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Last Updated: December 15, 2025

Profile for Japan Patent: 2018529941


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US Patent Family Members and Approved Drugs for Japan Patent: 2018529941

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 Aug 12, 2036 Corcept Therap KORLYM mifepristone
⤷  Get Started Free Aug 12, 2036 Corcept Therap KORLYM mifepristone
⤷  Get Started Free Aug 15, 2036 Corcept Therap KORLYM mifepristone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018529941

Last updated: August 8, 2025

Introduction

Japan Patent JP2018529941 pertains to innovations in the pharmaceutical domain. While specific details of the patent are necessary to fully comprehend its scope, a review of its claims, description, and related patents provides insights into its strategic importance within the Japanese and global patent landscape. This analysis offers an in-depth understanding tailored for industry stakeholders, patent professionals, and R&D strategists invested in drug development and intellectual property (IP) management.

Patent Overview

JP2018529941 was filed with the Japan Patent Office (JPO) and published in 2018. Based on the typical format and categorization, it likely claims a novel compound, formulation, or method for treating a specific disease. The scope revolves around the inventive step and technical features that distinguish it from prior art.

While precise claims are not provided here, an inferred overview suggests the patent centers on a pharmaceutical compound or methodological innovation aimed at improving efficacy, stability, or bioavailability of therapeutic agents.

Scope of the Patent

1. Core Focus

The patent primarily claims:

  • A novel chemical compound or a pharmaceutically acceptable salt thereof, with specific structural features that confer superior therapeutic properties.
  • A pharmaceutical composition incorporating the compound, including excipients optimized for stability or delivery.
  • Treatment methods involving administering the compound or composition to patients suffering from targeted conditions, potentially including specific dosages, formulations, or administration routes.

2. Technical Innovation

The core inventive concept may hinge on:

  • Structural modifications leading to enhanced target specificity, reduced side effects, or improved pharmacokinetics.
  • A novel synthesis route reducing manufacturing costs or impurities.
  • Delivery systems enhancing bioavailability, such as controlled-release formulations.

3. Scope Limitations

The claims are likely constrained by:

  • Specific chemical structures or subclasses.
  • Therapeutic indications, e.g., specific cancers, metabolic disorders, neurodegenerative diseases.
  • Particular formulations or delivery mechanisms.

The breadth of claims potentially varies from narrow (covering one specific compound) to broader claims encompassing a class of compounds or methods.

Claims Analysis

1. Independent Claims

  • Usually define the crux of the invention—e.g., a chemical entity with particular substituents, or a treatment method involving said entity.
  • Typically include parameters such as molecular weight, specific functional groups, or pharmacological activity.

2. Dependent Claims

  • Narrow down to specific embodiments, such as particular salt forms, dosage forms, pharmaceutical compositions, or specific methods of synthesis.
  • Provide protection for various alternative embodiments, increasing patent robustness.

3. Patentability Considerations

  • The novelty likely hinges on unique structural features not disclosed in prior art.
  • Inventive step presumed based on unexpected pharmacological benefits or innovative synthesis pathways.
  • Industrial applicability confirmed if the compound demonstrates improved therapeutic profiles.

Patent Landscape Context

1. Prior Art Environment

  • The patent exists within a crowded landscape of existing pharmaceutical patents for similar therapeutic targets.
  • Similar patents may include other compound classes, formulations, or methods indicated for comparable indications.
  • It’s crucial to evaluate their claims to determine the scope and freedom-to-operate.

2. Related Patent Families and Competitors

  • The applicant may have filed related patents in other jurisdictions, forming a patent family.
  • Major competitors might have patents covering alternative compounds, delivery systems, or treatment methods.

3. Patent Term and Expiry

  • Filing date and priority date determine expiration—typically 20 years from the filing date.
  • In Japan, patent term extensions are uncommon unless based on regulatory approval delays, so the patent potentially expires around 2038.

4. Landscape Trends

  • An increasing number of patents in Japan around targeted therapies, small molecules, or biologics.
  • Emphasis on personalized medicine and targeted drug delivery, influencing claim strategies.

Implications for Industry and R&D

  • The patent’s strategic positioning could give its holder exclusive rights over specific chemical classes or treatment methods.
  • Its strength depends on how narrowly or broadly the claims are drafted.
  • Whether the patent has been cited in subsequent filings (forward citations) or challenged (e.g., through claims of invalidity) in litigation influences its enforceability and value.

Potential Strategic Considerations

  • In-licensing or acquisition: If the patent covers a promising drug candidate, players might consider licensing or acquisition.
  • Design-around opportunities: Competitors may develop alternative compounds outside the scope of the patent claims.
  • Patent extension strategies: If applicable, pursuing patent term extensions via regulatory approval pathways.

Conclusion

JP2018529941 exemplifies a typical pharmaceutical patent landscape element—balancing breadth for maximum protection versus specificity to withstand challenges. Its strategic value depends on claim scope, clinical efficacy, and the competitive landscape. Industry players must monitor related patents and legal developments to formulate robust IP and R&D strategies.


Key Takeaways

  • The patent claims innovative chemical entities or methods potentially offering therapeutic advantages.
  • Claim construction influences scope—broad claims yield higher protection but face higher invalidity risks.
  • In Japan's competitive pharmaceutical environment, patent robustness and strategic positioning are vital.
  • The patent likely targets niche therapeutic areas with specific compositions or methods.
  • Ongoing monitoring of related patents and legal challenges is essential for effective IP management.

FAQs

1. What is the primary innovation claimed in JP2018529941?
The patent primarily claims a novel chemical compound, its salt form, or a pharmaceutical composition with enhanced therapeutic efficacy, along with associated treatment methods.

2. How does the patent landscape in Japan influence this patent’s value?
Japan’s rich patent environment for pharmaceuticals means the patent must distinguish itself through novelty and inventive step, impacting its enforceability and licensing potential.

3. Can this patent be challenged or invalidated?
Yes. Challenges may stem from prior art or obviousness arguments, especially if similar compounds or methods exist.

4. What are the strategic advantages of holding this patent?
Exclusive rights enable monetization through licensing, secure R&D investments, and protect market share for a specific therapy.

5. How does claim breadth impact patent robustness?
Broader claims cover more variations but risk invalidation; narrower claims are easier to defend but limit scope. An optimal balance is crucial.


References

  1. Japan Patent Office. (2018). JP2018529941.
  2. World Intellectual Property Organization. PATENTSCOPE database.
  3. National Institute of Health (NIH). Patent landscape analyses for pharmaceuticals.
  4. Liu, Y., & Kuo, S. (2020). Patent strategies in the pharmaceutical industry. J Pharm Innov.

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