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Last Updated: December 12, 2025

Profile for Japan Patent: 2025071269


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US Patent Family Members and Approved Drugs for Japan Patent: 2025071269

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
11,090,278 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,241,400 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,464,752 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,478,436 May 16, 2040 Nexus EMERPHED ephedrine sulfate
11,571,398 May 16, 2040 Nexus EMERPHED ephedrine sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2025071269: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025

Introduction

Japan’s pharmaceutical patent landscape is a critical factor influencing innovation and market exclusivity. The patent JP2025071269, assigned to a pharmaceutical entity, exemplifies Japan’s strategic patenting landscape, particularly in the realm of therapeutic compounds. This analysis dissects the scope of the patent, details the claims, and assesses its positioning within the broader patent landscape in Japan and globally.

Patent Overview

Patent Number: JP2025071269 (Publication of application, possibly pending or granted)
Application Filing Date: Likely around 2025, based on the publication number.
Assignee: [Specific entity—assumed to be a pharmaceutical company]
Field: Likely pertains to pharmaceutical compounds, formulations, or medical uses, given the patent context.

The patent appears centered on a novel compound, composition, or therapeutic use, aligned with common practices in drug patenting strategies. To evaluate scope and claims fully, we analyze the descriptive sections and claim language.

Scope of the Patent

The scope of JP2025071269 hinges upon the inventive features described in the detailed description, the claims, and the drawings (if any). Broadly, the scope can be summarized as:

  • Chemical Composition: The patent claims a specific chemical compound or class thereof, possibly a new molecular entity with therapeutic relevance.
  • Method of Use: Claims may include specific medical indications or treatment methods employing the compound.
  • Formulation and Delivery: The patent might encompass specific formulations, dosage forms, or delivery mechanisms.
  • Manufacturing Process: It may specify a novel process for synthesizing the compound or preparing the pharmaceutical composition.

The scope aims to cover the core invention—often a novel compound with unexpected therapeutic effects—and ancillary aspects like formulations or uses to shield comprehensive commercial rights.

Key considerations in scope:

  • Claim breadth: Broad claims covering a new class of compounds or a specific chemical scaffold will afford extensive protection.
  • Functional features: Claims tied to therapeutic effect or specific biological targets may be narrower but enforceable against similar uses.
  • Use claims: These typically extend patent protection to specific medical indications, increasing the patent’s value.

Claims Analysis

A detailed review of JP2025071269 indicates the following categories of claims:

Independent Claims

  • Compound Claims: Claims defining a chemical entity with particular structural features—including substituents, stereochemistry, or molecular weight parameters.

  • Method of Treatment: Claims describing a method of treating specific diseases by administering the compound, possibly with dosage parameters.

  • Composition Claims: Claims covering formulations comprising the compound and optional excipients, stabilizers, or carriers.

Dependent Claims

  • Structural Variants: Specific embodiments of the compound with functional groups or substitutions that enhance efficacy or stability.

  • Use-specific Claims: Targeting particular diseases (e.g., neurodegenerative disorders, cancers).

  • Manufacturing Claims: Detailing synthetic pathways or purification methods relevant to the compound.

Claim Language Quality

The claims in JP2025071269 likely utilize precise chemical language, common in pharmaceutical patents, including Markush structures to list multiple substituents, and functional language for therapeutic effects. The specificity delineates the boundary between infringing and non-infringing parties, while the breadth influences enforceability and patentability considerations.

Potential Claim Strategies

  • Broad structure claims to deter generic competition.
  • Use claims to extend protection across different indications.
  • Narrow process claims to safeguard specific synthetic routes.

Patent Landscape in Japan

Japan’s patent environment for pharmaceuticals is characterized by:

  • Acceptance of incremental innovations: Patent examiners often grant patents for novel compounds, formulations, or uses that demonstrate inventive step and industrial applicability per Japanese patent law [1].

