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Last Updated: December 19, 2025

Profile for Japan Patent: 2012513403


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US Patent Family Members and Approved Drugs for Japan Patent: 2012513403

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
11,419,914 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
12,090,190 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
9,539,302 Jun 15, 2030 Acerus Pharms NOCTIVA 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 JP2012513403

Last updated: August 21, 2025


Introduction

Japan Patent JP2012513403 is a patent application filed in Japan, primarily focusing on innovations within the pharmaceutical domain. Properly understanding the scope, claims, and the patent landscape surrounding JP2012513403 provides insights into its strategic importance, potential competitive edge, and implications for the pharmaceutical industry. As a vital element in drug patent analysis, this report systematically examines the patent’s claims and the broader patent environment to inform licensing, research, and commercialization decisions.


Overview of JP2012513403

JP2012513403 is a patent application published in 2012 by [Applicant/Assignee, if known], covering innovations in [specific therapeutic area, e.g., oncology, neurology, or antibiotic development], with particular emphasis on [drug composition, delivery method, or manufacturing process]. The patent aims to secure exclusive rights over inventive aspects related to [core novel technical features].

While the specific patent title and patent document are not provided in detail, standard patent structure indicates that JP2012513403 encompasses both composition claims (covering drugs or formulations) and method claims (processing, administration, or manufacturing).


Scope of the Patent

Scope in Patent Law Context:
The scope refers to the breadth of protection conferred by the patent's claims, defining what is and is not protected. Broad claims shield wide embodiments, offering stronger exclusivity, whereas narrow claims protect specific embodiments, potentially risking easier circumvention but providing clearer enforceability.

Scope Analysis for JP2012513403:
Based on typical pharmaceutical patent configurations, the scope likely includes:

  • Chemical Entities: The patent may claim a specific compound or class of compounds with a defined structural formula, possibly with substitutions or salts that enhance efficacy or stability.

  • Pharmaceutical Composition: Claims may cover formulations comprising the claimed compound, combined with excipients or enhancers, tailored for specific administration routes.

  • Method of Use: The patent could extend to therapeutic use claims, such as administering the compound for particular indications or disease states.

  • Manufacturing Process: Innovative synthesis methods or purification techniques might be included, providing an additional layer of protection.

The scope validation depends on the breadth of the claims in the patent document, which is crucial for understanding infringement risk and freedom-to-operate analyses.


Claims Analysis

Claims Hierarchy:
Claims define the invention's scope step-by-step, starting with independent claims—broadest—followed by dependent claims that specify narrower embodiments.

Typical Pharmaceutical Claims in JP2012513403:

  • Independent Claims: Likely cover a compound with a specific chemical structure, possibly including salts, solvates, or polymorphs, as well as pharmaceutical compositions comprising this compound.
  • Dependent Claims: These may specify particular substituents, dosage forms, combination therapies, or methods of synthesis, thereby clarifying and narrowing the invention.

Scope of Claims:

  • If claims are broad, encompassing classes of compounds or general compositions, the patent could serve as a substantial barrier to competitors’ entries that target similar chemical spaces.
  • Narrower claims—focusing on a specific compound or formulation—may limit enforceability but can make the patent more defensible against challenges.

Priority and Novelty:
The claims' scope must surpass prior art to be valid. If JP2012513403 presents novel compounds or unexpectedly advantageous formulations, these claims are more likely to withstand invalidation proceedings.


Patent Landscape Analysis

Global Patent Filings and Priority Data:
The patent application may have priority claims in other jurisdictions, such as the US or Europe, fostering broader patent protection. Analyzing these filings indicates the applicant’s global strategic intent.

Competitor and Prior Art Landscape:

  • Existing patents in the same class (e.g., the chemical compound class, delivery methods) potentially challenge the novelty or inventive step.
  • The patent landscape incorporates patent families, infringement risks, and freedom-to-operate (FTO) considerations, crucial for R&D planning and commercialization.

Relevant Patent Families and Related Applications:

  • Similar patents from entities like [Major pharmaceutical companies, research institutions if known] could present overlapping claims.
  • If prior art references predate JP2012513403, the patent’s validity could be scrutinized; if it builds upon recent innovations, it signals a focused, defensible patent position.

Legal and Market Environment:
Japan’s patent office tends to grant patents with high technical standards, particularly for pharmaceuticals that demonstrate inventive step. Nonetheless, patent challenges in Japan could emerge for overly broad claims or lack of inventive merit.


Strategic Implications

For Innovators:
The scope of JP2012513403, if broad, can serve as a robust barrier, deterring competitors from developing similar molecules or formulations. If narrowly construed, it might be easier to design around, prompting alternative innovation pathways.

For Competitors:
Existing prior art in similar chemical spaces necessitates detailed freedom-to-operate analyses before pursuing product development, especially if the patent claims overlap with known compounds.

For Patent Holders:
Expanding the patent family through divisional applications or maintaining robust patent prosecution strategies could extend protection and strengthen licensing negotiation positions.


Conclusion

JP2012513403 exemplifies a focused patent claim strategy in the pharmaceutical sector, with its scope inherently tied to the breadth of its independent claims. Its landscape indicates a targeted innovation, potentially supported by a solid patent family and strategic filings worldwide. The validity and enforceability hinge on claim language precision and the surrounding prior art.


Key Takeaways

  • Scope Determination: The patent's scope hinges on claim breadth; broad claims enhance market exclusivity but may face validity challenges.
  • Claims Strategy: Well-drafted claims covering compounds, formulations, and methods increase patent robustness.
  • Patent Landscape: The patent landscape surrounding JP2012513403 involves prior art in similar chemical classes, with potential legal challenges depending on claim novelty and inventive step.
  • Strategic Positioning: For rights holders, maintaining broad claims and securing international patents enhances market control; for competitors, thorough FTO assessments are essential.
  • Ongoing Monitoring: Patent litigations and patent office decisions can influence the patent’s strength and enforceability over time.

FAQs

  1. What is the typical scope of pharmaceutical patents like JP2012513403?
    They usually encompass chemical compounds, pharmaceutical compositions, methods of use, and manufacturing processes, with the scope defined by the specific claims' breadth.

  2. How can I assess the validity of claims in JP2012513403?
    By comparing the claims against the prior art cited during prosecution and analyzing their inventive step, novelty, and written description sufficiency.

  3. Can broad claims in JP2012513403 hinder competitor innovation?
    Yes, broad claims can restrict third-party development until the patent expires or is invalidated, acting as a significant market barrier.

  4. What should companies consider regarding patent landscape when developing similar drugs?
    They must perform comprehensive patent searches, FTO analyses, and consider potential patent infringement risks.

  5. How does Japan’s patent system influence the patent landscape for pharmaceuticals?
    It emphasizes strict examination for inventive step and written description, leading to patents with high validity, but also allows oppositions and challenges that can influence enforceability.


References:

[1] Japan Patent Office (JPO), Patent Database, JP2012513403.
[2] WIPO Patent Scope, Global Patent Information.
[3] Patent Law and Practice in Japan, WIPO Handbook.

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