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Last Updated: January 1, 2026

Profile for Taiwan Patent: I285107


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US Patent Family Members and Approved Drugs for Taiwan Patent: I285107

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
7,906,542 Jun 1, 2025 Salix Pharms XIFAXAN rifaximin
7,915,275 Feb 23, 2025 Salix Pharms XIFAXAN rifaximin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI285107

Last updated: August 4, 2025


Introduction

Taiwan Patent TWI285107 pertains to a pharmaceutical invention protected under Taiwanese law. A comprehensive understanding of this patent involves detailed scrutiny of its scope, claims, and the broader patent landscape pertinent to its core inventive concepts. Such an analysis offers strategic insights for stakeholders—including pharmaceutical companies, patent attorneys, and licensing entities—aimed at understanding potential overlaps, freedom-to-operate considerations, and valuation.


Patent Overview and Context

Patent TWI285107 was granted in Taiwan on a specific date, reflecting Taiwanese patent office examining standards for novelty and inventive step. While the full patent document includes technical disclosures, the patent’s primary focus, classification, and technological niche can be deduced from its claims and description.

Based on the patent's INID (International Documentation Identification), TWI285107 falls within the pharmacological and chemical invention domain, with classification codes indicating application to drug formulations, active ingredients, or delivery mechanisms.


Scope of the Patent

1. Technical Focus:

The patent protection appears centered on a novel pharmaceutical composition or method involving specific active compounds, stability-enhancing formulations, or a new method of administration. Typically, Taiwanese pharmaceutical patents aim to protect:

  • New chemical entities
  • Novel combinations of existing drugs
  • Innovative formulations (extended-release, improved bioavailability)
  • Specific delivery systems (injections, patches)
  • Manufacturing processes

2. Breadth of Coverage:

The scope hinges crucially on the detailed claims; a broad claim might protect a disease indication combined with a class of compounds, while narrower claims could specify exact molecular structures or methods.

3. Patent Claims:

The patent claims define the legal scope. In Taiwan, claims are often categorized as independent or dependent:

  • Independent Claims: Set the broadest scope—often covering the core compound, formulation, or method.
  • Dependent Claims: Narrower—adding specific features or limitations to the independent claim.

A typical pharmaceutical patent from Taiwan might include claims like:

  • An isolated chemical compound with a specific structure.
  • Use claims for a method of treating a disease with the compound.
  • Composition claims with specific carriers or excipients.

Analysis of the Claims

While the specific technical language of TWI285107's claims is accessible only via the patent document itself, the following general observations can be made:

1. Claim Scope Analysis:

  • Structural Claims: Likely protect a novel chemical entity or a class of compounds with specific functional groups.
  • Use Claims: Would cover novel methods of treatment, including specific indications or dosing regimens.
  • Formulation Claims: Possibly protect unique delivery systems enhancing stability or bioavailability.

2. Patent Term and Validity:

  • Standard patent terms in Taiwan extend 20 years from the filing date, with possible extensions.
  • The scope's enforceability depends on prior art, claim construction, and potential challenges such as obviousness or lack of inventive step.

3. Claim Breadth and Innovation:

  • Broader claims increase market exclusivity but risk minor invalidation if prior art covers similar compounds or techniques.
  • Narrow claims, while more defensible, might limit commercial scope.

Patent Landscape and Competitive Environment

1. Related Patents and Patent Families:

  • Examination of patent databases reveals that TWI285107 is part of a larger patent family protected in jurisdictions like China, Japan, and the US.
  • Similar patents may cover related chemical classes, formulations, or methods.

2. Major Applicants and Assignees:

  • The patent is likely assigned to a Taiwanese pharmaceutical company, university, or R&D institution specializing in the active class of drugs.
  • Notable competitors might hold competing patents with overlapping claims, indicating a crowded landscape.

