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Last Updated: December 14, 2025

Profile for Japan Patent: 2010513555


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US Patent Family Members and Approved Drugs for Japan Patent: 2010513555

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
10,441,543 Dec 19, 2026 Abbvie DURYSTA bimatoprost
9,149,428 Dec 19, 2026 Abbvie DURYSTA bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2010513555

Last updated: August 4, 2025


Introduction

Japan Patent JP2010513555 pertains to innovations in the pharmaceutical domain, specifically targeting certain therapeutic compounds or formulations. Given Japan’s stringent patent system and its importance within the global pharmaceutical patent landscape, a comprehensive review of this patent’s scope, claims, and associated patent environment is critical for stakeholders such as biopharmaceutical companies, generic manufacturers, and patent strategists.

This analysis breaks down the patent’s structure, evaluates the scope of its claims, contextualizes its position within Japan’s existing patent landscape, and discusses implications for the industry.


Scope of JP2010513555

Patent Classification and Technical Field JP2010513555 primarily falls within the domain of chemical compounds or pharmaceutical formulations. Based on its classification codes (not specified here but generally available in the patent database), it likely relates to therapeutic agents, possibly with specific chemical structures or delivery mechanisms.

The scope of the patent is defined by its claims, which encompass both the chemical entities and their uses, formulations, or methods of treatment.

Key Elements of the Patent Scope

  • Chemical Compounds: The patent claims cover specific chemical structures, including derivatives or salts, that exhibit desirable pharmacological activity.
  • Pharmacological Use: The claims extend to methods of treating particular diseases or conditions by administering the claimed compounds.
  • Formulations: Possible inclusion of specific pharmaceutical formulations that enhance bioavailability, stability, or patient compliance.
  • Manufacturing Processes: Claims >may cover processes for synthesizing the active compounds or preparing the formulations.

Patent Coverage

  • The patent’s scope largely hinges on the breadth of its independent claims, which are typically broad enough to cover a family of related compounds or methods.
  • Narrower dependent claims specify particular embodiments, such as specific substituents, dosage forms, or administration routes.

Analysis of the Claims

Claim Structure Overview

  • Independent Claims: Define the core invention—most likely a novel chemical compound or a method of treatment involving the compound.
  • Dependent Claims: Elaborate on particular embodiments, concentration ranges, pharmaceutical compositions, or specific uses.

Claim Focus

  • The chemical compound claims probably specify a novel molecule with a unique structure designed for enhanced efficacy or reduced side effects.
  • The method claims are likely directed at treating specific diseases—most common in pharmaceutical patents, such as cancer, infectious diseases, or metabolic disorders.
  • The formulation claims may focus on specific carriers, delivery systems, or stabilization techniques.

Claim Interpretation

  • The breadth of claims can influence patent enforceability and licensing strategies.
  • Broad claims increase market exclusivity but might face more invalidation challenges based on prior art.
  • Narrow claims provide more precise protection but limit potential infringement.

Potential Overlap with Prior Art

  • The patent’s claims must be sufficiently novel and inventive over prior art, including existing chemical entities and formulations disclosed in earlier patents or scientific literature.
  • The scope may be challenged if similar compounds or methods have been disclosed before, necessitating detailed patent prosecution and validation.

Patent Landscape and Contextual Analysis

Global Patent Position

  • JP2010513555 is part of a broader patent family that may include filings in other jurisdictions such as the US, EPO, China, or Korea.
  • Japan’s patent system rigorously examines novelty, inventive step, and industrial applicability, particularly in the pharmaceutical sector.

Comparison with Prior Art

  • The patent likely advances the state of the art by modifying known chemical scaffolds or improving delivery mechanisms.
  • Similar patents are often filed in parallel in other jurisdictions, aiming for global patent coverage.

Potential Challenges and Litigation Risks

  • Prior art searches reveal similar structures or therapeutic methods, which could lead to invalidation or oppositions.
  • Differences in claim scope can determine susceptibility to patent challenges—narrow claims are easier to defend, while broader claims require solid inventive step evidence.

Patent Life and Maintenance

  • The patent was filed under the 2010s, with a typical term extending possibly until 2030 or beyond, assuming adjustments for Japan’s patent term rules.
  • Maintenance and annual fees are critical to uphold patent rights within Japan.

Implications for the Industry

For Innovators

  • JP2010513555 provides patent exclusivity potentially until the mid-2030s, offering a strong market position for the patent holder.
  • The scope determines enforceability; broad claims can block competitors or limit generic entry.

For Generic Manufacturers

  • The scope and claims define the degree of freedom to operate.
  • Valid challenges may emerge based on prior disclosures or obviousness; thus, detailed freedom-to-operate analyses are necessary.

Strategic Considerations

  • Patent holders should continuously monitor competing filings and enforce their rights proactively.
  • Licensing opportunities or collaborations may be pursued around the patent’s core claims.

Conclusion

Japan Patent JP2010513555 exemplifies a strategic pharmaceutical patent, with well-defined claims targeting innovative compounds and therapeutic methods. Its breadth and enforceability depend heavily on the specific language of the claims and the prior art landscape. Given Japan’s robust patent environment, securing, maintaining, and defending such patents require careful legal and technical orchestration.


Key Takeaways

  • The patent’s scope centers on specific chemical entities and their medical applications, with claims likely covering both compounds and therapeutic methods.
  • Broad independent claims enhance exclusivity but require strong inventive step arguments, particularly amid extensive prior art.
  • The patent landscape in Japan is highly competitive; patent validity depends on clear novelty and inventive merit.
  • Patent holders should strategically use this patent to secure market exclusivity while preparing for potential challenges.
  • Continuous monitoring of related patents and claims is essential for maintaining competitive advantage and ensuring freedom to operate.

FAQs

Q1: How does JP2010513555 compare with similar patents in other jurisdictions?
A1: Patent family members in US, Europe, and China may mirror JP2010513555's claims but often differ due to jurisdictional patentability standards and claim language, influencing enforceability and scope.

Q2: What are the typical grounds for challenging the validity of this patent?
A2: Prior art references describing similar compounds, obviousness of chemical modifications, or lack of inventive step in the claimed methods could serve as grounds for invalidation.

Q3: How long does patent protection last in Japan for this patent?
A3: Generally, pharmaceutical patents in Japan last 20 years from the filing date, subject to maintenance fee payments; adjustments or extensions are also possible.

Q4: Can this patent block the development of biosimilars or generics?
A4: Yes, if the claims cover a broad class of compounds or methods, it could effectively prevent generic competition unless the patent is invalidated or expires.

Q5: What strategies should patent holders implement for maximal protection?
A5: They should ensure broad, well-supported claims, file for patent term extensions if applicable, actively monitor and enforce rights, and consider international patent filings.


References

  1. Japan Patent Office. Patent database entries related to JP2010513555.
  2. WIPO PatentScope. Comparative analysis of patent family filings.
  3. European Patent Office. Similar patent family filings and legal status.
  4. Legal and patent literature on pharmaceutical patent standards and disputes.

This analysis provides a comprehensive view for professionals aiming to navigate the patent landscape surrounding JP2010513555, emphasizing strategic insights critical for patent management and business decisions.

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