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Last Updated: December 13, 2025

Profile for Taiwan Patent: I800759


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US Patent Family Members and Approved Drugs for Taiwan Patent: I800759

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
10,278,969 Dec 11, 2034 Helsinn Hlthcare TRUSELTIQ infigratinib phosphate
11,160,804 Dec 11, 2034 Helsinn Hlthcare TRUSELTIQ infigratinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI800759

Last updated: October 5, 2025


Introduction

Taiwan patent TWI800759 pertains to a pharmaceutical invention registered within Taiwan’s Intellectual Property Office (TIPO). The patent’s scope, claims, and its position within the global patent landscape offer valuable insights for industry participants, including pharmaceutical innovators, generic manufacturers, and legal professionals. This analysis aims to elucidate the patent's scope through detailed claim interpretation, contextualize it within the broader patent environment, and assess potential implications for market and R&D strategies.


Patent Overview

TWI800759 claims to an innovative drug composition or method related to a specific API (Active Pharmaceutical Ingredient), formulation, or therapeutic application. While the exact title and detailed description are not provided here, typical scope assessments hinge on the patent claims' language, which defines the legal protection boundaries.

Based on usual patent drafting practices, the core claims likely cover:

  • The chemical composition, including specific molecular structures or derivatives.
  • A novel formulation, perhaps with improved bioavailability, stability, or targeted delivery.
  • A method of manufacturing such compositions.
  • Therapeutic uses or indications based on the composition.

Scope and Claims Analysis

1. Independent Claims

An independent claim in patent TWI800759 likely asserts a novel drug composition or process. Typically, independent claims are broad to maximize protection, often covering:

  • A pharmaceutical composition comprising a specific active agent, possibly with particular excipients or carriers.
  • A method of treating a specific condition using the claimed composition.
  • A chemical entity with a defined structural formula and specific substitution patterns.

Assessment:
The breadth of the independent claims determines the patent's scope. If claims encompass a broad class of compounds or formulations, they may restrict generic entry across multiple variants. Otherwise, narrowly defined claims focus protection on specific embodiments.

2. Dependent Claims

Dependent claims refine the independent claims, potentially emphasizing:

  • Specific dosage forms (e.g., tablets, injections).
  • Concentration ranges of the active ingredient.
  • Stability-enhancing features.
  • Manufacturing steps or process parameters.

Assessment:
Dependent claims fortify the core protection and provide fallback positions in infringement analysis.

3. Claim Construction and Interpretative Nuances

  • Structural Definitions: The precise chemical structures or features claimed influence patent enforceability.
  • Functional Features: Claims that specify functions (e.g., improved bioavailability) impact the scope.
  • Market and Therapeutic Claims: Claims extend to therapeutic methods or uses, which may involve second or use patents.

Patent Landscape Context

1. Global Patent Environment

  • Priority and Family Members: It’s common for companies to file patent families across multiple jurisdictions—e.g., China, US, Europe—to secure broad protection.
  • Competitor Patents: Existing patents in related drug classes may influence the scope, with potential overlaps or freedom-to-operate issues.
  • Ease of Infringement: The specificity of claims affects the likelihood of design-arounds or patent challenges.

2. Patent Expiry and Lifecycle

  • If TWI800759 is a standard or mid-term patent, its expiration date (often 20 years from the filing date) positions it within a competitive age.
  • Secondary patents (e.g., supplementary, formulation-specific) can extend commercial protection or complicate generic entry.

3. Patent Validity and Enforceability

  • Taiwan’s patent examination standards are rigorous, but patent challenges or oppositions could threaten validity.
  • Prior art searches in the chemical and pharmaceutical fields, including international patent databases, could uncover overlapping inventions.

Implications for Stakeholders

  • Innovators: The broadness of TWI800759’s claims could deter generic development, offering market exclusivity.
  • Generics Manufacturers: Narrow claims or expiry date may present opportunities for biosimilars or generics.
  • Legal & IP Professionals: Precise claim language warrants detailed claim charting and infringement analysis.
  • Business Strategy: Patent strength influences licensing, collaborations, and market entry timing.

Conclusion

The scope of Taiwan patent TWI800759 appears to protect a specific drug composition or method, with potential breadth depending on claim language. Its position within the patent landscape depends on its relation to global patent families, competing patents, and the strategic timing of patent filings. Thorough litigation or freedom-to-operate analyses require detailed claim interpretation and a comprehensive prior art review.


Key Takeaways

  • Claim Breadth and Specificity: The scope hinges on whether claims are broad (chemical class or therapeutic class) or narrow (specific formulation or process).
  • Patent Family and International Strategy: Analyzing corresponding family patents helps gauge global protection and market exclusivity.
  • Competitive Landscape: Overlapping patents or prior art could lead to challenges; monitoring competitors' patent portfolios is critical.
  • Lifecycle Management: The patent’s expiry and secondary patents influence long-term market presence.
  • Infringement Risk and Licensing: Clear claims facilitate enforcement; ambiguity may open loopholes or lead to litigation.

FAQs

1. What is the significance of claim scope in pharmaceutical patents?
Claim scope determines the extent of legal protection. Broader claims can block generic entry across multiple formulations or compounds, while narrow claims protect specific embodiments but limit enforceability.

2. How does Taiwan patent TWI800759 compare with international patents?
Assessment requires analyzing corresponding patent families. If similar patents exist in the US or Europe with broader coverage, they could influence enforcement or licensing strategies.

3. What factors influence the validity of a patent like TWI800759?
Key factors include novelty, inventive step, adequate disclosure, and absence of prior art. Patent challenges can target any of these areas.

4. How do secondary patents affect the patent landscape?
Secondary patents—covering improvements, formulations, or specific uses—extend market exclusivity beyond the primary patent expiry and complicate competition.

5. What are the strategic implications for pharmaceutical companies holding such patents?
They can leverage patent protection for market exclusivity, negotiate licensing deals, or coordinate patent filings across jurisdictions to strengthen global rights.


Sources

[1] Taiwan Intellectual Property Office (TIPO). Patent status and public records.
[2] WIPO Patentscope. International patent family analysis.
[3] Patent examination guidelines, Taiwan IPO.
[4] Industry reports on pharmaceutical patent strategies.

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