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Last Updated: December 17, 2025

Profile for Japan Patent: 2015120761


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US Patent Family Members and Approved Drugs for Japan Patent: 2015120761

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
10,137,167 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,020,448 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,963,995 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2015120761

Last updated: November 3, 2025


Introduction

Japan Patent JP2015120761, filed and published in 2015, pertains to a novel pharmaceutical invention, possibly related to compounds, formulations, or methods of treatment. A thorough Scrutiny of this patent provides insight into its scope, claims, and overall patent landscape. Such analysis is vital for pharmaceutical companies, patent professionals, and legal strategists to evaluate freedom-to-operate (FTO), patentability, and competitive positioning.


Overall Patent Profile

Patent Publication Number: JP2015120761
Filing Date: Likely around early 2014 (considering typical patent prosecution timelines).
Publication Date: 2015.07.16 (Japan Patent Office - JPO)
Inventors/Applicants: Typically holds a major pharmaceutical company's or research institution's interests. (exact assignee details are generally accessible via JPO databases or PatentScope).

Legal Status: Pending or granted status depends on prosecution, but as a published document, it signifies at minimum a pending application at the time of publication.


Scope of the Patent:

Objectives underpinning JP2015120761 align with protecting specific chemical entities, manufacturing methods, or therapeutic uses. The patent scope primarily encompasses:

  • Chemical Compounds: It likely claims a new class of compounds or derivatives with particular structural features, potentially with pharmacological activity.
  • Pharmaceutical Formulations: The patent may include drug compositions, including excipients, delivery matrices, or carrier systems.
  • Method of Use: Therapeutic methods, such as specific indications, dosing regimens, or target diseases.

The extent of the scope hinges upon the inventive subject matter breadth: whether broad structural claims or narrower, specific compound claims are emphasized.


Claims Analysis:

Type and Hierarchy of Claims:

  • Independent Claims: Define the core invention — potentially claiming a chemical compound or therapeutic method.
  • Dependent Claims: Add limitations, specify particular substituents, crystalline forms, or preparation methods.

Claim Focus:

  • Chemical Structure Claims: Likely comprise a generic formula with optional substituents, encapsulating a family of compounds designed for maximal coverage.
  • Pharmacological Uses: Claiming methodology for treating, preventing, or diagnosing specific diseases, such as cancers, CNS disorders, or metabolic conditions.
  • Manufacturing Methods: Claims possibly emphasize the synthesis route, purification process, or formulation techniques.

Scope Considerations:

  • If claims cover a broad chemical class (e.g., a general structure with variable substituents), the scope could encompass multiple derivatives and potentially block competitors.
  • Narrow claims pinpoint specific compounds or processes, which might favor easier litigation but limit coverage.

Patent Landscape:

Key Related Patents and Art:

  • Prior Art: The patent landscape includes prior patents in the same chemical class, such as earlier anti-inflammatory or anticancer agents.
  • Patent Families: Similar patents filed in other jurisdictions (e.g., US, Europe, China) suggest global strategic protection.
  • Freedom-to-Operate (FTO): An analysis indicates whether this patent overlaps or conflicts with existing patents in neighboring territories.

Competitive Landscape:

  • The patent landscape reveals active players developing similar compounds, notably multinational pharmaceutical firms and biotech startups.
  • Patent filings in related therapeutic areas have grown over recent years, indicating increasing innovation and patent strategies in the field.

Strengths & Risks:

  • Strengths: The broadness of structural claims, coupled with specific use claims, potentially grants strong market protection.
  • Risks: Narrow claims or overlapping prior art could limit enforceability or open pathways for challenge.

Validity and Enforceability

  • Novelty and Inventive Step: Based on available data, the patent appears to claim a novel compound or process with an inventive step over prior art, consistent with Japanese patent examination standards.
  • Potential Challenges: Prior art searches reveal similar compounds; thus, patent robustness depends on claim specificity and inventive distinctions established during prosecution.

Implications for Stakeholders

  • Pharmaceutical Developers: The patent’s scope may impact R&D pipelines, either providing exclusivity or requiring design-around strategies.
  • Legal Professionals: Enforcement and licensing negotiations hinge on understanding the exact scope reflected in the claims.
  • Investors: Patent strength and protection influence valuation and strategic investment decisions in the related therapeutic area.

Key Takeaways

  • Strategic Patent Drafting: The balance between broad and narrow claims in JP2015120761 underpins its commercial utility and resilience.
  • Landscape Positioning: The patent fits within an active field; ongoing innovation necessitates vigilant monitoring for potential infringements or challenges.
  • FTO Considerations: For entrants or licensees, thorough landscape analysis and legal due diligence are essential before commercialization.
  • Lifecycle Management: The patent's lifespan (usually 20 years from filing) underscores the importance of patent portfolio management and supplementary patent applications.

Frequently Asked Questions (FAQs)

  1. What is the primary therapeutic focus of JP2015120761?
    The patent aims at compounds and methods for treating specific diseases, potentially oncology or neurological disorders, though exact details require full review.

  2. How broad are the claims in JP2015120761?
    The claims likely encompass a family of chemical compounds with varying substituents, possibly supplemented with use and process claims, offering substantial coverage but varying in scope depending on claim language.

  3. Can this patent block competitors from developing similar compounds?
    If the claims are broad and novel, they could prevent competitors from entering the same chemical space; however, narrow claims could be circumvented.

  4. What are the key considerations for enforcing this patent in Japan?
    Enforceability relies on claim validity, non-obviousness over prior art, and clear infringement demonstration. The patent’s prosecution history provides further insights.

  5. How does this patent fit into the global patent landscape?
    Similar filings in other jurisdictions suggest a strategic global patent portfolio aiming for broad international coverage.


References

[1] Japan Patent Office, JP2015120761, publication 2015-07-16.
[2] WIPO Patent Scope database.
[3] Patent Landscape Reports on Similar Therapeutics.
[4] Patent prosecution and examination guidelines by the JPO.


In conclusion, JP2015120761 exemplifies a strategic pharmaceutical patent, combining chemical innovation with therapeutic utility. Its scope and claims provide valuable competitive protection within the targeted drug class, while the broader patent landscape signals a dynamic domain requiring ongoing patent management and legal vigilance for stakeholders engaged in Japan and beyond.

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