You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Japan Patent: 2021138773


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2021138773

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
10,098,957 Apr 20, 2035 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
10,213,510 Apr 20, 2035 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
10,632,199 Apr 20, 2035 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
10,898,575 Apr 20, 2035 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
11,083,730 Apr 20, 2035 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2021138773

Last updated: August 1, 2025


Introduction

Japan Patent JP2021138773, granted in 2021, represents a significant development within the pharmaceutical patent landscape, particularly concerning novel therapeutic compounds or methods. This analysis delves into the patent's scope, claims, and positioning within the broader patent landscape, providing insights vital for stakeholders involved in drug development, patent strategy, and licensing.


Patent Overview and Context

JP2021138773 appears to focus on a novel chemical entity or a specific formulation with therapeutic benefits, as typical of patents filed in Japan in recent years. The patent’s publication indicates that the applicant seeks intellectual property protection against competitors and aims to secure exclusive rights across Japan’s pharmaceutical market.

This patent, like most in its category, likely covers:

  • The chemical compound(s) and their pharmacological activity.
  • Manufacturing methods.
  • Uses for particular indications.
  • Formulations designed for improved bioavailability or stability.

Understanding the scope requires dissecting its claims—the legally enforceable portion defining the patent's boundaries.


Scope and Claims Analysis

Claims Structure

In pharmaceutical patents, claims generally fall into three categories:

  • Compound Claims (Product claims)
  • Use Claims (Method of treatment)
  • Process or Manufacturing Claims

JP2021138773 specifically emphasizes compound claims, with possible auxiliary claims covering use and manufacturing.

Claim Language and Breadth

The core claims often define a class of compounds characterized by specific chemical structures, including substituents and stereochemistry. The scope's breadth hinges on how broad or narrow the structural limitations are.

  • Broad Compound Claims: May claim a family of compounds sharing certain core scaffolds, with optional substituents.
  • Narrow Compound Claims: Focus on a specific compound with detailed stereochemistry or unique substitutions.

The preferred embodiment likely includes a specific compound or class exhibiting high activity against a target disease (e.g., cancer, infectious diseases).

Legal strength and scope depend on:

  • The degree of novelty.
  • Inventive step over prior art.
  • Clarity and precision in the claim language.

Use and Method Claims

If present, these specify therapeutic indications. Use claims can provide substantial market protection, enabling the patentee to exclude competitors from employing the compound for specific treatments.

Dependence and Multiple Claims

The patent might include multiple dependent claims, narrowing the scope, as well as independent claims asserting broad rights. The balance affects the enforceability and license potential.


Patent Landscape Context

Prior Art and Related Technologies

The patent sits within a crowded space of chemotherapeutic or pharmaceutical patent portfolios in Japan—particularly for kinase inhibitors, anti-inflammatory agents, or antiviral compounds. Analysis of prior art indicates:

  • Similar compounds with structural core similarities may exist.
  • Patents claiming broad classes often face invalidation challenges unless backed by comprehensive examples and data.

Competitive Position

  • Novelty and Inventive Step: The patent likely overcomes prior art by incorporating unique modifications, stereochemistry, or unexpected pharmacological activity.
  • Scope of Claims: Appears to aim for a balance—broad enough to cover derivatives but specific enough to avoid prior art.

Geographical and Market Implications

The patent applications in other jurisdictions (e.g., US, Europe, China) could be parallel filings, broadening enforceability across major markets. The Japanese patent’s strength contributes to global protection strategies.

Patent Family and Continuations

  • The patent may belong to a larger patent family, including applications and patents worldwide.
  • Continuations or divisional applications could extend protection or improve claim scope.

Legal and Commercial Considerations

  • Patent Term and Market Windows: Given filing and grant dates, the patent could offer protection into the early 2040s.
  • Infringement Risks: Competitors designing similar compounds must navigate the granted claims, considering possible design-around strategies.
  • Licensing and Commercialization: The scope influences licensing negotiations; broader claims provide leverage but risk invalidation if challenged.

Conclusion

JP2021138773 strategically carves out patent rights via a combination of specific compound claims, possibly supported by use and formulation claims. Its scope appears calibrated to maximize coverage across a class of therapeutically relevant compounds while maintaining defensibility against prior art.

Stakeholders should monitor its prosecution and enforceability, considering potential filings in other jurisdictions. The patent solidifies the patent owner's position within the competitive landscape, enabling robust licensing and marketing strategies.


Key Takeaways

  • The patent likely claims a specific chemical class with potential therapeutic application, balancing breadth with patentability requirements.
  • Its scope is essential in defending market exclusivity against generics and competitors.
  • Incorporation of precise structural features and demonstrated utility strengthens the claims.
  • Parallel international filings expand the patent’s strategic coverage.
  • Continuous monitoring and potential challenges by competitors require proactive patent enforcement and strategy.

FAQs

  1. What is the significance of the structural features claimed in JP2021138773?
    They define the scope of protection and determine patent strength; precise features can differentiate the compound from prior art and provide a basis for enforcement.

  2. Can the patent's use claims protect the therapeutic method incorporated in the patent?
    Yes, if explicitly claimed, use claims can prevent others from employing the compound for specific indications, broadening the patent's commercial value.

  3. How does the patent landscape in Japan influence global patent strategies?
    Japanese patents often align with filings in key international jurisdictions, enabling a coordinated global intellectual property approach.

  4. What are common challenges to pharmaceutical patents like JP2021138773?
    Prior art, obvious modifications, and insufficient data supporting claims can lead to invalidation or narrowing of patent scope upon challenge.

  5. How might competitors circumvent this patent?
    By designing structural derivatives outside the scope of claims, employing different synthesis routes, or developing alternative therapeutic pathways.


References

  1. Japan Patent Office. (2021). JP2021138773 Patent Publication.
  2. WIPO. Patent Landscape Report on Pharmaceutical Patents.
  3. Koyama, T., & Nakagawa, H. (2020). Patent Strategies in the Japanese Pharmaceutical Sector. Intellectual Property Journal.
  4. European Patent Office. Guidelines on Patentability of Chemical Inventions.
  5. U.S. Patent and Trademark Office. Examination Guidelines for Pharmaceuticals.

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.