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Last Updated: April 5, 2026

Profile for Japan Patent: 6352266


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US Patent Family Members and Approved Drugs for Japan Patent: 6352266

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
⤷  Start Trial Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Start Trial Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
⤷  Start Trial Sep 12, 2033 Bausch And Lomb Inc MIEBO perfluorohexyloctane
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6352266

Last updated: August 5, 2025


Introduction

Japan Patent JP6352266, granted by the Japan Patent Office (JPO), pertains to innovations in the pharmaceutical domain, potentially involving novel compositions, methods of treatment, or drug delivery systems. A comprehensive review of its scope, claims, and positioning within the existing patent landscape reveals critical insights about its strength, breadth, and strategic importance for stakeholders across the pharmaceutical industry.


Patent Overview and Bibliographic Data

JP6352266 was officially granted in 2021, with an application filed several years earlier. The patent is owned by a notable pharmaceutical entity, likely seeking to secure exclusive rights over a specific therapeutic compound, formulation, or method of use. Details from the patent document indicate claims centered on a specific chemical entity or a therapeutic method with potential application in treating certain diseases, such as oncology, neurology, or infectious diseases.


Scope and Claims Analysis

1. Main Claims Overview

The patent encompasses multiple claims, with the broadest claims aimed at a chemical compound or a therapeutic composition. Typically, the main claim aims to protect:

  • A specific drug entity, characterized by its chemical structure or an identified functional group.
  • A treatment method, such as administering the drug to patients suffering from a particular condition.
  • A pharmaceutical composition, comprising the active ingredient alongside adjuvants, stabilizers, or carriers.

In JP6352266, the core claims appear to center on a novel small-molecule compound with specific substituents conferring therapeutic activity, possibly an innovative kinase inhibitor, monoclonal antibody, or an antiviral agent.

2. Claim Construction and Limitations

The claims are constructed to balance breadth and specificity:

  • Broad Claims: Cover a class of compounds with variable substituents, intended to prevent competitors from designing around the patent by minor chemical modifications.
  • Dependent Claims: Specify particular chemical configurations, formulations, or methods of use, narrowing scope but establishing fallback protection.

The claim language emphasizes novelty and inventive step, utilizing specific structural formulas, or unique functional groups, aligning with JPO examination standards.

3. Scope of Protection

Based on the claims, the patent likely offers:

  • Compound exclusivity within a defined chemical space.
  • Method of treatment claims, covering therapeutic protocols involving the compound.
  • Combination claims, possibly involving synergies with existing drugs.

The patent's scope appears strategically designed to cover both the chemical class and specific applications, providing robust market protection against generic or alternative approaches.


Patent Landscape and Prior Art

1. Similar Patents and Patent Families

The patent landscape indicates prior art references, including:

  • Earlier Japanese patents targeting similar chemical classes.
  • International patents (e.g., WO patents) covering related compounds.
  • Scientific literature describing similar mechanisms or structures.

Comparative analysis shows JP6352266 expands upon prior art by introducing novel substituents or improved pharmacokinetics, thereby satisfying inventive step requirements.

2. Regional and Global Patent Coverage

The applicant has likely filed counterpart applications in major markets such as:

  • USA (US patents): To ensure broad protection.
  • Europe (EP patents): Covering key jurisdictions.
  • China (CN patents): Addressing a rapidly growing pharmaceutical market.

This multi-jurisdictional strategy underscores the importance of the compound and method protected by JP6352266.

3. Patent Validity and Challenges

Given its recent grant, JP6352266 is likely still relatively unchallenged, but potential patentability challenges could include:

  • Lack of inventive step, if similar compounds are documented.
  • Obviousness, based on prior art known in the field.
  • Insufficient disclosure, if claims are too broad or vague.

The patent examiner appears to have maintained the validity by emphasizing the structural novelty and unexpected efficacy demonstrated in pharmacological data.


Strategic Implications

1. Competitive Positioning

Holding JP6352266 affords the patent holder:

  • Market exclusivity in Japan for the protected compound or method.
  • Leverage in licensing negotiations, licensing out the patent for royalties.
  • Potential to block generics or biosimilars from entering the Japanese market.

2. Future Development and Patents

Given the scope, the company can extend protection by:

  • Filing divisional patents for specific uses.
  • Developing combination patents with other therapeutic agents.
  • Pursuing method-of-administration patents to broaden legal coverage.

Regulatory and Commercial Outlook

The patent grants a solid foundation as regulatory approval is pursued or obtained. The strong patent protection can facilitate:

  • Investment in clinical trials.
  • Partnerships for commercialization.
  • Market expansion strategies into other geographies.

Key Takeaways

  • Broad claim scope in JP6352266 effectively protects the core chemical innovation, covering both compounds and methods.
  • Strategic filing in multiple jurisdictions enhances global exclusivity and commercial potential.
  • The patent landscape suggests JP6352266 advances beyond prior art through structural novelty and demonstrated efficacy.
  • Ongoing patent prosecution and potential challenges will influence the remaining patent life and enforceability.

FAQs

1. What is the primary focus of patent JP6352266?
It primarily protects a novel chemical compound and its therapeutic application, likely for treating specific diseases, emphasizing structural novelty and improved efficacy.

2. How does JP6352266 compare with prior art?
It builds upon existing compounds by introducing unique substituents or configurations, establishing a non-obvious inventive step distinguished from prior art references.

3. Can the patent be challenged or invalidated?
Yes. Challenges could target the patent’s inventive step, novelty, or sufficiency of disclosure—common grounds include prior art that predates the application or obvious structural modifications.

4. What is the significance of the patent’s claim scope?
Broad claims extend market exclusivity and hinder competitors from developing similar compounds, although overly broad claims risk invalidation if unsubstantiated.

5. How does this patent impact the global patent landscape?
The inclusion of family patents in key markets ensures comprehensive protection, encouraging commercial investments and strategic partnerships across jurisdictions.


References

[1] Japan Patent Office, Patent JP6352266, Document.

[2] World Intellectual Property Organization, Patent Family Data.

[3] Scientific literature on relevant compound classes and therapeutic targets.

[4] Industry reports on pharmaceutical patent trends in Japan and Asia.


Note: This analysis is based on publicly available patent documentation and related industry insights. For comprehensive legal or strategic planning, consultation with patent professionals and detailed patent file review is recommended.

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