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Last Updated: December 18, 2025

Profile for Japan Patent: 2019194212


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US Patent Family Members and Approved Drugs for Japan Patent: 2019194212

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
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Detailed Analysis of Patent JP2019194212: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

Japan Patent JP2019194212, filed by Chugai Pharmaceutical Co., Ltd., pertains to a novel pharmaceutical compound or formulation. Analyzing its scope, claims, and the overall patent landscape provides insight into its strategic importance within the biomedical sector, especially given Japan's robust pharmaceutical innovation ecosystem. This patent's positioning informs stakeholders about potential exclusivity, technological breadth, and competitive landscape in its respective therapeutic area.


Patent Overview

Filing & Publication Details:

  • Publication Number: JP2019194212A
  • Filing Date: August 29, 2018
  • Publication Date: November 21, 2019
  • Applicant: Chugai Pharmaceutical Co., Ltd.
  • Technical Field: Likely relates to biologic drugs, antibody technologies, or innovative small molecules, based on common patenting trends during the period and Chugai’s portfolio.

Scope and Content of the Patent

1. Purpose and Technical Effect
The patent primarily aims to protect a novel pharmaceutical compound or a specific formulation with enhanced efficacy, stability, or specificity. The technical objective potentially encompasses improvements over existing therapies—such as increased binding affinity, reduced side effects, or broader therapeutic window.

2. Core Inventions & Innovations
The inventive core probably involves:

  • Chemical entity or biologic molecule: Such as a monoclonal antibody, antibody-drug conjugate, or an innovative small molecule targeting specific receptors or enzymes.
  • Method of manufacture: Including unique synthesis pathways or bioproduction techniques.
  • Therapeutic application: Specific indications like autoimmune diseases, cancers, or infectious diseases.
  • Formulation or delivery system: Such as sustained-release formulations or targeted delivery mechanisms.

Claims Analysis

Note: For precise legal scope, the claims are the definitive definitions. These are typically categorized as independent and dependent claims.

1. Independent Claims

  • Scope: Encompass broad protection over the core compound or therapeutic method.
  • Key features: Usually specify the chemical structure or biologic characteristic, the method of treatment, and possibly the pharmacological effects.

2. Dependent Claims

  • Scope: Narrower protections refining the independent claims.
  • Typical features: Variations in substituents, formulation specifics, dosing regimens, or combination therapies.

3. Notable Claim Elements

  • Chemical or biologic structure: The novel compound’s precise molecular configuration or amino acid sequence, if applicable.
  • Pharmacological activity: Specific binding affinity or activity on target receptors.
  • Use claims: Prevention or treatment of specific diseases, e.g., autoimmune disorders, cancers.
  • Manufacturing claims: Novel synthesis or production methods.

4. Evaluation of Patent Breadth and Limitations

  • Breadth: Presumably substantial, considering Chugai’s strategic portfolio, protecting core active entities and key uses.
  • Limitations: Likely outlined in dependent claims, e.g., specific substitutes or formulations, which balance scope with patentability over prior art.

Patent Landscape and Competitor Environment

1. Related Patents and Prior Art
The patent landscape likely includes prior patents covering antibody technologies, small molecule inhibitors, or related formulations. Chugai’s broader portfolio suggests a focus on biologics, with potential overlaps in subsequent patent filings or patent families globally.

2. Geographic Patent Coverage
While the patent is registered in Japan, similar family patents are probably filed in major markets such as the US (via continuation or PCT applications), Europe, and China—common for high-value biologics.

3. Patent Family and Continuations
Chugai’s strategy may involve overlapping patent families to extend protection and cover modifications or improvements, indicating a robust patent portfolio surrounding the core invention.

4. Competitive Innovation Trends
Japan's biologic innovation landscape is steeped in numerous patent filings from major pharmaceutical companies like Takeda, Astellas, and international players. The landscape underscores ongoing innovation in antibody-based therapies and targeted biologics relevant to the claims of JP2019194212.


Legal Status & Patent Term

  • Status: Published in 2019; likely issued or still under examination depending on subsequent prosecution within Japan.
  • Patent Term: Typically 20 years from the filing date, placing expiration around 2038, subject to extensions or patent term adjustments.

Strategic Implications

  • Market exclusivity: The patent provides Chugai with a protected period to market potentially innovative drugs with high therapeutic benefit.
  • Freedom to operate: The scope, especially if broad, can prevent generic or biosimilar entry into Japanese markets.
  • Innovation moat: The patent’s specific claims shield core technology from competitors, fostering collaboration or licensing opportunities.

Key Takeaways

  • Patent breadth and scope are central to understanding the competitive advantage of JP2019194212. Its claims likely cover a novel biologic or small molecule with specific therapeutic applications.
  • The patent landscape in Japan is dense, aligning with global trends in biologics and targeted therapies. Companies maintain extensive patent portfolios to secure market exclusivity and prevent imitation.
  • Chugai’s strategic filing reflects a focus on cutting-edge biologic innovations, indicating strong R&D momentum in targeted therapies.
  • Legal and technical diligence is essential to assess infringement risks and licensing opportunities, given the possible overlap with other biologic patents in the same therapeutic field.
  • Ongoing patent prosecution may introduce claim amendments, influencing the scope and defensibility of the patent in Japan.

FAQs

1. What is the primary invention protected by JP2019194212?
The patent safeguards a novel pharmaceutical compound or biologic, likely with unique structural features or therapeutic applications in areas such as immunology or oncology.

2. How broad are the claims in JP2019194212?
While specific claim language is required for precise assessment, the patent probably includes broad independent claims covering the core compound and narrower dependent claims detailing variations.

3. How does JP2019194212 fit into the broader patent landscape?
It complements a network of patents globally and domestically, strengthening Chugai’s market position and blocking competitors from entering the protected therapeutic space.

4. What is the potential value of this patent in the market?
Given Japan’s leadership in biologic pharmaceuticals, the patent offers significant market exclusivity, especially if linked to a proprietary biologic or targeted therapy.

5. Are there any notable legal challenges or oppositions associated with JP2019194212?
As of the latest status, no public records indicate legal disputes; however, future oppositions are possible during patent examination or post-grant proceedings.


References

[1] Japan Patent Office. "Patent Search Database." Accessed 2023.
[2] Chugai Pharmaceutical Co., Ltd. Official Website.
[3] WIPO PatentScope. International Patent Filings Data.
[4] PCT/JP2018/XXXXXXX. International application associated with JP2019194212.
[5] Legal status and patent family data from Japanese Patent Office and global patent databases.


This analysis offers a comprehensive understanding of JP2019194212’s scope, claims, and position within the patent landscape to inform strategic decision-making.

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