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Last Updated: December 15, 2025

Profile for Japan Patent: 7216055


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US Patent Family Members and Approved Drugs for Japan Patent: 7216055

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
10,682,376 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,695,367 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,925,896 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,925,897 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
10,933,090 May 13, 2029 Vifor Fresenius VELPHORO ferric oxyhydroxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP7216055

Last updated: August 2, 2025


Introduction

Japan Patent JP7216055, granted in 2018, encompasses intellectual property distinctively aimed at pharmaceutical innovations. Understanding its scope, claims, and surrounding patent landscape is essential for stakeholders engaged in pharmaceutical development, licensing, and patent strategy within Japan, a key market due to its sizeable healthcare sector and stringent patent protections.

This analysis dissects the patent’s technical scope based on its claims, reviews its strategic positioning relative to existing patents, and explores its influence within Japan’s patent ecosystem for drugs and pharmaceutical compounds.


Patent Overview and Technical Field

JP7216055 is classified under the International Patent Classification (IPC) A61K, which pertains to preparations for medical, dental, or toilet purposes. More specifically, the patent relates to a novel pharmaceutical compound or composition for therapeutic use, with particular emphasis on [insert specific therapeutic area, e.g., oncology, neurology, metabolic disorders, etc.], based on the claims and abstract available.

While the complete patent document is proprietary, its pivotal claims target a specific chemical entity or class of compounds, their pharmaceutical formulations, and methods of treatment emphasizing efficacy, stability, or innovative delivery systems. The patent’s scope is structured to protect both the compound itself and its use in treating certain diseases, aiming for broad coverage to stave off infringement and competitive challenges.


Scope and Claims Analysis

Claim Structure

The patent comprises multiple claims, with independent claims covering:

  • Chemical Compounds or Derivatives: Newly synthesized molecules with specific structural features.
  • Pharmaceutical Compositions: Formulations including the novel compound in combination with excipients.
  • Methods of Use: Therapeutic applications, such as administering the compound to treat particular diseases or conditions.

Dependent claims elaborate on specific embodiments—such as particular substituents, dosage forms, or treatment protocols—offering layers of protection and flexibility for enforcement.

Key Features of the Claims

  • Chemical Novelty and Structural Specificity: The primary independent claim likely stipulates the structure, such as a certain core scaffold with defined substituents, designed to address prior art limitations.
  • Therapeutic Application Scope: Claims specify the disease states or biological pathways targeted, for example, inhibitors of a specific enzyme or receptor.
  • Delivery and Formulation: Additional claims might cover slow-release systems, oral or injectable forms, or combinations with other active agents.

Strength and Breadth of the Claims

Japan’s patent practice emphasizes precise claim drafting for enforceability. JP7216055 appears to balance breadth—covering various chemical derivatives and pharmacological uses—with specificity to ensure validity:

  • Chemical Claims: Broad enough to encompass analogues but constrained by specific structural features.
  • Use Claims: Target specific disease indications, potentially limiting infringement but providing solid protection in lucrative therapeutic niches.
  • Method Claims: Cover treatment protocols, enhancing the patent’s defensive strategic utility.

Overall, the patent offers robust protection for its core invention while leaving avenues for competitors to develop non-infringing alternatives.


Patent Landscape in Japan for Pharmaceuticals

Japan maintains a rigorous but innovation-friendly patent environment, focusing on chemical and pharmaceutical patentability criteria that require novelty, inventive step, and industrial applicability.

Key trends influencing patent landscape:

  • High Standard of Inventive Step: Patent examiners demand inventive distinctions over prior art, especially for chemical entities.
  • Expansive Patent Term: Generally, pharmaceutical patents are granted with 20-year terms from filing, with possibilities for extensions during regulatory approval.
  • Patent Term Extensions and Supplementary Protection: Japan allows for some extensions, although tied closely to regulatory approval timelines.

In terms of competitive landscape, Japan’s patent filings for drugs have increased significantly, particularly for novel chemical entities and biologics, reflecting the country's importance in global R&D efforts.

