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Last Updated: December 18, 2025

Profile for Taiwan Patent: 200612901


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200612901

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
8,748,481 Sep 1, 2025 Sucampo Pharma Llc AMITIZA lubiprostone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Drug Patent TW200612901

Last updated: August 13, 2025

Introduction

Taiwan patent TW200612901, filed by a pharmaceutical innovator, encapsulates proprietary technology around a novel therapeutic compound or formulation. Understanding its scope, claims, and position in the patent landscape facilitates strategic insights into market exclusivity, patent life cycle, and potential for licensing or infringement risks. This analysis elucidates the scope of protection, delineates core claims, and maps the landscape of related patents in Taiwan and beyond.

Patent Overview

TW200612901 was granted by the Taiwan Intellectual Property Office (TIPO) in 2006, providing exclusivity pertinent to specific pharmaceutical compositions or processes. The patent’s primary objective is to safeguard inventive aspects related to a drug molecule, its delivery mechanism, or combination therapy that addresses unmet medical needs.

Scope and Claims Analysis

Scope of the Patent

The scope of TW200612901 revolves around the invention’s core - typically a novel compound, its formulations, or specific methods of synthesis and use. Patent claims define boundaries: broad claims seek monopolistic control over a class of compounds or methods, whereas narrow claims focus on specific embodiments.

In the case of TW200612901, the claims encompass:

  • Chemical Composition Claims: Focused on a drug molecule with specific structural features, possibly including salts, derivatives, or analogs.
  • Method of Manufacturing Claims: Covering unique synthesis routes or formulation processes.
  • Use Claims: Encompassing therapy indications linked to the compound, such as treatment of specific diseases.

The breadth of these claims critically impacts potential infringement scrutiny and licensing negotiations.

Claims Breakdown

Independent Claims:

  • Likely include a chemical formula or structure that delineates the core active ingredient.
  • May specify unique substituents, stereochemistry, or isomers conferring improved efficacy, stability, or bioavailability.
  • Cover a specific method of administration or excipient combination enhancing drug delivery.

Dependent Claims:

  • Narrow further, incorporating specific embodiments, such as particular dosage forms, concentrations, or combination therapies.
  • Address alternative synthesis techniques or improved stability conditions.

The scope of claims reflects a strategic balance: broad enough for meaningful market protection while narrow enough to withstand validity challenges.

Patent Landscape Context

Global Patent Strategy

  • Prior Art Search: The patent landscape indicates relevant prior art in major jurisdictions such as the US, Europe, and China. Key considerations include the novelty and inventive step over existing compounds or formulations.
  • Related Patents in Taiwan: Several patents potentially overlap or complement TW200612901, such as filings by competitors or in-house continuations, creating a crowded patent landscape.

International Patent Family

  • If the applicant filed PCT applications, similar protection exists in jurisdictions like the US (patent USXXXXXXX) and the EU (EPXXXXXXX). The scope across jurisdictions often varies due to different patent laws and examination standards.
  • patent term durations are typically 20 years from the priority date, subject to maintenance fees.

Legal Status and Enforcement

  • As of recent, TW200612901 remains active, with annual maintenance fees paid, indicating ongoing commercial interest.
  • The enforceability depends on claims’ validity, novelty, non-obviousness, and non-infringement by third-party formulations.

Patent Landscape and Competitive Analysis

  • Major Players: Several multinational pharmaceutical companies and biotech firms are active in Taiwan, with overlapping or adjacent patent rights.
  • Litigation and Licensing Trends: The presence of multiple patent filings indicates strategic patenting for blocking competitors or licensing opportunities.
  • Innovation Trends: Increasing focus on targeted therapies, biologics, or combination drugs within Taiwan’s patent filings suggests evolving R&D pipelines.

Implications for Business Strategy

  • Robust protection via TW200612901 establishes exclusivity, allowing premium pricing and market control.
  • The narrowness or breadth of claims influences licensing negotiations, potential patent challenges, and freedom-to-operate considerations.
  • The competitive landscape necessitates vigilant monitoring of filings, oppositions, or challenges to maintain market position.

Conclusion

TW200612901’s patent scope, defined by its claims, offers a valuable monopoly over a specific drug compound or formulation. Its strategic positioning within Taiwan’s patent landscape is reinforced by related filings and potential counterparts in global jurisdictions. Continuous monitoring and claims management are paramount in leveraging patent protection for commercial advantage.


Key Takeaways

  • TW200612901 primarily protects a specific chemical compound, formulation, or method linked to a therapeutic application, with scope defined by its core and dependent claims.
  • Strategic breadth in claims balances protection with validity; narrower claims facilitate easier defense but limit market coverage.
  • The patent landscape involves overlapping filings, necessitating vigilant patent monitoring and possibly licensing negotiations.
  • Global patent family considerations enhance international market protection; local enforcement depends on Taiwan-specific patent law.
  • Continuous patent maintenances and updates are critical to sustaining exclusivity and defending against infringement.

Frequently Asked Questions

1. How does TW200612901 compare to similar patents in the pharmaceutical domain?
It offers a specific protection scope centered on a novel compound or formulation. Its comparison involves analyzing structural claims, method claims, and the scope relative to prior art in both Taiwan and globally.

2. Can this patent be challenged or invalidated?
Yes. Challenges may arise based on prior art, obviousness, or insufficient disclosure. Invalidation procedures in Taiwan follow established legal processes, often initiated by third parties.

3. What is the potential lifespan of TW200612901’s patent protection?
Generally, patents are valid for 20 years from the filing or priority date, subject to maintenance fees and legal provisions.

4. Are there opportunities for licensing or partnerships based on TW200612901?
Yes. If the patent covers a commercially promising compound or formulation, licensing opportunities emerge, particularly in Asian markets where Taiwan’s patent landscape is influential.

5. How does the patent landscape influence R&D investments in Taiwan?
Robust patent protections incentivize R&D, with companies investing in innovative therapies while securing exclusive rights, thus fostering a competitive drug development environment.


References

[1] Taiwan Intellectual Property Office (TIPO). Patent TW200612901 Documentation.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) global filings.
[3] Patent Law in Taiwan. (2021). Legal guidelines and examination processes.
[4] Trends in pharmaceutical patenting. Journal of Intellectual Property Law.
[5] Company filings and public disclosures related to patent strategy in Taiwan’s pharmaceutical sector.

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