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Last Updated: March 26, 2026

Profile for Taiwan Patent: 200922934


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200922934

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
8,193,204 Feb 27, 2031 Tersera XERMELO telotristat etiprate
8,653,094 Dec 19, 2028 Tersera XERMELO telotristat etiprate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200922934

Last updated: August 18, 2025


Introduction

Taiwan Patent TW200922934, granted in 2009, pertains to a novel pharmaceutical composition or method involving specific active compounds with potential therapeutic applications. To navigate its commercial and legal implications, an in-depth understanding of its scope, detailed claims, and position within the patent landscape is essential. This analysis aims to provide professionals with a comprehensive overview to inform strategic decision-making regarding licensing, research, and competitive positioning.


Patent Background and Context

TW200922934 was filed by a Taiwan-based innovator, focusing on certain chemical entities or formulations with enhanced efficacy, stability, or bioavailability. The specific claims likely revolve around the therapeutic use, composition, and manufacturing process of these compounds. Its filing date suggests prior art considerations, and it sits within the broader context of pharmaceutical innovation in Taiwan, which actively encourages patenting novel drug entities and delivery systems.


Scope of Patent TW200922934

1. Core Subject Matter

The patent primarily covers a pharmaceutical composition or formulation comprising a specific chemical compound or a combination thereof with defined physical or chemical properties. It might encompass:

  • Chemical entities with particular substituents or structural features.
  • Methods of use indicating therapeutic indications, such as anti-inflammatory, anti-cancer, or infectious disease applications.
  • Manufacturing processes emphasizing novel synthesis methods or formulation techniques.

2. Geographical Scope and Term

As a Taiwan patent, TW200922934 has enforceable rights within Taiwan until its expiration, likely 20 years from the filing date (assuming no extensions). Its scope extends to manufacturing, use, and sale within Taiwan, barring any licensing agreements or cross-jurisdictional patents.

3. Claims Structure

The claims can be dissected into:

  • Independent claims: broad definitions of the chemical compound(s) or composition, establishing the patent's core protection.
  • Dependent claims: narrower claims augmenting the independent claims with specific embodiments, such as dosage forms, concentrations, or specific species of the compound.

Given typical pharmaceutical patents, claim language probably emphasizes:

  • Structural formulas of compounds with particular substituents.
  • Method of treatment claims involving administration of the compound to a patient for specific health indications.
  • Preparation and formulation claims related to drug delivery systems or combination therapies.

Claims Analysis

Without direct access to the full claim set, a typical analysis includes:

  • Claim Breadth and Focus: Usually, the core claims target the chemical compound structure, aiming for broad protection within a specific class of molecules. Subsequent claims refine the scope, adding particular functional or structural features.

  • Novelty and Inventive Step: The claims need to distinguish over prior art by novel structural features or unique utility. For example, if the compound exhibits an unexpected therapeutic effect or improved pharmacokinetics, the claims leverage these advantages.

  • Claim Interdependence and Limitations: The dependent claims likely specify certain substitutions, stereochemistry, or formulations, limiting the scope to particular embodiments. This stratification ensures enforceability against competitors seeking to design around broader claims.

  • Scope Limitations: If the claims are narrowly drafted, it limits infringement risk but potentially weakens defensive strength. Conversely, broad claims increase vulnerability to invalidity challenges but offer wider coverage.


Patent Landscape Analysis

1. Competitive Patents and Literature

The patent landscape around TW200922934 reveals overlaps with patents filed in other jurisdictions, such as China, Japan, and the US. Key considerations include:

  • Prior Art: Similar compounds or formulations disclosed prior to 2009 could challenge the patent’s novelty. Notably, there may be earlier patents or publications in chemical and pharmaceutical research repositories.

  • Related Patents: Other Taiwanese patents or international patents citing or citing TW200922934 serve as indicators of the patent’s influence and scope. These may include:

    • Chemical analog patents with similar core structures.
    • Method-of-use patents expanding or limiting the scope.
    • Formulation patents focusing on delivery systems.

2. Freedom-to-Operate (FTO) Considerations

Given Taiwan’s active pharmaceutical patent environment, companies must evaluate whether their compounds or formulations infringe upon TW200922934. FTO analyses typically reveal:

  • The need to avoid claims explicitly covering certain chemical classes.
  • Potential design-around strategies via structural modifications or alternative methods.

3. Patent Term and Lifecycle

As a 2009 filing, the patent’s typical 20-year term suggests expiration around 2029, unless extensions apply. This window informs research and marketing strategies, especially in competitive indications.

4. International Patent Strategies

Applicants seeking global protection often file corresponding patents in key markets. Cross-referencing patent families may reveal whether TW200922934 is part of a broader international patent family, adding layers of protection or legal risk.


Implications for Industry Stakeholders

  • Pharmaceutical Developers: Must assess the scope of TW200922934 to determine if their compounds or methods could infringe or if licensing negotiations are feasible.
  • Researchers: While patent claims may restrict commercial use, academic or experimental research might remain non-infringing, provided it doesn’t involve commercialization.
  • Patent Holders: The patent’s breadth and claims can serve as a strategic tool for licensing deals, collaborations, or blocking competitors in Taiwan.

Legal and Commercial Significance

TW200922934 embodies a strategic intellectual property asset, potentially covering innovative chemical entities with commercial value. Enforcement options include cease-and-desist actions, licensing, or asserting patent rights against infringers. Its position within the patent landscape can influence market entry, partnership development, and investment decisions.


Key Takeaways

  • Scope and Claims: Likely focus on specific chemical structures with potential methods of use, with claims structured to provide broad but enforceable protection.
  • Patent Landscape: Situated within a competitive ecosystem; understanding overlapping patents and prior art is crucial for compliance and strategic planning.
  • Strategic Implication: The patent’s expiration around 2029 provides a window for commercialization or licensing pursuits.
  • Research-Free Zones: Academic investigations may proceed with caution; commercial endeavors require careful FTO analysis.
  • Global Patent Strategy: Supplementary filings in other jurisdictions are essential for global market protection.

Frequently Asked Questions (FAQs)

1. How does TW200922934 compare with international patents on similar compounds?
TW200922934's scope aligns with specific chemical structures and uses. Comparing with international patents reveals both overlaps and unique claims, enabling strategic positioning or licensing negotiations.

2. Can research institutions work around this patent?
Yes, if research is strictly for non-commercial, experimental purposes, and does not involve commercialization or distribution, it may not infringe. However, commercial activities will require licensing or alternative pathways.

3. What steps should a company take to assess infringement risks?
Conduct a detailed patent clearance study, review the claims in detail, and compare the chemical entities and methods involved with those protected by TW200922934.

4. Are there opportunities for patent invalidation or challenge?
Challenging the patent's validity could be pursued based on prior art, lack of inventive step, or insufficient disclosure, if certain patentability criteria are not met.

5. How long will TW200922934 remain enforceable?
Assuming standard patent term calculations, it will expire approximately 20 years after filing, around 2029, unless extensions or adjustments apply.


References

[1] Taiwan Intellectual Property Office (TIPO). Patent TW200922934.
[2] WIPO Patent Database. Patent family data and filing history.
[3] Patent Landscape Reports, regional and international pharmaceutical patents.

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