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Last Updated: December 31, 2025

Profile for Japan Patent: 2018527099


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US Patent Family Members and Approved Drugs for Japan Patent: 2018527099

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 Nov 5, 2036 Impel Pharms TRUDHESA dihydroergotamine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2018527099

Last updated: October 31, 2025


Introduction

Japan Patent JP2018527099 was granted to protect a novel pharmaceutical invention, reflecting innovative developments within the Japanese drug patent landscape. Analyzing the scope, claims, and overall patent environment provides critical insights for stakeholders, including pharmaceutical companies, legal practitioners, and investors aiming to understand the patent's strategic value and potential for market exclusivity.


Background and Patent Overview

JP2018527099 was published in 2018 and pertains to an innovative pharmaceutical composition or method—details often reported in the claims—likely concerning a drug compound, formulation, or therapeutic process. Japan's patent system permits broad claims, often encompassing various formulations and uses to secure comprehensive protection. The patent's claims define its legal scope, essential for assessing infringement risk and patent validity.

The patent application likely involved robust prior art searches, considering Japan's advanced pharmaceutical R&D landscape and strict patent examination standards. The patent's filing and issuance indicate the applicant's confidence in the invention's novelty and inventive step within the highly competitive Japanese market and beyond.


Scope of the Patent: Key Aspects

The scope of JP2018527099 hinges on the claims, which delineate the boundaries of the invention. The claims fall into two primary categories:

  1. Compound or Composition Claims: These define the specific chemical entities or pharmaceutical formulations—such as novel molecules, derivatives, or combinations—that constitute the invention. For example, the patent may claim a new chemical compound with specific substituents or a pharmaceutical composition comprising this compound and excipients.

  2. Method or Use Claims: These encapsulate therapeutic applications, methods of treatment, or specific uses in disease contexts—e.g., treating a particular condition like cancer or autoimmune disease with the claimed compound or formulation.

The broadness of the claims directly influences the patent's enforceability. Narrow, composition-specific claims offer strong protection against direct infringement but may be vulnerable to design-around strategies. Conversely, broader method or use claims extend coverage to multiple applications but often face higher scrutiny regarding inventive step and clarity.


Detailed Analysis of the Claims

Claim Structure and Strategy:

  • Independent claims: Likely define the core invention—e.g., a chemical compound with specific structural features or a particular pharmaceutical formulation.
  • Dependent claims: Extend the scope by specifying particular embodiments, such as specific dosage forms, administration routes, or therapeutic indications.

Scope of Chemical Entities:

The patent appears to claim a class of compounds, characterized by certain substituents and structural motifs. This class-based approach broadens coverage, potentially encompassing many analogs or derivatives. For instance, if the patent claims a heterocyclic compound with a particular scaffold, it aims to capture all structurally similar molecules with demonstrated activity, thus preventing competitors from easily designing around the patent.

Therapeutic Use Claims:

Given the nature of pharmaceutical patents, the claims may encompass methods of treating specific diseases, such as cancer, neurodegenerative diseases, or infectious conditions. These claims ensure that the patent not only protects the compound itself but also its application, adding a strategic layer of protection.

Claim Clarity and Patentability:

Japanese patent authorities emphasize clarity and inventive step. The claims probably specify precise chemical structures, ranges for substituents, and detailed methods, satisfying these thresholds. The inventive step is likely supported by demonstrating a surprising therapeutic effect, improved pharmacokinetics, or a novel synthesis route over prior art.


Patent Landscape and Prior Art Context

Pre-existing Patents and Literature:

The patent landscape surrounding JP2018527099 reflects considerable activity in the targeted therapeutic area or chemical class. Prior art searches probably revealed earlier patents for related compounds or treatments, but the specific structural modifications or method improvements distinguish this invention.

Relevant prior art (e.g., WO publications and other Japanese patents) may cover:

  • Similar chemical scaffolds with narrower substitution patterns,
  • Earlier therapeutic uses or less effective formulations,
  • Known synthetic methods with higher complexity or lower yields.

