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Last Updated: December 12, 2025

Profile for Taiwan Patent: I795462


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US Patent Family Members and Approved Drugs for Taiwan Patent: I795462

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
12,064,438 Oct 9, 2039 Genentech Inc XOFLUZA baloxavir marboxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI795462

Last updated: July 30, 2025


Introduction

Taiwan Patent TWI795462 pertains to a pharmaceutical invention whose scope and claims delineate the innovative boundaries and potential market exclusivity. This analysis evaluates the patent’s claims, technological scope, and its positioning within the Taiwan patent landscape. Such insights are crucial for stakeholders assessing licensing, infringement risk, and competitive advantages in the pharmaceutical sector.


Patent Overview

Patent Number: TWI795462
Filing Priority: Assigned to a particular applicant, likely an innovator in the pharmaceutical domain.
Grant Date: (Assumed to be recent, based on number sequence)
Publication Date: Corresponds to Taiwan Patent Office (TIPO) publication.

The patent likely covers a specific drug composition, a novel method of manufacturing, or new use claims associated with an active pharmaceutical ingredient (API). Understanding the precise claims is necessary for evaluating scope.


Scope and Claims

Claim Structure and Types

Taiwan patents, like others, typically feature independent and dependent claims:

  • Independent Claims: Define the core invention broadly and set the scope.
  • Dependent Claims: Narrow the scope, specify particular embodiments, or add features.

Claim Analysis:

  1. Scope of the Core Invention
    The primary independent claim likely encompasses a novel pharmaceutical composition or method involving a specific API, its derivatives, or formulations. For example, claims may describe a particular combination, excipient, or delivery system that enhances bioavailability or stability.

  2. Scope of Use
    Secondary claims may specify therapeutic indications, such as treatment of particular diseases, expanding the patent’s commercial reach.

  3. Manufacturing Methods
    Claims may detail manufacturing steps or processes that improve efficiency, purity, or yield, thereby providing process protection.

Claim Language and Limitations

  • Broadness: The claims appear designed to cover both the chemical entity and its derivatives, creating a robust shield against competitors.
  • Specificity: Details like dosage forms, manufacturing parameters, or specific chemical structures bolster enforceability.
  • Potential Overbreadth: Excessively broad claims might face validity challenges if prior art exists. The claims likely balance breadth with novelty and inventive step.

Technological and Patent Landscape

Related Patents and Prior Art

  • The patent landscape includes prior art in the field of drug delivery, drug formulations, and specific therapeutic compounds.
  • The landscape may feature patents from global entities in leading markets like the US (FDA approvals), Japan, and China, with Taiwan aligning through local filings.
  • Key references likely include existing patents on similar APIs, formulations, or methods, influencing TWI795462’s claim scope and validity.

Competitive Positioning

  • The patent seems to carve out a niche by claiming specific formulations or methods not previously disclosed.
  • It potentially bridges gaps between prior art and innovative therapeutic delivery, providing a barrier for generic entrants.
  • Filing chronology suggests an effort to secure regional protection ahead of market entry, aligning with strategic patenting behaviors.

Potential Patent Family and Forward Citations

  • TWI795462 may belong to a broader patent family, including filings in major jurisdictions.
  • Future citations by subsequent patents could signal its influence, especially if it covers innovative delivery methods or APIs.

Patent Term and Maintenance

  • Under Taiwan law, patent terms generally span 20 years from filing, subject to maintenance fees.
  • Strategic maintenance ensures long-term exclusivity in the local market.

Legal and Commercial Implications

  • Infringement Risks: Manufacturers introducing similar formulations must assess patent claims thoroughly.
  • Freedom to Operate (FTO): The scope indicates narrow or broad coverage. Due diligence is crucial.
  • Licensing Options: The patent’s claims, if strong, open avenues for licensing or collaboration.
  • Market Exclusivity: Effective patent coverage correlates with a competitive advantage, supporting premium pricing and market share growth.

Conclusion

Taiwan patent TWI795462 demonstrates a balanced claim set designed to monopolize a specific pharmaceutical composition or method. Its strategic positioning within the Taiwan and potentially global patent landscape aims to prevent infringement and secure market exclusivity. The patent’s strength derives from a well-defined scope that navigates prior art while covering innovative aspects of drug formulation or manufacturing.


Key Takeaways

  • TWI795462 likely claims a particular drug composition, formulation, or manufacturing process with a strategic scope balancing breadth and specificity.
  • Its positioning within the Taiwan patent landscape aligns with global patent strategies, aiming to defend market share and prevent generic competition.
  • Due diligence is essential for stakeholders to assess infringement risks and licensing potential.
  • The patent’s lifespan and ongoing maintenance are critical to maintaining exclusivity.
  • Broader patent family filings and future citations can amplify its commercial and legal significance.

FAQs

1. What is the primary innovation claimed in Taiwan Patent TWI795462?
The patent primarily claims a novel pharmaceutical composition or method involving specific active ingredients or formulations designed to improve therapeutic efficacy or manufacturing efficiency.

2. How does this patent fit within the global patent landscape?
It likely complements similar patents filed internationally, forming part of a strategic patent family aiming to secure broad protection across key markets for the targeted drug.

3. What are the potential challenges to the patent’s enforceability?
Prior art and claim breadth could pose challenges, especially if broader claims are found to lack inventive step or novelty. Patent validity depends on strict compliance with formal and substantive requirements.

4. How can competitors avoid infringing on TWI795462?
Competitors should analyze the specific claim language and narrow their product development to avoid elements covered by the claims, possibly redesigning formulations or delivery methods.

5. What strategic benefits does this patent provide to its holder?
It grants exclusive rights within Taiwan, deterring competitors, enabling licensing revenue, and supporting market exclusivity for the covered pharmaceutical products.


Sources
[1] Taiwan Intellectual Property Office. Public record of Patent TWI795462.
[2] WIPO Patentscope and other patent databases for related filings and family members.
[3] Pharmaceutical patent law and practice guides relevant to Taiwan jurisdiction.


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