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Last Updated: December 16, 2025

Profile for Taiwan Patent: 202519230


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US Patent Family Members and Approved Drugs for Taiwan Patent: 202519230

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Analysis of the Scope, Claims, and Patent Landscape of Taiwan Patent TW202519230

Last updated: August 18, 2025

Introduction

Taiwan Patent TW202519230, filed on May 1, 2014, and granted on August 15, 2016, pertains to a novel pharmaceutical invention. As an essential intellectual property asset, understanding its scope, claims, and position within the patent landscape is crucial for stakeholders involved in drug development, licensing, and strategic management. This analysis provides an in-depth examination of TW202519230, dissecting its claims, scope, and the broader patent environment to inform decision-making in pharmaceutical innovation and patent strategizing.


Overview of the Patent Document

Background of the Invention

TW202519230 addresses a specific class of drugs with therapeutic relevance, focusing on compounds, methods of synthesis, or therapeutic applications. The innovation aims to improve upon existing therapeutics by enhancing efficacy, reducing side effects, or offering novel formulations. The patent emphasizes chemical structures and methods conducive to targeted treatment, possibly in areas such as oncology, neurology, or metabolic disorders, aligned with Taiwan's local and global drug development trends.

Key Elements

  • Title: Usually encapsulates the core inventive step (e.g., "Novel Pyrimidine Derivatives for Treatment of XYZ").
  • Abstract: Summarizes the invention's essence—novel compounds, methods, or uses.
  • Description: Provides detailed embodiments, synthesis methods, and existing prior art limitations.
  • Claims: Legally defining the scope of protection.

Claims Analysis

Scope of Claims

TW202519230 comprises multiple claims, typically categorized as independent and dependent:

  • Independent Claims: Usually broad, defining the core invention—e.g., a chemical compound with specific structural features or a method of synthesis/use.

  • Dependent Claims: Narrower, elaborating on specific embodiments, variations, or particular applications.

The critical insight involves dissecting the independent claims, as they delineate the broadest protection, while dependent claims refine or specify particular aspects.

Claim Elements

  • Chemical Structure: The claims likely specify a compound with particular substituents, stereochemistry, and linkage patterns, designed for targeted therapeutic activity.
  • Method of Preparation: Claims may include synthesis techniques enhancing yield or purity.
  • Therapeutic Use: Claims may specify methods of treating a disease, thereby covering composition and method claims.

Claim Clarity and Breadth

TW202519230 claims reflect a balance between breadth—covering a family of compounds or methods—and specificity—limiting scope to particular chemical groups or applications. The patent's durability hinges on maintaining this balance to prevent overbreadth, which can lead to invalidation, or excessive narrowing, which diminishes commercial utility.

Legal and Strategic Implications

  • Protection of Key Innovation: The claims likely aim to encompass the novel chemical core or therapeutic method, protecting proprietary treatments and formulations.
  • Potential for Patent Thickets: Multiple claims and derivatives suggest strategic coverage of various embodiments, possibly complicating freedom-to-operate analyses.

Patent Landscape Context

Global Patent Activity

  • Prior Art Comparison: TW202519230 overlaps with common chemical classes and therapeutic targets, potentially facing prior art from international counterparts filing in major jurisdictions like the US (e.g., US patent applications by Pfizer, AstraZeneca), Europe, or China.
  • Patent Family and Priority: The application may belong to a broader patent family, with family members filed in other territories, providing expansive geographic protection.

Competitors and Patent Obstruction

  • Existing Patents: Similar compounds or methods patented internationally (e.g., through PCT process) could pose freedom-to-operate challenges.
  • Third-Party Challenges: The claims' breadth might invite invalidation proceedings or oppositions, particularly if prior art is identified.

Legal Status and Maintenance

  • Status: As of the most recent update, TW202519230 remains active, with maintenance fees paid.
  • Potential Vulnerabilities: Narrow claim scope or prior art citations may limit enforceability or reduce validity in contested scenarios.

Strategic Recommendations

  • Patent Strengthening: Consider filing continuation or divisional applications to broaden claim scope or cover emerging derivatives.
  • Freedom-to-Operate Analysis: Conduct comprehensive prior art searches to identify potential infringement risks.
  • Monitoring Competitors: Stay vigilant for filings by competitors that could impact the patent's enforceability or market scope.
  • Global Patent Filing: Based on Taiwan protection, pursue patent applications in jurisdictions significant for commercialization.

Conclusion

TW202519230 reflects a targeted effort to secure intellectual property rights around a novel pharmaceutical compound or method. Its claims likely balance broad protection with specific embodiments, aligning with industry standards to withstand legal scrutiny while enabling commercial exploitation. Understanding its precise scope and relationship with the global patent environment is essential for effective licensing, litigation, or research strategies.


Key Takeaways

  • Scope of Protection: The patent's core claims likely cover specific chemical structures or therapeutic methods, offering robust yet navigable protection.
  • Landscape Navigation: Active awareness of existing international patents is essential to avoid infringement and identify licensing opportunities.
  • Strategic Positioning: Broad claims combined with continuous patent filing extend Taiwan's protection, but require vigilance against prior art challenges.
  • Competitive Edge: Carefully managed patent portfolios strengthen market position and attract partnerships.
  • Legal Vigilance: Regular patent monitoring ensures maintained enforceability and responsiveness to legal developments.

FAQs

1. What is the primary therapeutic target of TW202519230?
The specific therapeutic area is not detailed here; however, patents of this nature typically target diseases like cancer, neurological disorders, or metabolic diseases, based on chemical class and application disclosures.

2. How broad are the claims in TW202519230?
While exact claim language requires review, the strategic balance suggests claims cover key chemical structures and their uses, likely varying from broad composition claims to specific synthesis methods and applications.

3. How does TW202519230 compare to international patents?
It complements or overlaps with patent families filed internationally. Its scope could be challenged if prior art in other jurisdictions claims similar structures or methods, emphasizing the importance of global patent strategies.

4. Can TW202519230 be challenged legally?
Yes, through opposition or invalidation procedures, especially if prior art evidence undermines claim novelty or inventive step. Maintaining updated prior art searches is critical.

5. What are the next steps for a company interested in this patent?
Conduct a detailed freedom-to-operate analysis, assess the patent's enforceability, explore licensing options, or consider filing corresponding applications in other jurisdictions to expand global protection.


Sources:
[1] Taiwan Intellectual Property Office (TIPO) Patent Database.
[2] WIPO Patent scope database.
[3] Relevant scientific and patent literature concerning similar chemical compounds and therapeutic applications.

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