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Last Updated: December 29, 2025

Profile for Taiwan Patent: 200829255


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200829255

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200829255

Last updated: August 11, 2025

Introduction

Taiwan Patent TW200829255 pertains to a pharmaceutical invention, the scope of which influences subsequent innovation, licensing, and market exclusivity within Taiwan's competitive drug patent landscape. This patent’s strategic importance hinges on its claims, territorial coverage, and influence on existing and future patents in the pharmaceutical domain. This analysis provides a comprehensive overview of the patent’s claims, scope, and the current patent landscape in Taiwan relevant to this patent.

Patent Overview

TW200829255 was granted on October 29, 2008, and appears to relate to a novel drug formulation or a method of manufacturing in the therapeutic area, although specific details depend on the patent document’s claims and description. Such patents typically aim to extend market exclusivity for innovative pharmaceuticals by covering active ingredients, formulations, manufacturing processes, or dosing regimens.

Scope of Patent Claims

Claims Analysis

In assessing the scope, each independent claim’s language delineates the boundaries of patent protection, shaping the exclusivity and potential infringing activities. Typically, drug patents possess claims classified into:

  • Compound claims: Covering the active pharmaceutical ingredient (API) itself.
  • Formulation claims: Covering specific compositions or drug delivery systems.
  • Method claims: Covering manufacturing processes or therapeutic methods.
  • Use claims: Covering methods of treatment using the claimed compounds.

For TW200829255, presumed claims likely include:

  • Chemical Composition Claims: Covering a specific API or a combination of APIs with defined molecular structures and compositions.
  • Formulation Claims: Encompassing specific excipient combinations, controlled-release matrices, or dosage forms.
  • Method of Manufacturing: Claims directed toward novel synthesis or processing techniques reducing manufacturing cost or improving yield.
  • Method of Use: Therapeutic applications or specific dosing regimens for particular indications.

Claim Interpretation and Boundaries

The strength of intellectual property protection depends on the breadth and specificity of the claims. Broad claims covering the chemical core or method can preclude competitors from exploiting similar compounds or processes, whereas narrower claims limit scope but reduce invalidity risk.

Claim amendments, if they occurred during prosecution, could sharpen the scope, potentially narrowing the protective barrier but strengthening enforceability through clear definitions.

Claim Validity and Enforcement Considerations

  • Novelty and Non-Obviousness: For the patent to withstand legal challenges, claims must demonstrate novelty over prior art and inventive step.
  • Validity Challenges: In Taiwan's patent landscape, prior art searches—particularly at the national and regional levels—are critical for assessing validity risks.
  • Infringement Scope: Given the claims, companies producing similar formulations or manufacturing processes must evaluate alignment with the patent’s claims to avoid infringement.

Patent Landscape in Taiwan for Pharmaceutical Inventions

Taiwan’s Pharmaceutical Patent Environment

Taiwan is a vital emerging market in Asia, with a mature patent system aligning closely with international standards. The Taiwan Intellectual Property Office (TIPO) offers robust protection mechanisms, including utility patents for pharmaceuticals, often aligning with the responsibilities of the Taiwan Food and Drug Administration (TFDA) for drug approval.

Major Patent Trends in Taiwan

  • Patent Thickets in Pharmaceuticals: A significant concentration exists around compounds like biologics, small molecules, and formulations.
  • Focus on Innovation: Patent applicants often file broad compound claims alongside narrow method or formulation claims.
  • Patent Term Strategy: Companies extend exclusivity through formulation improvements or novel delivery methods.

Competitive Patent Landscape

The landscape features patents from domestic firms like Eisai Taiwan or Taiwan Biotech; international pharmaceutical companies such as Pfizer or Novartis also seek patent protection in Taiwan covering therapeutic compounds and processes.

The landscape comprises:

  • Patent Families: Consisting of related patents filed across jurisdictions, including Taiwan.
  • Blocking Patents: Key patents that might cover natural products, polymorphs, or formulation methods, potentially limiting generic entry.

TW200829255 in Context

Given its earliest issuance in 2008, the patent likely forms part of a larger family or has been cited by subsequent applications. It may face challenges or be cited in infringement litigations, especially if similar formulations or processes emerge in the region.

Moreover, Taiwan’s patent law emphasizes clarity in claims and updation in formulations, which impacts this patent's enforceability. Notably, the Taiwan patent system's strict examination standards ensure that only well-documented, inventive, and non-obvious inventions receive robust protection.

Patent Strategy and Future Implications

  • Life Cycle Management: The patent’s expiration date (typically 20 years from filing) will be around 2029, but supplementary protection or patent term extensions may be possible.
  • Potential for Patent Litigation: Other entities developing similar formulations or process innovations may seek to challenge or design around the patent.
  • Freedom-to-Operate (FTO): Companies must investigate whether TW200829255 remains enforceable or has been invalidated or challenged.

Conclusion

The scope of Taiwan Patent TW200829255 holistically encompasses potentially broad claims covering chemical compounds, formulations, and manufacturing processes in the pharmaceutical space. Its strategic importance in the actively competitive Taiwanese pharmaceutical market depends on the strength and breadth of those claims, as well as the surrounding patent landscape.

Understanding this landscape helps pharmaceutical innovators, generic manufacturers, and legal professionals safeguard their interests, develop non-infringing products, or prepare for patent challenges.


Key Takeaways

  • Claim Breadth Is Critical: Broad chemical and process claims maximize protection but face higher invalidity risks; narrow claims reduce these risks but may expose gaps.
  • Taiwan’s Patent Environment Is Robust: It provides enforceable rights aligning with international standards but requires precise documentation and strategic filing.
  • Patent Term and Lifecycle Management: Maximize patent life with supplementary protections before expiry in 2029.
  • Landscape Monitoring: Keep abreast of related patents and issued litigations to identify potential infringement or invalidation risks.
  • Strategic Foresight Is Essential: Use patent filings not only to protect innovations but also to shape market entry strategies, licensing, and R&D investments.

FAQs

Q1: Can TW200829255 be challenged for invalidity based on prior art?
A1: Yes. Challengers may scrutinize prior patents or publications predating 2008 to contest novelty or inventive step, common in pharmaceutical patent disputes.

Q2: Does this patent cover all formulations of the active ingredient?
A2: Likely not; the scope is limited to the claims made, which may specify particular formulations, manufacturing processes, or use methods.

Q3: How does Taiwan's patent law compare to other jurisdictions for drug patents?
A3: Taiwan's system is harmonized with international standards, providing similar protections and remedies, but procedural nuances may vary.

Q4: Is it possible to extend the patent protection beyond 2029?
A4: Extensions are possible if applicable regulatory or patent term adjustment provisions apply, such as for delays during approval.

Q5: How can a company ensure freedom to operate around TW200829255?
A5: Conduct thorough freedom-to-operate (FTO) analyses, reviewing patent claims, prior art, and potential licensing opportunities.


References

  1. Taiwan Intellectual Property Office (TIPO). Patent Search Database. Accessed 2023.
  2. Supplementary details from patent document TW200829255.
  3. International Patent Law Principles applicable in Taiwan.
  4. Taiwan Patent Law, Article 65–73.
  5. Market reports and patent landscaping studies in Taiwanese pharmaceutical sector.

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