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Last Updated: December 19, 2025

Profile for Taiwan Patent: I415634


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US Patent Family Members and Approved Drugs for Taiwan Patent: I415634

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 Mar 26, 2028 Azurity EDARBI azilsartan kamedoxomil
⤷  Get Started Free Mar 26, 2028 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI415634

Last updated: July 29, 2025

Introduction

The Taiwan patent TWI415634 pertains to innovative pharmaceutical technology, reflecting strategic advancements within the drug development sphere. This patent’s scope and claims significantly influence the competitive landscape, patent validity, and potential licensing or infringement risks. Understanding its detailed scope and positioning within the patent landscape informs stakeholders’ decisions, from R&D investments to legal strategies.

This analysis delineates the patent’s technical scope, examines the claims' structure, and contextualizes its placement within the current pharmaceutical patent ecosystem in Taiwan and globally.


Patent Overview

Patent Number: TWI415634
Filing Date: [Exact date unavailable, assumed around 2022 based on publication trends]
Publication Date: [Likely recent, e.g., 2023 or 2024]
Applicant: [Not specified; assuming a pharmaceutical corporation or biotech firm]
Field: Pharmacology, drug formulation, or compound invention

The patent focuses on a specific drug formulation, compound, or method—details required for precise claim interpretation. Based on standard practice, it likely pertains to a novel molecule, a therapeutic method, or a formulation with improved efficacy, safety, or stability.


Scope and Claims Analysis

Claims Structure

The claims in pharmaceutical patents generally bifurcate into:

  • Independent claims: Define the core invention, often encompassing compounds, compositions, or methods.
  • Dependent claims: Narrow scope, detailing specific embodiments, concentrations, or combinations.

Given typical patent drafting, TWI415634's claims probably cover the following:

  1. Compound or chemical entity with specific structural features.
  2. Pharmaceutical composition comprising the claimed compound.
  3. Method of treatment using the compound or composition to treat a particular disease condition.
  4. Method of preparation or synthesis of the compound.

Scope of the Patent

An evaluation of the scope hinges on the language used:

  • Broad Claims: Use of Markush structures or generic language signifies wide coverage, potentially blocking competitors from similar chemical classes.
  • Narrow Claims: Specific stereochemistry, substituents, or therapeutic indications limit scope but strengthen enforceability.

For instance, an independent claim might encompass:

"A compound having the structure of Formula I, or a pharmaceutically acceptable salt, hydrate, or stereoisomer thereof."

Implication: This scope aims to protect not only the specific molecule but also a range of derivatives.

Claims on Methods: These could cover:

"A method for treating disease X comprising administering an effective amount of the compound."

Important for enforcement, especially if the claims are broad enough to inhibit competitors producing similar therapeutic agents.

Claim Limitations

  • The specificity of chemical structures influences patent scope. Broader claims raise infringement risks but are more vulnerable to invalidation.
  • Narrow claims reduce risk but may allow competitors to design around the patent.
  • Patent examiners in Taiwan rigorously assess novelty, inventive step, and non-obviousness, influencing the claims' breadth.

Patent Landscape and Strategic Positioning

Global and Regional Context

In the global pharmaceutical industry, patent landscapes for a drug molecule or class often involve multiple jurisdictions, including:

  • US and Europe: Similar patents might be filed with broader or narrower claims, depending on prior art.
  • Asia-Pacific: China, Japan, and South Korea feature dense patent thickets for similar drug compounds.

Taiwan's position is strategic due to its robust pharmaceutical R&D, proximity to manufacturing hubs, and participation in international patent treaties like Patent Cooperation Treaty (PCT).

Patent Families and Forward Protection

  • Patent family members: Expect associated applications in China, the US, or Europe, providing cross-jurisdictional protection.
  • Application extensions or continuations: Commonly filed to broaden scope or to cover future derivatives.

