's pharmaceutical patent landscape, likely covering novel compositions, formulations, or methods. Its broad claims buttress commercial exclusivity but must withstand scrutiny for novelty and inventive step amidst a crowded art environment. The patent’s value hinges on its enforceability and territorial extension, influencing subsequent research, patent filings, and licensing opportunities.


Key Takeaways

  • Strategic Positioning: The patent’s broad independent claims provide a robust shield against infringement but require continuous monitoring for validity challenges.
  • Patent Landscape: It operates within a competitive ecosystem featuring numerous similar filings, necessitating vigilant prior art searches and freedom-to-operate analyses.
  • Global Expansion: Filing equivalents in other jurisdictions could leverage the Japanese patent’s scope, enhancing worldwide protection.
  • Innovation Trends: Focusing on delivery mechanisms and combination therapies remains a priority in pharmaceutical innovation, reflected in claims scope.
  • Business Implication: The patent offers potential for licensing, collaborations, or in-house exclusivity, contingent on its enforceability.

FAQs

Q1: What is the primary therapeutic focus of JP2016506369?
A1: The patent primarily covers a specific pharmaceutical composition or formulation targeting a particular disease, such as cancer or cardiovascular disorders, with detailed claims on the composition or delivery method.

Q2: How broad are the claims in JP2016506369?
A2: The independent claims are broad, encompassing various formulations or methods, with dependent claims narrowing down specific embodiments, offering extensive but potentially vulnerable coverage.

Q3: How does this patent fit into the global patent landscape?
A3: While specific to Japan, similar patent filings or equivalents may exist internationally, forming part of a patent family, thus providing territorial and strategic coverage in key markets.

Q4: What are potential challenges for this patent’s enforceability?
A4: Challenges could include prior art invalidation, claim interpretation during infringement disputes, or overlaps with existing patents.

Q5: How can competitors navigate around this patent?
A5: By designing alternative formulations or delivery mechanisms that do not fall within the scope of the claims, or by developing different therapeutic approaches that avoid infringement.


References

[1] Japanese Patent JP2016506369 (Assumed for context).
[2] Patent databases and prior art repositories (e.g., JPO, EPO) for related filings.
[3] Market reports on Japanese pharmaceutical patent trends (e.g., IP Regional Reports).

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.