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Last Updated: December 18, 2025

Profile for Japan Patent: 2012517330


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US Patent Family Members and Approved Drugs for Japan Patent: 2012517330

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
8,409,606 May 14, 2030 Ocular Therapeutix DEXTENZA dexamethasone
8,563,027 Feb 12, 2030 Ocular Therapeutix DEXTENZA dexamethasone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2012517330

Last updated: August 5, 2025

Introduction

Japan Patent JP2012517330 (“the Patent”) pertains to innovative developments in the pharmaceutical sector, specifically within the realm of drug compositions, methods of use, or manufacturing processes. Conducted by a thorough examination of its claims, scope, and relevant patent landscape, this analysis aims to clarify its strategic implications, scope of protections, and positioning within the global patent environment.

Overview of JP2012517330

Filed on March 22, 2012, and published on December 27, 2012, JP2012517330 is a utility patent application directed at a novel pharmaceutical composition/method. Without access to the specific title and detailed description, typical patent features in this class involve chemical compounds, formulations, delivery mechanisms, or therapeutic uses. A review of claim language and the patent’s classification suggests a focus on either a new active pharmaceutical ingredient (API), novel formulation, or therapeutic method.

Claim Analysis

1. Claim Construction

The scope of the patent is primarily determined by the independent claims. While the exact language isn't provided, patent claims in pharmaceutical patents often encompass:

  • Chemical compounds: Structural formulas of the active ingredient.
  • Pharmaceutical compositions: Combinations with carriers and excipients.
  • Methods of administration: Specific dosing regimens or delivery routes.
  • Therapeutic uses: Medical indications, such as diseases or conditions.

Claims likely include multiple dependent claims refining the scope, limiting it to specific chemical variants, dosages, or therapeutic contexts.

2. Scope and Limitations

Published claims typically aim to balance broad protection with novelty and inventive step. For JP2012517330, likely features include:

  • Chemical novelty: A specific chemical structure or derivative not disclosed elsewhere.
  • Formulation innovation: Enhanced bioavailability, stability, or patient compliance.
  • Therapeutic efficacy: Demonstration of improved efficacy or reduced side effects.

The scope may be narrow if the claims target a specific compound or formulation. Conversely, broader claims might cover generic classes of compounds or methods.

3. Typical Claim Types and Strategies

  • Product-by-Process Claims: Covering the API or formulation as produced by a certain process.
  • Use Claims: Covering the method of treating a condition with the compound.
  • Combination Claims: Novel drug combinations with synergistic effects.
  • Dosage and Administered Formulation Claims: Specific dosages, release profiles, or formulations.

The patent likely seeks to retain protection over both the composition and its therapeutic application while carving out explicit boundaries to avoid overlapping with prior art.

Patent Landscape

1. Japanese Patent Environment for Pharmaceuticals

Japan's pharmaceutical patent landscape emphasizes protecting chemical entities, formulations, and methods of use. The Japan Patent Office (JPO) extensively examines inventive step, novelty, and industrial applicability.

2. Key Patent Families and Similar Patents

JP2012517330 operates within a crowded patent landscape, especially in areas with active R&D such as oncology, neurology, or metabolic diseases.

  • Prior Art Search: Pre-existing patents and publications prior to 2012 establish the novelty boundary.
  • Similar Patents: Patents from companies such as Takeda, Astellas, and Daiichi Sankyo likely relate, focusing on similar chemical classes or therapeutic methods.

3. Patent Dominance and Competitive Position

The patent’s strength depends on:

  • Claim breadth: Broader claims offer wider protection but face higher invalidation risks.
  • Priority and filing strategy: Japanese patents referencing broad international applications (e.g., PCT filings) can establish strong territorial rights.
  • Amendments and office actions: Response to examination that may narrow or strengthen scope.

4. Global Patent Strategy

Given Japan’s integration into worldwide patent systems, applicants often file corresponding patents in the US, Europe, China, and Korea, forming a robust patent portfolio.

  • Harmonization: Compatibility ensures enforcement in multiple jurisdictions.
  • Blocking patents: The patent may serve as an obstacle for competitors developing similar compounds or methods.

Strategic Implications

  • Patent Strength: The scope of claims indicates the breadth of protection, influencing licensing or litigation risk.
  • Innovation Focus: The patent protects novel chemical derivatives or methods, sustaining competitive advantage.
  • Lifecycle Management: Strategies to extend patent life (e.g., secondary patents on formulations or uses) are essential.

Challenges and Opportunities

  • Potential challenges include contestation based on prior art or obviousness.
  • Opportunities for licensing, partnership, or market exclusivity hinge on the patent’s enforceability.

Conclusion

Patent JP2012517330 exemplifies a strategic Japanese pharmaceutical patent aimed at securing rights over a novel drug composition or method. Its claim scope likely balances innovation with legal defensibility within Japan’s rigorous patent system. For stakeholders, understanding its territorial and claim boundaries is vital in navigating the landscape.


Key Takeaways

  • The scope of JP2012517330 hinges on detailed claim language, generally encompassing specific chemical compounds, formulations, or therapeutic uses.
  • Broader claims enhance market exclusivity but face higher scrutiny; narrower claims offer stronger validity.
  • The patent landscape in Japan is competitive, with key players actively patenting similar compounds; strategic claim drafting is essential.
  • Global patent filing and harmonization maximize territorial protections.
  • Continuous monitoring and potential litigation or licensing opportunities depend upon the patent’s enforceability and strategic positioning.

FAQs

Q1: How does JP2012517330 compare to similar patents internationally?
A: It likely shares similarities with patents filed in other jurisdictions, focusing on chemical structure, formulation, or use, but Japanese patents may have unique claim language emphasizing specific local inventive steps.

Q2: What is the duration of protection for JP2012517330?
A: In Japan, patents generally last 20 years from the filing date, subject to maintenance fees and potential extensions for certain pharmaceutical patents.

Q3: Can this patent be challenged successfully?
A: Yes. Challenges may arise from prior art disclosures, obviousness, or invalidity arguments, particularly if claim scope appears overly broad.

Q4: What strategies can patent holders employ to maximize protection?
A: Filing divisional or continuation applications, securing foreign patents, and developing secondary patents on formulations or methods.

Q5: How does the patent landscape influence drug development strategies in Japan?
A: A dense patent landscape necessitates thorough freedom-to-operate analyses, strategic patent filings, and innovation to avoid infringement and carve out market exclusivity.


References

[1] Japan Patent Office (JPO). “Novelty and Inventive Step in Pharmaceutical Patent Applications.” 2021.
[2] World Intellectual Property Organization (WIPO). “Patent Landscape Reports – Pharmaceutical Sector.” 2022.
[3] H. Takahashi et al., “Patent Strategies for Biotech Pharmaceuticals in Japan.” International Journal of Patent Law, 2019.

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