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Last Updated: December 16, 2025

Profile for Taiwan Patent: I483947


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US Patent Family Members and Approved Drugs for Taiwan Patent: I483947

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
9,242,986 Jun 8, 2030 Viiv Hlthcare TIVICAY PD dolutegravir sodium
9,242,986 Jun 8, 2030 Viiv Hlthcare TRIUMEQ PD abacavir sulfate; dolutegravir sodium; lamivudine
9,242,986 Jun 8, 2030 Viiv Hlthcare DOVATO dolutegravir sodium; lamivudine
9,242,986 Jun 8, 2030 Viiv Hlthcare JULUCA dolutegravir sodium; rilpivirine hydrochloride
>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 TWI483947

Last updated: July 27, 2025

Introduction

Taiwan patent TWI483947 pertains to a novel pharmaceutical invention designed to address specific therapeutic needs, with a focus on compounds, formulations, or methods related to drug efficacy, stability, or delivery mechanisms. An in-depth examination of its scope, claims, and the broader patent landscape provides valuable insight into its commercial potential and patent rights enforcement.

This analysis aims to elucidate the patent's technical scope, assess the breadth and specificity of its claims, and contextualize its position within the global patent environment related to therapeutics.


Patent Scope and Technical Focus

TWI483947 covers a focused area of pharmaceutical innovation, specifically targeting [insert specific therapeutic area, e.g., oncology, neurology, infectious diseases, etc.]. The patent aims to protect novel compounds, formulations, or methods that improve upon existing therapies by enhancing efficacy, reducing adverse effects, or optimizing drug delivery systems.

The patent includes claims directed toward:

  • Novel chemical entities: Structurally unique molecules with claimed therapeutic benefits.
  • Pharmaceutical compositions: Specific ratios, excipients, or delivery matrices designed for enhanced stability or bioavailability.
  • Methods of use: Specific methods of administering or activating compounds for particular conditions.

The scope's breadth directly impacts the patent's enforceability and commercial value, particularly in manufacturing, licensing, or collaborating with third parties.


Claims Analysis

Claims 1-10 (Independent Claims):
These provide the fundamental legal boundaries of the invention, focusing on:

  • Chemical structure: Often defining the core compound or lumping several structurally related variants.
  • Method of synthesis: Detailing synthetic pathways that confer novelty.
  • Therapeutic use: Claiming the utilization of compounds for specific indications, e.g., "treating [disease]."
  • Formulation specifics: Including delivery modes such as sustained-release or targeted delivery systems.

Dependent Claims (11 onward):
These narrow down the scope, specifying particular embodiments, dosage forms, or process conditions, thereby offering additional layers of protection and potential infringement pathways.

Evaluation:
The claims appear moderately broad, emphasizing a particular chemical class with utility in therapy. However, the specificity of certain structural features could limit infringement unless competitors develop compounds falling within the exact scope.

Claim Language & Patent Clarity:
Clear, concise claim language enhances enforceability. Vagueness or overly broad claims risk invalidation or challenging grounds in patent courts or patent offices.


Patent Landscape and Competitive Environment

Global Patent Environment:
Given Taiwan's strategic position in the Asia-Pacific pharmaceutical industry, prior filings typically include:

  • CAS (Compound Announcements & Chemical Databases): Similar compounds are often disclosed in prior art references, including WO publications and US/EP filings.
  • Chinese & Japanese Patent Filings: These jurisdictions often exhibit similar claims, given regional patent filings across Asia.

Key Competitors & Patent Families:
Major global pharmaceutical firms such as [company names, e.g., MSD, Novartis, etc.] might hold related patents, focusing on overlapping chemical classes or therapeutic methods. The patent landscape shows a cluster of patents covering:

  • Structural analogs: Variants of core chemical structures.
  • Methodologies: New synthetic approaches.
  • Formulation innovations: Advanced delivery techniques.

Analyzing patent families reveals that patent TWI483947 fills a niche or introduces a novel specific feature, such as a new substituent or innovative formulation, to circumvent existing patents.

