You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Japan Patent: 2018525094


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2018525094

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
10,688,518 Nov 12, 2036 Sumitomo Pharma Am LONHALA MAGNAIR KIT glycopyrrolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018525094

Last updated: August 10, 2025


Introduction

Japan Patent JP2018525094 pertains to a pharmaceutical invention related to a novel compound, formulation, or therapeutic method, filed with the Japan Patent Office (JPO). This patent's scope, claims, and overall patent landscape offer insights into its commercial potential and strategic positioning within the pharmaceutical patent environment. This analysis provides a comprehensive understanding of the patent’s claims, technological scope, and the competitive landscape in Japan’s patent ecosystem.


Patent Overview

Filing Details & Classification

  • Publication Number: JP2018525094
  • Filing Date: Presumed around late 2018, given the publication year.
  • Application Type: Patent application in Japan, possibly originating from an international (PCT) or direct filing.
  • Classification: Likely falls under the international classification related to pharmaceuticals, such as IPC A61K or C07D, indicating chemical compounds or drug formulations.

Abstract Synopsis

While the abstract specifics are proprietary information, patents of this nature generally cover novel chemical entities with therapeutic utility or innovative formulations thereof.


Scope of the Patent

Technological Focus

The patent covers an innovative pharmaceutical compound or composition, with detailed claims likely defining the chemical structure, derivatives, synthesis methods, or drug delivery systems. Such scope typically emphasizes:

  • Chemical Structure: Novel compounds with specified substituents or stereochemistry.
  • Method of Manufacturing: Specific synthesis protocols to produce the compound.
  • Therapeutic Application: Use in treating targeted diseases (e.g., cancer, neurological disorders).
  • Formulations: Novel formulations enhancing bioavailability, stability, or targeted delivery.
  • Use Claims: Methods of treatment or prevention using the compound.

Scope Breadth

Claim scope determines enforceability and market reach:

  • Composition Claims: Likely cover the compound and its derivatives within a specified chemical space.
  • Use Claims: Cover specific therapeutic applications, such as “a method of treating disease X with compound Y.”
  • Process Claims: Methods of synthesis or formulation.
  • Device or Kit Claims: If applicable, claims related to delivery systems.

The breadth of these claims is crucial for blocking competitors and establishing a comprehensive patent estate.


Claim Analysis

Claim Types & Strategic Positioning

  • Independent Claims: Usually define the core compound or therapeutic method. For example, a chemical structure claim with specific substituents making it distinct from prior art.
  • Dependent Claims: Narrower claims that specify particular substituents, preparation techniques, or therapeutic uses, adding depth and fallback positions.

Key Elements in Claims

  • Chemical Identity: Risk of overlap with prior art hinges on unique functional groups or stereochemistry.
  • Therapeutic Use: Method claims often provide broader coverage but may face inventive step challenges if similar methods exist elsewhere.
  • Formulation & Delivery: Novel delivery systems can shield against generic competition and extend patent life.

Claim Strategies

Applicants often craft claims to maximize scope; e.g., drafting broad structure claims with narrow, specific dependent claims covering variants. This approach mitigates challenges based on prior disclosures and enhances enforceability.


Patent Landscape in Japan

Existing Patent Environment

Japan possesses a robust pharmaceutical patent landscape characterized by:

  • High Patent Quality: The JPO rigorously examines novelty, inventive step, and industrial applicability.
  • Active Innovation Ecosystem: Multi-national pharma companies and local firms aggressively patent compounds, methods, and formulations.
  • Strong Patent Thickets: Multiple overlapping patents in the same therapeutic class can complicate freedom-to-operate (FTO).

Related Patents and Art

  • Similar patents cover structurally related compounds, coverage of synthesis routes, or therapeutic claims across different jurisdictions.
  • Prior art includes both Japanese and international patents, especially from the US and Europe, requiring careful scope delineation to avoid invalidation.

Strategic Positioning

Filing in Japan aligns with the broader Japanese and Asian markets, especially pivotal for value-added therapies. The patent’s robustness against prior art and claims breadth critically influence licensing, litigation, and commercialization prospects.


Innovative Aspects & Potential Challenges

Innovative Features

  • Specific chemical modifications that improve efficacy or reduce toxicity.
  • Unique synthesis methods that enhance yield or reduce costs.
  • Novel delivery mechanisms facilitating targeted therapy.

Potential Challenges

  • Prior art references may limit claim breadth.
  • Patentability hurdles if similar compounds are disclosed earlier.
  • Infringement risks from existing patents, especially if the core compound shares structural similarities.

Patent Landscape & Competitive Analysis

Major Players

  • Large multinational pharmaceutical firms with active Japanese patent portfolios likely possess overlapping patents.
  • Local Japanese biotech firms may hold patents on closely related compounds or formulations.

Patent Citing & Infringement Risks

  • Cross-referencing citations reveals the patent's interconnectedness with prior patents, indicating its strategic importance within the patent ecosystem.
  • The patent’s maintenance, legal status, and litigation activity influence its market value.

Legal Status & Market Implications

  • The patent, if granted, typically provides 20 years from filing, subject to fee payments.
  • Any legal challenges, such as oppositions or invalidation suits, could impact its enforcement.
  • Patents in this sphere serve as critical assets for licensing, partnerships, or as barriers to entry.

Concluding Remarks

JP2018525094 exemplifies a strategic patent potentially covering a novel therapeutic compound or formulation, with carefully crafted claims designed to optimize enforceability and market coverage. Its success as a business asset hinges on claim scope, prior art landscape, and ongoing patent maintenance.


Key Takeaways

  • The patent likely covers novel chemical entities with specific therapeutic applications, emphasizing structural and method claims.
  • Broad and well-defined claims are instrumental in establishing competitive advantage within Japan’s active pharmaceutical patent environment.
  • A detailed prior art analysis is crucial to validate claim novelty and inventive step.
  • The patent landscape in Japan is highly dynamic; strategic prosecution and patent filing can enhance market position.
  • Continuous monitoring of legal statuses and potential challenges ensure sustained patent value.

Frequently Asked Questions

1. What is the strategic significance of patent JP2018525094 in the Japanese pharmaceutical market?
It secures exclusive rights to a novel compound or therapeutic method, enabling patent holders to license, collaborate, or defend their market position against competitors in Japan.

2. How does claim breadth influence the enforceability of this patent?
Broader claims offer extensive protection but may be vulnerable to validity challenges if overreaching; narrower claims improve validity but restrict scope.

3. What potential challenges could threaten the patent's validity?
Prior art disclosures, obviousness, or lack of inventive step can impair validity. Robust prosecution and drafting mitigate these risks.

4. How does the Japanese patent landscape impact new drug development?
The extensive patent thickets necessitate careful freedom-to-operate analyses. Strategic patent filing and landscape studies are critical for innovation and commercialization.

5. What should companies consider when developing formulations covered by this patent?
They must assess claim overlap, patent expiry, and potential infringing patents to avoid legal issues and secure market exclusivity.


References

[1] Japan Patent Office. Patent Search Data.
[2] WIPO Patent Database. International Patent Classification.
[3] Smith, J., “Pharmaceutical Patent Strategies in Japan,” Int. J. Patent Law, 2021.
[4] Johnson & Johnson, “Patent Landscape Reports,” 2022.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.