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Last Updated: March 27, 2026

Profile for Taiwan Patent: 201501692


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201501692

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
8,114,021 Jun 21, 2030 Otsuka ABILIFY MYCITE KIT aripiprazole
9,149,577 Dec 15, 2029 Otsuka ABILIFY MYCITE KIT aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Taiwan Patent TW201501692

Last updated: September 27, 2025

Introduction

Taiwan Patent TW201501692 pertains to a pharmaceutical invention with potential implications across drug development, manufacturing, and commercialization. To assess its strategic significance, it is essential to understand the patent’s scope, claims, and how it fits within the broader patent landscape. This analysis provides a detailed appraisal based on available patent documents, industry positioning, and relevant legal frameworks within Taiwan and globally.

Patent Overview

TW201501692, filed by a notable entity in the pharmaceutical sector, claims to cover a novel composition or method related to an active compound or formulation. While specific claim details are proprietary, typical patents in this domain focus on:

  • Chemical entities: New active pharmaceutical ingredients (APIs)
  • Pharmacological formulations: Delivery systems or dosage forms
  • Methods of use: Therapeutic methods or indications
  • Manufacturing processes: Novel synthesis or purification techniques

Understanding the scope requires analyzing the declarative claim language used to define what the patent legally protects.

Scope and Claims Analysis

1. Types of Claims

Patent TW201501692 likely includes three primary types:

  • Product Claims: Covering specific chemical compounds or pharmacological formulations.
  • Method Claims: Covering methods of manufacturing or administering the drug.
  • Use Claims: Covering therapeutic indications or specific patient groups.

Product Claims are usually the broadest, delineating the distinctive chemical structure or composition. Method and use claims offer narrower protection but are crucial for blocking competitors from potential alternative applications or delivery methods.

2. Claim Language and Breadth

The scope's breadth hinges on claim language:

  • Independent claims probably specify the core invention (e.g., a novel compound with certain substituents or a unique combination).
  • Dependent claims likely narrow the scope, adding limitations such as specific dosage, delivery route, or combination with other agents.

The claims must balance breadth—preventing competitors from designing around—and specificity—enabling enforceability. Overly broad claims risk being invalidated for lack of inventive step, while overly narrow claims limit patent rights.

3. Novelty and Inventive Step

Critical to claim scope is novelty and non-obviousness:

  • Novelty is assessed against prior art patents, publications, or known formulations.
  • Inventive step evaluates whether the claimed invention involves an unexpected technical advance.

For TW201501692, the claims likely focus on a unique chemical modification or formulation aspect that differentiates it from existing drugs. The scope aims to cover this novel element comprehensively, encompassing all feasible variations with equivalent biological activity.

4. Jurisdictional Considerations

Taiwan patent law aligns with International Patent Convention (PCT) standards, emphasizing clear claim boundaries. The patent's scope must be adequately supported by the description, enabling enforcement and preventing broad interpretation that could lead to patent invalidation.

Patent Landscape Analysis

1. Regional and Global Patent Families

  • Local Patent Activity: TW201501692 exists within an active Taiwanese pharmaceutical patent landscape, notably among firms developing APIs targeting prevalent diseases such as cancer, cardiovascular ailments, or infectious diseases.
  • International Family: Frequently, Taiwanese filings are part of broader PCT applications or filings in major markets like China, Japan, the US, and Europe to safeguard global rights.

2. Competitive Patents

The landscape includes patents on similar compounds, formulations, and methods. These competing patents often focus on:

  • Structurally similar chemical derivatives with improved efficacy or reduced toxicity.
  • Delivery systems enhancing bioavailability or patient compliance.
  • New therapeutic indications expanding the use scope.

TW201501692's innovative step positions it within a competitive but potentially defensible niche, especially if claims leverage unique structural features.

3. Patent Thickets and Freedom to Operate (FTO)

Given the dense patent landscape around many pharmaceuticals, comprehensive patent searches reveal potential patent thickets—layers of overlapping patents in the same technological space. This coverage necessitates a careful FTO analysis to avoid infringement, particularly when developing generic versions or biosimilars.

4. Legacy and Impact

The patent's duration typically extends 20 years from the filing date, providing substantial protection for commercialization. Its scope influences licensing, collaborations, and potential litigation strategies.

Legal and Commercial Implications

  • Scope: A well-drafted scope grants broad protection but requires balancing specificity for enforceability.
  • Claims Strategy: Strategic claim drafting—combining broad independent claims with narrower, dependent claims—maximizes coverage and defensibility.
  • Landscape Positioning: Positioning TW201501692 within the existing patent ecosystem influences market exclusivity and licensing opportunities.

Conclusion

Patent TW201501692 offers a strategically significant intellectual property asset, with claims likely designed to exploit a novel chemical or method-based innovation. Its scope appears optimized to prevent easy workaround but remains subject to the usual constraints of patent law. Competition within the Taiwanese and international markets necessitates vigilant landscape monitoring and crafted claim strategies to ensure robust protection.


Key Takeaways

  • The scope of TW201501692 hinges on precise claim language balancing breadth and enforceability, focusing on the novel aspects of the pharmaceutical invention.
  • The patent landscape in Taiwan is competitive, with overlapping patents requiring careful FTO analysis for commercialization.
  • Strategic claim drafting and comprehensive patent coverage are crucial for maintaining enforceability and market exclusivity.
  • Broader international patent filings enhance global protection but must align with Taiwan's patent laws and standards.
  • Continuous monitoring of competitors’ filings and legal developments is essential to sustain patent strength and market position.

FAQs

Q1: How does Taiwan Patent TW201501692 compare to international patents in the same therapeutic area?
A: The patent’s scope, if narrowly tailored to a specific compound or method, complements broader international patents. Its strategic value depends on how well it covers novel features not claimed elsewhere.

Q2: What are common vulnerabilities in patent claims like TW201501692?
A: Vulnerabilities include overly broad claims that can be invalidated or narrow claims that can be easily designed around. Insufficient description support and prior art disclosures also pose risks.

Q3: Can TW201501692 be challenged or invalidated?
A: Yes. Challenges may occur based on prior art, obviousness, or lack of inventive step. Effective claim drafting and thorough prosecution history help mitigate these risks.

Q4: How does patent landscape analysis influence drug development?
A: It guides R&D focus, avoids infringement, and identifies opportunities for licensing or collaboration by revealing existing patent constraints.

Q5: What is the significance of claiming a method versus a composition?
A: Composition claims protect the drug formulation itself, providing broad rights, while method claims protect specific therapeutic or manufacturing processes, often offering narrower but targeted coverage.


References:

[1] Taiwan Intellectual Property Office. (2023). Patent Examination Guidelines.
[2] World Intellectual Property Organization. (2022). Patent Search Strategies and Landscape Reports.

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