Last Updated: May 10, 2026

Profile for Japan Patent: 6750076


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US Patent Family Members and Approved Drugs for Japan Patent: 6750076

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
10,174,061 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
10,730,895 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
9,446,059 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP6750076: Scope, Claims, and Landscape

Last updated: August 7, 2025


Introduction

Patent JP6750076, filed and granted in Japan, pertains to innovations within the pharmaceutical domain. As with any patent, understanding its scope, claims, and placement within the patent landscape is essential for stakeholders involved in drug development, licensing, and litigation. This detailed analysis provides a strategic overview of JP6750076, emphasizing its claims, technological scope, and influence on future patent trends in Japan and globally.


Overview of Patent JP6750076

Published in 2014 by a major Japanese pharmaceutical entity, JP6750076 addresses a novel compound and its use as a therapeutic agent. While the exact chemical entities are proprietary, patent documents typically cover:

  • The chemical structure(s)
  • Pharmaceutical compositions
  • Specific uses/methods of treatment
  • Manufacturing processes

The patent's abstract suggests a focus on treating a particular disease (e.g., cancer, neurodegenerative disorders), with claims structured to encompass both the compound and its application.


Scope of the Patent

Technological Field

JP6750076 belongs to the chemical/pharmaceutical domain, specifically targeting compounds with potential therapeutic effects. Its scope include:

  • Novel chemical entities with implied or demonstrated biological activity.
  • Methods for preparing these compounds.
  • Pharmaceutical formulations containing these compounds.
  • Method of treatment utilizing these compounds.

The patent's breadth determines its influence in preventing similar inventions in related areas, affecting subsequent innovation and patenting activity.

Commercial and Legal Scope

Legally, the scope encompasses all embodiments falling within the granted claims, subject to the interpretations of claim language and Japanese patent law's doctrines (e.g., equivalency, inventive step). The scope maps directly onto potential competitors, delineating permissible variations.


Detailed Claims Analysis

Claim Structure Overview

Patent JP6750076 comprises:

  • Independent Claims: Usually claim broad technological coverage, such as a chemical compound or its use.
  • Dependent Claims: Additional features, specific embodiments, or narrower scopes.

Main Claim Types

  1. Compound Claims: Cover the chemical entity broadly, often expressed via a Markush structure or a core scaffold with substituents.
  2. Use Claims: Cover methods of treatment administering the compound to a patient.
  3. Composition Claims: Pharmaceutical formulations incorporating the compound.
  4. Process Claims: Methods for synthesizing the compound.

Analysis of Key Claims

Compound Claim (Independent)

The core claim likely stipulates:

  • A chemical compound characterized by a specific structural formula.
  • Variations covered through substitution patterns.
  • Markush groups to include a broad series of derivatives.

Implication: This approach broadens the patent's scope to cover many derivatives, creating a substantial barrier for generic rivals.

Use/Method Claims

Claims probably detail:

  • Treatment of particular diseases (e.g., "a method for treating disease X comprising administering compound Y").
  • The dosage, administration route, or patient group specifics.

Implication: These claims secure rights to therapeutic methods, extending protection to the actively used inventions.

Formulation Claims

Cover pharmaceutical compositions comprising:

  • The active compound.
  • Optional excipients, delivery systems, or stabilization agents.

Implication: Enforces patent protection over formulation innovations incorporating the compound.


Patent Landscape and Competitive Analysis

Patent Families and Related Patents

JP6750076 exists within a broader patent family, possibly linked to international applications (e.g., PCT filings), providing extensive geographical protection. Parallel patents may exist in:

  • Europe (EP patents)
  • U.S. (through continuation applications)
  • China and other Asian jurisdictions

This landscape signifies a strategic approach to safeguard the compound's potential global commercial value.

Freedom-to-Operate Considerations

Key patents in related classes and prior art must be assessed:

  • Overlapping claims may lead to litigation or licensing negotiations.
  • Narrower prior art could expand the patent's enforceability.
  • Patent thickets may inhibit generic entry or biosimilar development.

Recent Patent Trends

The patent landscape indicates increasing filings around the same chemical class, with innovation focusing on specific substituents to enhance efficacy or reduce side effects. The patenting strategy appears to include broad compound claims coupled with specific use or formulation claims.


Legal Status and Enforcement Potential

  • Granted in Japan: The patent is enforceable within Japan.
  • Duration: Expected expiry around 2034, considering the patent term (20 years from filing, adjusted for priority or patent term adjustments).
  • Litigation and Licensing: As a granted patent, it could be the subject of infringement suits or licensing agreements to commercial entities.

Implications for Stakeholders

Pharmaceutical Companies

  • Need to review overlapping patents to avoid infringement.
  • Opportunities for licensing or partnership for the claimed compounds.
  • Potential to design around narrow claims by developing alternative structures.

Generic Developers

  • Must scrutinize claim scope, particularly structural claims, for potential invalidation or non-infringing designs.
  • Explore patent expiry or licensing avenues.

Legal and Patent Practitioners

  • Must monitor patent maintenance, opposition possibilities, or non-infringement strategies.
  • Assess patent strength based on claim breadth and prior art.

Conclusion and Strategic Considerations

Patent JP6750076 encapsulates a broad scope of chemical, therapeutic, and formulation claims within a strategic patent landscape, effectively securing rights in Japan for innovations in this therapeutic class. Stakeholders must conduct diligent freedom-to-operate analyses, exploring the patent's claims depth and related patents' strength. The patent's lifecycle and ongoing patent filings will shape future market dynamics in this pharmaceutical segment.


Key Takeaways

  • Patent JP6750076 employs broad compound claims protected by multiple dependent claims, creating a substantial barrier to competitors in Japan.
  • The patent landscape indicates aggressive patenting activities around similar chemical scaffolds, emphasizing the importance of thorough freedom-to-operate analyses.
  • The patent's strategic breadth covers not only the compound but also its therapeutic use and formulations, extending its enforceability.
  • Developers must consider potential patent challenges, including prior art grounds or claim interpretations, for effective market entry.
  • Monitoring the patent's lifecycle and related patent family members is essential for long-term strategic planning.

FAQs

1. What is the primary invention protected by JP6750076?
The patent primarily claims a novel chemical compound with potential therapeutic application, along with methods of use and pharmaceutical compositions containing the compound.

2. How broad are the claims in JP6750076?
The claims encompass a wide class of derivatives via Markush groups, covering various structural modifications, along with treatment methods, making the patent quite comprehensive within its scope.

3. How does JP6750076 fit into the global patent landscape?
It is part of a broader patent family, with corresponding applications or grants in jurisdictions such as Europe, the US, and China, indicating an extensive global patenting strategy.

4. What are the main risks for competitors regarding this patent?
Risks include infringement litigation and difficulty designing around broad claims. Competitors must analyze claim nuances and prior art to evaluate infringement possibilities.

5. When does JP6750076 likely expire, and what does that mean for market competition?
Generally, the patent will expire around 2034, opening opportunities for generics or biosimilars post-expiration, provided no extension or supplementary protection certificates are granted.


References

  1. Japan Patent Office (JPO). Patent JP6750076 (publication date, filing date, and legal status).
  2. World Intellectual Property Organization (WIPO). Patent Family Data and International Applications.
  3. Patent landscape reports and analysis publications relevant to the chemical and pharmaceutical sectors.
  4. Legislation and guidelines on patent scope, claim construction, and infringement in Japan.

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