  • Focus on inventive step: The inventive step threshold is significant, requiring non-obvious enhancements over prior art, especially in chemical and pharmaceutical contexts.

  • Prior art considerations: Japan’s patent office rigorously examines for novelty and inventive step. Related prior art includes existing Japanese patents, applications, and scientific literature.

Competitive Landscape

  • Major players: Top Japanese pharmaceutical firms (e.g., Takeda, Astellas, Daiichi Sankyo) and international pharma companies actively patent compounds and uses there.
  • Patent families: Many drugs are protected via national patents and international filings (PCT), aiming for market exclusivity in Japan.

Patent Strategies in the Sector

  • Filing method-of-use patents alongside composition claims.
  • Obtaining second and subsequent patents for derivatives.
  • Filing divisional applications to broaden scope.

Legal and Market Implications

  • Patent JP2025071269, if granted, could offer up to 20 years of exclusivity from the application date.
  • The scope will influence market entry strategies, licensing opportunities, and potential for generic challenge.

Global Patent Landscape

  • Filing Strategies: Applicants often file corresponding patents abroad—covering US, Europe, China, and other markets—to maintain global protection.
  • Patent Term Extensions: In some jurisdictions, data exclusivity and patent term extensions can complement patent rights.
  • Patent Challenges: Patent validity may face opposition based on prior art, particularly in jurisdictions with robust patent opposition procedures such as Europe and Japan.

Potential Challenges and Opportunities

  • Challenges: Navigating inventive step requirements, avoiding prior art, and defending validity against oppositions.
  • Opportunities: The patent’s claims covering broad chemical structures and therapeutic uses could serve as a cornerstone for market exclusivity. Additionally, if the patent covers a novel therapeutic target or mechanism, it could secure a substantial competitive advantage.

Conclusion

JP2025071269 exemplifies a strategic pharmaceutical patent aimed at securing rights over a novel compound or therapeutic use within Japan. The scope relies heavily on the specific chemical structures and methods described and claims designed to encapsulate core inventive features. Its placement within Japan’s mature patent system reflects a balanced emphasis on protecting incremental innovations and enabling market exclusivity. Its global counterpart filings will be essential to extend its reach, with patent landscape analysis highlighting the importance of comprehensive patent procurement strategies.


Key Takeaways

  • The scope of JP2025071269 likely encompasses specific chemical structures, therapeutic methods, and formulations, tailored to maximize patent protection.
  • Clear, well-drafted claims focusing on structural novelty and therapeutic utility underpin enforceability and competitive advantage.
  • Japan’s patent landscape favors incremental innovations, emphasizing inventive step and industrial applicability.
  • Strategic patent filings across jurisdictions are crucial to safeguard the compound’s commercial potential.
  • Ongoing patent examination and potential opposition proceedings could influence the patent’s strength and market lifespan.

FAQs

1. How broad are the claims typically in pharmaceutical patents like JP2025071269?
Claims can range from narrow, compound-specific claims to broader, class-based claims covering an entire chemical scaffold, depending on the applicant’s strategy and the patent office’s examination.

2. What are the common challenges in patenting pharmaceutical compounds in Japan?
Challenges include demonstrating inventive step over existing prior art, defining clear and specific claims, and avoiding prior disclosures that could invalidate the patent.

3. How does Japan’s patent law affect pharmaceutical patent enforcement?
Japan’s patent law emphasizes inventive step and industrial applicability, with patent courts actively adjudicating disputes to uphold valid patents and invalidate weak ones.

4. Are method-of-use claims effective in Japan?
Yes, method-of-use claims are recognized and can provide valuable protection, particularly when the novel therapeutic indication offers commercial exclusivity.

5. How important is international patent filing for pharmaceutical innovations originating in Japan?
Highly important, as global markets require patent protection in multiple jurisdictions to prevent generic entry and maximize commercial value of innovations.


References

[1] Japan Patent Office (JPO). Guidelines for Examination of Patent Applications.

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