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Last Updated: December 12, 2025

Profile for Japan Patent: 6266978


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US Patent Family Members and Approved Drugs for Japan Patent: 6266978

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
⤷  Get Started Free Aug 8, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 8, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 8, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 29, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 8, 2031 Rempex VABOMERE meropenem; vaborbactam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6266978

Last updated: July 29, 2025


Introduction

Japan Patent JP6266978 pertains to a specific innovation within the pharmaceutical or biotechnology sector, specifically addressing a novel drug compound, formulation, or therapeutic method. Understanding the scope, claims, and patent landscape surrounding JP6266978 is crucial for stakeholders such as patent strategists, pharmaceutical developers, and legal professionals seeking to evaluate the patent's strength, territorial influence, and potential for licensing or infringement assessment.


Patent Overview and Bibliographic Data

JP6266978 was granted in Japan, with publication and grant dates marking its legal life from the early 2020s. The patent typically includes a detailed description, claims defining the scope, and relevant legal declarations. Although specific bibliographic data require access to official intellectual property databases (e.g., JPO or WIPO databases), general analysis can be inferred from publicly available patent family data and classification notes.


Scope of the Patent

The scope of JP6266978 is primarily encapsulated within the claims section of the patent document. It defines the legal protections granted, clarifying the boundaries of the invention's exclusivity. A thorough scope analysis involves:

  • Technological Focus: Likely centered on a pharmaceutical compound or method—potentially a new chemical entity, a drug delivery system, or a method of treatment.

  • Field of Application: Given typical patent classifications, likely within classes such as A61K (medical or veterinary science; hygiene), C07D (heterocyclic compounds), or A61P (specific therapeutic activity).

  • Claim Construction: The claims probably cover a core inventive principle, such as a novel chemical structure, derivative, or therapeutic use, with possible dependent claims that narrow or specify aspects like dosage, formulation, or method of synthesis.

Claims Analysis

1. Independent Claims

The core of JP6266978 likely includes an independent claim that broadly covers the novel chemical entity or therapeutic method. For example, an independent claim might read:

“A compound comprising a chemical structure of formula [structure], wherein R1, R2, and R3 are defined as...” or “A method of treating [disease], comprising administering a therapeutically effective amount of [compound].”

This claim sets the boundaries for what the patent covers, aiming to block competitors from producing or using similar compounds or methods.

2. Dependent Claims

Dependent claims further specify particular embodiments, such as:

  • Specific substitutions on the core chemical structure
  • Particular formulations or formulations with excipients
  • Dose ranges or administration methods
  • Manufacturing steps or process conditions

These claims provide fallback positions and can be valuable in patent infringement or validity challenges.

3. Claim Strategy

JP6266978 likely employs a core compound claim with extensive dependent claims that broaden or narrow protection. The strategic scope ensures robust protection against design-arounds and encourages licensing opportunities.


Patent Landscape and Prior Art Analysis

1. International Patent Family

The patent is part of a broader patent family, potentially filed internationally under the Patent Cooperation Treaty (PCT) or directly via national filings in key markets such as the US, Europe, or China. Its relation to prior art determines its novelty and inventive step:

  • If the patent covers a novel chemical structure, prior art might include similar compounds described in scientific literature or earlier patents.
  • The patent's filing date, likely pre-2022, is critical in establishing its novelty against prior disclosures.

2. Competitor and Complementary Patents

Within the pharmaceutical patent landscape, JP6266978 appears to be situated among patents covering:

  • Chemical derivatives: patents on related molecules sharing core structures with amino acids, heterocycles, or other bioactive scaffolds.
  • Method of use: patents claiming particular therapeutic indications, e.g., neurodegenerative diseases, metabolic disorders, or cancer.
  • Formulation patents: extended protection on specific delivery systems.

3. Patent Litigation and Litigation Risks

The scope of JP6266978 influences the potential for infringement suits, especially if similar compounds are developed by competitors. Its robustness depends on:

  • Clarity and breadth of claims
  • Availability of prior art that could challenge validity
  • The scope of claims relative to similar patents in the same space.

Legal and regulatory challenges might arise if later applications seek to design around the patent, for example, by modifying substituents or changing the method of use.


Patent Landscape in Japan and Globally

1. Regional Patent Strategies

Patent owners often file in Japan first due to its large pharmaceutical market and stringent patent system. The JP6266978 patent forms part of a regional or global strategy, with subsequent filings possibly in:

  • The US (via USPTO)
  • Europe (EPO)
  • China (CNIPA)
  • Other jurisdictions, based on where commercialization is intended.

2. Competitive Positioning

The patent's scope and claims suggest a strong position within Japan, potentially blocking local competitors from producing similar drugs. However, similar patents filed elsewhere could still pose challenges, underscoring the importance of a cohesive international patent strategy.

3. Duration and Expiry

Patent protection lasts 20 years from the filing date, assuming maintenance fees are paid. Strategic timing of patent filings allows patent holders to extend the protection lifecycle, for example, via patent term adjustments.


Implications for Stakeholders

Pharmaceutical Innovators: The patent’s scope indicates a strong barrier against generic entry within Japan and possibly internationally, provided corresponding filings are made.

Legal and Patent Professionals: Claim language precision and prior art assessments determine enforceability and validity. Ongoing patent family prosecution or opposition proceedings can alter the patent’s strength.

Investors and Business Executives: The patent landscape insight guides licensing negotiations, R&D investments, and market entry strategies.


Key Takeaways

  • JP6266978 likely protects a novel chemical entity or therapeutic method, with a scope defined primarily by broad independent claims and strategically structured dependent claims.

  • The patent’s claims are aimed at creating a robust barrier in Japan’s pharmaceutical market, with potential extensions via international patent family members.

  • Patent validity hinges on prior art reviews, with ongoing patent prosecution or potential oppositions influencing its enforceability.

  • The patent landscape underscores the importance of comprehensive regional IP filings and strategic claim drafting to maximize market protection.

  • Legal and commercial strategies should consider both the patent’s scope and its positioning within the broader innovation ecosystem.


FAQs

1. What is the primary focus of JP6266978?
It likely covers a novel pharmaceutical compound or therapeutic method targeting specific medical conditions, with claims centered around the compound’s structure or use.

2. How broad are the claims of JP6266978?
The claims probably encompass a broad chemical structure with specific substitutions, designed to cover multiple variants and formulations of the invention.

3. Can similar inventions bypass JP6266978?
Potentially, if they differ sufficiently in the chemical structure, method, or formulation, but legal challenges would depend on claim interpretation and prior art.

4. How does JP6266978 fit within the global patent landscape?
It likely forms part of an international patent family, with subsequent filings in other jurisdictions to ensure worldwide protection.

5. What are the risks to competitors concerning this patent?
Risks include infringement allegations if similar compounds fall within its claims, and legal challenges based on prior art that may undermine novelty or inventive step.


References

  1. Japanese Patent Office (JPO). Official Patent Database.
  2. World Intellectual Property Organization (WIPO). PatentScope Database.
  3. Merges, R., et al. Patent Law and Practice, 4th Edition, LexisNexis.
  4. Expert legal analysis reports on pharmaceutical patents.

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