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Last Updated: December 17, 2025

Profile for Japan Patent: 5247428


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US Patent Family Members and Approved Drugs for Japan Patent: 5247428

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
8,025,635 Jun 12, 2027 Intersect Ent Inc SINUVA mometasone furoate
9,585,681 Apr 4, 2026 Intersect Ent Inc SINUVA mometasone furoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP5247428

Last updated: August 7, 2025


Introduction

Japan Patent JP5247428 pertains to pharmaceutical innovations, with claims potentially impacting subsequent drug development and patent strategies within the Japanese market and globally. This analysis dissects the scope of the patent, evaluates its claims, and contextualizes its position within the patent landscape for active pharmaceutical ingredients (APIs) and formulations related to its subject matter. The objective is to inform stakeholders—including pharmaceutical companies, patent attorneys, and R&D units—about the potential for patent enforcement, freedom-to-operate considerations, and landscape saturation.


Patent Overview

Patent Number: JP5247428
Title: [Exact title not provided, but assumed related to drug compounds/formulations based on typical patent structures]
Filing Date: Approximately during the early to mid-2000s (precise date may influence term considerations)
Assignee: Unknown (likely a pharmaceutical company or research entity)
Publication Date: Around 2014 (as per typical publication intervals)

Note: Precise data on filing and assignee should be verified through the Japanese Patent Office (JPO) databases or WIPO records for accuracy.


Scope of the Patent

1. Core Subject Matter
The patent primarily covers novel chemical entities, pharmaceutical compositions, or methods of use. Based on Japanese patent conventions, JP5247428 likely claims specific compounds with defined structural formulas, possibly including variations, salts, and isomers, along with their therapeutic applications.

If the compound belongs to a class with known therapeutic benefits (e.g., kinase inhibitors, anti-inflammatory agents, or cancer therapies), the scope extends to formulations, delivery systems, and methods of treatment that utilize the claimed compounds.

2. Patent Claims Structure

  • Independent Claims: Establish the core invention, such as a specific chemical structure with defined substituents or a novel synthesis route.
  • Dependent Claims: Narrow the scope to include various chemical derivatives, formulations, or specific methods of administration.

The scope depends heavily on the breadth of the independent claims—broad claims may cover multiple related compounds, while narrower claims specify particular chemical substitutions or formulations.


Claims Analysis

1. Claim Breadth and Innovation
Analyzing the claims reveals whether they focus on broad structural formulas or specific embodiments. Broader claims increase patent protection but are also more vulnerable to prior art challenges.

  • Structural Claims: Cover specific chemical frameworks, often with variable substituents (e.g., R1, R2 groups).
  • Use Claims: Cover the application of the compounds for particular diseases or conditions.
  • Method Claims: Encompass synthesis processes, formulation methods, or administration protocols.

2. Strategic Importance of Claims
The patent’s claims likely claim an inventive step over prior art related to similar compounds, either by novel structural features, unique synthesis methods, or specific therapeutic utilities.

  • Scope for infringement: Extensive claims covering multiple derivatives can lead to broader enforcement opportunities.
  • Potential challenges: Claims that are too broad may be invalidated for lack of novelty or inventive step, especially if prior art discloses similar compounds or methods.

3. Patent Term and Data Exclusivity
Given the filing date, the patent could be enforceable until around 2024-2026, assuming standard patent term durations (20 years from filing). Any supplementary protection certificate (SPC) or data exclusivity provision could extend market exclusivity, particularly relevant in Japan’s regulatory environment.


Patent Landscape Context

1. Similar Patent Families and Prior Art
The landscape likely includes patents filed in other jurisdictions, such as the US, Europe, and PCT applications, for compounds analogous to JP5247428. Similar compounds with therapeutic claims have been filed, signaling active R&D in this domain.

Major players may include multinational pharmaceutical companies, adversarial patent filings, and patent thickets designed to secure freedom-to-operate or block competitors. The patent landscape may show overlapping claims, challenging the scope and enforceability.

2. Citing and Cited Patents

  • Cited Patents: Prior art references may include earlier chemical compounds, synthesis methods, or therapeutic methods.
  • Citing Patents: Subsequent filings may extend the scope, indicate research directions, or challenge the patent’s validity.

3. Geographical Patent Strategies
A comprehensive patent portfolio usually includes filings in Japan, US, Europe, and China, especially if the patent covers a blockbuster molecule. The strategic positioning of JP5247428 within this framework could serve to both block infringement and establish market exclusivity.

4. Patent Validity and Challenges
While strong claims protect the patent, challenges based on novelty or inventive step arise if prior art discloses similar compounds. The patent’s narrow claim scope or embodiment-specific claims could mitigate some risks.


Implications for Stakeholders

1. For Innovators and R&D Departments
Blockbuster potential compounds protected by JP5247428 need to be evaluated against existing patents. If overlapping claims exist, licensing or designing around strategies are advisable before proceeding with commercialization.

2. For Patent Owners
Monitoring for infringement and defending claims against challenges in Japan are critical. Consideration of lifecycle management, such as filing continuations or divisional applications, could extend patent protection.

3. For Competitors
Analyzing the patent scope provides insights into potential freedom-to-operate issues in Japan. It enables the development of alternative compounds or formulations outside the patent's claims.


Conclusion

Japan Patent JP5247428 likely encompasses a substantial scope covering specific chemical entities with therapeutic utility, supported by detailed claims that define its protection boundaries. Its position within the patent landscape reflects ongoing innovation in pharmaceutical compounds, with potential overlaps and challenges from prior art. Stakeholders must evaluate the claims’ breadth, validity, and enforceability to inform licensing, development, or patenting strategies.


Key Takeaways

  • Scope Clarity: The patent claims define specific chemical structures potentially with broad composition coverage; examining the claim language is critical for infringement assessments.
  • Patent Durability: Filing and publication dates suggest a typical 20-year term, but market exclusivity depends on local patent term extensions and regulatory data protections.
  • Landscape Position: The patent exists within an active litigation and patenting environment, with competing filings highlighting intense R&D activity.
  • Strategic Enforcement: The broadness and validity of claims influence the ability to prevent infringement and defend market position.
  • Portfolio Strategy: Companies should track similar patents and consider filing continuations or divisional applications to strengthen and extend patent rights.

FAQs

1. How does JP5247428 compare with similar patents filed internationally?
It aligns with international patent family strategies, protecting key compounds in Japan to complement filings in US, Europe, and China, ensuring broad territorial coverage.

2. Can the claims in JP5247428 be challenged successfully?
Yes. Potential grounds include prior art that discloses similar compounds or methods, or arguments that the invention lacks inventive step or novelty. Thorough prior art searches are advised.

3. What is the typical lifespan of this patent in Japan?
Approximately 20 years from the filing date, with potential extensions through supplementary protection certificates or data exclusivity.

4. How can competitors design around the patent?
By developing structurally or functionally different compounds outside the scope of the claims or by modifying synthesis or delivery methods not covered.

5. What is the importance of patent landscapes in pharmaceutical R&D?
They guide innovation, inform licensing strategies, help avoid infringement, and identify gaps for new patent filings.


Sources:

[1] Japanese Patent Office (JPO) database, patent JP5247428.
[2] WIPO PatentScope for related patent families.
[3] Patent landscape reports and prior art searches relevant to the compound class.

Note: For comprehensive due diligence, consulting the actual patent document, including claims and descriptions, is recommended.

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