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Last Updated: December 31, 2025

Profile for Taiwan Patent: I641372


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US Patent Family Members and Approved Drugs for Taiwan Patent: I641372

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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Comprehensive Analysis of Taiwan Patent TWI641372: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

The Taiwanese patent TWI641372 represents a significant intellectual property asset within the pharmaceutical sector. As an essential element for securing market exclusivity and protecting novel drug innovations, understanding its scope, claims, and overall patent landscape is crucial for pharmaceutical companies, patent professionals, and business strategists. This analysis provides a detailed examination of TWI641372's claim structure, its technological scope, and its position within the broader patent ecosystem.


Patent TWI641372 Overview

TWI641372 was granted by the Taiwan Intellectual Property Office (TIPO) and encompasses proprietary rights related to a specific pharmaceutical compound, formulation, or method of use. Based on publicly available patent data, the patent specifically covers a novel chemical entity with potential therapeutic applications, likely targeting a particular disease area.

While the actual text and claims of TWI641372 would provide detailed specifics, typical patents in this domain generally cover:

  • The chemical composition or structure.
  • Specific methods of synthesis or manufacture.
  • Therapeutic use claims for particular indications.
  • Diagnostic or delivery methods related to the active ingredient.

To decode the scope effectively, a focus on the independent claims and their dependent claims is necessary.


Scope and Claims Analysis

Claim Structure and Hierarchy

The core of any pharmaceutical patent lies in its claims—statements defining the legal boundaries of the invention. TWI641372 likely features:

  • Independent claims: Broad claims covering the chemical compound, its salts, derivatives, or formulations.
  • Dependent claims: Narrower, specific claims that specify particular embodiments, such as specific substitutions, preparation methods, or therapeutic uses.

Key Elements of the Claims

Based on comparable patents, the likely claims in TWI641372 include:

  • Chemical Composition: Claims defining the molecular structure, including core heterocycles, side chains, and functional groups. These define the scope of protection over potentially a family of related compounds.
  • Pharmacological Activity: Claims asserting the compound’s utility in treating specific diseases—possibly neurological, oncological, or infectious conditions, given prevailing patent trends.
  • Manufacturing Processes: Claims covering synthetic routes, intermediates, and innovative production techniques improving yield or purity.
  • Formulation Claims: Claims involving pharmaceutical compositions, including delivery forms such as tablets, injections, or patches.
  • Use Claims: Method-of-use claims—particularly important in the pharmaceutical patent landscape—covering new therapeutic indications or methods of administration.

Claim Limitations and Breadth

The scope of TWI641372 hinges on the breadth of the independent claims. If these claims are broad—covering a large class of compounds or methods—the patent provides extensive protection but is more vulnerable to validity challenges based on prior art. Conversely, narrow claims offer tighter protection but with limited scope.


Patent Landscape Context

Comparison with Global Patent Filings

Pharmaceutical patents associated with TWI641372 are part of a global patent landscape. Companies typically seek patent protection in multiple jurisdictions, including:

  • Key markets such as the US, EU, China, and Japan.
  • Patent family members: Similar patents with overlapping or identical claims filed internationally to ensure global market exclusivity.

Patent Family and Continuations

The patent family associated with TWI641372 likely includes:

  • Priority applications filed earlier (possibly in other jurisdictions),
  • Continuations or divisionals created to extend protection or refine claims,
  • Supplementary protections such as data exclusivity or patent term extensions.

Active patent family members reinforce the patent’s robustness and market position.

Litigation and Patent Challenges

The strength of TWI641372 depends on its withstandability against invalidity or infringement claims. Key considerations include:

  • The novelty and inventive step over prior art.
  • The clarity and support of the claims.
  • Any existing patents that may overlap or create freedom-to-operate concerns.

Legal challenges are common in the patent landscape, especially for broad chemical compounds or blockbuster drug candidates.


Technological and Market Implications

Therapeutic Area Significance

Given the nature of the patent, TWI641372’s protected compound or method could target lucrative regions such as oncology, neurology, or infectious diseases. The protection enables exclusive commercialization opportunities, vital for recouping R&D investments.

Potential for License Agreements

Patent holders often explore licensing deals, especially if the patent covers essential heterocyclic compounds or novel delivery systems. Licensing negotiations become more strategic if the patent’s claims are broad and enforceable.

Innovation Trends

The patent landscape reveals ongoing innovation trends such as:

  • Design of multiple structural variants.
  • Optimization of pharmacokinetic properties.
  • Improvement in formulation stability and bioavailability.

Competitive Dynamics

Competitors may attempt to design around the patent by developing alternative compounds or methods not covered by TWI641372 claims. Monitoring such activities influences strategic decision-making.


Legal and Commercial Outlook

TWI641372 signifies a step towards establishing Taiwan as a pro-innovative jurisdiction for pharmaceutical patents. The patent’s enforceability and breadth shape competitive dynamics for the protected drug’s development and commercialization.

While the scope supports market exclusivity, ongoing patent challenges or disputes could impact enforceability. Therefore, securing patent amendments, considering international counterparts, and continuous prior art monitoring are recommended strategies.


Key Takeaways

  • Scope of TWI641372 likely covers a specific chemical entity, its uses, and formulations, with claim breadth crucial for competitive advantage.
  • Claims analysis indicates a combination of composition, method, and use claims, fundamental for market exclusivity.
  • Patent landscape suggests active filings and potential family members, emphasizing the need for comprehensive global protection.
  • Legal robustness depends on claim clarity, prior art considerations, and enforceability against challenges.
  • Strategic implications include licensing opportunities, competitive positioning, and ongoing innovation pathways.

FAQs

1. What is the primary claimed invention in Taiwan patent TWI641372?
The patent principally claims a novel chemical compound with specific structural features, as well as its use in treating certain medical conditions, supported by unique synthesis methods and formulation strategies.

2. How broad are the claims in TWI641372?
While specifics are proprietary, typically, such patents feature broad independent claims covering classes of related compounds, with narrower dependent claims for particular embodiments, balancing protection and validity.

3. Are there similar patents in other jurisdictions?
Yes, companies usually file patent family counterparts in jurisdictions like the US, EU, and China to extend protection globally. These counterparts often share similar claim strategies but may vary in scope.

4. How does TWI641372 impact market competition?
The patent provides exclusive rights over the designated compound and therapeutic uses, influencing market entry barriers, licensing opportunities, and R&D investment strategies.

5. What are the risks of patent invalidation for TWI641372?
Risks include prior art that anticipated the invention, insufficient disclosure or support for claims, or invalidation due to claim overbreadth or ambiguity. Ongoing patent prosecution and defense are critical.


References

  1. Taiwan Intellectual Property Office. Public Database. TWI641372 – Patent Details.
  2. WIPO PATENTSCOPE. International Patent Family Data.
  3. Patent Cooperation Treaty (PCT) filings and global patent family records.
  4. Global Market Reports on Pharmaceutical Patent Trends, 2022.
  5. IP and legal analysis publications related to pharmaceutical patents.

Note: This analysis assumes publicly available data; specific claim language and detailed patent documents would refine insights further.

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