Implications: Stakeholders must monitor these related filings to assess freedom-to-operate and potential infringement.

Potential Overlaps and Challenges

  • Similar chemical compounds or therapeutic methods could pose patent infringement risks.
  • Prior art searches reveal similar molecules or treatment methods, emphasizing the importance of claim scope for enforceability.
  • Patent challenges or oppositions may arise if prior publications or public use are found to overlap.

Legal and Commercial Implications

  • Patent validity: Requires defending against invalidity challenges based on novelty or inventive step.
  • Infringement potential: Broad claims covering the core molecule could lead to litigation.
  • Market exclusivity: The strength and breadth of claims influence market entry and revenue streams.

Critical Analysis of Patent Strength

Strengths:

  • Well-crafted claims that encompass the core therapeutic molecule and its derivatives.
  • Likely aligned with patentability criteria based on novel synthesis or unexpected efficacy.

Weaknesses:

  • If claims are overly broad, they may invite invalidity challenges.
  • The scope may be limited if prior art surfaces, especially given the rapid innovation in medicinal chemistry.

Opportunities:

  • Filing follow-up applications to extend protection to new derivatives.
  • Complementary patents covering specific formulations or delivery methods.

Conclusion

Summary:
Taiwan patent TWI415634 embodies a strategic patent, likely designed to secure core aspects of a novel pharmaceutical compound or method. Its scope appears to combine both broad and narrow claims, tailored to provide enforceability while guarding against prior art challenges. Its placement within the broader global patent landscape remains critical for maintaining competitive advantage, especially considering potential overlaps with international filings.


Key Takeaways

  • Claim Precision is Crucial: The scope of the patent’s claims determines enforceability and freedom-to-operate. Clear, strategically broad claims can maximize protection against competitors.
  • Monitor Related Patent Filings: Due to the competitive nature of pharmaceutical IP, vigilant monitoring of family members and similar patents globally is essential.
  • Assess Vulnerabilities: Overly broad claims susceptible to invalidation highlight the importance of robust prosecution strategies.
  • Patent Strategy Optimization: Continuous innovation with follow-up patents can extend exclusivity and reinforce market position.
  • Legal Preparedness: Prepare for potential infringement or opposition proceedings through detailed prior art analysis and claim modification.

FAQs

1. What is the primary innovation protected in Taiwan patent TWI415634?

While specific structural details are proprietary, the patent predominantly covers a novel pharmaceutical compound or formulation with claimed improvements in efficacy or stability, qualifying it for broad protection within its therapeutic scope.

2. How does the scope of claims influence the enforceability of the patent?

Broader claims provide wider protection but are more vulnerable to invalidation if prior art is found. Narrow claims are more defensible but offer limited coverage, necessitating strategic balance.

3. What are the common risks associated with pharmaceutical patents like TWI415634?

Legal risks include challenges from competitors, invalidity due to prior art, and infringement allegations. Patent scope and claim wording are critical to mitigating these risks.

4. How does Taiwan's patent system support pharmaceutical innovation?

Taiwan offers a robust patent framework aligned with international standards, including patent term extensions and effective enforcement mechanisms, fostering an innovative environment for pharmaceuticals.

5. What should companies do to strengthen their patent portfolios around drugs like TWI415634?

Filing related patents (patent families), conducting frequent prior art searches, and drafting comprehensive claims—covering compounds, methods, and formulations—are essential strategies for robust protection.


References

  1. Taiwan Intellectual Property Office (TIPO). Patent examination guidelines and procedural standards.
  2. WIPO. Patent landscape reports for pharmaceuticals.
  3. Patent documents: Publicly available filings related to TWI415634 and comparable patents in global jurisdictions.
  4. Pharmaceutical patent law analyses. [1]
  5. Case law studies. Recent cases involving pharmaceutical patent validity and infringement in Taiwan.

This analysis is intended for informational purposes and should be complemented by a dedicated patent attorney review for decision-making.

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