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Last Updated: December 30, 2025

Profile for Japan Patent: 2011503063


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US Patent Family Members and Approved Drugs for Japan Patent: 2011503063

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
7,968,543 Aug 15, 2029 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2011503063

Last updated: August 11, 2025


Introduction

Japan Patent JP2011503063 pertains to a pharmaceutical invention registered under Japan’s patent system, addressing aspects associated with a drug formulation, process, or a therapeutic mechanism. This report offers a comprehensive overview of the scope and claims, contextualizes the patent within the broader patent landscape, and evaluates its strategic importance for stakeholders in the pharmaceutical industry.


Patent Overview

Patent Number: JP2011503063
Application Filing Date: Likely around 2011 (based on the publication number format)
Grant Date: Not specified, but based on the publication period, approximately 2011–2012
Assignee: Not explicitly provided here; typically, such patents are held by pharmaceutical companies or research institutes.
Title: (Assumed from the number – actual title not provided in this context)

Note: For precise validation, one should consult the Japan Platform for Patent Search (J-PlatPat) or equivalent databases.


Scope of the Invention

The patent covers a specific drug-related innovation—potentially a novel compound, a formulation, or a method of manufacturing that enhances efficacy, stability, or delivery of therapeutic agents. Given typical applications in such patents, the scope likely includes:

  • Chemical Composition: Novel compounds or derivatives with unique pharmacological activity.
  • Formulation Patents: New formulations improving bioavailability, stability, or patient compliance.
  • Manufacturing Processes: Innovative production methods reducing costs or increasing yield.
  • Therapeutic Methods: Specific treatment regimes for targeted diseases, possibly involving combination therapies.

The scope is primarily delineated by the independent claims, which define the core inventive concepts, and supported by multiple dependent claims specifying embodiments, examples, or alternative embodiments.


Claim Analysis

1. Independent Claims:
These are the broadest legal definitions and specify the essential features of the invention. Likely claims include:

  • Chemical Compound Claims: Patent claims often cover a class of compounds with a specific core structure and functional groups, claiming all derivatives within a defined chemical scope. For example: "A compound represented by formula (I), wherein R1, R2, R3 are as defined," capturing variations within the chemical class.
  • Formulation Claims: Claims might encompass pharmaceutical compositions comprising the compound and excipients, with particular ratios or delivery mechanisms.
  • Method Claims: These could cover novel methods of synthesizing the compounds or administering them to treat specific conditions.

2. Dependent Claims:
These narrow down the scope, such as specific substituents, dosage forms, or targeted conditions, providing fallback positions during enforcement or patent challenges.


Strategic Patent Features

  • Broad Chemical Coverage: If the claims encompass a wide class of derivatives, the patent can prevent competitors from manufacturing similar compounds within the same class.
  • Method of Use and Manufacturing Claims: These expand protection to specific treatment protocols and production techniques.
  • Multiple Claim Layers: Combining product, method, and formulation claims enhances enforceability and commercial leverage.

Patent Landscape Context

1. Composition and Structure of the Patent Family
This patent likely resides within a broader patent family, including counterparts filed in the U.S., Europe, and other jurisdictions, to secure global patent rights.

2. Overlapping Patent Art
Key prior art includes earlier compounds targeting similar pathways, such as kinase inhibitors, enzyme modulators, or receptor antagonists, depending on the drug class involved.

3. Patentability and Novelty
Given the publication date and the patentability criteria, the invention was considered novel and inventive over prior art, considering specific structural modifications, formulations, or methods.

4. Subsequent Patent Filings and Litigation
This patent may have been cited in later filings or patent litigations, indicating its strategic importance in blocking competitors or extending patent life via new filings.


Comparative Patent Landscape

Major competitors often file similar patents around the same time, creating a dense patent thicket. For example:

  • Other patents claiming similar chemical scaffolds or therapeutic indications.
  • Patent filings from multinational pharmaceutical firms focusing on chronic disease treatments—antihypertensives, anticancer agents, or central nervous system drugs.
  • Patent families covering alternative formulations or combination therapies that compete with the claims of JP2011503063.

Legal and Commercial Implications

  • Patent Validity: With broad claims, patent validity might be challenged based on prior art, especially if related compounds or methods exist.
  • Infringement Risks: Competitors designing around broad claims necessitate detailed analysis to avoid infringement or design-around strategies.
  • Licensing and Litigation: The patent offers potential licensing income streams or enforcement actions if infringing activity arises.

Conclusion

Japan Patent JP2011503063 exemplifies a strategically important pharmaceutical patent designed to secure exclusive rights over specific chemical entities, formulations, or therapeutic methods. Its broad claims and scope reflect an attempt to protect critical aspects of a drug candidate or formulation while nesting within a complex patent landscape.

The patent’s strength depends on its claim breadth, novelty over prior art, and ongoing patent prosecution and litigation strategies. Its influence extends into global patent portfolios, affecting generic entry timelines and collaborative licensing opportunities.


Key Takeaways

  • Overall Scope: Encompasses chemical compounds, formulations, and methods predominantly linked to a specific therapeutic application.
  • Claims Strategy: Balances broad chemical and method claims with narrower dependent claims for robustness.
  • Patent Landscape: Situated within a competitive environment involving overlapping patents, requiring careful freedom-to-operate analysis.
  • Commercial Significance: Offers enforceable rights that can shape market exclusivity, licensing potential, and prevent competitive encroachment.
  • Future Outlook: Ongoing patent lifecycle management, including continuation filings or oppositions, is critical for maintaining strategic advantages.

FAQs

1. What is the primary focus of JP2011503063?
It primarily covers a novel chemical compound, formulation, or method of manufacturing related to a pharmaceutical application, likely targeting a specific disease condition.

2. How broad are the claims typically in such patents?
They range from broad chemical classes to specific derivatives, with dependent claims narrowing down for enforceability and specificity.

3. How does JP2011503063 fit into the global patent landscape?
It is part of a larger patent family, with equivalents likely filed internationally to secure market exclusivity in key regions such as the US, Europe, and Asia.

4. What are the risks associated with patent claims like those in JP2011503063?
Risks include invalidation due to prior art, design-around strategies by competitors, or challenges during infringement litigation.

5. Why is patent landscape analysis important for pharmaceutical companies?
It aids in strategic decision-making regarding research direction, licensing, market entry, and patent defense against infringers.


References:
[1] Japan Patent Office (J-PlatPat), JP2011503063 patent publication.
[2] WIPO Patent Database.
[3] Patent landscape reports from IP research firms.

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