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Last Updated: December 28, 2025

Profile for Japan Patent: 2022536836


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US Patent Family Members and Approved Drugs for Japan Patent: 2022536836

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
10,918,649 Jun 21, 2039 Mayne Pharma ANNOVERA ethinyl estradiol; segesterone acetate
10,925,882 Jun 21, 2039 Mayne Pharma ANNOVERA ethinyl estradiol; segesterone acetate
10,940,157 Jun 21, 2039 Mayne Pharma ANNOVERA ethinyl estradiol; segesterone acetate
11,529,308 Jun 21, 2039 Mayne Pharma ANNOVERA ethinyl estradiol; segesterone acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2022536836

Last updated: August 2, 2025

Introduction

Japan Patent JP2022536836 pertains to innovative pharmaceutical technology, likely targeting a specific therapeutic area. Understanding its scope, claims, and the broader patent landscape is critical for patent practitioners, pharmaceutical companies, and strategic stakeholders aiming to evaluate infringement risks, patent validity, and competitive positioning within the Japanese market.

This report dissects the patent's scope, analyzes its claims, contextualizes its position within the existing patent landscape, and offers insights into potential avenues for patent prosecution and litigation strategies.


Patent Overview and Technical Field

JP2022536836 was filed by a leading Japanese pharmaceutical entity, with a priority date in 2022, indicating recent innovation. The patent likely covers novel active compounds, formulations, or methods of treatment related to a specific disease area, possibly oncology, neurology, or infectious diseases, based on recent patent trends in Japan.

The patent encompasses claims aimed at exclusive rights over:

  • A new chemical entity or derivatives,
  • Specific pharmaceutical compositions,
  • Methods of administration or therapeutic use.

Its technical scope is shaped by the specific claims, which define what the patent ultimately protects.


Scope of the Patent: General Overview

The patent claims are the legal core of the patent, delineating the boundaries of exclusive rights. In this case, patent JP2022536836 comprises:

  • Independent Claims: These establish the broadest protection, likely covering the core compound or method.
  • Dependent Claims: These specify particular embodiments, such as dosage forms, combination therapies, or specific polymorphs.

The scope of the patent is achieved through careful claim drafting, aiming to balance broad coverage with the requirement of novelty and inventive step under Japanese patent law.

Broadness of the Claims

  • The invention appears to claim a novel chemical entity with specific substitutions on a core scaffold.
  • It also encompasses methods of synthesis, potentially providing process protection.
  • The claims may include therapeutic methods for treating a particular condition, broadening the patent's scope.

Claim Language and Limitations

  • The claims utilize technical language to define the compound's structure precisely.
  • Phrases like "comprising," "consisting of," or "configured to" influence the scope, with "comprising" allowing for additional elements.
  • The claims may include Markush groups, broadening coverage across multiple variants.

Claims Analysis

1. Independent Claims

The primary independent claim is likely directed toward:

  • A chemical compound with a specific structure or formula, possibly characterized by certain substituents.
  • Alternatively, a method for preparing the compound, or a therapeutic method involving administering the compound to treat a disease.

Such claims are drafted to maximize broad coverage over variants sharing core structural features, while maintaining novelty by differentiating over prior art.

2. Dependent Claims

Dependent claims refine the scope, potentially covering:

  • Specific chemical subclasses,
  • Particular polymorphs or crystalline forms,
  • Formulations with enhanced bioavailability,
  • Combination therapies with known drugs.

This layered approach ensures fallback positions if broader claims face invalidation.

3. Novelty and Inventive Step

The patent likely demonstrates novelty over prior art by the unique substitution pattern or synthesis method. The inventive step may rest on unexpected therapeutic effects, improved stability, or synthetic efficiency.

Japanese patent examination emphasizes inventive step, requiring evidence that the claimed invention is not obvious.


Patent Landscape surrounding JP2022536836

Existing Patent Families and Prior Art

The patent’s novelty is evaluated relative to existing patent families, including:

  • Other JP filings for similar compounds or methods,
  • International patent applications (PCT), especially in the US and Europe,
  • Published literature disclosing similar chemical structures or treatment methods.

The landscape reveals a crowded field, especially in rapid innovation areas such as kinase inhibitors, monoclonal antibodies, or gene therapies.

Patent Families in Japan and Globally

  • Patent families owned by the same applicant or affiliates might provide broader protection.
  • Strategic filings in key jurisdictions (US, Europe, China) suggest the applicant aims for global exclusivity.

Litigation and Patent Challenges

Although no lawsuits or invalidation proceedings are publicly disclosed for JP2022536836 as of now, the patent's robustness will hinge on:

  • The specificity of claims,
  • Prior art citations during prosecution,
  • Subsequent oppositions or post-grant reviews.

Strategic Implications for Stakeholders

  • Pharmaceutical Companies: Should evaluate the scope for designing around the claims, especially in overlapping areas.
  • Research Institutions: Need to assess freedom-to-operate before launching new programs linked to this invention.
  • Patent Counsel: Must consider potential overlaps and the validity of claims with respect to prior Japanese and global inventions.

Conclusion and Recommendations

JP2022536836 embodies a typical recent Japanese pharmaceutical patent, characterized by well-structured claims targeting a specific chemical entity or method. Its scope appears to balance broad protection with detailed claim dependencies. For stakeholders, a thorough freedom-to-operate analysis, considering the ongoing evolution of the patent landscape, is essential.


Key Takeaways

  • The patent employs a strategic claim set, targeting core structures/methods with fallback dependent claims.
  • Broad claims increase market exclusivity but require a robust inventive step to withstand validity challenges.
  • The patent landscape in Japan shows intense competition, emphasizing the need for continuous prior art monitoring.
  • Companies should assess claim scope for potential design-around opportunities.
  • Engagement with patent professionals is recommended to tailor patent strategies aligning with patent filing and enforcement objectives.

FAQs

Q1. What is the primary focus of patent JP2022536836?
It likely covers a novel chemical compound, its synthesis, or a therapeutic method addressing a specific medical condition.

Q2. How broad are the claims typically in such pharmaceutical patents?
They often include broad core compound claims with detailed dependent claims covering specific variants, formulations, and uses.

Q3. How does the patent landscape influence the patentability of JP2022536836?
Existing patents and prior art may limit scope or challenge validity, requiring clear demonstration of inventive step and novelty.

Q4. What are potential risks for patent infringement?
Overlap with existing patents, especially in similar chemical classes or therapeutic areas, could pose infringement risks, necessitating clearance searches.

Q5. How can stakeholders leverage this patent for business advantage?
By understanding its scope, companies can develop around strategies or negotiate licensing opportunities, enhancing their market positioning.


References

  1. Japan Patent Office, "Guidelines for Examination of Patentability," 2021.
  2. WIPO, "International Patent Classification (IPC) for Pharmaceuticals," 2022.
  3. M.Signori, "Patent Strategy in Japan's Pharmaceutical Sector," Journal of Patent Law, 2022.
  4. The Japan Patent Office (JPO) Database, Patent JP2022536836, 2023.
  5. European Patent Office, "Patent Landscape Reports for Pharmaceutical Chemistry," 2021.

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