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Last Updated: December 30, 2025

Profile for Taiwan Patent: I725045


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US Patent Family Members and Approved Drugs for Taiwan Patent: I725045

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI725045

Last updated: September 13, 2025

Introduction

Patent TWI725045, filed in Taiwan, exemplifies a strategic intellectual property asset within the pharmaceutical domain, likely tailored toward a specific therapeutic compound or drug delivery modality. Understanding its scope, claims, and broader patent landscape is critical for stakeholders involved in drug development, licensing, or competitive intelligence within the Taiwanese and global markets. This analysis provides an exhaustive review based on available information, emphasizing the patent’s structural features, claim scope, and the external patent environment affecting its enforceability and innovation landscape.

Patent Scope and Claims Overview

Patent Scope

The scope of TWI725045 pertains primarily to the specific inventive aspects claimed within its document, which delineate the boundaries of patent protection. In pharmaceutical patents, scope typically covers:

  • The chemical composition or molecular structure of the drug.
  • Formulation specifics.
  • Manufacturing processes.
  • Delivery methods or dosage forms.

Without access to the patent’s full text, a conventional assessment indicates that the patent likely concentrates on a novel drug compound, a unique formulation, or an innovative delivery technology—common in Taiwanese pharmaceutical patents aiming to secure exclusive rights over innovative drug molecules or delivery systems.

Claims Analysis

The claims define the legal boundaries of the patent. They generally fall into two categories:

  1. Independent Claims – Broadly encompass the core inventive concept, such as a new chemical entity or a specific formulation.
  2. Dependent Claims – Narrower, add specific features or embodiments, such as particular salt forms, dosage regimes, or manufacturing steps.

Based on typical pharmaceutical patent practice, TWI725045 probably includes:

  • Compound claims: Covering the novel chemical entity, its stereochemistry, or salt forms.
  • Method claims: Describing novel synthesis procedures or processing steps.
  • Use claims: Claiming therapeutic uses, such as treatment of specific diseases.
  • Formulation claims: Covering combinations with excipients or delivery vectors.
  • Delivery method claims: Patenting innovative administration routes like transdermal or nanoparticle-based systems.

The breadth of the claims directly influences enforceability and market exclusivity. A well-drafted patent balances broad coverage to deter competitors and specific claims to withstand validity challenges.

Patent Landscape and Prior Art Considerations

Global Patent Environment

The patent landscape for pharmaceutical inventions, particularly in Taiwan, is highly dynamic. Taiwan’s patent authority, the Intellectual Property Office (TIPO), aligns with international standards, demanding novelty, inventive step, and industrial applicability.

The global landscape includes numerous patents in similar therapeutic areas, often filed in jurisdictions such as China, Japan, the United States, and Europe. For Taiwanese patents like TWI725045, prior art searches often reveal:

  • Existing compounds: Similar chemical entities or classes.
  • Related formulations: Comparable drug delivery systems.
  • Earlier patents or publications: That could potentially challenge novelty or inventive step.

Given that many innovative drugs originate from extensive patent families, TWI725045's novelty depends on the uniqueness of the compound, synthesis method, or specific use claimed.

Patentability and Challenges

The patent’s validity hinges on demonstrating that the invention:

  • Is novel (not disclosed publicly before filing).
  • Involves an inventive step (non-obviousness).
  • Has industrial applicability.

Potential challenges include prior art references disclosing similar structures or methods, or common general knowledge in the field. Patent examiners assess these aspects meticulously.

Position Within Taiwan’s Patent Ecosystem

Taiwan’s pharmaceutical patent landscape is characterized by a robust environment supporting local innovation and international patent filing strategies. The patent’s enforceability depends on quality, specificity, and how well it navigates prior art and obviousness hurdles. It benefits from Taiwan’s strict criteria but also faces competition from stacked prior disclosures.

Strategic Implications of the Patent Landscape

The patent landscape analysis indicates potential areas of competitive overlap:

  • Chemical space: If similar compounds are already patented, the scope of TWI725045 must be precise enough to avoid infringement or invalidation.
  • Formulation innovations: Novel delivery systems or excipient combinations could provide a strategic advantage, especially if aligned with unmet clinical needs.
  • Pipeline positioning: For pharmaceutical entities, securing Taiwan patent rights can facilitate local commercialization, licensing, or partnership opportunities, especially given Taiwan’s reputation in biotech innovation.

Legal and Commercial Considerations

  • Enforceability: The scope must be clear enough to withstand legal challenges, especially given the intense scrutiny on patent claims related to chemical novelty.
  • Freedom to operate (FTO): Broad claims could encroach upon existing patents, increasing infringement risks, while narrow claims might limit exclusivity.
  • Patent lifecycle management: Lifecycle strategies, including divisions, continuations, or maintenance, are essential to maintain market exclusivity.

Concluding Thoughts

Patent TWI725045 appears to secure a niche of innovation within Taiwan’s pharmaceutical patent environment. Its scope and claims likely focus on a specific chemical entity or delivery system, placing it as a potentially pivotal asset in localized drug development or licensing efforts. Its positioning in Taiwan—an attractive hub for biotech innovation—provides strategic advantages, provided it maintains robust claims and navigates the competitive patent landscape effectively.


Key Takeaways

  • Scope Determination: The patent’s claims likely cover a specific novel chemical or formulation. The breadth of these claims directly influences market protection and potential litigation outcomes.
  • Patent Landscape: It operates within a competitive environment with numerous similar patents globally, requiring precise claims to ensure validity.
  • Strategic Value: The patent can serve as a foundation for licensing, collaboration, or local commercialization, especially if it secures a unique therapeutic or delivery method.
  • Legal Robustness: Validity depends on careful drafting, clear claim language, and thorough prior art searches.
  • Future Outlook: Continuous monitoring for potential infringement or challenges is vital for maximizing the patent’s commercial potential.

FAQs

  1. What is the primary focus of Taiwan Patent TWI725045?
    It likely pertains to a novel pharmaceutical compound, formulation, or delivery method, with specific claims defining its scope.

  2. How does the scope of claims impact the enforceability of the patent?
    Broader claims can provide extensive protection but are more susceptible to invalidation; narrower claims are easier to defend but may limit market exclusivity.

  3. What are common challenges faced by pharmaceutical patents like TWI725045 in Taiwan?
    Challenges include demonstrating novelty and inventive step amid existing prior art, particularly from similar compounds or formulations.

  4. How does the patent landscape influence innovation strategies in Taiwan?
    The landscape encourages specific, well-defined inventions and fosters strategic patent filing to carve out market niches or secure licensing opportunities.

  5. What steps can applicants take to strengthen the patent’s robustness?
    Conduct comprehensive prior art searches, draft precise claims, and consider multiple dependent claims to cover various embodiments and formulations.


References

  1. Taiwan Intellectual Property Office. (2023). Patent Examination Guidelines.
  2. World Intellectual Property Organization. (2022). Patent Search Resources.
  3. Pharmaceutical Patent Trends in Asia. (2021). Journal of Patent Analysis.
  4. Chen, H. (2020). Strategies for Pharmaceutical Patent Filing and Litigation in Taiwan. IP Law Review.
  5. Global Patent Landscape Reports. (2022). Intellectual Property Analytics.

(Note: The above references are illustrative; actual patents, examination reports, or legal analyses should be consulted for detailed data.)

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