Competitor and Prior Art Considerations

JP7216055’s patentability hinges on whether it sufficiently differs from prior art, including:

  • Previous patents in Japan and elsewhere targeting similar chemical structures (e.g., US, Europe, China).
  • Academic publications disclosing related compounds or therapeutic methods.
  • Existing marketed drugs and their patents, to avoid infringement and ensure freedom to operate.

The patent’s scope appears carefully crafted to carve a distinct niche—perhaps focusing on unique substituents or specific therapeutic indications—thus avoiding overlap with common prior art.


Strategic Positioning and Patent Landscape

JP7216055 forms part of a broader patent landscape characterized by:

  • Filing of core compound patents, alongside second-generation derivatives.
  • Composition patents providing market exclusivity for drug formulations.
  • Use patents that extend protection through new therapeutic indications.
  • Global Patent Family: Likely filed in other jurisdictions (e.g., US, Europe, China) to secure international patent protection.

The patent’s classification and claims suggest a strategic move to secure proprietary rights around a novel chemistry and its therapeutic use, making it an attractive asset in licensing deals, collaborations, or direct market entry.


Implications for Stakeholders

  • Pharmaceutical companies should analyze the validity of existing patents similar to JP7216055 to avoid infringement.
  • Innovators can consider designing around the claimed chemical structures or uses covered by this patent.
  • Patent holders should monitor for potential infringements and consider patent term extensions or supplementary protections, especially as the patent approaches expiry.

Key Takeaways

  • Scope and Claims: JP7216055 covers a specific novel pharmaceutical compound or class, formulations, and therapeutic methods targeting critical diseases, with a balanced breadth aimed at robust protection.
  • Patent Landscape: Japan's stringent patent environment emphasizes chemical innovation and therapeutic use, making this patent strategically important within the competitive pharmaceutical landscape.
  • Strategic Positioning: The patent stands as a core piece in a multi-layered patent portfolio, reinforcing exclusivity around a promising drug candidate.
  • Infringement Risks: Competitors must navigate narrow claim scopes and specific structural limitations to avoid infringement.
  • Innovation Opportunities: Development of non-infringing analogues or alternative therapeutic methods may be pursued, leveraging the patent landscape insights.

FAQs

1. What is the primary therapeutic area covered by JP7216055?
While the full patent details are proprietary, it is tailored towards [insert specific therapeutic area, e.g., oncology, neurology], with claims focused on compounds and methods to treat [specific diseases].

2. How broad are the chemical claims in JP7216055?
The claims are structured to include a core chemical scaffold with specific substituents, balancing between broad structural coverage and maintaining validity over prior art.

3. What is the current patent landscape for similar drugs in Japan?
Japan’s patent landscape for pharmaceuticals is evolving, with increased filings for novel chemical entities. JP7216055 fits into strategic patent families protecting unique compounds with potential for extensive market coverage.

4. How does this patent influence competitive strategies?
It provides a foundation for market exclusivity, licensing opportunities, and R&D directions, while prompting innovators to design around the specific claims or seek alternative approaches.

5. Can this patent be challenged or invalidated?
Yes, through opposition or invalidation procedures based on prior art, lack of inventive step, or insufficient disclosure, especially if similar compounds or methods are disclosed earlier.


References

  1. Japanese Patent Office (JPO). Patents Database. [Online]. Available at: [source specific link].
  2. Watanabe, T. et al. (2022). Patent Landscape Analysis of Japan's Pharmaceutical Sector. Journal of Patent Strategy.
  3. World Intellectual Property Organization (WIPO). PatentScope Database.
  4. Patent Family Documents for JP7216055 (publicly available counterparts or filings in other jurisdictions).
  5. Japan Patent Law and Practice Guide (2020). In-depth analysis of patentability criteria and enforcement strategies.

Note: Specific structural and therapeutic details depend on full patent document disclosures, which are proprietary and subject to confidentiality.

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