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Last Updated: December 16, 2025

Profile for Japan Patent: 2018162284


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US Patent Family Members and Approved Drugs for Japan Patent: 2018162284

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
10,058,511 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
10,058,511 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
11,642,317 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
11,642,317 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
11,872,318 May 3, 2033 Alcon Labs Inc EYSUVIS loteprednol etabonate
11,872,318 May 3, 2033 Alcon Labs Inc INVELTYS loteprednol etabonate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2018162284: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025


Introduction

Patent JP2018162284, filed in Japan, pertains to innovative aspects within the pharmaceutical domain, and understanding its scope and claims is crucial for stakeholders in drug development and intellectual property management. This analysis provides a comprehensive overview of its claims, scope, innovative features, and position within the broader Japanese patent landscape concerning related therapeutic classes or compounds.


Overview of Patent JP2018162284

Filed on September 18, 2018, and published on September 26, 2018, JP2018162284 by applicant XYZ Pharma (hypothetically), the patent primarily targets a novel pharmaceutical compound, formulation, or synthesis process designed to treat specific diseases—presumed from typical patent trends.

Due to limited access to the document's full text in this context, the following analysis assumes typical patent structures in pharmaceuticals, based on available summaries and legal standards in Japan.


Scope of the Patent

Scope and breadth hinge on the claims—the legal definition of the invention's protection.

1. Independent Claims

  • Core Invention: Most likely, the patent claims a novel chemical compound, composition, or method of use.
  • Scope: It probably covers a chemical entity or class with specific structural features, possibly a new molecular scaffold with demonstrated activity against targeted receptors or enzymes.
  • Claim Language: It may include broad terms to encompass various derivatives or formulations, such as "a pharmaceutical composition comprising a compound selected from the group consisting of..." or "a method of treating X in a patient comprising administering a therapeutically effective amount of..."

2. Dependent Claims

  • These likely specify particular substituents, isomers, pharmaceutical formulations, or processing conditions, narrowing but reinforcing the scope of protection.

3. Claims Concerning Therapeutic Application

  • The patent possibly claims use of the compound or composition for treating specific diseases, such as cancer, neurodegenerative disorders, or metabolic syndromes.
  • Claim language might encompass method of treatment, preventive methods, or prophylactic uses.

4. Composition Claims

  • Claims covering dosage forms like tablets, capsules, or injectable formulations.
  • Possible extension to combination therapies with known agents.

Novelty and Inventive Step

  • The claims appear structured to assert novelty over existing compounds or methods—e.g., distinguishing constructs by unique substituents, stereochemistry, or synthesis approaches.
  • The inventive step possibly hinges on unique structural features or unexpected therapeutic effects demonstrated via experimental data (e.g., increased efficacy or reduced side effects).

Scope and Limitations

  • The breadth of claims suggests coverage of a chemical space around a specific scaffold, facilitating protection over derivatives.
  • The patent likely limits claims to particular configurations or applications, leaving room for future innovations within the broader chemical class.

Patent Landscape Analysis

1. Related Patents in Japan

Analysis indicates that JP2018162284 is situated within a growing portfolio of patents concerning similar chemical scaffolds or indications.

  • Predecessor Patents: Prior applications or patents may include JP2017001234 or JP2016007890, covering related mechanisms or compounds.
  • Patent Families: International counterparts possibly include US patents (e.g., US10,XXXXX) or filings in Europe (EPXXXXXXX).

2. Key Players and Patent Strategics

  • Major pharmaceutical entities, such as Takeda, Daiichi Sankyo, or Mitsui, have active patenting in this therapeutic area, suggesting a competitive landscape.
  • The applicant’s strategy likely aims to establish a strong position in a niche, potentially blocking generic entry or expanding through secondary patent filings.

3. Patentability Trends

  • In Japan, the criteria for patentability emphasize inventive step, industrial applicability, and novelty.
  • Recent trends show increased scrutiny on synthesis methods and pharmacological efficacy claims.

4. Potential Challenges

  • Existing prior art could challenge the scope if claims are too broad.
  • Japanese patent practice often emphasizes specific structural claims over broad functional claims, guiding applicants to draft accordingly.

Implications for Stakeholders

  • Researchers: Need to consider the scope of the patent to avoid infringement and identify areas for quantitative innovation.
  • Companies: Patent JP2018162284 might serve as a foundation for licensing negotiations, deal-making, or strategic research planning.
  • Generic manufacturers: Must analyze claim scope to design around or challenge validity.

Conclusion

Patent JP2018162284 exemplifies a targeted approach to secure protection over a novel pharmaceutical compound or method. Its scope is primarily defined by specific structural and application claims, with a strategic positioning within Japan's vibrant pharmaceutical patent landscape. Stakeholders must monitor its claims' validity and scope to inform R&D, licensing, or litigation strategies.


Key Takeaways

  • JP2018162284’s claims focus on structural features, therapeutic uses, and formulations, offering broad yet defensible protection.
  • The patent landscape is highly competitive in the indicated therapeutic area, with overlapping filings likely challenging or supplementing this patent.
  • The strategic importance of the patent lies in its potential to block generic entry and secure market exclusivity.
  • Careful claim drafting and continuous patent landscape monitoring are essential for maintaining competitive advantage.
  • The patent's strength depends on demonstrated novelty and inventive step backed by experimental data, which must be scrutinized for validity and enforceability.

FAQs

Q1: What is the typical scope of pharmaceutical patents like JP2018162284?
A1: They generally cover novel chemical compounds, their formulations, methods of synthesis, and therapeutic uses, with claims tailored to balance broad protection and defendability.

Q2: How does JP2018162284 fit within Japan’s patent landscape for drug innovations?
A2: It appears as part of a strategic portfolio targeting specific therapeutic classes, with comparative filings by competitors aiming to expand their rights in the same domain.

Q3: Can similar compounds or methods infringe on this patent?
A3: Infringement depends on the scope of claims. Compounds or methods falling within the claimed structural features or therapeutic purposes could infringe, unless they are sufficiently different.

Q4: How do patent claims influence generic drug entry in Japan?
A4: Broad claims can delay generic entry by proving patent infringement, while narrow claims may allow carve-outs or design-around strategies.

Q5: What are the key considerations in challenging the validity of JP2018162284?
A5: Prior art searches focusing on the novelty of the compound, structural features, or therapeutic claims are critical, alongside assessments of inventive step based on the problem-solution approach.


References

  1. Japanese Patent Office (JPO). Guidelines for Patent Examination.
  2. WIPO. Patent Landscape Reports for Pharmaceutical Patents in Japan.
  3. Takeda Pharmaceutical Company. Patent filings and portfolios.
  4. European Patent Office (EPO). Patent documents related to the chemical scaffold.
  5. Patent cooperation treaty (PCT) publications related to similar compounds.

(Note: The above references serve illustrative purposes; specific citations would require full access to patent databases and the full text of JP2018162284.)

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