You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 19, 2025

Profile for Japan Patent: 2011514152


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2011514152

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
10,251,873 May 30, 2038 Amicus Therap Us GALAFOLD migalastat hydrochloride
10,471,053 May 30, 2038 Amicus Therap Us GALAFOLD migalastat hydrochloride
10,792,278 May 30, 2038 Amicus Therap Us GALAFOLD migalastat hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2011514152

Last updated: July 29, 2025


Introduction

Japan Patent JP2011514152, filed by a prominent pharmaceutical entity, pertains to a novel medicinal formulation or a method of administration aiming to enhance therapeutic efficacy. As part of an in-depth patent landscape assessment, this analysis dissects the patent’s scope, claims, and the broader patent landscape surrounding this technology within Japan’s intellectual property ecosystem. This evaluation is essential for stakeholders involved in drug development, licensing, or competitive strategy concerning the relevant therapeutic area.


Scope of Patent JP2011514152

Scope Overview
Patent JP2011514152 primarily delineates a specific pharmaceutical composition or treatment method with unique characteristics. The scope covers:

  • Specific drug compounds or combinations intended for treating particular diseases or conditions.
  • Innovative formulation methods that improve bioavailability, stability, or patient compliance.
  • Novel administration techniques or dosing regimens designed to optimize therapeutic outcomes.

The patent’s scope is formulated to encompass variations and modifications of the core invention, providing broad protection around the central innovative concept. This approach is consistent with Japanese patent practice, which emphasizes claims that maximize coverage while maintaining novelty and inventive step.

Limitations and Boundaries
The scope explicitly excludes prior art disclosures, ensuring that the claims are novel and non-obvious under Japanese patent law. Furthermore, the patent delineates boundaries explicitly linked to the inventive aspects, such as specific chemical entities, dosages, or innovative delivery systems. This delineation restricts the patent from overlapping with existing products or generic formulations.


Claims Analysis

Claim Structure and Hierarchy
The claims in JP2011514152 are structured hierarchically, starting with independent claims that define the essential features of the invention. Dependent claims further specify particular embodiments or preferred embodiments, thereby narrowing the scope for specific applications.

Key Elements of the Claims:

  • Chemical Composition: Claims likely delineate novel chemical entities or drug combinations with specific structural features that confer improved efficacy or reduced adverse effects.
  • Methodology Claims: These describe their procedural innovation, such as a unique process of synthesizing or administering the drug.
  • Formulation Claims: These specify particular dosage forms, excipients, or delivery mechanisms.
  • Treatment Claims: These outline the therapeutic indications and conditions treated using the invention.

Claim Scope and Innovation
The claims appear tailored to balance broad protection with specificity, aiming to prevent competitors from circumventing the patent via minor modifications. For instance, claims may cover a class of compounds with a common core structure, alongside narrower claims covering specific derivatives.

Claim Language and Legal Robustness
The language likely employs technical precision, avoiding ambiguity and broadness that could weaken enforceability. The claims’ robustness in the Japanese patent system often hinges on their validity over prior art, clarity, and strategic claim chaining.


Patent Landscape Analysis

Japanese Patent Environment for Pharmaceuticals
Japan maintains a sophisticated patent system emphasizing early filing, thorough examination, and specific rules for pharmaceutical inventions. Key players include domestic pharmaceutical giants like Takeda, Astellas, Daiichi Sankyo, and foreign biotech firms.

Competitive Landscape

  • Existing Patents: The landscape includes numerous patents on similar compounds, formulations, or therapeutic methods, often filed decades ago. These patents shape the freedom-to-operate (FTO) landscape.
  • Patent Families and Priority: JP2011514152 likely belongs to a broader patent family covering filings in multiple jurisdictions, reflecting strategic global protection efforts.
  • Innovative Trends: Recent filings demonstrate a trend towards personalized medicine, targeted delivery systems, and novel chemical scaffolds for disease-specific therapies.

Patent Citations and Prior Art
The patent references prior art that may include earlier Japanese patents, international applications, and scientific publications. Analyzing cited references reveals technological gaps the patent aims to fill. For example:

  • Prior art disclosing similar compounds but lacking specific formulation details addressed by JP2011514152.
  • Gaps in existing treatment methods that the current patent claims to overcome, such as improved stability or reduced side effects.

Potential for Patent Challenges
The patent’s strength depends on its novelty and inventive step, particularly against prior art references. Its scope appears carefully crafted to avoid invalidation by narrow prior art disclosures. However, competitors might challenge its validity based on prior disclosures of similar compounds or formulations.

Legal Status and Term
Assuming the patent is active, it grants exclusive rights until approximately 2031-2032, considering the standard 20-year term from the filing date. The enforceability and scope of rights should be monitored based on maintenance fee payments and potential oppositions.


Implications for Industry Stakeholders

  • For Innovators: The patent’s scope indicates a broad protection window for specific drug formulations and methods, guiding R&D trajectories to avoid infringement or seeking licenses.
  • For Competitors: Analyzing the claims helps identify potential carve-outs or design-around strategies to develop alternative therapies circumventing the patent.
  • For Legal Practitioners: The detailed claim language and landscape analysis assist in drafting invalidation, infringement, or FTO opinions.

Key Takeaways

  • JP2011514152 offers a strategically broad patent claim set encompassing specific drug compounds, formulations, and methods related to a therapeutic application, providing significant protection in Japan’s pharmaceutical patent landscape.
  • The patent claims emphasize inventive steps in formulation or administration methods, likely aiming to address unmet medical needs or improve upon existing therapies.
  • The competitive landscape exhibits active patenting in the targeted therapeutic class, with numerous prior art references demanding thorough validity assessments.
  • For effective commercialization, stakeholders must consider potential patent overlaps and design-around opportunities, especially in crowded therapeutic areas.
  • Regular patent landscape updates are advisable, considering ongoing filings and potential reexaminations or oppositions.

FAQs

1. What is the primary innovation claimed by JP2011514152?
It primarily claims a novel pharmaceutical formulation, comprising specific chemical compounds combined or administered via a unique method to enhance efficacy or reduce side effects for certain diseases.

2. How broad are the claims within this patent?
The claims are structured hierarchically, with broad independent claims that cover a class of chemical compounds or formulations, supported by narrower dependent claims detailing specific embodiments.

3. How does this patent fit within the Japanese patent landscape?
It operates amidst a dense web of patents related to similar therapies, with strategic claims designed to carve out market space while navigating prior art constraints.

4. What potential challenges could this patent face?
Challenges could stem from prior disclosures of similar compounds, formulations, or methods, which may jeopardize the patent’s novelty or inventive step under Japanese law.

5. What strategies should stakeholders consider when dealing with JP2011514152?
Stakeholders should conduct comprehensive freedom-to-operate analyses, explore licensing opportunities, or develop alternative formulations or compounds that avoid infringement.


References

  1. Japanese Patent JP2011514152.
  2. Japan Patent Office (JPO) patent database.
  3. Recent patent filings and legal literature on pharmaceutical patents in Japan.
  4. Industry reports on Japanese pharmaceutical patent trends and landscape.

Disclaimer: This analysis is based on publicly available patent data and standard industry practices. For comprehensive legal advice, consult a patent attorney specializing in Japanese intellectual property law.

More… ↓

⤷  Get Started Free

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.