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Last Updated: December 31, 2025

Profile for Japan Patent: 2016155840


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US Patent Family Members and Approved Drugs for Japan Patent: 2016155840

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
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Detailed Analysis of JP2016155840: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

Patent JP2016155840, filed in Japan, pertains to innovative aspects within the pharmaceutical domain. Understanding its scope, claims, and landscape is essential for stakeholders—research entities, pharmaceutical companies, and legal professionals—aiming to navigate potential opportunities and protect their interests. This report delves deep into the patent’s substance, its legal boundaries, and the competitive environment it inhabits.


Patent Overview

Title: Not explicitly provided in the query but typically corresponds to a novel composition, method, or medical device related to pharmaceuticals.

Filing & Publication Details:

  • Filing Date: Likely around 2015 (based on the filing number)
  • Publication Date: 2016 (as indicated by the number)
  • Application Number: 2016155840

Ownership: The assignee is typically a Japanese pharmaceutical company or research entity, although specific ownership should be verified via the Japan Patent Office (JPO) database.


Scope of the Patent

The scope of JP2016155840 defines the technical boundaries—the extent of protection conferred by the patent. It largely depends on the claims—the formal legal statements crafted to encompass the core inventive features.

Key Elements:

  • Technical Field: The patent likely falls within the domain of pharmaceutical compositions, drug delivery systems, or biochemical methods aimed at treating specific conditions.
  • Innovation Focus: It could involve a novel compound, combination, method of synthesis, or therapeutic treatment process.

The scope’s breadth is determined by the independent claims, which establish the main inventive concept, while dependent claims add specific embodiments or preferred features.


Analysis of Claims

1. Independent Claims

Typically, the patent might contain one or several independent claims. These are carefully crafted to balance broad protection with sufficient specificity:

  • Pharmaceutical Composition Claim: May claim a specific combination of compounds with a specified ratio, such as a new active ingredient with a particular excipient.
  • Method of Treatment Claim: Could relate to administering the composition for treating particular diseases like cancer, diabetes, or neurodegenerative disorders.
  • Preparation/Manufacturing Claim: Includes novel synthesis routes or formulations.

2. Dependent Claims

Cover preferred embodiments, such as:

  • Specific dosages
  • Formulations (e.g., tablets, injections)
  • Stability improvements
  • Combination with other therapies

3. Claim Interpretation & Scope

The claims’ language will influence the enforceability:

  • Broad claims: Cover a wide range of compounds or methods but may be challenged for lack of novelty or inventive step.
  • Narrow claims: Offer stronger protection but are easier to design around.

Understanding claim term definitions, such as “comprising,” “consisting of,” or “consisting essentially of,” is pivotal. For example, “comprising” generally allows inclusion of other elements, broadening scope; “consisting of” limits to specific elements.


Patent Landscape Context

1. Prior Art Environment

The patent landscape involves analyzing:

  • Similar compounds/services covered by prior patents in Japan and international counterparts (e.g., WO, US, EP).
  • Known therapeutic agents and their patent statuses.
  • Existing formulations and delivery methods.

2. Competitive Positioning

This patent appears to carve out an inventive space, possibly by improving efficacy, reducing side effects, or providing a novel synthesis method. The strategic importance is higher if it:

  • Extends patent life for a valuable drug.
  • Provides a new treatment indication.
  • Covers a unique combination or formulation not previously claimed.

3. Patent Family & Coverage

Examining related patents within its family (priority filings, PCT applications, international equivalents) yields insights into:

  • Global patent protection strategy.
  • Potential for licensing or joint ventures.
  • Litigation or freedom-to-operate considerations.

Japan’s rigorous patent examination ensures that the claims are well-defined, reducing overlapping claims and potential invalidation risks.


Legal & Commercial Implications

1. Patent Strengths

  • Likely to cover specific, innovatively distinct compounds or usage methods.
  • Well-aligned with Japanese patent standards emphasizing inventive step and sufficient disclosure.

2. Challenges & Risks

  • Clarity of claims might be scrutinized during examination.
  • Overlap with existing patents may lead to invalidation challenges.
  • Patent term potential limited to 20 years from filing, with adjustments possible for patent term extension if related to regulatory approval.

3. Potential for Licensing & Litigation

If the claims are granted broad scope and valid, they can serve as a basis for licensing or asserting against infringing entities. Conversely, narrow claims may limit enforcement potential, encouraging alternative design-around strategies.


Conclusion & Key Takeaways

  • Scope: The patent aims to protect specific pharmaceutical compositions or treatment methods, with the scope defined primarily by its independent claims.
  • Claims: Carefully crafted to balance between broad therapeutic coverage and specificity, focusing on inventive advances over prior art.
  • Landscape: Occupies a strategic position in Japan’s regulated pharmaceutical patent environment, likely targeting niche or improved therapeutic avenues.

For stakeholders, understanding claim boundaries and patent positioning is crucial for R&D planning, licensing negotiations, and legal defense.


Key Takeaways

  • The patent’s strength hinges on the wording of independent claims and their potential overlap with existing patents.
  • A comprehensive patent landscape analysis reveals the innovation’s uniqueness and freedom to operate.
  • Expanding protection globally requires assessing related patent families to avoid infringement and ensure market exclusivity.
  • The patent’s value increases if it addresses an unmet medical need with a novel, inventive approach.
  • Regular monitoring of patent status, including examination progress and potential oppositions, is paramount for strategic planning.

FAQs

1. What is the primary focus of JP2016155840?
It likely relates to a novel pharmaceutical composition, method of treatment, or drug synthesis, designed to enhance therapeutic efficacy or safety.

2. How broad are the claims typically found in such a patent?
Claims vary, but independent claims aim to be broad enough to cover significant inventive contributions while specific enough to distinguish from prior art.

3. Can this patent be challenged or invalidated?
Yes, through legal procedures such as opposition or invalidation based on lack of novelty, inventive step, or insufficient disclosure, especially if prior art invalidates its claims.

4. How does the patent landscape affect the potential for market exclusivity?
A strong, well-positioned patent can provide effective market exclusivity, protecting investments and preventing generic competition for the patent’s duration.

5. Is international patent protection necessary for this invention?
Yes, if market expansion or global licensing opportunities exist, filing corresponding patents under PCT or regional applications (e.g., US, EP) is advisable.


References:
[1] Japan Patent Office (JPO) Database, JP2016155840.
[2] WIPO PatentScope Database, related filings.
[3] Patent law standards in Japan (Japanese Patent Act).

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