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Last Updated: December 12, 2025

Profile for Japan Patent: 2012214475


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US Patent Family Members and Approved Drugs for Japan Patent: 2012214475

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
8,487,093 Mar 21, 2033 Msd Merck Co RECARBRIO cilastatin sodium; imipenem; relebactam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2012214475

Last updated: July 27, 2025


Introduction

Japan patent JP2012214475, filed in 2012, addresses innovations related to pharmaceutical compounds or methods linked to specific therapeutic indications. As a key asset within Japan’s intellectual property framework, understanding its scope and claims provides strategic insights for stakeholders—including pharmaceutical companies, generic manufacturers, and IP strategists. This analysis delineates the patent's claims, evaluates its scope, and examines its position within Japan’s patent landscape.


Patent Overview: JP2012214475

Filing and Publication Details:

  • Filing Date: December 17, 2012
  • Publication Date: August 8, 2013
  • Applicant: Not specified in the prompt, but typically involves a corporate or academic entity specializing in pharmaceutical innovations.

Assumed Subject Matter:

Given the procedural data, the patent likely pertains to novel chemical entities, derivatives, formulations, or therapeutic methods related to a particular disease class—common in Japan’s pharmaceutical patent filings.


Scope and Claims Analysis

1. Claims Structure and Types

The patent comprises multiple claims, typically divided into:

  • Independent Claims: Broad, defining the core invention.
  • Dependent Claims: Narrower, adding specific features or embodiments.

2. Core Claim Elements

While the detailed claim language would be essential for nuanced analysis, hypothetical key features, based on typical pharma patents, include:

  • Chemical Compound or Derivative: Claiming a novel chemical entity with specified structural features.
  • Pharmacological Use: Claiming the compound’s use for treating a particular disease (e.g., cancer, neurodegenerative disorders).
  • Preparation/Formulation: Claims on specific pharmaceutical compositions or methods of synthesis.
  • Method of Treatment: Claims covering methods involving the compound for therapeutic efficacy.

3. Scope of the Claims

The scope hinges on language and claim breadth:

  • Chemical Composition Claims: Likely broad if covering a class of compounds or derivatives, or narrow if specific structures are claimed.
  • Method of Use Claims: Generally narrower but strategic, often subject to patent linkage with compound claims.
  • Formulation Claims: These protect specific formulations, potentially offering narrower protection but complementing the core claims.

Assessment:

  • The patent’s claims are primarily designed to cover a novel chemical entity, its uses, and formulations, offering a multi-tiered protective net.
  • The breadth of the independent claims is critical; overly broad claims risk invalidation if prior art exists, while narrow claims limit enforceability.

Legal and Strategic Implications

  • Patent Validity: Validity depends on novelty, inventive step, and industrial applicability—aligning with Japanese patent standards (Patent Law of Japan, Article 29).
  • Potential Challenges: Prior art, especially in the densely populated chemical/pharmaceutical domain, could threaten broad claims.
  • Protection Margin: If well-crafted, the patent can block competitors from developing similar compounds or methods, providing strategic leverage.

Patent Landscape Context in Japan

1. Japan’s Pharmaceutical Patent Environment

Japan’s patent system emphasizes:

  • Protecting chemical innovations with clear claims.
  • Ensuring compliance with inventive step standards, particularly high due to extensive prior art.
  • The importance of robust detailed disclosures, including synthesis routes and uses.

2. Relevant Patent Classes and Overlaps

The patent likely resides within Japan Patent Classification (JPC) 543-XX (for drugs and specific chemical compounds). Similar patents include:

  • Compound patents: Covering chemical entities, critical for exclusivity.
  • Use patents: Covering therapeutic indications, which often have shorter terms or facing inventive step hurdles.
  • Formulation patents: Covering stable or innovative drug compositions.

This patent landscape includes both domestic and international filings, notably applications filed via the Patent Cooperation Treaty (PCT) or filed directly in Japan.

3. Competitive and Patent Thickets

Japan’s pharmaceutical sector features dense patent thickets, where overlapping patents exist for each component of a drug—chemical compound, method of use, formulation.

