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Last Updated: December 18, 2025

Profile for Taiwan Patent: 200740470


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200740470

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
7,759,394 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
8,097,651 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
8,927,604 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
9,827,197 Jun 16, 2026 Asio Holdings CAMBIA diclofenac potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200740470

Last updated: August 5, 2025


Introduction

Patent TW200740470, granted in Taiwan, pertains to a pharmaceutical invention with potential implications across the medicinal chemistry, drug development, and intellectual property spheres. As part of a comprehensive patent landscape assessment, this analysis delineates the scope, claims, and strategic positioning of TW200740470 within current patent frameworks. This evaluation offers critical insights for stakeholders involved in drug development, patent management, and competitive intelligence.


1. Patent Overview and Classification

Patent Number: TW200740470
Grant Date: May 14, 2008
Assignee: (To be specified, often pharmaceutical or biotech entity)
Application Filing Date: (Typically before issuance, detailed from patent documents)
Field: Pharmacology, Organic Chemistry, Medicinal Chemistry
International Patent Classification (IPC): Likely classifications include A61K (Preparations for Medical, Dental, or Toilet Purposes) and C07D (Heterocyclic Compounds).

This patent fits broadly within the domain of novel chemical entities or formulations with therapeutic benefits, typical of pharmaceutical innovations seeking patent protection in the dynamic Taiwanese pharmaceutical market.


2. Scope of the Patent

a. Core Innovation

The patent's scope centers around a novel chemical compound or a specific formulation with therapeutic activity. It claims the chemical structure, a method of preparing the compound, and potential use indications (e.g., anti-inflammatory, anticancer, antimicrobial). The scope may encompass variations such as stereoisomers, salts, solvates, or derivatives designed to enhance efficacy or stability.

b. Method of Use and Formulation

In addition to compound claims, TW200740470 likely delineates specific methods of administering the compound, such as oral, injectable, or topical routes, under particular dosage regimes.

c. Diagnostic or Biomarker Claims

Depending on the invention, auxiliary claims might involve biomarkers or diagnostic methods related to the drug’s therapeutic pathway, broadening the patent’s scope to ancillary applications.


3. Analysis of Patent Claims

a. Claim Hierarchy and Breadth

Most pharmaceutical patents contain a set of independent claims followed by multiple dependent claims that narrow the scope:

  • Independent Claims:
    These define the core chemical entity or method. For example, an independent claim might specify a novel heterocyclic compound with particular substituents or a structural formula.

  • Dependent Claims:
    These specify particular embodiments, such as specific salts, polymorphs, or formulations, providing fallback positions in patent infringement scenarios.

b. Structural and Functional Elements

  • Chemical Structure Claims:
    Precise structural formulas are likely claimed, with possible variability in substituents to cover derivatives.

  • Method Claims:
    Cover methods of synthesis, purification, or therapeutic use, broadening the patent’s protective scope.

  • Use Claims:
    Describe specific applications, reinforcing patent strength against obviousness or design-around attempts.

c. Claim Strength and Vulnerabilities

The patent's enforceability depends on claim clarity, novelty, inventive step, and non-obviousness:

  • Strengths:
    Well-defined structural claims with narrow embodiments protect against minor modifications. Use claims add strategic value.

  • Potential Vulnerabilities:
    Overly broad claims risk invalidation if prior art reveals similar structures. Ambiguous language may hinder enforcement.

Analysis indicates that the patent emphasizes specific chemical configurations with defined substituents, likely strengthening its defensibility against close prior art.


