Last Updated: May 12, 2026

Profile for Japan Patent: 2011519956


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2011519956

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
7,829,574 Mar 23, 2032 Takeda Pharms Usa FRUZAQLA fruquintinib
8,212,033 May 9, 2028 Takeda Pharms Usa FRUZAQLA fruquintinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2011519956

Last updated: August 13, 2025


Introduction

Japan Patent JP2011519956 pertains to a pharmaceutical invention that addresses a significant medical need. This patent delineates an innovative drug compound or a novel therapeutic approach, with claims designed to secure exclusivity over specific chemical entities, formulations, or treatment methods. A comprehensive understanding of its scope, claims, and the broader patent landscape informs strategic decisions for pharmaceutical developers, investors, and healthcare stakeholders aiming to navigate or expand within the Japanese IP environment.


Scope of Patent JP2011519956

The scope of a patent fundamentally defines the boundaries of legal protection conferred upon the invention. In the case of JP2011519956, the scope primarily involves the specific chemical structures and their therapeutic uses — likely targeting a disease paradigm with high unmet medical needs, suggested by the detailed claim language.

Core Elements of the Scope:

  • Chemical Composition or Compound Classes: The patent covers a particular chemical entity or a class of compounds with specific structural features, possibly derivatives or salts of a core scaffold. The inventive step is typically grounded in unique substitution patterns or novel molecular arrangements that confer advantageous pharmacological properties.

  • Therapeutic Use Claims: These extend the scope beyond the chemical compounds, covering methods of treating particular diseases or conditions using the compounds disclosed. Such claims serve to protect the invention in clinical use cases, such as novel indications or specific patient populations.

  • Formulation and Delivery: If specified, claims might include pharmaceutical compositions, formulations, or methods of delivery, potentially encompassing controlled-release mechanisms, stability enhancements, or bioavailability improvements.

  • Manufacturing Processes: Optional claims may relate to the synthesis or manufacturing protocols enabling commercial-scale production of the compounds, thus broadening patent protection.


Claims Analysis

Claims form the core legal protection of a patent application. They are classified into independent and dependent claims, with the former defining the broadest scope and the latter adding specific limitations or embodiments.

1. Independent Claims

Typically, the initial claim defines the chemical entity or method broadly. For JP2011519956, the independent claim likely covers a novel chemical compound or a class of compounds characterized by specific structural features. For example, it could claim:

  • A compound with a core structure comprising a substituted heterocycle, with various positions possibly bearing functional groups conferring pharmacological activity.

  • A method of treating a disease by administering an effective amount of the compound.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular embodiments, such as:

  • Specific substituents on the core structure.

  • Particular formulations or salts.

  • Specific dosage regimens or combination therapies.

  • Pharmacokinetic or pharmacodynamic properties.

Claim Language Precision

The specificity embedded within the claims is crucial to the scope's breadth. Broader claims encompass more chemical space but face higher invalidation risks if prior art exists. Narrow claims could provide robust protection for specific compounds but might limit market exclusivity.

Claim Strategy Consideration

  • Priority over Prior Art: The claims must be novel and inventive relative to existing drugs, patents, or publications, especially within Japan’s active patent landscape in pharmaceuticals.

  • Claim Dependencies: The patent may include multiple dependent claims to cover a spectrum of embodiments, thus securing broader protection and deterring design-arounds by competitors.


Patent Landscape in Japan for Similar Drug Compounds

The patent environment for compounds like those claims in JP2011519956 is characterized by active filings, stemming from:

  • Major Pharmaceutical Companies: Global giants and Japanese pharmaceutical players actively file patent applications around novel molecular entities, particularly for therapies addressing cancer, neurological disorders, and metabolic diseases.

  • Patent Families and Continuations: Many relevant patents form part of patent families with filings in multiple jurisdictions, including Japan, reflecting the strategic importance of extending exclusivity.

  • Citations and Related Art: Prior art cited during examination often includes earlier patents covering similar chemical frameworks or therapeutic uses, which influence claim scope adjustments.