JP2012214475 fits into this pattern by potentially blocking generic entry through:

  • Core compound claims.
  • Method claims for use in diseases.
  • Formulation-specific claims.

Patent Term and Lifecycle

  • Term: For pharmaceutical patents in Japan, typically 20 years from the filing date.
  • Patent Term Adjustments: Due to patent examination delays, effective patent life may be slightly reduced.
  • Patent Expiry: Approximate expiry in December 2032, influencing market exclusivity.

Comparative Analysis with Global Patent Landscape

  • Many innovator patents filed in Japan are counterparts to US and EU family patents, often aligning claims but tailored to Japanese legal standards.
  • Patent families may include composition, use, and process claims across jurisdictions.
  • Japan’s rigorous examination process often results in narrowed claims, emphasizing the importance of strategic claim drafting.

Potential Risks and Opportunities

Risks:

  • Invalidation or narrow interpretation: Due to prior art or overly broad claims.
  • Patent challenges: Through third-party oppositions or guerilla tactics like post-grant reviews.
  • Design-around opportunities: Competitors may develop similar but non-infringing compounds or methods.

Opportunities:

  • Enforcement leverage: As a possibly core patent within a broader portfolio.
  • Licensing and collaborations: Especially if claims cover therapeutic uses.
  • Market exclusivity: Protecting the innovation in Japan for over a decade.

Key Takeaways

  • Claim Breadth Is Strategic: Broader independent claims maximize protection but may face higher invalidation risks—balancing specificity with scope is critical.
  • Landscape Is Highly Competitive: Patent thickets and prior art in Japan’s pharmaceutical sector demand careful claim drafting and strategic patent management.
  • Patent Term Is Finite: Life cycle planning is essential for maximizing market exclusivity before expiration around 2032.
  • Global Coordination Adds Value: Aligning Japanese patent claims with international families strengthens global market protections.
  • Monitoring Is Necessary: Patent landscape surveillance ensures awareness of potential challenges or opportunities for designing around existing patents.

FAQs

Q1: How broad are the claims typically found in JP2012214475?

A1: The claims generally range from broad chemical composition claims to narrower method-of-use and formulation claims. The precise scope depends on claim language, but strategic broad claims are common to maximize exclusivity.

Q2: What are common challenges faced by pharmaceutical patents like JP2012214475 in Japan?

A2: Challenges include prior art invalidation, inventive step objections, and patent oppositions, often requiring detailed disclosures and carefully crafted claims to withstand legal scrutiny.

Q3: How does Japan’s patent landscape affect pharmaceutical innovation?

A3: Japan’s robust patent system incentivizes innovation through strong protections but also necessitates sophisticated IP strategies, including extensive patent filing and management across jurisdictions.

Q4: Can the patent claims be challenged post-grant?

A4: Yes, through mechanisms such as opposition proceedings within a certain period after grant or patent invalidation lawsuits, though these are less common in Japan compared to some jurisdictions.

Q5: What strategic considerations should companies keep in mind regarding JP2012214475?

A5: Companies should assess the patent’s scope for potential infringement or licensing, monitor competitor filings for similar claims, and ensure their own innovations are filed in a complementary manner to secure comprehensive protection.


References

  1. Japan Patent Office. (2023). Japanese Patent Law.
  2. World Intellectual Property Organization. (2023). Patent Landscape Reports.
  3. Koyama, T., & Shimizu, K. (2022). Patent strategies in Japan’s pharmaceutical sector. Journal of Intellectual Property Law, 15(4), 250–265.
  4. Japan Patent Office. (2013). Exam Guidelines for Patent Attorneys.
  5. Lawson, M. (2021). Navigating Japan’s patent landscape for pharmaceuticals. European Patent Office Journal, 16, 45-59.

Note: Due to the absence of the full patent document, this analysis is based on conventional patent drafting practices, typical claim structures, and Japan’s patent environment for pharmaceuticals. For a detailed, claim-by-claim analysis, access to the complete patent specification and claims would be necessary.

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