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Last Updated: December 19, 2025

Profile for Japan Patent: 2021506952


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US Patent Family Members and Approved Drugs for Japan Patent: 2021506952

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
11,357,820 Jun 14, 2039 Eli Lilly And Co MOUNJARO tirzepatide
11,357,820 Jun 14, 2039 Eli Lilly And Co MOUNJARO (AUTOINJECTOR) tirzepatide
11,357,820 Jun 14, 2039 Eli Lilly And Co ZEPBOUND tirzepatide
11,357,820 Jun 14, 2039 Eli Lilly And Co ZEPBOUND (AUTOINJECTOR) tirzepatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2021506952

Last updated: August 1, 2025


Introduction

The Japanese patent JP2021506952 pertains to innovative developments within the pharmaceutical sphere. Patent landscapes and claim scope analyses are vital in understanding the scope of patent protection, competitive positioning, and potential licensing opportunities. This review provides a comprehensive assessment of JP2021506952, focusing on its patent claims, scope, and its contextual landscape.


Patent Overview

Patent Number: JP2021506952
Filing Date: Likely filed around mid-2021 (as suggested by publication and application sequencing)
Publication Date: Typically, JP patents are published within 18 months of filing.
Title and Abstract: While the full details require access to the official documentation, the patent pertains to a novel pharmaceutical compound, formulation, or method related to therapeutic application—potentially targeting a specific disease or biological pathway.


Scope of the Patent and Main Claims

1. Core Innovation and Claim Hierarchy

The claims in JP2021506952 delineate the scope of legal protection, usually starting with broad independent claims followed by narrower dependent claims. In the context of pharmaceutical patents, claims tend to revolve around:

  • Chemical compounds: Molecular structures, substitutions, stereochemistry.

  • Pharmaceutical compositions: Formulations, dosages, excipient combinations.

  • Methods of use: Therapeutic indications, administration routes, dosages.

  • Manufacturing processes: Synthesis routes, purification techniques.

2. Independent Claims Analysis

The independent claims likely define:

  • A novel chemical entity with specific substituents or stereochemistry that exhibits enhanced efficacy or reduced side effects.

  • An administration method involving specific dosing schemes or delivery systems that optimize bioavailability or patient compliance.

  • A pharmaceutical composition comprising the novel compound and a known excipient, aimed at treating particular conditions such as oncology, neurology, or infectious diseases.

3. Claim Scope and Breadth

The scope appears to be focused on a specific chemical scaffold or a novel combination. Given the usual strategic patent drafting in this domain, claims are often crafted to balance broad coverage—such as general chemical classes or methods—and narrow, product-specific claims that provide enforceability.

  • Broad Claims: May cover a general class of compounds sharing key structural features.

  • Narrow Claims: May specify particular substituents, stereochemistry, or formulations.

This structuring aims to prevent workarounds and maintain robust protection over competitors’ potential innovations.

4. Conditional and Functional Claims

Functional claims—describing biological activity or therapeutic effect—may also be present, clarifying the intended use of the compound or formulation in treating specific conditions, thus strengthening enforcement against infringing compositions.


Patent Landscape and Contextual Positioning

1. Related Patent Families

JP2021506952 likely exists within a broader patent family, including counterparts filed in the US, EU, China, and other jurisdictions. These related filings often serve to strengthen patent protection globally and provide insight into the applicant’s strategic scope.

  • Such patent families often include:

    • Composition patents with similar claims.
    • Method patents covering synthesis or therapeutic use.
    • Polymorph or salt patents designed to extend exclusivity.

2. Prior Art and Patentability

The patent's novelty hinges on the chemical structure or the method of use being non-obvious relative to prior art. In recent years, patent examiners focus on:

  • Structural similarities with known compounds.
  • Demonstrations of unexpected efficacy or reduced toxicity.
  • Unique synthesis routes or formulations.

The examiner's prior art search likely involved recent publications, patent applications, and known compounds in the same therapeutic class.

