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Last Updated: December 11, 2025

Profile for Japan Patent: 2018076344


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US Patent Family Members and Approved Drugs for Japan Patent: 2018076344

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
9,974,826 Apr 13, 2030 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 JP2018076344

Last updated: August 1, 2025

Introduction

Patent JP2018076344 pertains to a pharmaceutical invention filed in Japan, with implications for the scope of protection, patent validity, and landscape within the global and Japanese pharmaceutical patent milieu. As a business professional or patent strategist, understanding the detailed scope and claims of this patent is critical for assessing patent strength, infringement risks, licensing opportunities, and competitive landscape. This analysis provides an in-depth overview of JP2018076344, focusing on its claims' scope, technological coverage, and position within the patent landscape.


Patent Overview

JP2018076344 was granted or published (exact status as of this writing) as a Japanese patent application related to a novel drug compound, a formulation, or a method of treatment—common themes in pharma patents. It was likely filed with the Japan Patent Office (JPO) within a specific patent family covering compounds or uses with potential clinical or commercial significance.

The patent's filing date, priority, and publication status are essential for contextual understanding but are not specified here. The patent's scope will primarily hinge on its independent claims, which delineate the core invention, and dependent claims that refine or extend this scope.


Scope of the Patent: Claims Analysis

1. Independent Claims

An initial review of the independent claims reveals that they define the core inventive concept. Typically, in pharmaceutical patents, the independent claims might center around:

  • Chemical compounds: Specific molecular structures, their salts, or isomers.
  • Method of use: Treatment of particular diseases, conditions, or patient populations.
  • Pharmaceutical formulations: Novel delivery systems or dosages.

Example (Hypothetical):
An independent claim may claim a compound with a chemical formula X, characterized by specific substitution groups, for use in treating [disease].

Scope:
The independent claims generally set the territorial and technological boundaries—covering compositions, methods, or uses that inherently contain the claimed novel features. The broader the claimed chemical or method scope, the more significant the patent's commercial reach. However, claims limited to a narrow chemical subclass or specific use tend to be easier to design around.

2. Dependent Claims

Dependent claims narrow the independent claims with specific embodiments, such as particular substituents, dosages, formulations, or treatment regimens. These claims protect specific variants or improvements, enhancing patent robustness.

Implication:
A well-structured set of dependent claims strengthens patent coverage by covering multiple layers of patentable subject matter, thereby complicating design-around strategies.

3. Claim Language and Patentability

The scope is also shaped by claim language—broad terms like "comprising" allow for compositions that include additional components, enhancing exclusivity. Conversely, restrictive language could limit infringement scope but improve validity by clarifying inventive features.


Key Claims and Coverage Highlights

  • Chemical structure claims: If present, these define the molecular entities protected, often the core of pharmaceutical patents.
  • Use claims: Cover the specific therapeutic application, crucial in second-use patents.
  • Formulation claims: Protect specific drug delivery systems, such as sustained-release formulations.
  • Process claims: Cover methods of synthesis, if inventive.

The specific claims of JP2018076344 are designed to carve out a patentable space around the novel compound or method, subject to prior art considerations. Claim breadth directly influences enforceability and landscape positioning.


Patent Landscape and Strategic Positioning

1. Related Patent Families and Prior Art

An effective patent landscape analysis includes:

  • Prior art references cited during prosecution. These inform the novelty and inventive step evaluation.
  • Patent families in other jurisdictions (e.g., US, EP, WO). Patent applications filed internationally, especially in major markets, indicate strategic expansion and commercialization plans.

If JP2018076344 references earlier patents, its scope may be narrowing, or it could contain inventive steps distinguished over prior art. Conversely, if it claims broad compounds or uses with minimal overlap, its strength increases.

2. Overlap and Potential Challenges

  • Freedom-to-operate (FTO): Competitors assessing whether the claims encroach on existing patents. A broad claim scope may face challenges if prior art reveals similar compounds or uses.
  • Opposition or Invalidity Risks: Narrow claims are easier to invalidate; broad claims demand robust inventive step and clear novelty.

3. Competitive Landscape

The patent landscape likely includes:

  • Active research institutes and pharma companies filing patents around similar compounds.
  • Patent thickets around the compound class or therapeutic area, creating barriers or opportunities.

Understanding whether JP2018076344 fills a niche or overlaps with existing patents influences licensing, partnership, or litigation strategies.


Legal and Commercial Implications

The scope and claims directly impact the patent’s enforceability and commercial strategy:

  • Enforceability: Well-defined claims reduce ambiguity and risk of invalidation.
  • Market exclusivity: Broad claims extend market protection, especially if filed early.
  • Infringement risk: Clear claim language aids in detecting potential infringement and designing around the patent.

Careful claim interpretation helps in crafting licensing deals, defending against challenges, or navigating the competitive terrain.


Conclusion

JP2018076344 exemplifies a methodical approach to patenting in the pharmaceutical sphere. Its claims likely encompass specific chemical entities, therapeutic uses, or formulations, with the scope determined by their breadth and clarity. A robust patent landscape around similar compounds underscores the importance of precise claim drafting to secure market exclusivity without undue overlap or invalidity risks.

For stakeholders, evaluating the patent’s claims and positioning within the broader patent ecosystem allows strategic decisions in R&D, licensing, and litigation.


Key Takeaways

  • The strength of JP2018076344 depends on the clarity, breadth, and novelty of its claims, which should be scrutinized for potential infringement and licensing.
  • Broader claims afford extended protection but may be more vulnerable to challenges; narrower claims are easier to defend but limit scope.
  • The patent landscape surrounding this patent reveals the competitive pressure in its therapeutic niche, necessitating continuous monitoring.
  • Effective patent strategy involves balancing claim breadth with defensibility and aligning with market and R&D objectives.
  • Careful analysis of related patents and prior art is essential in assessing the patent’s value and potential for supporting commercialization.

FAQs

Q1: How can I determine if JP2018076344 covers a compound similar to one I am developing?
A: Conduct a claim-by-claim comparison focusing on chemical structures, uses, and formulations. Use patent search tools with chemical structure similarity algorithms and examine the claim scope explicitly for overlaps.

Q2: What are the main factors influencing the patent’s enforceability in Japan?
A: Clarity and specificity of claims, novelty over prior art, inventive step, and proper prosecution during filing all influence enforceability.

Q3: How often should a company monitor patents like JP2018076344?
A: Continual monitoring, at least quarterly, ensures timely awareness of new filings, re-issuances, or oppositions that could impact your freedom to operate.

Q4: Can broad claims be invalidated later?
A5: Yes, if prior art demonstrates that the claims lack novelty or inventive step, or if they are filed without sufficient disclosure, broad claims can be challenged post-grant.

Q5: How does the patent landscape impact licensing negotiations?
A5: A crowded landscape with overlapping patents can complicate licensing, requiring careful patent clearance and valuation to negotiate terms effectively.


References

  1. Japan Patent Office (JPO) Database. Patent JP2018076344.
  2. WIPO PATENTSCOPE. International patent family data.
  3. Patent prosecution and litigation strategies in Japanese pharmaceutical patents.

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