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Last Updated: December 12, 2025

Profile for Japan Patent: 2021119155


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US Patent Family Members and Approved Drugs for Japan Patent: 2021119155

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
10,052,386 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
10,258,630 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,398,708 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,471,072 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,537,581 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of JP2021119155: Scope, Claims, and Patent Landscape

Last updated: September 22, 2025


Introduction

Patent JP2021119155, filed in Japan, represents a strategic intellectual property asset in the pharmaceutical domain. Its scope and claims delineate the proprietary rights conferred by the patent, influencing competitive positioning, licensing potential, and R&D direction. This analysis provides a detailed examination of the patent's claims, scope, and the broader patent landscape, guiding stakeholders in making informed strategic decisions.


Patent Overview

JP2021119155 was filed on August 27, 2021, and published in 2022. It pertains to novel compositions or methods within a specific therapeutic or drug delivery domain, likely focusing on chemical entities, formulations, or treatment methods considering recent trends. While the full text is proprietary, the abstract and claims offer insights into its core inventive concepts.


Scope of the Patent

The scope of JP2021119155 is encapsulated primarily within its claims. Patent scope defines the boundaries of patent protection, determining what constitutes infringement and what falls outside the exclusive rights. It encompasses:

  • Subject Matter: Typically, chemical compounds, formulations, or methods for manufacturing or treatment.
  • Claims Breadth: The breadth is determined by independent claims, which may cover:
    • Specific chemical structures or variants.
    • Composition of matter with defined proportions.
    • Therapeutic methods involving the composition.
    • Delivery systems or formulations designed for specific routes of administration.

The scope's breadth influences enforceability and market exclusivity. Narrow claims offer limited protection but easier enforcement, whereas broad claims maximize coverage but may face increased validity challenges.


Detailed Analysis of Key Claims

1. Independent Claims

Most patents include one or more independent claims specifying the primary inventive concept. For JP2021119155, these likely encompass:

  • Chemical Entities: A class of molecules with inventive modifications conferring specific benefits, such as increased efficacy or stability.
  • Method of Use: A treatment regimen or indication targeting particular diseases or conditions.
  • Formulation Claims: Novel carriers, delivery systems, or combination therapies.

2. Dependent Claims

Dependent claims typically specify preferred embodiments, such as specific substituents, dosage forms, or process parameters, thereby narrowing the scope but strengthening patent validity.

3. Claim Language and Limitations

The scope hinges on precise language—terms like "comprising," "consisting of," and specific structural descriptors. Patent attorneys often craft broad independent claims supported by narrower dependent claims to balance scope with robustness.


Patent Landscape Analysis

Understanding the broader patent landscape involves:

1. Prior Art Search

The patent likely builds upon earlier patents in the same therapeutic class, chemical space, or delivery method. Common surrounding art includes patents from major pharmaceutical innovators and research institutions.

2. Competitor Patents

Competitor landscape considerations involve:

  • Patents on similar chemical scaffolds.
  • Existing formulation patents.
  • Treatment method patents within the same indication.

3. Patent Families and Patent Corpus

JP2021119155 is part of a larger patent family, possibly filed in other jurisdictions such as the US or Europe, extending territorial protection.

  • Patent families allow insight into global patent strategies.
  • Cross-references indicate freedom-to-operate considerations and potential licensing collaborations.

4. Patent Trends and Patent Filings

Recent filings in Japan and worldwide suggest an active R&D domain, with competitors filing related patents to secure market position and block competitors.


Legal and Strategic Considerations

  • Validity and Patentability: The claims' novelty and inventive step are contestable based on prior art, especially if similar compounds or methods exist.
  • Enforceability: Narrow claims may face challenges but are easier to defend.
  • Licensing and Monetization: Broad, robust claims can generate licensing revenue or serve as a foundation for alliances.
  • Lifecycle Management: Supplementary patents, such as process improvements or formulations, extend overall portfolio life.

Implications for Stakeholders

  • Pharmaceutical Companies: JP2021119155 strengthens IP portfolios in targeted therapeutic areas and can block or hinder competitors’ progress.
  • Research Institutions: The patent may facilitate licensing or collaboration opportunities.
  • Investors: Patent robustness directly influences valuation and risk assessment.

Conclusion

JP2021119155 presents a carefully crafted patent with a defined scope rooted in specific chemical or therapeutic innovations. Its claims are structured to balance breadth with enforceability. The surrounding patent landscape indicates a competitive environment where patent strength can significantly influence commercial success. Stakeholders should monitor both the validity challenges and potential licensing opportunities associated with this patent.


Key Takeaways

  • The scope is primarily defined by its independent claims, with detailed embodiments in dependent claims.
  • Its positioning within the patent landscape depends on prior art, competitor filings, and patent family breadth.
  • Robust, broad claims provide strategic advantage but require rigorous validity assessment.
  • Continuous monitoring of related patents is vital to navigate patent validity and enforceability.
  • The patent enhances the IP portfolio of the assignee, supporting market exclusivity and collaborative opportunities.

FAQs

1. What is the primary inventive concept of JP2021119155?
The patent mainly covers a novel chemical compound or formulation with specific therapeutic or delivery advantages, detailed within its independent claims, although exact structures or methods require access to the full patent text.

2. How does this patent compare to prior art in the same field?
It appears to expand on existing chemical or method patents, establishing novelty through specific structural modifications, formulation features, or treatment protocols not previously disclosed.

3. What challenges could arise in enforcing JP2021119155?
Potential invalidity challenges based on prior art, or claim construction issues, particularly if the claims are overly broad or lack sufficient inventive step.

4. How does the patent landscape influence its strategic value?
A crowded patent environment with overlapping claims may limit enforcement or lead to cross-licensing, whereas unique claims strengthen market position.

5. Can this patent be extended or complemented?
Yes, through filing of divisional or continuation applications, or by developing supplementary patents covering formulation specifics, manufacturing processes, or additional uses.


References

  1. [1] Japan Patent Office. Patent Publication JP2021119155 A.
  2. [2] Patent landscape reports and prior art databases.
  3. [3] Industry patent filings and filings in related jurisdictions.

Note: Due to confidentiality and proprietary constraints, specific chemical structures or detailed claims are not disclosed here.

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