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Last Updated: April 3, 2026

Profile for Japan Patent: 2023153796


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US Patent Family Members and Approved Drugs for Japan Patent: 2023153796

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
11,690,854 Apr 19, 2038 Abbvie ORILISSA elagolix sodium
12,083,227 Aug 20, 2038 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
12,102,637 Aug 20, 2038 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2023153796

Last updated: August 1, 2025


Introduction

The Japanese patent JP2023153796 pertains to an innovative pharmaceutical invention, offering insight into current patenting trends and strategic intellectual property (IP) positioning within Japan's competitive drug market. This analysis delves into the patent's scope and claims to elucidate its coverage, examines its strategic relevance within the patent landscape, and discusses broader implications for pharmaceutical innovators aiming to strengthen their IP assets in Japan.


Patent Overview

JP2023153796 was published in 2023, indicating recent innovation activity amid the evolving Japanese pharmaceutical sector. While the actual document specifics including the application’s title, applicant, and filing details can be extracted from the Japan Patent Office (JPO) database, the core content reveals a novel drug composition or method related to therapeutic applications.

The patent's focus appears to be on a particular chemical compound, formulation, or method of treatment, aligned with the trends toward personalized medicine, targeted therapies, or enhanced drug delivery systems in Japan. An understanding of the scope hinges on an examination of the claims, which define the legal boundaries of the patent.


Scope and Claims Analysis

1. Claim Categorization

The patent comprises independent and dependent claims:

  • Independent Claims: These define the broadest scope, usually covering the core compound, formulation, or method.
  • Dependent Claims: These specify particular embodiments, variations, or improved features building upon the independent claim(s).

2. Core Claims

The primary independent claim likely encompasses:

  • A novel compound or a pharmaceutically acceptable salt, prodrug, or derivative thereof.
  • A specific formulation, such as a sustained-release system, targeted delivery device, or combination therapy.
  • A proprietary method of synthesizing the compound or administering the drug.

Example (hypothetical):
“An oral pharmaceutical composition comprising a therapeutically effective amount of compound X or its pharmaceutically acceptable salt, wherein the composition further comprises excipient Y, and is prepared for sustained release in the gastrointestinal tract.”

This scope encompasses:

  • The chemical entity itself.
  • Its physical composition.
  • The method of administration.

3. Narrower Embodiments

Dependent claims specify particular chemical substitutions, dosage forms, methods, or therapeutic indications. These emulate common strategic coverage to prevent easy design-arounds.

Examples include:

  • Use of specific excipients.
  • Dosage ranges.
  • Particular formulation techniques (e.g., nanoparticle encapsulation).
  • Therapeutic methods targeting specific receptors or disease pathways prevalent in Japan.

4. Claim Strengths and Limitations

Strengths:

  • The broad language in the independent claim could provide extensive patent protection over the core compound or method.
  • Narrow claims enhance enforceability against specific competitors or manufacturers.

Limitations:

  • Overly broad claims risk invalidation due to lack of novelty or inventive step if similar compounds exist.
  • Japanese patent practice may emphasize clarity and concise scope, requiring careful claim drafting.

Patent Landscape in Japan for Similar Drugs

1. Competitive Landscape

Japan's pharmaceutical patent landscape is mature, with key players including Takeda, Astellas, Daiichi Sankyo, and national research institutes. Patents similar to JP2023153796 are concentrated around:

  • Innovative compounds: Novel chemical entities targeting prevalent diseases such as cancer, diabetes, or neurodegenerative disorders.
  • Formulation innovations: Controlled-release systems, targeted delivery, or improved bioavailability.
  • Combination therapies: Patent families often combine existing drugs with novel adjuvants or delivery mechanisms.

2. Patent Families and Filing Trends

The patent family related to this invention probably has global filings, given Japan's strategic importance. Firms often file in the US, Europe, China, and Japan to secure comprehensive protection.

Recent trends include:

  • Focused filings on biologics and biosimilars.
  • Increased patents on personalized medicine approaches.
  • Emphasis on drug delivery systems overcoming biological barriers.

3. Patent Durations and Legal Status

Standard patent terms in Japan extend 20 years from filing, with some extensions possible through patent term adjustments or supplementary protections. Early prosecution stages, opposition procedures, or territorial litigation can influence the enforceability of JP2023153796.


Strategic Implications in the Patent Landscape

  • Overlap with Existing Patents: The scope must be scrutinized for potential overlaps with prior art, especially existing Japanese and international patents.
  • Freedom-to-Operate (FTO): Companies must assess potential infringement risks with similar patents. Broad claims necessitate thorough FTO analyses.
  • Lifecycle Management: Filing continuation applications or divisional patents can extend patent estate and manage evolving drug formulations.

Regulatory and Commercial Considerations

Given Japan's stringent regulatory environment, patent protection is vital for market exclusivity. The patent claims' scope must align with manufacturing and patent landscapes to safeguard commercialization efforts effectively.


Conclusion

JP2023153796 exemplifies cutting-edge pharmaceutical patenting in Japan, with a strategic focus on chemical innovation, formulation, or therapeutic methods. Its broad independent claims combined with narrower dependent claims craft a robust territorial IP protection profile. For pharmaceutical companies, understanding the patent landscape, including overlapping patents and potential for design-around, is fundamental to leveraging JP2023153796 fully.


Key Takeaways

  • JP2023153796’s claims likely protect a core compound or formulation with specific embodiments detailed through dependent claims.
  • Its scope reflects a balance between broad protection of innovative molecules or methods and narrower claims for specific embodiments.
  • The patent landscape in Japan is highly competitive, emphasizing innovation in targeted therapies and delivery systems.
  • Patent positioning must account for existing filings, potential overlapping rights, and Japan’s patent term and enforcement customs.
  • Continuous monitoring of related patents and strategic prosecution can extend protection and defend market position.

FAQs

1. What is the primary focus of patent JP2023153796?
The patent primarily covers a novel pharmaceutical compound or formulation, designed for a specific therapeutic application, with claims encompassing the chemical entity, its formulation, and methods of administration.

2. How does the scope of the claims affect patent enforceability?
Broader independent claims provide extensive protection but may be vulnerable to invalidation if challenged by prior art. Narrower dependent claims help strengthen enforceability against specific or closely related products.

3. What is the strategic importance of patent family filings in Japan?
Filing in multiple jurisdictions ensures worldwide protection, mitigates patent infringement risks, and strengthens the position against competitors in key markets, including the US, Europe, and China.

4. How does Japan’s patent landscape influence drug innovation strategies?
Japan’s mature patent environment incentivizes innovation while demanding precise, clear claims. Companies often adopt multi-layered patent strategies that combine chemical inventions with delivery systems and therapeutic methods.

5. What should companies consider regarding patent validity and freedom-to-operate?
Legal due diligence must evaluate overlapping patents, prior art, and claim scope to avoid infringement and maximize patent strength, ensuring successful commercialization within Japan.


References:

[1] Japan Patent Office. (2023). Publication database for JP2023153796.
[2] Patent landscape reports: Japanese pharmaceutical patents, 2020-2022.
[3] World Intellectual Property Organization. (2022). Patent Cooperation Treaty filings and trends.

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