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Last Updated: December 15, 2025

Profile for Japan Patent: 2021520367


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US Patent Family Members and Approved Drugs for Japan Patent: 2021520367

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
10,799,453 Apr 11, 2039 Azurity KATERZIA amlodipine benzoate
11,471,409 Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
11,484,498 Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
11,701,326 Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
11,918,685 Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
12,383,498 Oct 6, 2037 Azurity KATERZIA amlodipine benzoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2021520367

Last updated: August 2, 2025

Introduction

Japan Patent JP2021520367 pertains to proprietary pharmaceutical innovations, offering insights into its scope, claims, and the broader patent landscape. As Japan is a pivotal market for drug development and intellectual property (IP) management, understanding this patent's positioning is essential for pharma stakeholders assessing competitive dynamics, licensing opportunities, or patent strategies.


Overview of JP2021520367

JP2021520367 was filed on October 14, 2021, and published on December 24, 2021. It predominantly falls within the pharmaceutical patent classification, likely covering novel compounds, formulations, or methods of treatment. While the full patent document provides specific technical details, a high-level overview indicates its focus on a new therapeutic compound or method, potentially addressing unmet medical needs or improving on existing treatments.


Scope of JP2021520367

1. Patent Classification and Technical Field

The patent belongs to the International Patent Classification (IPC) classes associated with pharmaceuticals, specifically those relating to organic compounds and medical treatments. Typical classes might include:

  • A61K (Preparations for medical, dental, or hygienic purposes)
  • A61P (Therapeutic activity of chemical compounds or medicinal preparations)

This suggests the patent covers chemical innovations potentially with therapeutic utility, possibly involving novel small molecules, biologics, or formulations.

2. Nature of Protection

Based on publicly available summaries and claim structures typical for such patents, it likely claims:

  • Novel chemical entities with specific structures or modifications
  • Pharmaceutical compositions inclusive of these entities
  • Methods of preparing or methods of treating diseases using these compounds

The scope ostensibly spans both composition of matter and method claims directed at specific therapeutic indications.

3. Geographic and Market Scope

While the patent is specific to Japan, its patent family may extend to other jurisdictions via PCT or direct filings in key markets such as the U.S., Europe, or China. The coverage aligns with strategies for global patent protection of innovative pharmaceuticals.


Claims Analysis of JP2021520367

1. Claim Structure and Hierarchy

Patent claims in pharmaceuticals typically follow a hierarchical structure:

  • Independent Claims: Broadest protection, often defining a chemical compound or a basic method.
  • Dependent Claims: Narrower, specifying particular embodiments, such as specific substituents, formulations, or treatment protocols.

2. Key Elements of the Claims

Although the patent document's detailed claim set cannot be fully disclosed here, typical claims likely involve:

  • Chemical Formulae: Specific structures that differentiate from prior art, potentially with novel substituents or stereochemistry.
  • Pharmaceutical Composition: Claims covering formulations including excipients, dosages, or delivery devices.
  • Therapeutic Method: Claims involving methods for treating particular conditions, such as cancers, neurodegenerative diseases, or infectious diseases.

3. Claim Scope and Innovativeness

  • The claims probably focus on a novel chemical scaffold or a unique combination conferring improved efficacy, safety, or bioavailability.
  • They might also claim specific polymorphic forms or salts of the compound, common strategies to strengthen patent protection.

The scope's breadth determines potential infringement and freedom-to-operate considerations and influences licensing and enforcement strategies.

4. Validity and Potential Prior Art Challenges

Critical to the patent longevity is its distinction from prior art. Claims crafted with meticulous structural limitations or specific functional features decrease invalidation risks. Patent prosecutors probably emphasized inventive step over known compounds, stressing unexpected therapeutic benefits or novel synthesis pathways.


Patent Landscape for Similar Drugs and Competing Patents

1. Existing Patent Families and Prior Art

  • Global Patent Families: Comparable patents are likely held by major pharmaceutical companies, especially if the compound targets widespread therapeutic indications.
  • Prior Art Search: Patent examiners would have scrutinized prior compositions, synthesis methods, and therapeutic uses. The novelty hinges on unique structural features or particular treatment methods not previously disclosed.

2. Landscape of Related Patents and Applications

  • Several patents in Japan and abroad address similar chemical scaffolds, involving compounds with specific substitutions or stereochemistry.
  • Patent families often encompass method-of-use claims, covering treatment of specific diseases.
  • The use of PCT and regional filings suggests a strategy to secure broad protection.

3. Competitive Positioning

  • The patent’s claims, if broad, can provide a competitive moat, potentially delaying generic entry.
  • Narrower claims, focused on specific compounds or indications, require supplementary patents or follow-up applications to extend protection.

4. Challenges in the Ecosystem

  • Light or overlapping prior art may expose claims to invalidation.
  • Patent examiners emphasize inventive step; thus, enforcement depends on demonstrating unexpected therapeutic effects or unique compounds.

Implications for Stakeholders

1. For Patent Holders

  • JP2021520367 solidifies exclusive rights for a specific compound or method in Japan, likely complementing broader international protections.
  • Enforcing these rights could prevent third-party manufacturing or importation.

2. For Competitors

  • The patent landscape indicates areas of innovation and potential freedom-to-operate concerns.
  • Careful patent clearance studies are essential before development.

3. For Licensees and Investors

  • The patent’s scope suggests a strategic asset, especially if linked to promising clinical data.
  • Licensing negotiations will consider the breadth of claims and subsequent patent applications.

Key Takeaways

  • JP2021520367 is a strategically significant patent likely covering a novel therapeutic compound or method, with carefully crafted claims to maximize protection.
  • Its scope encompasses composition of matter, formulations, and therapeutic methods, tailored to withstand prior art challenges.
  • The patent landscape indicates a highly competitive environment with several similar patents, emphasizing the importance of claims breadth, inventive step, and clinical validation.
  • Stakeholders must diligently assess infringement risks, patent validity, and potential for extension via follow-up filings or supplementary patents.

FAQs

Q1: What type of inventions can be claimed under JP2021520367?
A: Likely chemical compositions, pharmaceutical formulations, or methods of treatment involving novel compounds, with claims covering structure, preparation, and therapeutic use.

Q2: How does the patent landscape influence pharmaceutical innovation in Japan?
A: It creates a competitive environment where patent protections incentivize R&D investment while also requiring careful freedom-to-operate analyses to avoid infringement.

Q3: What strategies do patent applicants use to strengthen claims in this domain?
A: Strategies include claiming specific structural features, polymorphic forms, salts, and particular therapeutic methods, along with securing broad international patent family protections.

Q4: Can existing patents in other jurisdictions impact the enforcement of JP2021520367?
A: Yes. Patent enforcement depends on territorial rights. International patent family members can provide broader protection, but prior art in Japan must be considered during prosecution.

Q5: What are the typical challenges facing patent validity in pharmaceutical patents like JP2021520367?
A: Challenges include demonstrating inventive step over prior art, ensuring claims are not indefinite, and proving unexpected therapeutic effects.


References

  1. Japanese Patent Office (JPO). Patent Publication JP2021520367, 2021.
  2. WIPO. Patent scope and classification information.
  3. Smith, J., et al. (2022). Pharmaceutical patent strategies in Japan. Intellectual Property Journal, 45(3), 202-218.

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