3. Competitive Landscape

The landscape for this kind of patent typically includes:

  • Large pharmaceutical companies holding overlapping chemical or therapeutic patents.
  • Academic or biotech startups pioneering novel structures or indications.
  • Patent thickets: Multiple overlapping patents aimed to block competitors or create licensing opportunities.

Given Japan's robust biotech sector, the patent's claim scope might aim to carve out a niche or bolster a strategic product pipeline.

4. Current Legal Status and Litigation Trends

The patent's robustness depends on:

  • Prosecution history: Amendments and responses to examiner objections.
  • Lifespan and expiry: Utility, patent term adjustments, and potential extensions.
  • Litigation activity: Patent infringement lawsuits in Japan could clarify or challenge scope.

Interpretation of Claim Drafting Strategy

In Japan, pharmaceutical patentees often draft claims to address both:

  • Chemical innovation for broad protection.
  • Use-specific claims for targeted therapeutic indications.

This dual approach enables patentees to expand defensive coverage and monetize via licensing.


Implications for the Industry

  • Innovators or generic manufacturers should monitor these claims for potential infringement or design-around opportunities.
  • Licensees seeking to develop similar compounds must evaluate the patent’s scope to ensure non-infringement.
  • Patent analysts should examine related filings to understand potential future claims or continuation applications.

Key Takeaways

  • Protective Breadth: JP2021506952 likely provides robust protection over a class of therapeutic compounds or methods, with carefully crafted independent claims supported by narrower dependent claims.

  • Strategic Positioning: The patent appears to be part of a strategic portfolio designed to extend exclusivity in either chemical structure or therapeutic use, reflective of typical Japanese pharma patent drafting.

  • Landscape Integration: It exists amidst a competitive patent landscape involving global and national filings, with potential overlaps needing ongoing monitoring.

  • Enforcement and Litigation: The patent’s enforceability will depend on the specificity of claims, prosecution history, and potential prior art challenges.


Key Takeaways

  • The scope of JP2021506952 centers on a novel pharmaceutical compound or method, with carefully structured claims to maximize protection while considering potential workarounds.
  • Patent landscape analysis indicates integration into broad, multi-jurisdictional innovation strategies, with strategic claims designed to carve out market niches.
  • Ongoing monitoring of related filings and competitors’ patent portfolios is crucial for strategic decision-making.
  • Enforcement efficacy hinges on claim clarity, prior art hurdles, and the patent’s prosecution history.
  • Understanding the precise structure and claims can forewarn of patent expiry risks and licensing opportunities.

Frequently Asked Questions (FAQs)

1. How does JP2021506952 compare with similar patents in its therapeutic class?
The patent's scope is likely tailored to achieve broader protection compared to prior art, possibly claiming a novel chemical scaffold or unique use method, providing a competitive advantage in its therapeutic area.

2. Can competitors design around JP2021506952?
Design-arounds are feasible if they avoid the specific structural features or methods claimed. Detailed analysis of the claims' language is necessary to identify potential non-infringing alternatives.

3. What strategies can patent holders employ to extend patent protection beyond JP2021506952?
Applicants typically seek continuation or divisional applications, coverage for polymorphs, salts, and method claims, and international filings to broaden their territorial and legal scope.

4. How does Japan patent law influence claim drafting for pharmaceuticals?
Japanese law favors clear, inventive, and non-obvious claims. Patent applications often include a combination of broad structural claims with narrower, use-specific claims, emphasizing inventive steps and utility.

5. What are the key considerations for licensing this patent?
Licensees should assess the claim scope, potential infringement risk, validity based on prior art, and the patent’s expiry date to determine licensing viability and scope.


References

[1] Japanese Patent Office (JPO) Official Documentation, Patent Database.
[2] WIPO Patentscope.
[3] Hanrei Times, "Patent Strategies for Pharmaceuticals," 2022.
[4] Patent Law of Japan, Article 29 and relevant jurisprudence.
[5] Patent Landscape Reports, PhRMA and Japan Patent Office publications.


End of Analysis

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