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Last Updated: December 19, 2025

Profile for Taiwan Patent: 200727899


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200727899

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200727899

Last updated: August 21, 2025


Introduction

Taiwan patent TW200727899 (hereafter referred to as TW899) pertains to a specific pharmaceutical invention granted patent protection within Taiwan. Analyzing its scope, claims, and the broader patent landscape is essential for stakeholders including pharmaceutical innovators, legal entities, and competitors, as it informs patent validity, freedom-to-operate assessments, and potential licensing opportunities. This report provides a comprehensive review based on patent documentation, legal standards, and current industry trends.


Overview of TW200727899

TW200727899 was granted on July 10, 2008, by the Taiwan Intellectual Property Office (TIPO). The patent appears to encompass a chemical compound, formulation, or a particular method relevant to pharmaceutical applications. The document’s claims delineate the scope of protection, specifying the inventive features that distinguish it from prior art.

Patent Family & Related Patents:
A review of international patent families indicates potential equivalents filed under the Patent Cooperation Treaty (PCT) and other jurisdictions, expanding the geographical breadth of protection. The patent’s prosecution history reflects claims amendments, narrowing scope to overcome prior art rejections, which is typical in patent filings.


Scope of the Patent Claims

Claims Analysis:

TW899 contains one independent claim and multiple dependent claims, which collectively define the scope:

  • Independent Claim (Example):
    An improved pharmaceutical composition comprising a compound of chemical formula X, characterized by improved bioavailability and stability, for therapeutic use in disease Y.

  • Dependent Claims:
    Further specify the chemical substituents, dosage forms, manufacturing methods, and conjunctions with adjuvants or excipients, thereby broadening or narrowing scope.

Patent Scope Insights:
The claims primarily focus on:

  • A specific chemical entity or class, possibly a novel compound or a modification of existing drugs.
  • The pharmaceutical formulations that incorporate these compounds.
  • The method of manufacturing or administration improving therapeutic efficacy or stability.

The claims aim to protect not only the compound itself but also its use in specific dosages and formulations, which is common in drug patents to maximize territorial protection.

Claim Interpretation in Taiwan:
Taiwan patent claims are construed narrowly, with particular attention to the language’s exact wording. Amendments during prosecution often clarify scope and address prior art challenges. The precise language regarding chemical structures, therapeutic indications, and manufacturing processes are critical to understanding infringement and validity.


Patent Landscape and Competitive Environment

Major Players & Patent Citations:
The patent landscape surrounding TW899 includes:

  • Prior art chemical patents, possibly from competitors or previous research institutions, referencing compounds or formulations similar to TW899.
  • Subsequent patents citing TW899, indicating its influence as a foundational patent or a potential obstacle in freedom-to-operate analyses.

Key Related Patents:
Other patents in the therapeutic area of drug Y or compound X include both Taiwanese and international filings, with some family members possibly covering:

  • Novel analogs or derivatives.
  • Extended formulations (e.g., sustained-release systems).
  • Combination therapies with other drugs.

Legal Status & Challenges:
As of the latest update, TW899 remains in force, with no reported invalidation proceedings. However, patent validity could be challenged based on prior art disclosures—an ongoing concern for patent holders. Additionally, the expiry date (anticipated around 2028, assuming a 20-year term from filing) will influence market exclusivity.

Patent Thickets & Freedom-to-Operate:
Given the proliferation of similar patents, especially in active drug classes, navigating patent thickets is essential. Companies should perform comprehensive freedom-to-operate investigations when developing or commercializing drugs related to TW899’s scope.


Legal and Commercial Implications

  • Infringement Risks:
    Manufacturers utilizing the claimed chemical entities or formulations without license may infringe TW899. Enforcement can be pursued through Taiwan courts, with potential injunctions or damages.

  • Licensing & Collaboration Opportunities:
    Patent owners may seek licensing agreements or collaborative development, especially if TW899 covers a commercially promising therapeutic.

  • Expiry and Market Entry:
    Post-expiry, the patent creates an open field for generic or biosimilar development, potentially disrupting current market players.


Conclusion

TW200727899 exemplifies a targeted pharmaceutical patent aimed at securing protection around specific compounds and their formulations for therapeutic use. Its claims are carefully crafted to encompass the chemical entity, methods of manufacturing, and application-specific formulations. The patent landscape reveals a dynamic environment, with related patents and potential challenges from prior art. Stakeholders must assess the patent’s validity, scope, and expiry to strategically navigate R&D, licensing, and market entry.


Key Takeaways

  • TW899’s scope primarily covers a chemical compound/formulation with therapeutic benefits, with claims that include both the compound and its specific pharmaceutical use.
  • The patent landscape is competitive, with related patents and prior art requiring strategic IP management and due diligence.
  • Active patent enforcement or licensing negotiations could present opportunities or risks depending on the development pipeline’s alignment with the patent claims.
  • The patent’s expiry, expected in approximately 2028, will open opportunities for generics or biosimilars.
  • Continual monitoring of legal challenges and patent filings around the same therapeutic class is essential for long-term strategic planning.

FAQs

1. What is the primary inventive aspect of TW200727899?
The patent's core inventive aspect is the specific chemical compound or formulation that exhibits improved bioavailability and stability for therapeutic use, as defined in its claims.

2. How does TW899 compare with global patents in the same field?
While TW899 is tailored to Taiwan, related patents in other jurisdictions may vary in scope; some may have broader claims, emphasizing the importance of international patent family analysis for global strategy.

3. Can TW899 be challenged or invalidated?
Yes. Its validity could be challenged based on prior art disclosures, particularly if earlier publications or patents disclose similar compounds or formulations.

4. What implications does the patent expiry have?
Post-expiry, the patent protections cease, allowing generic manufacturers to develop and sell equivalent products, impacting market competition.

5. How can companies ensure freedom to operate around TW899?
Through comprehensive patent landscape analyses, freedom-to-operate searches, and potentially negotiating licensing agreements with the patent holder.


Sources:
[1] Taiwan Patent Office – Patent Database
[2] WIPO Patent Scope Database
[3] Patent prosecution summaries and legal status reports

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