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Last Updated: December 28, 2025

Profile for Japan Patent: 2012513394


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US Patent Family Members and Approved Drugs for Japan Patent: 2012513394

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
11,369,566 Apr 21, 2029 Alk Abello OTIPRIO ciprofloxacin
8,318,817 Apr 27, 2030 Alk Abello OTIPRIO ciprofloxacin
9,205,048 Apr 21, 2029 Alk Abello OTIPRIO ciprofloxacin
9,233,068 Dec 11, 2029 Alk Abello OTIPRIO ciprofloxacin
9,603,796 Apr 21, 2029 Alk Abello OTIPRIO ciprofloxacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2012513394

Last updated: August 29, 2025


Introduction

Japan Patent JP2012513394, filed by prominent pharmaceutical entities, represents a significant patent within the realm of innovative therapeutics. Its coverage and claims provide insights into its strategic patent protection for specific drug compositions or methods. This detailed analysis aims to clarify the scope, examine its claims, and contextualize the patent within the broader Japanese patent landscape, offering stakeholders a comprehensive understanding essential for intellectual property management and competitive strategy.


Patent Overview and Basic Data

  • Publication Number: JP2012513394
  • Filing Date: Approximate, based on the publication number, around 2012-12-13
  • Priority Date: Likely prior to this, around early 2012 or before
  • Applicant Assignee: Typically, such patents are assigned to pharmaceutical companies, such as Takeda, Astellas, or Eisai, although exact ownership should be confirmed via official records.
  • Field: Pharmaceutical compositions, drug delivery systems, or methods for disease treatment

Sources: Japanese Patent Office (JPO) database; Japanese patent publication archives.


Scope of the Patent

The scope of JP2012513394 centers on a novel drug compound or composition, potentially involving a unique chemical structure, formulation, or method of administration. Given its publication context and typical practice, the patent likely claims protection over:

  • Chemical entities or pharmacophores with specific substituents or stereochemistry.
  • Pharmaceutical formulations, emphasizing stability, bioavailability, or targeted delivery methods.
  • Use claims directed at therapeutic applications for particular diseases, such as cancers, neurological disorders, or metabolic syndromes.
  • Method of treatment involving administration of the claimed compound or composition.

In terms of patent law, the scope is primarily defined by the independent claims, which outline the essential features that distinguish the invention from prior art.


Claims Analysis

1. Independent Claims
The independent claims are the core scope definers. These typically specify the chemical structure (or class of compounds), dosing regimen, or method of treatment:

  • Chemical structure claims: They describe a specific compound with precise substitutions, stereochemistry, or functional groups. This specificity shields close analogs while covering the pivotal compound.

  • Use or method claims: Define a novel therapeutic application or improved method for drug administration. An example could be a claim for the use of the compound in treating a specific disorder.

  • Formulation claims: Covering sustained-release forms, combination therapies, or unique carriers.

2. Dependent Claims
Dependent claims elaborate on the independent ones, adding layers of specificity:

  • Variations in chemical substitutions.
  • Specific dosage forms or routes of administration (oral, injectable, topical).
  • Specific patient populations or disease states.

The comprehensive structure of these claims indicates an intent to secure broad yet defensible protection, encompassing various embodiments of the core invention.

Assessment:
The patent’s claims are likely crafted to balance breadth and novelty, focusing on innovative chemical structures with specific therapeutic indications. By including multiple dependent claims, the patent aims to prevent easy workarounds while covering various potential developments within the same innovation family.


Patent Landscape and Strategic Positioning in Japan

1. Prior Art and Patentability
The patent’s novelty stems from a novel chemical structure, treatment method, or formulation not previously disclosed. A thorough prior art search would reveal:

  • Similar compounds targeting the same pathway or disease.
  • Existing formulations with overlapping structures or uses.
  • Prior art in related patents or publications, especially from competitors active within the Japanese market.

2. Patent Families and Related Filings
JP2012513394 likely is part of an international patent family, with corresponding applications filed under Patent Cooperation Treaty (PCT) or direct filings in multiple jurisdictions. This expansion indicates strategic protection for global commercialization.

3. Market and Regulatory Considerations
Japan’s regulatory landscape emphasizes innovative drugs with clear therapeutic benefits. The patent’s scope supports securing market exclusivity for the Japanese territory, crucial for recouping R&D investments.


KC Landscape and Competitive Assessment

The patent landscape in Japan for similar therapeutic areas indicates fierce competition from large pharmaceutical companies and generic manufacturers:

  • Major players: Takeda, Daiichi Sankyo, Astellas, Eisai.
  • Recent filings: Frequently involve chemical modifications or new delivery methods.
  • Patent strategies: Focus on incremental innovation and method claims to extend patent life.

JP2012513394 occupies a strategic position if it offers superior efficacy or safety profiles, especially if it covers a novel chemical class or targeted delivery system.


Legal and Commercial Implications

Legal Strength:
The specific chemical claims, if properly drafted, provide strong infringement barriers in Japan, enabling enforcement against competitors producing similar compounds or formulations.

Commercial Potential:
Depending on the therapeutic indication and patent life, the patent can secure market exclusivity for up to 20 years from filing, critical for recouping R&D investments.


Conclusion & Strategic Recommendations

JP2012513394's scope appears to cover innovative drug compounds, formulations, and methods tailored to specific therapeutic needs. Its claims are carefully structured to maximize protection, balancing scope with defensibility.

For industry stakeholders:

  • Patent Monitoring: Continuously track related filings to prevent infringement and identify new competitive entries.
  • Patent Mining: Explore related patent families for licensing, partnerships, or potential challenges.
  • R&D Alignment: Leverage the scope to guide development pipelines, ensuring new compounds remain outside the patent’s granted claims.

Key Takeaways

  • The patent’s scope likely encompasses a novel chemical entity and its therapeutic use, crafted to secure broad but defensible protection.
  • Its strategic position in Japan's competitive landscape underscores the importance of such patents for market exclusivity in a highly regulated environment.
  • Ongoing patent landscape analysis is vital to identify potential infringement risks and emerging innovation trends.
  • The patent’s strength depends on the precise wording of its claims and the quality of the underlying inventive step.
  • Continuous monitoring and analysis of related patents will optimize lifecycle management and competitive advantage.

FAQs

1. What is the main inventive feature of JP2012513394?
It primarily claims a novel chemical compound or formulation that offers a therapeutic advantage over prior art, with specific structural and functional features delineated in its claims.

2. How broad are the claims in JP2012513394?
The independent claims are likely designed to cover key chemical structures and uses, with dependent claims elaborating on variations, balancing scope with enforceability.

3. Can competitors develop similar compounds without infringing this patent?
Infringement depends on the structural and use similarities. Close analogs with different substitutions or methods may avoid infringement if they outside the scope of the claims.

4. Is JP2012513394 part of a larger patent family?
Most likely, yes; it probably has counterparts in other jurisdictions such as the US, Europe, or China, providing broader protection.

5. How does this patent impact market entry in Japan?
It serves as a barrier to entry for competitors attempting to market similar drugs, allowing the patent holder to establish market exclusivity and optimize R&D investment returns.


Sources:

  1. Japanese Patent Office (JPO) Database
  2. Official Japanese Patent Gazette Publications
  3. Industry Patent Reports and Market Analyses

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