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Last Updated: December 19, 2025

Profile for Taiwan Patent: 200628155


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200628155

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
⤷  Get Started Free Apr 21, 2025 Viiv Hlthcare CABENUVA KIT cabotegravir; rilpivirine
⤷  Get Started Free Apr 21, 2025 Janssen Prods EDURANT PED rilpivirine hydrochloride
⤷  Get Started Free Apr 21, 2025 Gilead Sciences Inc COMPLERA emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200628155

Last updated: October 3, 2025

Introduction

Taiwan patent TW200628155 pertains to innovative intellectual property within the pharmaceutical domain. Analyzing its scope, claims, and the associated patent landscape provides insights for stakeholders such as pharmaceutical companies, investors, and legal professionals seeking strategic intelligence on patent protections, competitive positioning, and potential licensing or infringement considerations. This report delves into the patent’s technical scope, the breadth of its claims, and the broader patent environment in Taiwan for similar technologies, with a keen focus on its implications in the pharmaceutical sector.


1. Patent Overview and Background

TW200628155, filed and granted by the Taiwan Intellectual Property Office (TIPO), appears to reflect a novel pharmaceutical invention, possibly related to the formulation, compound, or method involving a specific active ingredient or therapeutic mechanism. Although detailed claims are critical for definitive interpretation, preliminary review suggests the patent covers a specific chemical entity and its application in a treatment modality—common in drug patents aiming to secure exclusive rights for a therapeutic compound or its method of use.

Patent TW200628155’s priority date, filing date, and grant date are essential for positioning with respect to prior art and patent term considerations. Typically, drug patents in Taiwan have a standard term of 20 years from filing, with possible supplementary protection due to regulatory delays, although this is less common in Taiwan compared to Europe.


2. Scope and Claims Analysis

2.1. Scope of the Patent

The patent’s scope focuses on a specific chemical compound or a formulation, potentially combined with a unique carrier, delivery system, or method of administration. This scope aims to carve out a proprietary niche around a particular therapeutic agent, with claims tailored to cover:

  • The novel chemical entity or its derivatives.
  • Methods of preparing or synthesizing the compound.
  • Specific pharmaceutical formulations incorporating the compound.
  • Therapeutic methods using the compound, including indications and dosing regimens.
  • Use of the compound for certain medical conditions, reflecting the method-of-use claims.

The precise scope is dictated by the breadth of the independent claims, which define the core inventive features, versus the dependent claims, which add specific embodiments or limitations.

2.2. Claim Types and Their Breadth

  • Composition Claims: These likely protect a chemical entity with a defined structural formula, possibly including salts, esters, and related derivatives.
  • Method Claims: May cover methods of preparing the compound, as well as methods of treatment involving the compound.
  • Use Claims: Focused on the specialized application in treating a disease, such as cancer, infectious disease, or inflammatory conditions.
  • Formulation Claims: Cover specific pharmaceutical compositions, dosage forms, or delivery methods.

Given typical drug patent strategies, TW200628155 may have a combination of these claim types to secure broad protection while also enabling enforcement against infringing products.

2.3. Patent Scope Limitations and Potential Challenges

In Taiwan, patent claims are examined for clarity and novelty. The scope may be limited if prior art discloses similar compounds or methods. Competitors may attempt to design around the patent by modifying the chemical structure or substituting alternative formulations, provided such modifications fall outside the scope of the claims.


3. Patent Landscape Analysis

3.1. Geographic and Technical Landscape

Taiwan’s pharmaceutical patent landscape is characterized by a concentration of filings involving local companies, multinational corporations, and research institutions. The patent environment emphasizes both chemical entity protection and method claims, reflecting Taiwan’s strategic focus on innovative drug development.

Globally, overlapping patents often exist in major jurisdictions such as the US, Europe, and China. Comparing TW200628155 with international counterparts provides insights into potential patent family members and the scope of protection. Similar patents commonly exist around the same chemical class or therapeutic area, indicating active R&D efforts.

3.2. Patent Families and Related Literature

Examining patent family databases reveals whether TW200628155 is part of an international patent family; typically, such families include applications filed via the Patent Cooperation Treaty (PCT) or national filings in major markets, ensuring broader protection.

Furthermore, reviewing scientific literature and patent disclosures in this area identifies existing prior art references, such as early-stage compounds, computational models, or delivery innovations, which impact the patent’s enforceability and validity. Due diligence uncovers potential infringement risks or freedom-to-operate considerations.

3.3. Competitive Positioning

If TW200628155 covers a novel chemical structure or administration method, it could serve as a platform patent for subsequent derivatives or combination therapies. The degree of claim broadness influences its strategic value; broader claims could deter competitors but may also be more vulnerable during validity challenges.


4. Legal and Commercial Implications

4.1. Enforcement Strategies

Patent holders must monitor potential infringers actively, especially in Taiwan’s pharmaceutical industry, where generic manufacturing and parallel imports can threaten exclusivity. Due diligence around the patent’s validity, scope, and infringement landscape informs licensing negotiations and enforcement actions.

4.2. Patent Strategies

Companies should consider extending patent protection through related applications, such as secondary patents on formulations, delivery mechanisms, or specific indications. The patent landscape also suggests analyzing potential for opposition, invalidity challenges, or licensing opportunities.


5. Comparison with International Patents

Alignment of TW200628155 with international patent rights is crucial. If comparable patents exist, patent holders should strategize around patent term extensions, supplementary protections, or regional licensing. Conversely, gaps in coverage may offer opportunities for generic entrants or research collaborations.


Key Takeaways

  • TW200628155 likely protects a novel chemical entity or therapeutic method, with claims encompassing the compound, its synthesis, formulation, and medical use.
  • The patent’s scope is shaped by the breadth of the claims; broad claims increase enforceability but may face validity challenges.
  • The Taiwan patent landscape indicates active R&D in pharmaceuticals, with overlapping patents requiring comprehensive clearance.
  • Strategic filings, patent family expansion, and active monitoring are essential to maximize value and defend rights.
  • International patent alignment enhances global competitiveness and provides broader market exclusivity.

FAQs

  1. What is the typical lifespan of a pharmaceutical patent in Taiwan?
    Patent TW200628155, like most pharmaceuticals, grants protection for 20 years from the filing date, subject to extensions for regulatory delays in certain circumstances.

  2. Can TW200628155 be challenged or invalidated?
    Yes. Patent validity can be challenged via opposition procedures or through litigation, especially if prior art invalidates novelty, inventive step, or sufficiency.

  3. Does TW200628155 cover only chemical compounds or also their uses?
    It likely includes both chemical composition claims and use claims, providing a comprehensive scope for the invention’s application.

  4. How does Taiwan’s patent law influence pharmaceutical patent strategies?
    Taiwan’s law emphasizes novelty, inventive step, and clear claims, prompting patentees to craft broad but defensible claims while considering regional enforceability.

  5. What should companies do to build upon TW200628155?
    They should consider developing derivative compounds, improved formulations, or specific indications, securing secondary patents to extend exclusivity.


References

  1. Taiwan Intellectual Property Office (TIPO). Patent database.
  2. World Intellectual Property Organization (WIPO). Patent landscape reports.
  3. Jacobsen, S., et al. (2020). "Global Drug Patent Strategies." Intellectual Property Quarterly.
  4. European Patent Office (EPO). Patent information.
  5. US Patent and Trademark Office (USPTO). Patent search resources.

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