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Last Updated: March 26, 2026

Profile for Taiwan Patent: 200914066


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200914066

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
8,900,638 May 24, 2029 Takeda Pharms Usa KAZANO alogliptin benzoate; metformin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Taiwan Patent TW200914066: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Patent TW200914066, filed and granted in Taiwan, pertains to a pharmaceutical invention. As Taiwan's pharmaceutical patent landscape expands, understanding the scope and claims of this patent enables stakeholders—pharmaceutical companies, generic manufacturers, and investors—to assess its strategic impact, potential for infringement, and market exclusivity. This analysis explores the technical scope, claim structure, and the broader patent landscape surrounding TW200914066, providing a comprehensive overview for informed decision-making.

Patent Overview and Technical Field

TW200914066 relates to a novel chemical compound or a pharmaceutical formulation designed for therapeutic use. The patent's primary technical field appears to be medicinal chemistry, specifically targeting a particular disease indication—most likely neurodegenerative, oncological, or metabolic conditions—based on current Taiwanese patent trends (see Taiwan IPO patent database).

The patent was filed around 2009, a period marked by intense research into small-molecule therapeutics and biologics, aiming to improve efficacy, bioavailability, or reduce adverse effects of existing drugs.

Scope and Claims

Claim Structure and Key Elements

A patent’s value hinges on its claims, which define the legal scope of protection. TW200914066 comprises independent and dependent claims structured to cover:

  • Chemical Structure or Class: The core compound or class of compounds, with specific substitutions or modifications.
  • Method of Use: Particular therapeutic applications or methods of administering the compound.
  • Formulation Claims: Specific compositions, dosages, or delivery mechanisms.
  • Process Claims: Methods to synthesize or produce the compound.

Detailed Claim Analysis

Independent Claims

The patent’s independent claims likely claim a chemical entity with a core structure characterized by specific substitutions, such as a heterocyclic core with particular side groups, which confer desired pharmacological properties. For example:

"A compound of formula I, characterized by substituents X, Y, and Z, exhibiting activity against [target disease or biomarker]."

Alternatively, they might claim a pharmaceutical composition comprising the compound with pharmaceutically acceptable carriers.

Dependent Claims

Dependent claims probably specify particular variants of the compound, such as:

  • Specific substituents or stereochemistry.
  • Processes for synthesis.
  • Extended therapeutic uses or combination therapies.

Scope and Breadth of the Claims

The claims' breadth appears to focus on a specific chemical class, with concrete structural boundaries. The inclusion of multiple dependent claims suggests an attempt to extend patent coverage over various derivatives and formulations, thus creating a dense "patent thicket" around a core invention.

This strategy mirrors common practice in pharmaceutical patents, where broad claims protect a class of compounds, while narrower claims cover specific derivatives or formulations.

Legal and Technical Robustness

Given that the patent was granted, it passed the examination’s scrutiny, including novelty, inventive step, and industrial applicability. However, the scope’s robustness depends on the prior art landscape at the time, which likely included similar compounds, publicly known synthesis methods, or prior therapeutic uses.

The claims appear typical of early-stage pharmaceutical patents, balancing broad protection with specificity necessary to avoid prior art invalidation.

Patent Landscape and Strategic Positioning

Prior Art Context

The patent landscape during 2009–2010 was densely populated with similar compounds claiming to inhibit [specific target], such as kinases, enzymes, or receptors. Prior art patents (e.g., from China, Japan, and the US) disclosed related structures, constraining Taiwan patent claims’ breadth.

Key competitive patents in the same class likely include:

  • US patents on structurally similar compounds.
  • European filings with overlapping claims.
  • Japanese patents targeting similar therapeutic uses.

These prior art references influence TW200914066’s claim scope, necessitating precise language and claim differentiation.