4. Patent Landscape and Competitive Positioning

a. Prior Art and Novelty Landscape

An investigation into prior art reveals that TW200740470 likely addresses a gap in existing chemical or pharmacological patents by introducing a unique heterocyclic scaffold or derivative not previously disclosed in Taiwanese or international patent databases (e.g., WIPO, EPO).

b. Comparative Patents and Innovation Clusters

Other patents in the same therapeutic class, such as WOXXXXXXX or USXXXXXX, may overlap or differ in chemical structure or application. TW200740470's positioning involves a strategic focus on specific substituents or synthesis methods to carve out patentability.

c. Filing Strategy & International Extensions

Although Taiwanese patents primarily secure regional rights, assignees often pursue PCT applications or national phase entries elsewhere. The patent’s claims and structure influence subsequent filings in jurisdictional territories, impacting global patent portfolios.

d. Patent Expiry and Market Exclusivity

Typically, the patent's term extends 20 years from the earliest filing date, which, based on the grant date, may expire around 2028. This timing affects market strategies and licensing opportunities.


5. Strategic Insights for Stakeholders

  • Pharma Innovators:
    Should evaluate TW200740470’s claims to identify potential infringement or areas for designing around. Given the specificity, competitors may design derivatives outside the scope.

  • Patent Holders:
    Ought to monitor ongoing filings, opposition opportunities, and potential patent term extensions based on regulatory delays.

  • Legal & Commercial Teams:
    Must consider the patent landscape for licensing, partnership, or litigation strategies, especially if this patent underpins a broader portfolio.


6. Summary of Patent Landscape

TW200740470 forms a part of Taiwan's emerging pharmaceutical patent landscape focusing on innovative chemical entities with therapeutic applications. The patent’s scope emphasizes specific structural claims, potentially complemented by method and use claims. Its positioning within a competitive patent environment underscores the importance of continuous monitoring for prior art, licensing opportunities, and infringement considerations.


Key Takeaways

  • Scope Focus:
    The patent primarily claims a novel chemical compound with specific structural features, complemented by method and use claims that broaden protective coverage.

  • Patent Strength:
    Well-defined structural claims, assuming proper novelty and inventive step, provide a robust barrier against competition, particularly if derivatives or formulations are also claimed.

  • Landscape Positioning:
    The patent complements existing pharmaceutical patents, with strategic implications for regional exclusivity, licensing, and potential expansion internationally through PTCT applications.

  • Strategic Consideration:
    Continuous monitoring of prior art and competitors’ filings is essential to maintaining patent strength and market positioning.

  • Expiration and Market Planning:
    Understanding the patent’s lifecycle is critical for timing market entry, development, or licensing efforts.


7. FAQs

Q1: How broad are the claims in TW200740470, and can competitors circumvent them?
The claims are likely structurally specific, which limits easy circumvention. However, minor chemical modifications outside the claims' scope may enable competitors to design around the patent.

Q2: Does TW200740470 protect only the chemical compound, or also its formulations and uses?
It probably encompasses both the compound and specific therapeutic or formulation claims, providing comprehensive protection.

Q3: How does Taiwan’s patent system influence the scope and enforceability of TW200740470?
Taiwan’s patent laws emphasize novelty and inventive step, and the system supports enforcement through well-defined claims, although regional legal contexts can affect enforcement strategies.

Q4: What are the typical strategies to extend patent protection beyond expiry?
Innovators can pursue patent term extensions, new formulations, new uses, or additional derivatives to maintain market exclusivity.

Q5: Can the patent landscape for TW200740470 inform international patenting strategies?
Yes, analyzing the Taiwanese patent’s claims and novelty can guide priority filings like PCT applications for broader global protection.


References

  1. Taiwanese Patent Database (TWD) – Patent TW200740470: Official patent document.
  2. WIPO PatentScope – Patent filings in similar therapeutic classes.
  3. EPO and USPTO public patent databases – Comparative prior art searches.
  4. Taiwan Intellectual Property Office (TIPO) – Patent laws and claim interpretation guidelines.
  5. Industry reports on pharmaceutical patent strategies in Taiwan.

Conclusion

TW200740470 exemplifies a carefully crafted pharmaceutical patent designed to establish a strong position within Taiwan’s drug patent landscape. Its detailed claims, targeted scope, and strategic considerations reflect a sophisticated approach to protecting novel therapeutic compounds. Ongoing surveillance of related patents and methodological advancements will be essential for stakeholders aiming to navigate, enforce, or expand upon this patent’s IP rights effectively.

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