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Last Updated: March 26, 2026

Profile for Japan Patent: 2016532655


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US Patent Family Members and Approved Drugs for Japan Patent: 2016532655

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 Oct 7, 2034 Impax CREXONT carbidopa; levodopa
⤷  Start Trial Oct 7, 2034 Impax CREXONT carbidopa; levodopa
⤷  Start Trial Oct 7, 2034 Impax CREXONT carbidopa; levodopa
⤷  Start Trial Oct 7, 2034 Impax CREXONT carbidopa; levodopa
⤷  Start Trial Oct 7, 2034 Impax CREXONT carbidopa; levodopa
⤷  Start Trial Oct 7, 2034 Impax CREXONT carbidopa; levodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2016532655

Last updated: August 8, 2025


Introduction

Japan Patent JP2016532655, filed on May 20, 2015, and published on November 24, 2016, represents a significant patent in the pharmaceutical landscape, particularly aligning with innovations related to medicinal compounds or drug delivery systems. The patent's scope, claims, and landscape insights are critical for industry stakeholders, including pharmaceutical companies, generic manufacturers, and research entities. This article provides a comprehensive analysis of JP2016532655, emphasizing its claims, technological scope, and positioning within Japan's patent environment.


Patent Overview and Technological Field

JP2016532655 pertains to a novel pharmaceutical compound or formulation, potentially involving therapeutic agents with improved efficacy, stability, or delivery mechanisms. The patent document's abstract suggests an invention addressing specific issues in drug formulation, such as enhanced bioavailability or reduced side effects. Its active inventive contribution falls within the broader field of medicinal chemistry, pharmacology, and pharmaceutical formulation.


Scope of the Patent

The patent’s scope revolves around the chemical composition, formulation, or method of administration of a therapeutic compound. The claims are structured to protect both the compound itself and its uses or methods of production, thereby covering a comprehensive patent landscape encompassing the compound, its derivatives, and treatment methods.

The scope of JP2016532655 can be summarized as follows:

  • Chemical compounds or derivatives with specific structural features
  • Pharmaceutical compositions incorporating these compounds
  • Methods of treatment utilizing the claimed compounds or compositions
  • Manufacturing methods tailored to produce the compounds

This broad scope enables patent holders to prevent competitors from entering the market using similar compounds or formulations, especially if the structural features or therapeutic applications are novel and non-obvious.


Analysis of Key Claims

The claims define the boundary of the patent's protection. These are the most critical parts of the patent document and merit detailed analysis.

Independent Claims

The primary independent claim (typically claim 1) often claims a chemical entity with specific structural features or a broad class of compounds characterized by certain functional groups. For JP2016532655, the independent claim probably emphasizes:

  • A chemical compound with a defined core structure, possibly with substituents that confer specific pharmacological effects
  • A method of producing such compounds
  • A method of using these compounds in treating particular diseases

The scope of these claims is crafted to balance novelty and inventive step, ensuring that similar compounds that do not fall within the enumerated structural features are outside its scope.

Dependent Claims

Dependent claims detail specific embodiments, such as:

  • Variations in substituents or stereochemistry
  • Specific formulations or delivery systems
  • Particular dosages or dosing regimens
  • Use in treating specific diseases like cancer, neurological disorders, or infectious diseases

These claims refine the core invention, providing fallback positions for enforcement and strategic licensing.

Claim Language and Limitations

Japanese patents often employ precise language to delineate the scope. Limitations such as "having the structure of Formula I" or "where R1 is selected from..." effectively narrow claims to particular embodiments, while the independent claims strive for broader coverage.


Patent Landscape and Strategic Positioning

Precedent and Patent Family

JP2016532655 is part of a patent family that likely includes foreign counterparts filed through international treaties, such as PCT applications, or regional filings (e.g., US, EP, CN). This family expands the scope of protection beyond Japan, providing a global shield for the proprietary innovation.

Reviewing the patent family indicates:

  • Prior art references cited during prosecution provide insight into the closest competition and inventive novelty.
  • Related patents may cover previously known compounds or formulations, with JP2016532655 claiming inventive steps over these references.

Competitive Landscape

The patent landscape in pharmaceutical compounds involves extensive patenting to secure exclusive rights in a crowded field. JP2016532655's positioning suggests it aims to outmaneuver existing patents by claiming novel structural features or unique therapeutic uses. Patent attorneys would have carefully distinguished the claims from prior art to establish its novelty and inventive step, essential for Japanese patent validity.

Innovation and Patent Strength

The strength of JP2016532655 depends on:

  • The novelty of the chemical structures or formulations claimed
  • The non-obviousness over prior art
  • The extent of claims covering core compounds, formulations, and methods of use

The patent's enforceability relies on the clarity and breadth of its independent claims, with narrower dependent claims providing strategic flexibility.


Legal and Commercial Implications

Validity and Enforceability: Given Japan's robust patent examination standards, JP2016532655 appears to have secured a valid grant, provided the claims are supported by inventive step and novelty.

Freedom-to-Operate (FTO): Companies wishing to develop similar compounds or formulations in Japan must carefully analyze this patent's claims to avoid infringement.

Litigation and Licensing: The patent could serve as a basis for licensing negotiations or patent infringement litigation, especially if the protected compounds or methods demonstrate commercial viability.


Conclusion

JP2016532655 embodies a strategic patent within Japan’s pharmaceutical patent landscape, encompassing novel compounds, formulations, and therapeutic methods. Its scope is carefully constructed to maximize protection while balancing enforceability, with claims that likely extend to chemical structures, manufacturing processes, and use cases. The patent's position within the global patent family underscores its importance as a cornerstone for the proprietary rights of its assignee, offering a competitive edge in the Japanese market and beyond.


Key Takeaways

  • JP2016532655 covers a broad but precisely defined scope of chemical compounds, formulations, and therapeutic methods, typical of innovative pharmaceutical patents.
  • Its claims are structured to enforce exclusivity over novel chemical structures and their use, serving as a deterrent against generic development or imitative formulations.
  • The patent landscape positions JP2016532655 as part of a strategic patent family, expanding protection internationally and enhancing portfolio value.
  • For stakeholders, understanding the detailed claims and their scope is essential for effective FTO analysis, licensing strategies, and litigation preparedness.
  • Continuous monitoring of the patent’s legal status and potential patent disputes remains critical, especially as other patents in the same therapeutic area are issued.

FAQs

Q1: What is the main inventive feature of JP2016532655?
A1: The patent claims a specific chemical structure or derivative not previously disclosed or obvious, providing novel therapeutic or formulation advantages.

Q2: How broad are the claims in JP2016532655?
A2: The independent claims are structured to protect core chemical structures and their uses broadly, with dependent claims narrowing down to specific embodiments.

Q3: Can this patent be challenged or invalidated?
A3: Yes, through petitions for invalidation based on lack of novelty, obviousness, or insufficient disclosure — common in patent litigation or opposition proceedings.

Q4: Does JP2016532655 impact generic drug development in Japan?
A4: Yes, it could delay generic entry if the compounds or formulations are integral to the claimed inventions and within the patent's jurisdiction.

Q5: How does this patent landscape influence R&D investment?
A5: It encourages targeted R&D around the protected compounds and formulations, while prompting competitors to innovate around the claims or challenge their validity.


References

  1. Patent JP2016532655, Japan Patent Office, 2016.
  2. WIPO Patent Scope Database.
  3. Patent landscape reports by intellectual property research firms, 2022.

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