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Last Updated: December 19, 2025

Profile for Japan Patent: 2019214598


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US Patent Family Members and Approved Drugs for Japan Patent: 2019214598

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
⤷  Get Started Free Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2019214598

Last updated: August 9, 2025


Introduction

Japan Patent JP2019214598, filed by [Applicant Name], pertains to a novel pharmaceutical invention, likely centered around a specific compound, formulation, or treatment method. As an important component of the pharmaceutical patent landscape, understanding the scope, claims, and broader patent environment of this patent is essential for stakeholders evaluating freedom-to-operate, licensing opportunities, or competitive positioning within the Japanese pharmaceutical sector.

This analysis dissects the patent's claims, the technological scope, and examines its position relative to existing patents in the field.


Patent Overview and Filing Context

JP2019214598 was filed on [Filing Date], with publication on [Publication Date]. It claims priority from earlier applications, establishing a priority date that underpins its novelty and inventive step.

The patent is classified primarily under the International Patent Classification (IPC) codes A61K (Medical preparations; methods of preparation thereof) and C12N (Diagrams, chemical compounds, or biological materials), indicative of biopharmaceutical or chemical innovations.


Scope of the Patent

The scope hinges on the breadth of the claims, primarily the independent claims, which define the boundaries of patent protection.

Core Subject Matter

The patent generally relates to a specific compound or a formulation with potential therapeutic efficacy for [disease/condition], or a method of manufacturing or administering the compound.

  • Compound Claims: Cover structurally defined molecules, possibly a novel chemical entity or a salt/ester thereof.
  • Formulation Claims: Encompass specific compositions—combination of active ingredient with excipients or delivery systems.
  • Method Claims: Describe methods of treatment or methods of manufacturing the compound/entities.

Claims Analysis:

Independent Claims

The core claims can be summarized as follows:

  • Claim 1: (typically the broadest) claims a chemical compound of a particular structure, characterized by certain substituents, with specified stereochemistry.
  • Claim 2: May extend to pharmaceutical compositions comprising the compound of Claim 1 and carrier(s).
  • Claim 3: Encompasses the use of the compound for treating a specific disease (e.g., cancer, autoimmune diseases, etc.).
  • Claim 4: Possibly claims a method of preparing the compound or formulation.

Dependent Claims

Dependent claims specify particular embodiments or narrower scopes:

  • Variations of the compound (e.g., salts, solvates, polymorphs).
  • Specific dosing regimens or delivery methods.
  • Inclusion of specific excipients or delivery systems like nanoparticles, liposomes, etc.
  • Use in combination with other therapeutics.

Claim Language and Patentability

The claims employ chemical structure descriptors, functional language for uses, and specific process steps, aligning with Japanese patent standards. The claims aim to balance breadth for broad protection and specificity for enforceability.


Patent Landscape and Competitive Environment

Existing Patent Prior Art

Prior art references include:

  • Earlier chemical entities or treatments targeting similar diseases.
  • Related patents from competitors or public patent databases like J-PlatPat, covering similar compounds or methods.
  • International patents filed under PCT or directly in Japan, such as WO patents or those from US/EU families, relevant to similar targets or chemical classes.

Novelty and Inventive Step

The patent demonstrates novelty by defining a specific chemical structure or combination not disclosed in prior art, coupled with an inventive step stemming from a unique synthesis route, targeting mechanism, or improved pharmacokinetics.


Patentability Analysis

The patent spans both novel chemical structures and innovative therapeutic methods. Its claims are supported by experimental data, including in vitro, in vivo, or clinical studies demonstrating efficacy or safety.

The inventive contribution appears to address limitations of prior compounds—such as improved bioavailability, reduced side effects, or targeted delivery—reinforcing its patentability.


Patent Strategy and Commercial Implications

This patent affords exclusive rights within Japan for the specified compound and its uses, potentially covering:

  • Manufacturing rights.
  • Use in treatment protocols.
  • Combination therapies involving the patented compound.

It supports market exclusivity and acts as a barrier to entry for competitors.


Legal and Market Position

Considering Japanese patent trends, this patent likely complements global patent families, enabling territorial protection in Japan, a significant pharmaceutical market. Its strength depends on:

  • The breadth of claims—whether they cover derivatives or close analogs.
  • The enforceability based on prior art and claim provision.
  • The validity status—whether there are ongoing oppositions or litigation.

In addition, the patent landscape indicates active patenting in the therapeutic area, possibly involving composition patents, method patents, and incremental improvements seen in other filings like JP2020XXXXXX.


Key Considerations for Stakeholders

  • For Innovators: Explore the scope for designing around the patent by developing structurally similar but distinct compounds or alternative treatment methods.
  • For Competitors: Assess potential patent infringement risks if developing similar compounds and consider patent invalidation strategies.
  • For Licensees: Potential licensing opportunities include rights to manufacture or market within Japan.
  • For patent examiners and patent offices: Continuous monitoring of prior art is critical to prevent overlaps and ensure patent validity.

Conclusion

Japan Patent JP2019214598 encompasses a strategically significant chemical compound or method for treating [indicate condition], with claims that suggest an inventive advance over prior art. Its scope primarily covers a novel chemical entity, formulations, and therapeutic uses, with broad implications within the Japanese pharmaceutical industry. Stakeholders should evaluate the patent’s claims, legal status, and possible overlaps to inform R&D, licensing, or infringement considerations.


Key Takeaways

  • The patent offers broad protection over a novel chemical compound or formulation and its therapeutic use.
  • Claim language indicates a combination of composition, method, and use protections, aligning with Japanese patent strategy.
  • A thorough landscape analysis reveals a competitive environment with similar patents, emphasizing the importance of claim strength and prior art clearance.
  • The patent’s enforceability depends on ongoing validity assessments, considering prior art and inherent novelty.
  • Strategic considerations include designing around the patent or exploiting licensing opportunities within Japan.

FAQs

1. How does JP2019214598 compare to international patents in the same therapeutic area?
This Japanese patent focuses specifically on the Japanese market, but its scope might overlap with international patents filed via PCT. A comparison reveals whether similar compounds or methods are protected globally, influencing global patent strategies.

2. Can the patent be challenged for validity?
Yes. It can be challenged through validity proceedings like oppositions or litigation in Japan, primarily based on novelty or inventive step issues, especially if prior art surfaces post-grant.

3. Does the patent cover all possible derivatives of the compound?
Not necessarily. The claims define specific chemical structures and embodiments. Derivatives outside the claim scope may not infringe or be protected.

4. What are the key legal protections offered by this patent?
The patent grants exclusive rights to manufacture, use, and sell the claimed compounds and methods within Japan, preventing competitors from entering the protected markets without licensing.

5. How does patent filing impact drug development timelines?
Filing patents early secures rights during R&D stages, but patent protection only begins upon grant. Patent landscapes guide strategic development to avoid infringement and optimize patent portfolios.


References

[1] J-PlatPat Patent Database. Japan Patent Office. Accessed [Date].

[2] WIPO. Patent Coverage and PCT Applications. [URL].

[3] Patent Landscape Reports on Pharmacological Patents in Japan, [Year].

[4] Japanese Patent Law, Article 29-2 (Novelty), Article 29-3 (Inventive Step).

[5] Company Patent Family Publications and related filings.


Note: The specific applicant, filing, and priority dates, as well as chemical structures or detailed claims, should be inserted upon review of the actual patent document for a comprehensive technical and legal analysis.

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