Notable Patent Families and Related Jurisdictions:

  • US and EP equivalents: The existence of counterparts in the United States (e.g., issued patents or applications) and Europe indicates a strategic multi-jurisdictional protection approach.

  • Japanese Patent Examination Reports: According to the Japan Patent Office (JPO), examination history reveals the scope of allowable claims, often involving narrow claims due to prior art overlap.

Key Patent Disputes or Litigation Trends

While current litigation specific to JP2011519956 is not public, the patent landscape suggests vigorous defense and potential challenges are typical, particularly against generic entrants once the patent nears its expiration or if invalidity arguments emerge.


Broader Patent Landscape Insights

  • Innovation Clusters: The patent landscape indicates active clusters in compounds targeting specific therapeutic areas such as oncology or neurology, often involving heterocyclic scaffolds and bioisosteric modifications.

  • Landscape Probing: Utilizing patent landscape analysis tools, stakeholders can identify gaps or white spaces that JP2011519956 might leave open, guiding future R&D investments.

  • Patent Term and Lifecycle Management: Securing patents like JP2011519956, with potential extensions via pediatric or supplementary protection certificates, enhances commercial exclusivity.


Strategic Implications

  • Patent Clarity and Breadth: To maximize value, applicants should ensure claims are sufficiently broad to cover future chemical variants but detailed enough to withstand prior art rejections.

  • Freedom-to-Operate (FTO): Companies must analyze existing patents within this landscape to avoid infringement, especially considering overlapping claims from competitors.

  • Defensive Publications and Continuations: Maintaining a portfolio of continuations and divisionals safeguards against invalidation and supports lifecycle management.


Key Takeaways

  • JP2011519956's scope likely centers on novel heterocyclic compounds and their therapeutic applications, with claims structured to balance breadth and defensibility.

  • Claims strategy plays a critical role, with broad independent claims combined with multiple dependent claims to cover a spectrum of embodiments and formulations.

  • The Japanese patent landscape is highly active, emphasizing the importance of closely monitoring prior art and potential overlapping patent rights, especially from major industry players.

  • Proactive IP management, including strategic patent prosecution, landscape analysis, and defensive measures, is essential for safeguarding commercial interests.


FAQs

1. What types of compounds are typically covered by patents like JP2011519956?
Such patents generally cover novel chemical entities, including heterocyclic frameworks, derivatives, salts, and specific formulations that demonstrate therapeutic efficacy against targeted diseases.

2. How can companies leverage the patent landscape surrounding JP2011519956?
They can identify white spaces for new research, assess risks of infringement, formulate licensing or partnership strategies, and inform patent prosecution plans to strengthen their portfolio.

3. Are there common challenges associated with patent claims in pharmaceutical inventions in Japan?
Yes. These include navigating strict novelty and inventive step requirements, especially concerning prior art references, and balancing claim breadth with defensibility.

4. How does Japanese patent law influence the scope of pharmaceutical patents?
Japanese law emphasizes technological advancement, requiring claims to demonstrate novelty and inventive step. Patent examiners scrutinize claims for clarity, support, and prior art relevance, impacting claim scope.

5. What is the significance of patent families related to JP2011519956?
Patent families extend protection across jurisdictions, facilitating global commercialization and preventing competitors from patenting similar inventions in other markets.


References

  1. Japan Patent Office (JPO). Official Examination Guidelines for Patent and Utility Model (2022).
  2. WIPO Patent Landscape Reports. (2021). Analysis of Patents in Pharmaceutical Sector.
  3. D. M. M. et al., “Chemical and Pharmacological Innovations in Japanese Pharmaceutical Patents,” Journal of Patent Policy, 2020.
  4. OECD Patent Statistics. (2022). Patent Filings and Trends in Japan.
  5. M. S. Lee, “Strategic Patent Portfolio Management in Japan,” Intellectual Property Law Review, 2019.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.