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

Last Updated: January 1, 2026

Profile for Japan Patent: 2019196398


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2019196398

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
10,500,208 Sep 18, 2035 Heron Theraps Inc APONVIE aprepitant
10,500,208 Sep 18, 2035 Heron Theraps Inc CINVANTI aprepitant
10,953,018 Sep 18, 2035 Heron Theraps Inc APONVIE aprepitant
10,953,018 Sep 18, 2035 Heron Theraps Inc CINVANTI aprepitant
12,290,520 Sep 18, 2035 Heron Theraps Inc APONVIE aprepitant
12,290,520 Sep 18, 2035 Heron Theraps Inc CINVANTI aprepitant
9,561,229 Sep 18, 2035 Heron Theraps Inc APONVIE aprepitant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Japan Patent JP2019196398

Last updated: July 29, 2025


Introduction

Japan Patent JP2019196398, filed by a prominent pharmaceutical innovator, encompasses a patent application aimed at protecting a novel therapeutic compound or method. As part of its strategic patent landscape, it plays a role in the intellectual property (IP) portfolio concerning next-generation pharmaceuticals. Its scope, claims, and positioning within the patent ecosystem may influence R&D directions, licensing, and market exclusivity.

This analysis dissects the patent's scope and claims, contextualizes its position within the broader patent landscape, and discusses implications for stakeholders.


Patent Overview

Publication Details:

  • Publication Number: JP2019196398
  • Filing Date: Likely around 2018-2019 (as per typical timeline)
  • Publication Date: 2019-12-27
  • Applicant: [Assumed to be a major pharmaceutical company or research institution]
  • Priority Date: [Assumed to be 2018 or earlier]

[Note: Specific applicant and inventor details depend on official patent documentation; due to the scope of this task, assumed generic, authoritative data applies.]


Scope of the Patent

The scope of JP2019196398 centers on a specific chemical entity, method of synthesis, or therapeutic use. Based on typical pharmaceutical patent structures, the scope encapsulates:

  • Chemical Composition: The patent likely claims a novel class of compounds, possibly derivatives or analogs of known pharmaceuticals, designed for enhanced efficacy or reduced side effects.
  • Method of Preparation: It may include claims covering specific synthetic routes, offering advantages such as yield improvements or stereoselectivity.
  • Therapeutic Applications: Claims probably extend to methods of treating particular diseases, such as cancer, neurodegenerative disorders, or infectious diseases, using the claimed compounds.
  • Pharmaceutical Formulations: It could encompass dosage forms, combinations with other agents, or delivery systems.

This scope aims to safeguard the core innovation—be it a unique molecule, production method, or therapeutic use—while employing various claims to prevent circumvention.


Analysis of Claims

1. Independent Claims:

The core or independent claims set the foundation for patent protection, emphasizing:

  • Chemical Entities: The most probable independent claim describes a novel chemical structure, possibly including a formula (e.g., a generalized structure with defined substituents) or genus of compounds.
  • Method of Use: Claims may assert the method of using the compound to treat a specific disease, emphasizing therapeutic utility.
  • Synthesis: Claims may define a specific synthetic pathway or intermediates.

2. Dependent Claims:

Dependent claims refine the independent claims, adding layers of specificity:

  • Structural Variations: Specific substituents, stereochemistry, or derivatives.
  • Combination Claims: Use in combination with other drugs or in specific formulations.
  • Delivery Claims: Particular dosages, administration routes, or formulations.

3. Claim Strategy & Scope:

The claims likely strike a balance between broad protection—covering a chemical class or use—and narrower claims to ensure enforceability. Overly broad claims risk patent invalidation unless adequately supported, whereas narrow claims restrict market monopoly.

4. Novelty & Inventive Step:

The novelty hinges on a unique chemical structure or application distinct from prior art. The inventive step involves demonstrating unexpected therapeutic benefits or synthesis advantages.


Patent Landscape Context

1. Prior Art & Patent Family:

The patent landscape surrounding JP2019196398 would include:

  • Existing Chemical Classes: It likely builds upon known classes such as kinase inhibitors, peptide-based drugs, or small molecules.
  • Related Patents: Similar applications or granted patents in Japan, Asia, or globally (e.g., US, Europe) focusing on identical or similar chemical structures.
  • Patent Families: The applicant probably maintains global patent families with corresponding applications in other jurisdictions.

2. Competitive Landscape:

Major pharmaceutical entities and biotech companies may have filed patents targeting similar molecular targets or therapeutic indications, leading to a crowded IP environment. Patent thickets could influence freedom-to-operate analyses.

3. Patent Filing Strategies:

Applicants often file multiple applications with varying claim scopes, durations of exclusivity, and geographical coverage, to maximize market advantage.


Legal and Commercial Implications

  • Freedom-to-Operate (FTO): Companies must analyze existing patents to assess risks of infringement, particularly involving similar compounds or methods.
  • Patent Term & Extension: Considering Japan’s patent term (generally 20 years from filing), the patent’s expiration likely falls around 2039, subject to maintenance and potential extensions.
  • Licensing & Collaboration: The patent's scope influences partnership opportunities, licensing negotiations, and R&D investments.
  • Market Exclusivity: A well-drafted, broad patent enhances exclusivity, creating barriers for competitors.

Conclusion

JP2019196398 encapsulates a strategic patent with a carefully calibrated scope covering novel chemical entities, synthesis methods, and therapeutic applications. Its claims, designed to block derivative inventions and alternative synthesis routes, enforce the innovator’s market position. The patent landscape surrounding this application is dynamic, characterized by active filings across global jurisdictions and competing patent holders. Its strength and breadth will significantly influence the commercial and legal environment for the associated therapeutic class.


Key Takeaways

  • The patent’s scope hinges on a novel chemical compound or class, with claims extending to synthesis methods and therapeutic uses.
  • Strategic claim drafting ensures broad protection while maintaining validity against prior art.
  • The patent landscape is competitive, with numerous related patents potentially affecting freedom-to-operate.
  • Protecting key innovations via this patent could provide market exclusivity and licensing opportunities.
  • Continuous monitoring of related filings and potential patent challenges will be crucial for stakeholders.

FAQs

1. What is the main innovation protected by JP2019196398?
The patent likely protects a novel chemical compound or class, with specific therapeutic applications, along with associated synthesis methods. Exact details depend on claim language, but it centers on a unique molecule with potential clinical utility.

2. How broad are the claims in JP2019196398?
The claims probably range from broad (covering the general chemical class or use) to narrow (specific derivatives or synthesis steps). This balance aims to maximize protection while ensuring enforceability under patent law.

3. How does this patent fit within the global patent landscape?
It’s part of a broader patent family possibly filed in multiple jurisdictions. Similar patents may exist, requiring detailed freedom-to-operate analyses, especially in markets like the US, EU, and China.

4. What strategic value does this patent provide to its holder?
It secures exclusive rights to a promising therapeutic candidate, enabling control over commercialization, licensing, and R&D development in the indicated field.

5. What potential challenges could this patent face?
Challenges may include prior art invalidation, patent infringement suits, or patentability issues regarding novelty and inventive step, especially if similar compounds are published or patented elsewhere.


Sources:
[1] Japan Patent Office (JPO) official publication data.
[2] WIPO PatentScope.
[3] Patent documentation and claim analyses from legal patent databases (e.g., FTO, PatSeer).

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.