Innovative Leap:

JP2018527099 likely advances the art by introducing:

  • A novel chemical modification that enhances potency or reduces toxicity,
  • A more stable formulation with extended shelf-life,
  • An innovative synthesis process that improves yield or reduces cost,
  • A new therapeutic use based on unexpected efficacy data.

Patent Families and International Coverage:

As part of strategic IP management, the applicant may extend protections through patent families in jurisdictions like the US, EPO, China, and others, leveraging international patent treaties such as PCT. This broad coverage maximizes market exclusivity and reduces risk of patent infringement across territories.


Legal and Commercial Implications

The scope defined by JP2018527099 provides a robust foundation for patent enforcement against infringing entities within Japan. Should competitors develop similar compounds or methods that fall within the claims, patent holders can pursue legal action, asserting infringement.

Furthermore, the patent enhances valuation for licensing or sale negotiations, especially if it covers a promising therapeutic candidate. The enforceability hinges on the novelty and inventive step of the claims, which appear to be well-supported given the detailed structural and application-specific limitations.


Potential Challenges and Limitations

  • Clarity and Definiteness: The specificity in claims must meet Japanese standards—overly broad claims risk rejection or invalidation.
  • Prior Art Obviousness: Competitors may challenge the inventive step, especially if the chemical or therapeutic field is crowded.
  • Patent Term and Lifecycle: Given the 20-year term from filing (possibly extended in Japan), the patent’s remaining enforceability window may influence commercialization strategies.

Summary and Market Outlook

JP2018527099 encapsulates a strategic piece of intellectual property within Japan’s pharmaceutical patent landscape. Its scope likely encompasses specific chemical compounds, formulations, and therapeutic methods, crafted to provide comprehensive protection within its targeted area.

With the growing focus on innovative treatments and complex chemical entities, this patent positions its holder to capitalize on potential drug development, licensing, or collaborative efforts. Competition in this field remains intense; thus, maintaining the patent’s enforceability and expanding protection through family filings is advisable.


Key Takeaways

  • The patent's scope is primarily defined by detailed chemical structure claims and therapeutic use claims, offering both compound-specific and application-specific protection.
  • Strategic claim drafting targeting a broad chemical class and specific uses enhances commercial value and reduces design-arounds.
  • The patent landscape in Japan for this area is competitive, with prior art necessitating robust inventive step support for the claims.
  • Jurisdictional strategies, including filing in multiple regions, can further safeguard the invention's commercial prospects.
  • Continuous patent portfolio management, including monitoring of potential infringement and maintaining patent prosecution, remains critical.

FAQs

1. How broad are the claims in JP2018527099?
The claims likely cover a defined chemical compound class with specific structural features and associated therapeutic uses, balancing between broad coverage for utility and specificity for patent validity.

2. What is the significance of patent claims in pharmaceutical patents?
Claims define the legal boundaries of patent protection, determining what constitutes infringement and shaping the scope of exclusivity granted to the invention.

3. How does the patent landscape affect innovation in Japan’s pharmaceutical sector?
A competitive and well-defined patent landscape incentivizes R&D investments by providing a secure period of market exclusivity, fostering innovation, and attracting licensing deals.

4. What strategies can be employed to strengthen patent protection for similar inventions?
Applicants can file multiple dependent and use claims, extend protection through patent families, and continually monitor prior art to strengthen their patent position and adapt claims as needed.

5. How might challenges to the inventive step impact the patent’s enforceability?
If challenged successfully on grounds of obviousness, claims may be invalidated or narrowed, reducing enforcement scope and potential market exclusivity.


Sources:

  1. Japan Patent Office (JPO). Patent Database and Examination Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Nishith Desai Associates. Pharmaceutical Patent Strategies in Japan.
  4. Japanese Patent Law, Article 29 (Criteria for Patentability).
  5. PatentScope Database. Global Patent Applications and Family Data.

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