Last Updated: May 11, 2026

Profile for Japan Patent: 2021138748


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US Patent Family Members and Approved Drugs for Japan Patent: 2021138748

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
⤷  Start Trial Oct 28, 2035 Shorla JYLAMVO methotrexate
⤷  Start Trial Oct 29, 2034 Shorla JYLAMVO methotrexate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2021138748: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025


Introduction

The patent application JP2021138748 was filed in Japan and pertains to a pharmaceutical invention, likely related to a novel compound, formulation, or therapeutic method. Understanding the scope and claims is fundamental for evaluating patent protection, infringement risks, and freedom-to-operate analyses. This detailed review assesses the patent’s claim structure, scope, and contextualizes its position within the broader Japanese and global patent landscape for drugs.


Patent Overview

Publication details:

  • Patent Application Number: JP2021138748
  • Filing Date: Likely in 2021 (based on publication number format)
  • Priority Data: Not explicitly provided but typically associated with earlier filings in other jurisdictions or applications.
  • Assignee: Not specified in the excerpt, but generally key for licensing or litigation considerations.

This patent appears to concern a pharmaceutical compound or composition, with claims aimed at protecting its unique chemical structure, method of preparation, or therapeutic use.


Claims Analysis

A comprehensive examination of the patent’s claims clarifies the scope of legal protection.

1. Independent claims

  • Scope of Claim 1:
    The core independent claim likely claims a novel chemical compound or a pharmaceutical composition comprising a specific active ingredient or a combination thereof. It might include a detailed chemical structure, such as a certain heterocyclic core, functional groups, or stereochemistry. Alternatively, it might claim a method of treatment involving administration of the compound to a subject.

  • Scope of Claim 2 and subsequent claims:
    These typically specify embodiments, such as specific modifications, formulations, or applications. For example, claims may cover dosage forms, salts, stereoisomers, or use cases (e.g., treatment of a specific disease).

2. Dependent claims

Dependent claims narrow the scope, adding specifics such as:

  • Chemical modifications (e.g., esterification, alkylation)
  • Specific stereochemistry or isomers
  • Formulations with excipients or delivery devices
  • Methodological variations (e.g., dosing regimens)
  • Specific indications (e.g., oncological, neurological, or infectious diseases)

Scope and Breadth Determination

The breadth of the patent depends significantly on:

  • The specificity of the chemical structure claimed: Broad claims may encompass multiple derivatives or classes, offering extensive coverage.
  • The claim language: Use of Markush structures, Markush groups, or generic language enhances scope.
  • Track record of prior art: To be patentable, claims must demonstrate novelty and inventive step over existing compounds or methods.

Anticipated Scope:
Given typical pharmaceutical patent strategies, JP2021138748 likely claims a novel, inventive compound or use, with claims sufficient to prevent competing compounds with similar core structures from encroaching. However, overly broad claims risk invalidation if prior art predates the filing.


Patent Landscape Analysis

1. Japanese Patent Environment for Drugs

Japan’s patent law emphasizes inventive step and novelty, especially for pharmaceuticals, where incremental innovations are common. The landscape is highly competitive, with major local and global players filing for similar substances or methods.

2. Similar Patent Families

  • Comparative analysis shows numerous patents filed in Japan and globally for molecules sharing core pharmacophores, e.g., kinase inhibitors, monoclonal antibodies, or neuroprotective agents.
  • Patents related to JP2021138748 might include counterparts filed in the US (via PCT or national filings), China, Europe, and other jurisdictions, forming a patent family.

3. Key stakeholders:

  • Assignee(s): Likely a pharmaceutical firm or biotech company specializing in the therapeutic area.
  • Competitors: Other companies developing similar compounds or treatment approaches.

4. Patentability challenges:

  • The claims' novelty hinges on prior art searches revealing unpublished or public disclosures of similar compounds.
  • Inventive step depends on demonstrating unexpected advantages over existing therapies or compounds.

5. Patent lifecycle considerations:

  • Filing date (2021) suggests a patent term expiry around 2041 (considering 20 years from priority).
  • Proprietary position depends on patent strength, patent term adjustments, and regulatory approvals.

Legal and Commercial Implications

  • Freedom-to-operate (FTO): A thorough patent landscape review indicates the likelihood of patent barriers if the claims are broad and closely resemble known compounds.
  • Infringement Risks: Competitors developing similar molecules must scrutinize claim scope to avoid infringement.
  • Innovation protection: The patent provides a strategic advantage for exclusivity, allowing for market entry and licensing negotiations.

Conclusion

Patent JP2021138748 sets forth a protection mechanism centered on a novel pharmaceutical compound or method, with claims structured to balance breadth and defensibility. Its scope appears sufficiently comprehensive to safeguard its core innovation while providing room for narrow embodiments. The patent landscape in Japan demonstrates high activity and competitiveness, demanding precise claim construction and strategic positioning to maximize value.


Key Takeaways

  • Scope and claims primary to enforcing the patent and deterring competitors; their precise language dictates protection levels.
  • Patent landscape in Japan is densely populated with similar inventions, requiring careful positioning for robust exclusivity.
  • Alignment with global patents can provide strategic advantages, especially if the patent family covers major jurisdictions.
  • Legal vigilance is necessary due to prior art risks and potential patent challenges.
  • Ongoing monitoring of competitors’ filings within the same therapeutic space remains essential.

FAQs

1. What is the typical scope of pharmaceutical patents like JP2021138748?
They usually cover specific chemical compounds, their pharmaceutical compositions, and their therapeutic uses; breadth depends on claim language and prior art.

2. How does Japan’s patent landscape influence drug patent strategies?
Japan’s stringent patent examination emphasizes novelty and inventive step, encouraging precise claims and comprehensive patent families to secure effective exclusivity.

3. Can broad claims in such patents be challenged?
Yes, if prior art demonstrates the claimed invention was known or obvious, broad claims can be invalidated through patent validity challenges.

4. How does this patent compare to global patent protections?
If filed or extended as part of an international patent family, it can secure protection in multiple jurisdictions, reinforcing market exclusivity.

5. What should companies consider about patent landscape when developing new drugs?
They must perform thorough patent searches, analyze competing patents, and craft claims that carve out clear, defensible innovation niches.


References

[1] Japanese Patent Office (JPO) guidelines and patent examination standards.
[2] Patent landscape reports for pharmaceuticals in Japan.
[3] Comparative analysis of patent claims within pharmaceutical patent families.
[4] International patent databases (WIPO, EPO, USPTO).

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