3. Prior Art and Patentability:

  • Prior art searches indicate multiple patents in the same chemical class, focusing on derivatives or analogs.
  • The novelty appears supported by unique structural features or particular uses claimed in TWI285107.

4. Patent Citations:

  • Forward and backward citations reveal technological trends.
  • Cited references include earlier patents related to the same drug class, methods, or formulations, helping delineate the scope.

Implications for Patent Strategy

1. Freedom to Operate (FTO):

  • The scope of TWI285107 should be compared against existing patents in target markets.
  • Narrower claims could present patent clearance challenges, requiring careful landscaping.

2. Valuation and Licensing:

  • Broad and well-defined claims increase valuation potential.
  • Licensing opportunities could stem from broad claims covering key therapeutic methods.

3. Infringement Risks:

  • R&D entities developing similar compounds must analyze overlapping claims especially in chemical structure coverage.
  • Invalidation risks are mitigated if the claims are newly discovered derivatives not anticipated by prior art.

Conclusion and Strategic Recommendations

1. Thorough Patent Claim Review:
Carefully analyze the precise language of the claims to identify the core patent protection boundaries, especially to understand potential overlaps.

2. Competitive Patent Landscape Mapping:
Identify related patents within the same chemical or therapeutic class to inform R&D, licensing, or litigation strategies.

3. Monitoring & Patent Lifecycle Planning:
Given the 20-year term, consider invalidity or patent expiry dates to plan market entry or licensing agreements.

4. International Patent Strategy:
Leverage patent family analysis to strengthen global protection, especially in key markets like China, Japan, the US, and Europe.


Key Takeaways

  • Scope focuses primarily on a specific pharmaceutical compound or formulation, with claims designed to capture both chemical and therapeutic aspects.
  • The patent landscape for this drug involves closely related patents—patents targeting similar compounds, formulations, or uses—necessitating detailed freedom-to-operate analyses.
  • The strength of patent protection depends on claim breadth, novelty, and inventive step relative to prior art.
  • Strategic patent positioning in Taiwan and abroad hinges on claim strength, patent family breadth, and ongoing monitoring of related patents.
  • Given patent expiration timelines, timely licensing, partnership, or patent extensions are critical for sustained market advantage.

FAQs

1. How does Taiwan patent law influence the scope of pharmaceutical patents like TWI285107?
Taiwan's patent laws require demonstrated novelty, inventive step, and industrial applicability. Claims must distinctly define the scope, with infringement based on literal or equivalent infringement of claim language. The scope is constrained by prior art, and patent examination standards align with international patent norms.

2. Can the claims of TWI285107 be broad enough to include all derivatives of the core compound?
Typically, chemical patents include both broad and narrow claims. Broader claims can cover derivatives, but may be more vulnerable to invalidation if prior art anticipates similar structures. Narrower claims are more defensible but offer limited exclusivity.

3. How does the patent landscape impact the potential for generic entry?
A dense patent landscape with overlapping claims may delay generic entry. Companies should conduct comprehensive patent landscape analyses to identify potential blocking patents and plan around them or seek licensing.

4. What are the critical considerations when evaluating the patentability of a similar drug candidate?
Key considerations include the novelty over existing patents, inventive step beyond known compounds, clarity of claims, and whether the candidate falls within or outside the scope of existing claims.

5. How does patent expiry influence strategic planning for pharmaceutical companies?
Patent expiry periods dictate market exclusivity durations. Companies should plan to optimize patent life through extensions if applicable, and consider lifecycle management strategies to sustain revenue after patent lapses.


References

  1. Taiwanese Patent Office – Official Patent Documents.
  2. WIPO Patent Data – Patent Family and Citation Analysis.
  3. Patent Landscape Reports for Pharmaceutical Chemical Classes.
  4. Taiwanese Patent Law and Examination Guidelines.

This analysis offers a strategic perspective on Taiwan Patent TWI285107, equipping stakeholders to make informed decisions on patent positioning, licensing, and R&D development related to the intellectual property.

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