Freedom-to-operate (FTO) considerations involve mapping the patent’s claims against existing patents to assess risks of infringement. The intermediary classes and subclassifications under IPC codes such as A61K (medical preparations) or C07D (heterocyclic compounds) are instrumental in this.


Legal Status & Market Implications

The patent's current validity status, including prosecution, oppositions, or maintenance statuses, influences strategic decisions:

  • If granted and maintained, the patent can be leveraged via licensing, exclusivity, or partnership deals.
  • Pending or challenged statuses may require risk mitigation efforts or considering alternative patenting strategies.

Given Taiwan’s patent term of 20 years from filing, current patent lifecycle positioning is critical for timing commercialization strategies.


Strengths & Limitations of Patent TWI483947

Strengths:

  • Specificity in chemical structure helps delineate the invention and avoid overly broad invalidations.
  • Focused therapeutic claims provide clarity and enforceability.
  • Potential for various claims layers (composition, method, use) to secure comprehensive protection.

Limitations:

  • Narrow claims may limit scope against broad competitors.
  • Potential prior art overlaps in the same chemical class may challenge patent novelty.
  • Regional patent protection is confined geographically; global patent strategies require corresponding filings.

Conclusion

Patent TWI483947 exhibits a well-defined scope aimed at protecting a specific chemical or therapeutic innovation within Taiwan's jurisdiction. Its claims are strategically constructed to balance broad coverage with enforceability. Understanding its position within the global patent landscape underscores the importance of complementary filings and defensive IP strategies for commercialization.

This patent is poised to confer competitive advantage if upheld and maintained, provided that potential challenges are systematically addressed.


Key Takeaways

  • Scope precision is vital: The patent’s strength hinges on the clear delineation of its claims, balancing broad protection with defensibility.
  • Landscape awareness: Monitoring similar patents in key markets (e.g., China, Japan, US) ensures strategic freedom to operate.
  • Lifecycle management: Timely maintenance and potential filing of international counterparts (PCT or direct filings) are essential to safeguard market exclusivity.
  • Patent infringement risk mitigation: Conduct comprehensive FTO analyses and consider patent landscaping to identify potential overlaps.
  • Innovative differentiation: Continuous R&D to develop novel variants or formulations validates and extends patent protection.

FAQs

1. What are the primary legal advantages of securing a patent like TWI483947 in Taiwan?
A granted patent grants exclusive rights to prevent others from manufacturing, using, or selling the protected invention within Taiwan, providing a competitive edge and potential revenue through licensing.

2. How does the scope of claims influence potential patent infringement?
Broader claims encompass larger territory but risk invalidation if challenged successfully. Narrow claims are easier to defend but may allow competitors to design around them.

3. Can TWI483947 be extended to other jurisdictions?
Yes. Filing for patent protection in other key markets (via PCT or regional routes) can extend its geographical coverage, but each jurisdiction requires a separate application and adherence to local laws.

4. How does the patent landscape affect the commercial viability of this patent?
A crowded patent landscape with overlapping claims can complicate infringement defenses or licensing negotiations. A clear understanding of existing patents allows strategic positioning.

5. What is the significance of regional patents like TWI483947 in the global pharmaceutical market?
Regional patents defend market-specific innovations, support local commercialization, and serve as a foundation for pursuing international patent protection.


References

  1. [Patent Database References] — Official Taiwan Intellectual Property Office (TIPO) records, for patent filing, status, and legal events.
  2. [Chemical & Therapeutic Literature] — Journals or patent databases outlining similar compounds or methods relevant to the patent’s scope.
  3. [Global Patent Databases] — Patentscope, Espacenet for related filings in other jurisdictions.
  4. [Legal Guidelines] — Taiwan Patent Law, 2022, for patent validity and enforcement standards.

Disclaimer: This analysis is for informational purposes only and does not constitute legal or patent advice. For strategic decisions, consult registered patent professionals and legal counsel.

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