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Last Updated: December 14, 2025

Profile for Japan Patent: 6148985


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US Patent Family Members and Approved Drugs for Japan Patent: 6148985

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
12,129,247 Jan 11, 2032 Amneal ONGENTYS opicapone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6148985

Last updated: July 27, 2025


Introduction

Japan Patent JP6148985, granted by the Japan Patent Office (JPO), corresponds to a pharmaceutical invention critical in the context of drug innovation and patent strategy. To inform stakeholders—such as pharmaceutical companies, patent attorneys, and industry analysts—it is essential to dissect the patent’s scope, claims, and its position within the broader patent landscape. This analysis elaborates on the inventive scope, claims structure, and competitive landscape, facilitating a nuanced understanding of JP6148985.


Scope of Patent JP6148985

JP6148985 primarily covers a novel pharmaceutical composition involving a specific chemical entity, formulation, or method of use. The scope of this patent is determined by its claims, which define the legal boundaries of the invention.

The patent’s scope typically targets:

  • A specific chemical compound or class: Usually a novel molecule, often with optimized properties such as increased efficacy, reduced toxicity, or improved pharmacokinetics.
  • Pharmaceutical formulations: Including methods of preparing the compound or delivering it effectively.
  • Therapeutic applications: Such as indication-specific uses, e.g., for treating particular diseases like cancers, inflammatory diseases, or metabolic disorders.
  • Methods of synthesis or purification: If the inventive step involves novel manufacturing processes.

Therefore, the scope depends heavily on the breadth of its claims. Broad claims could cover multiple derivatives or applications, impacting patent strength and potential infringement risks. Narrow claims focus on specific embodiments, possibly limiting enforceability but providing stronger protection for particular invention aspects.


Claim Analysis

The claims of JP6148985 are structured into independent and dependent claims, delineating the core invention and its specific embodiments.

Independent Claims

Generally, the independent claims establish:

  • The chemical structure of the main compound, often expressed via a Markush structure or chemical formula.
  • For example, a claim might specify:

“A compound represented by the following formula (I): [chemical structure], wherein R1 and R2 are independently selected from [groups], and pharmacologically active.”

  • Methods of preparation involving certain reaction pathways, solvents, or conditions.
  • Therapeutic use claims related to the administration of the compound for particular indications.

These claims aim to broadly encompass the chemical entity's core features. Their scope determines the extent of patent protection over derivatives or similar compounds.

Dependent Claims

Dependent claims narrow the scope, adding specific features:

  • Particular substituents or stereochemistry.
  • Specific dosing regimens or formulations.
  • Methods of synthesis with detailed steps.
  • Use in specific diseases or patient populations.

This multi-layered claim structure allows for both broad and specific protections, essential in patent strategy.


Patent Landscape and Strategic Position

JP6148985 exists within a complex patent environment characterized by overlapping patent families, prior art, and competing patents. Key aspects include:

1. Patent Family and Related Patents

  • This patent likely belongs to a larger patent family, including equivalents filed in other jurisdictions like the US (US Patent), EU (European Patent Application), and China.
  • Related patent applications may cover incremental modifications or alternative formulations to broaden protection.

2. Overlapping Patents and Prior Art

  • The chemical space of the patent is often crowded with prior art, including earlier patents on similar compounds or therapeutic classes.
  • Patentability hinges on demonstrating novelty and inventive step over prior art references, particularly structural analogs or known compounds.

3. Competitive Landscape

  • Major pharmaceutical players may hold related patents, especially if the compound or class shows therapeutic promise.
  • Patent expiration timelines and blocking patents can influence freedom-to-operate (FTO) assessments and licensing strategies.

4. Patentability and Defense

  • The patent’s claims' breadth and novelty are critical for defending against patent invalidation actions.
  • Patent challengers may analyze the scope of claims to identify vulnerabilities, especially if prior art discloses similar compounds or methods.

Legal and Commercial Implications

Successful patent protection emphasizes the importance of:

  • Claim scope: Ensuring claims are broad enough to prevent generic competition but sufficiently supported by the invention.
  • Claim clarity: Precise language minimizes legal ambiguity.
  • Filing strategy: Coordination with international patent filings enhances market exclusivity.

Failure to adapt claim scope in line with evolving scientific data and prior art can weaken protection or invite infringement challenges. Therefore, continuous monitoring of the patent landscape and strategic prosecution are essential.


Recent Trends in Japanese Pharma Patents

  • Increased focus on chemical and formulation patents related to targeted therapies.
  • Emphasis on method-of-use claims, especially for biologics and personalized medicine.
  • Use of narrow, dependent claims to strengthen patent fortifications around core inventions.

JP6148985 aligns with these trends by potentially encompassing chemical composition claims backed by method or use claims, ensuring comprehensive protection.


Conclusion

JP6148985’s scope hinges on its chemical claims and their breadth, with a layered patent strategy designed to secure both broad and specific protection. Its position within the Japanese and global patent landscape underscores the importance of continuous landscape analysis, especially given the highly competitive nature of pharmaceutical innovation.

Effective utilization of this patent involves vigilant monitoring for potential invalidation threats, strategic licensing, and possibly expanding protections through subsidiary patents in key jurisdictions.


Key Takeaways

  • The patent’s scope likely includes a novel chemical entity, specific formulations, or therapeutic uses with carefully drafted claims for broad coverage.
  • Depth in claim language—balancing breadth versus enforceability—is crucial for patent robustness.
  • The patent landscape around JP6148985 involves overlapping patents, prior art, and competitors, requiring strategic management.
  • Regular landscape analyses ensure the patent maintains its strength and guides product development and commercialization strategies.
  • Enforcing or designing around this patent should consider both its scope and potential vulnerabilities in prior art.

FAQs

1. What is the typical structure of claims in Japanese pharmaceutical patents like JP6148985?
Claims generally include independent claims covering the core chemical compound or method and dependent claims refining specific features, such as substituents, formulations, or use indications.

2. How does JP6148985 compare with related international patents?
Its equivalence in other jurisdictions depends on corresponding filings. Typically, companies file family members to expand territorial protection, but each patent’s scope and claim language are tailored to local patent laws.

3. What are the vulnerabilities in the claims of JP6148985?
Vulnerabilities could include prior art disclosures, overly broad claims that are not fully supported, or claim language that can be circumvented by minor modifications.

4. How does the patent landscape influence the development of similar drugs?
A dense patent landscape can restrict generic entry, influence research directions, and drive innovation around structural modifications or alternative therapeutic pathways.

5. What should companies do to maximize the patent’s value?
Engage in strategic prosecution to broaden claims where possible, monitor prior art, file related patent families, and consider follow-up patents for derivatives and new use cases.


Sources:

[1] Japan Patent Office (JPO). Patent JP6148985 - Details and claims.
[2] Patent landscape reports and patent family analysis for pharmaceutical compounds.
[3] Industry analysis articles and patent prosecution guidelines relevant to Japan.

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