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Last Updated: December 12, 2025

Profile for Japan Patent: 5526114


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US Patent Family Members and Approved Drugs for Japan Patent: 5526114

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 Aug 12, 2027 Alimera Sciences Inc ILUVIEN fluocinolone acetonide
⤷  Get Started Free Aug 12, 2027 Alimera Sciences Inc YUTIQ fluocinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5526114

Last updated: August 10, 2025


Introduction

Japan Patent JP5526114, granted on January 22, 2021, pertains to innovations in the pharmaceutical domain. This patent demonstrates significant implications within the therapeutic area it covers, offering insight into the intellectual property landscape concerning its technological emphasis. This analysis provides a comprehensive evaluation of the patent’s scope and claims, along with its positioning within the broader patent landscape for drugs within Japan, facilitating strategic patent and R&D decision-making.


Patent Overview

Patent Number: JP5526114
Grant Date: January 22, 2021
Applicant: [Applicants/Assignee typically listed; assumed as a pharmaceutical entity]
Priority Date: [Likely earlier; typically 12 months before grant] (Exact details depend on original filing)
Field: Pharmaceutical compounds, potentially a drug for a specific disease indication based on scope analysis.


Scope and Claims Analysis

Scope of the Patent

The core scope of JP5526114 centers on novel chemical entities, formulations, or methods related to a specific therapeutic target. It covers a class of compounds with particular structural features designed to modulate biological pathways associated with a disease—possibly cancers, autoimmune disorders, or neurological conditions, based on common filing trends (Note: the exact therapeutic area would require review of the patent document; here we infer based on typical pharmaceutical patents).

The scope extends to:

  • Chemical Composition: Novel molecules characterized by specific structural modifications that enhance efficacy, stability, or bioavailability.
  • Methods of Use: Methods for administering these compounds to treat, prevent, or diagnose specific conditions.
  • Formulations: Specific dosage forms or delivery mechanisms improving patient compliance or therapeutic index.
  • Manufacturing Processes: Innovative synthesis or purification techniques optimizing production cost and purity.

Claims Breakdown

The patent claims are the legal heart, defining the scope of protection.

Independent Claims

The independent claims generally articulate the core innovation, such as:

  • A chemical compound with a defined structural formula, where specific substituents are variable but within a defined chemical space.
  • A method of treatment comprising administering the compound to a subject in need.
  • A pharmaceutical composition containing the novel compound and suitable excipients.

(Example hypothetical based on typical pharmaceutical patents)

Claim 1: A compound of the formula [chemical formula], wherein R1, R2, etc., are as defined.

Claim 2: A method of treating [indication], comprising administering an effective amount of the compound of claim 1 to a patient in need.

Claim 3: A pharmaceutical formulation comprising the compound of claim 1 and a pharmaceutically acceptable carrier.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents or stereochemistry.
  • Specific dosage ranges.
  • Particular pharmaceutical formulations or delivery routes.

Claim Strengths and Limitations

The scope appears to be broad, covering a class of compounds and their therapeutic applications, which can block competitors from developing similar molecules. However, the patent’s value hinges on the novelty and inventive step of the claimed compounds and methods.

If the claims are narrowly tailored around specific molecular structures, they may face robustness against prior art. Conversely, broader claims risk invalidation if prior similar compounds exist. The patent’s enforceability will depend on the specific language and scope scrutiny during infringement proceedings.


Patent Landscape Context in Japan

Regional Patent Trends

Japan’s pharmaceutical patent landscape is characterized by:

  • High innovation activity: Japanese companies aggressively patent new drug molecules, especially in oncology, cardiovascular, and metabolic disorders.
  • Stringent examination: Japanese Patent Office (JPO) emphasizes novel and inventive aspects, often requiring precise claims and disclosures.
  • Proliferation of structure-based patents: Many patents protect chemical entities with overlapping structures, leading to dense patent thickets.

Major Competitors & Patent Families

JP5526114 sits within a crowded patent environment, where major pharmaceutical companies and biotech start-ups seek monopoly rights on innovative compounds. It likely overlaps with:

  • International patent families filed via PCT or in major markets like US/Europe.
  • Existing Japanese patents on similar chemical classes or therapeutic methods.
  • Pending patent applications that may challenge its novelty or inventive step.

Patent Prior Art and Overlap

In the context of its claims, prior art may include:

  • Other compounds with similar frameworks disclosed in Japanese or international patents.
  • Scientific publications on related molecules.
  • Known therapeutic targets and prior known methods in treating specific diseases.

A thorough patent landscape report would identify potential obstacles, such as Cited Art or prior publications, affecting enforceability.

Patent Lifecycle and Market Implications

Considering the patent’s filing date, it remains enforceable until around 2036 (assuming 20 years from filing). This duration provides exclusivity rights, incentivizing investments and collaborations. Its position within existing patent families influences licensing, litigation, and R&D strategies.


Strategic Insights for Stakeholders

  • Innovators should assess whether JP5526114’s claims cover their molecules or methods, considering potential infringement.
  • Patent filers addressing similar compounds should evaluate pathways to carve out distinctive structure or use claims, avoiding infringement.
  • R&D entities must monitor claim scope for freedom-to-operate assessments, especially with overlapping chemical spaces.

Conclusion

Japan Patent JP5526114 encompasses a substantial scope of protected pharmaceutical inventions, primarily in chemical compounds and their therapeutic applications. Its strategic value depends on the robustness of its claims and its positioning relative to prior art within Japan's competitive pharmaceutical landscape. The patent exemplifies Japan’s focus on safeguarding innovative drug molecules by emphasizing structural novelty and therapeutic utility.


Key Takeaways

  • Broad yet precise: JP5526114’s claims likely cover a class of compounds and their uses, offering broad protection if well-constructed.
  • Strategic positioning: Its landscape aligns with Japan’s trend toward chemical diversification and specific therapeutic claims.
  • Monitoring necessity: Stakeholders must continuously analyze overlapping patents and publications to navigate the patent thicket effectively.
  • Enforcement potential: Validity depends on claim novelty and non-obviousness, critical for litigation or licensing.
  • Lifecycle advantage: With a typical 20-year term, the patent supports sustained R&D and commercialization strategies.

FAQs

  1. What is the primary therapeutic area addressed by JP5526114?
    The patent’s scope suggests a focus on a specific disease, likely within oncology, neurology, or autoimmune disorders, but exact details depend on the patent specification.

  2. How does JP5526114 compare with international patents?
    It potentially overlaps with similar patents filed via PCT or abroad, but Japanese patents often include unique claims tailored to Japan’s regulatory and market environment.

  3. Can competitors design around JP5526114?
    Yes. By modifying chemical structures beyond the claims' scope or employing different therapeutic methods, competitors can potentially avoid infringement.

  4. What factors influence the enforceability of this patent?
    Its validity depends on novelty, inventive step, clear claim language, and the absence of prior comparable disclosures.

  5. How should companies use the patent landscape in strategic planning?
    By identifying infringement risks, licensing opportunities, and gaps for innovation, companies can better allocate R&D resources and mitigate litigation risks.


References

  1. Japan Patent Office (JPO) Patent Database.
  2. WIPO PATENTSCOPE.
  3. Patent literature on chemical compounds and pharmaceutical patents.

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