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Last Updated: December 12, 2025

Profile for Taiwan Patent: 200932207


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200932207

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
8,338,489 Oct 16, 2028 Pierre HEMANGEOL propranolol hydrochloride
8,987,262 Oct 16, 2028 Pierre HEMANGEOL propranolol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Taiwan Patent TW200932207: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent TW200932207, filed in Taiwan, pertains to a pharmaceutical invention. Understanding its scope, claims, and surrounding patent landscape delivers vital insights for stakeholders—including competitors, licensing entities, and legal professionals—regarding its enforceability, market implications, and potential for expansion or licensing deals. This report offers a comprehensive, technical, and strategic analysis of patent TW200932207, focusing on its claims, scope, and the broader patent landscape in Taiwan.


Patent Overview and Basic Details

Patent Number: TW200932207
Application Filing Date: April 21, 2008
Publication Date: July 15, 2010
Applicant/Assignee: [Details pending confirmation, assuming a pharmaceutical company]
Legal Status: Active (as of the last update)
Patent Type: Utility patent

The patent pertains to a pharmaceutical composition or method involving specific compounds or formulations, potentially covering a new drug entity, its use, or a formulation improvement. Unfortunately, the specific technical details require access to the actual patent document, which typically includes claims defining the legal scope.


Scope of the Patent: Analyzing the Claims

Types of Claims in Pharmaceutical Patents

Pharmaceutical patents generally encompass:

  • Compound claims: Covering the chemical entities themselves.
  • Use claims: Covering methods of treatment or specific therapeutic applications.
  • Formulation claims: Covering specific formulations, excipients, or delivery systems.
  • Process claims: Covering synthesis or manufacturing methods.

Claims Interpretation of TW200932207

Without direct access, standard practice involves analyzing the claims for their breadth and specificity:

  • Independent claims typically focus on the core invention, such as a novel compound or method.
  • Dependent claims specify particular variants, such as specific dosages, methods of administration, or compound derivatives.

Hypothetically, the patent likely includes:

  • Structural claims: Covering the chemical structure of a new molecule, possibly an innovative compound or derivative.
  • Use claims: Encompassing a method of treating a specific condition, e.g., a certain disease or disorder.
  • Formulation claims: Covering specific pharmaceutical compositions, with particular excipients or delivery systems.

Claim Scope and Potential Limitations

The breadth of claims influences enforceability:

  • Broad structural claims enable the patent-holder to prevent similar compounds with minor modifications.
  • Narrower use or formulation claims may be more vulnerable to design-around strategies.

In general, the claims likely aim to strike a balance between broad coverage of the chemical entity or method and specificity to withstand patent challenges.


Patent Landscape in Taiwan for Similar Drugs

Regional Patent Filings and Overlapping Patents

Taiwan's pharmaceutical patent landscape features a mix of:

  • Original drug patents from multinational corporations.
  • Patent applications testing the boundaries of claim scope, often overlapping with neighboring jurisdictions like China, Japan, and Korea.
  • Generic biology and formulations patenting, emphasizing incremental innovation.

Overlap and Potential Conflicts

Patent TW200932207 exists within a competitive environment, where:

  • Existing patents may cover similar chemical classes or therapeutic methods.
  • Active patent scape suggests ongoing innovation, increasing the likelihood of infringement disputes or licensing negotiations.

Innovation Trends

In Taiwan, innovation in pharmaceuticals gravitates toward:

  • Novel chemical entities (NCEs).
  • Targeted therapies, e.g., oncology, immunology.
  • Drug delivery systems improving bioavailability.

If TW200932207 involves an NCE or a significant formulation, it likely remains relevant amidst new patent filings.


Legal and Commercial Implications

Patent Validity and Enforceability

Key considerations include:

  • Novelty and inventive step: Ensuring the claimed invention is unique and non-obvious over prior art.
  • Proper scope: Claims must be neither overly broad nor overly narrow, to withstand legal scrutiny.
  • Maintenance: Correct procedural maintenance and renewal fees affirm active status.

Infringement Risks and Defense Strategies

Competitors developing similar molecules or methods must:

  • Carefully analyze claim language to avoid infringement.
  • Consider design-around strategies—such as structural modifications or different therapeutic targets.

Patent holders should monitor market activity for potential infringements and prepare enforcement or licensing negotiations accordingly.


Strategic Recommendations

  • For Innovators: To maximize protection, consider broadening claim scope while maintaining validity; file continuation applications for follow-up claims.
  • For Licensees: Conduct comprehensive freedom-to-operate (FTO) analyses pre-launch.
  • For Competitors: Analyze the patent claims precisely to identify potential loopholes or§ avenues for licensing or licensing negotiations.

Key Takeaways

  • Scope hinges on claim language: The strength and breadth of TW200932207 depend on specific claim definitions—broad compound claims offer extensive protection, but narrower claims may limit scope.
  • Competitive milieu: Taiwan’s active pharmaceutical patent scene indicates ongoing innovation, which can influence the patent’s enforceability and licensing landscape.
  • Interplay with global patents: Since Taiwan is part of the patent “triad,” overlapping patents from China, Japan, or other jurisdictions could influence freedom to operate.
  • Legal robustness: Ensuring novelty, inventive step, and precise claim language are essential for the patent’s longevity and enforceability.
  • Future strategic moves: Stakeholders should continuously monitor patent citations, amendments, and potential oppositions to gauge landscape shifts.

FAQs

Q1. What are the typical claim types in Taiwan pharmaceutical patents?
Answer: They generally include structural (compound-specific), use (method of treatment), formulation (delivery system), and process (manufacturing) claims.

Q2. How does Taiwan’s patent law affect pharmaceutical patent scope?
Answer: Taiwan’s patent law emphasizes novelty, inventive step, and industrial applicability, which influence claim scope and patent validity.

Q3. Can TW200932207 prevent competitors from developing similar drugs?
Answer: If the claims are sufficiently broad and valid, they can block similar compounds or methods; however, narrow claims may allow design-around strategies.

Q4. How does the patent landscape impact drug commercialization in Taiwan?
Answer: The landscape determines freedom-to-operate; overlapping patents may lead to litigation or require licensing.

Q5. What strategies can extend the patent life or strengthen protection?
Answer: Filing continuation or divisional applications, and broadening claim scope during prosecution, can enhance protection.


References

  1. Taiwan Intellectual Property Office (TIPO): Patent Law and Practice.
  2. WIPO Patent Navigator.
  3. Patent databases and legal case studies relating to Taiwanese pharmaceutical patents.
  4. Legal analysis reports in pharmaceutical patent law.

In summary, patent TW200932207 appears to encompass a significant innovation within Taiwan’s pharmaceutical landscape. Its scope and claims are central to its enforceability and commercial value—necessitating ongoing analysis as the patent environment evolves. Stakeholders must analyze specific claim language and monitor related filings to effectively leverage or navigate this patent’s landscape.

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