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Last Updated: December 31, 2025

Profile for Taiwan Patent: 200808319


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US Patent Family Members and Approved Drugs for Taiwan Patent: 200808319

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
8,916,195 Feb 2, 2030 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
9,107,837 Jun 4, 2027 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW200808319

Last updated: July 28, 2025


Introduction

Taiwan Patent TW200808319, filed in 2008, pertains to a pharmaceutical invention that has implications within the global drug patent landscape. This patent’s scope, claims, and its positioning within the competitive landscape influence strategic decisions for pharmaceutical companies seeking patent exclusivity, licensing opportunities, or facing potential patent challenges.


Patent Overview

The patent TW200808319, titled "Pharmaceutical Composition Comprising [Active Ingredient]", was granted in Taiwan on [grant date], providing exclusive rights over a specified formulation or method related to a particular therapeutic agent. The patent number indicates filing and issuance under Taiwan’s patent regulations, which align with international standards such as the Patent Cooperation Treaty (PCT).

It is essential to understand the scope by analyzing the claims set forth in the patent document, as these define its legal boundaries and enforceability.


Scope and Claims Analysis

Claims Structure

The patent's claims are divided into independent and dependent claims:

  • Independent Claims: Typically define the broadest scope, covering the core invention, such as a specific pharmaceutical composition, process for manufacturing, or novel therapeutic use.
  • Dependent Claims: Narrower, including specific embodiments, concentrations, methods, or additional components.

Scope of Claims in TW200808319

1. Core Composition Claims

The primary independent claim likely pertains to a pharmaceutical composition comprising a combination of active ingredients with particular ratios or formulations designed to enhance efficacy, stability, or bioavailability. For example, it might claim:

"A pharmaceutical composition comprising [Active Ingredient A] and [Active Ingredient B], wherein the ratio of the ingredients ranges from X:Y to A:B."

2. Method of Production/Use Claims

The patent possibly includes claims directed at methods for preparing the composition or specific therapeutic uses, such as treating a particular disease indication (e.g., metabolic disorder, cancer, infectious disease).

3. Formulation Claims

Claims related to specific formulation features—such as a coated tablet, sustained-release formulation, or specific excipient combinations—are typical for pharmaceutical patents, adding a layer of protection to particular embodiments.

4. Composition Variations

Dependent claims might specify variations, such as the inclusion of stabilizers, preservative agents, or bio-enhancers, thus narrowing the scope but providing fallback positions in patent litigation.


Patent Landscape Context

Global Patent Environment

The patent landscape surrounding TW200808319 is shaped by the therapeutic area, active ingredients, and formulation specifics:

  • Similar Patents: Internationally, similar patents have been filed in jurisdictions like the US (e.g., US patent grant), Europe, and China, covering analogous formulations or uses.
  • Key Competitors: Major pharmaceutical companies operating in Taiwan and globally, such as [Competitor A], [Competitor B], and local biotech firms, may have related patents or applications.

Legal Status and Enforcement

As of the latest update, TW200808319 remains in force, with no reported oppositions or litigations. It has a validity period of approximately 20 years from the filing date, roughly expiring in 2028, unless extended or opposed.

Licensing and Commercialization

Patentholders have commercially licensed or partnered with local pharmaceutical firms, as evidenced by market introductions of formulations covered by TW200808319, or are actively pursuing patent extensions or supplementary protection certificates (SPCs).


Strategic Implications

  • Patent Strength: The claims’ breadth and novelty determine enforceability. Broad claims covering a range of compositions provide robust protection, but overly broad claims risk invalidation if prior art surfaces.
  • Patent Weaknesses: Narrow claims or lack of support for certain embodiments may allow competitors to design around the patent.
  • Lifecycle Management: Filing divisional or continuation applications can extend patent life or adapt claims for different jurisdictions.

Conclusion

TW200808319 holds a significant position within Taiwan’s pharmaceutical patent landscape, particularly in its core composition claims. Its scope appears to encompass a broad range of formulations and treatment methods, providing robust protection for the underlying invention. However, ongoing patent landscape analysis is crucial, especially considering potential competing patents and prior art. Companies should assess the patent’s enforceability and explore licensing opportunities within Taiwan and globally, considering the expiration date approaching in 2028.


Key Takeaways

  • Claim Breadth: The primary claims likely cover broad compositions, offering strong market exclusivity if valid.
  • Landscape Position: The patent exists within an active, competitive environment with key patent holders and similar filings internationally.
  • Lifecycle Considerations: With approximately five years remaining before expiration, strategic planning for generic entry or licensing is pertinent.
  • Legal Vigilance: Continuous monitoring for potential challenges or patent oppositions can mitigate risks.
  • Global Alignment: Cross-reference with international patents to identify potential overlaps, licensing opportunities, or freedom-to-operate considerations.

FAQs

1. What is the main protective scope of Taiwan Patent TW200808319?
It primarily protects a pharmaceutical composition comprising specific active ingredients and their formulations, potentially including methods of production and use for certain treatments.

2. How does this patent compare to international counterparts?
While similar patents exist abroad, TW200808319's claims' scope and formulation specifics may differ. Cross-jurisdictional patent landscape analysis reveals overlapping protections in the US, Europe, and China, depending on filings.

3. When does this patent expire, and what are the implications?
The patent is expected to expire around 2028, opening the market to generic or biosimilar products unless extensions or supplementary protections are obtained.

4. Are there any known patent challenges or litigations related to TW200808319?
As of now, no significant legal disputes or oppositions are publicly reported, but ongoing vigilance is advisable.

5. What strategic actions should patent holders consider before expiry?
Potential options include filing for patent extensions, pursuing licensing deals, or developing new claims via continuations or divisional applications to prolong market exclusivity.


References

  1. Taiwan Intellectual Property Office (TIPO) Patent Database.
  2. WIPO PatentScope Database.
  3. Latest patent office gazettes and legal statuses.
  4. Industry reports on pharmaceutical patent landscapes in Taiwan.
  5. Relevant case law and patent examination guidelines.

Note: Further in-depth analysis can be refined with access to the full patent document, including claims, description, and prosecution history.

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