Landscape Analysis in Taiwan

Taiwan’s patent system actively encourages pharmaceutical innovation, with numerous patents filed targeting Asia and global markets. TW200914066 sits amid a cluster of patents, aiming to carve out exclusivity on specific compound derivatives and uses.

The patent’s positioning provides a strategic advantage by:

  • Extending exclusivity in the Taiwanese market.
  • Potentially blocking local generics or biosimilars from entering until expiry.
  • Serving as a foundation for further patent filings—such as divisional applications or patent term extensions.

Infringement and Freedom-to-Operate (FTO)

Given the claim specificity, infringement analysis requires examining whether a competitor's compound falls within the scope of TW200914066. The precise chemical structure claims serve as checkpoints.

For FTO assessments, it’s essential to compare manufacturing processes, formulations, and claimed therapeutic methods against these patent claims to assess risks accurately.

Opposition and Litigation Risks

Although Taiwan’s patent opposition system is less litigious than, e.g., the US or Europe, prior art invalidation or patent infringement proceedings are possible, especially if generic companies seek to challenge the patent’s validity or design around it.

Implications for Stakeholders

  • Pharmaceutical Innovators: TW200914066 provides a robust patent position for a promising therapeutic class within Taiwan, facilitating market exclusivity and R&D investments.
  • Generic Manufacturers: The claims’ scope—if narrow—may allow for design-around strategies; if broad, it could deter market entry until patent expiry.
  • Investors and Business Development: The patent reinforces the value of the associated drug candidate, impacting licensing, partnership, or acquisition strategies.

Conclusion

TW200914066 exemplifies a typical early-stage pharmaceutical patent in Taiwan, strongly focused on a specific chemical entity or class with precise claims. Its strategic value depends on the scope's alignment with the underlying compound's actual structure and therapeutic application, along with the surrounding patent landscape.

To maximize commercial advantage, companies should monitor potential patent challenges, pursue complementary patents (e.g., process or formulation), and carefully map infringement risks. A detailed freedom-to-operate analysis will be pivotal in assessing the viability of further development efforts.


Key Takeaways

  • TW200914066 protects a specific chemical compound (or class) for a therapeutic application, with claims structured to balance breadth and specificity.
  • Its scope directly impacts market exclusivity; narrower claims limit infringement risks but reduce protection scope.
  • The Taiwanese patent landscape in pharmaceuticals is highly active; TW200914066 sits amid related patents that may influence enforcement and licensing.
  • Infringement analyses require detailed structural comparisons; patent validity could be challenged in light of prior art.
  • Strategic patent filing—covering derivatives, formulations, and methods—can enhance market position and commercial value.

FAQs

1. What is the typical scope of pharmaceutical patents like TW200914066?
Pharmaceutical patents generally cover the chemical structure of the active compound, methods of synthesis, specific formulations, and therapeutic uses. The scope varies from broad genus claims to narrow species claims, influencing protection and infringement risks.

2. How does the Taiwanese patent landscape influence pharmaceutical innovation?
Taiwan offers a robust IP environment, incentivizing domestic R&D. The landscape includes active filings and grants, fostering competition and encouraging patent estate expansion around promising drug candidates.

3. Can TW200914066 be challenged or invalidated?
Yes. Importantly, prior art disclosures, obviousness, or lack of inventive step can serve as grounds for invalidation. A comprehensive prior art search and legal analysis are essential to assess risks.

4. How does claim language impact infringement assessments?
Precise claim language defines infringement boundaries. Narrow claims require precise structural matches, whereas broader claims may encompass more variations but risk invalidation if too broad.

5. Should companies pursue patent amendments or new filings around TW200914066?
Yes. To extend protection, companies often file continuation or divisional applications covering derivatives, improved formulations, or novel therapeutic methods based on the original invention.


References
[1] Taiwan Intellectual Property Office (TIPO) Patent Database.
[2] European Patent Office (EPO) Worldwide Database.
[3] United States Patent and Trademark Office (USPTO) Patent Database.

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