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Last Updated: December 28, 2025

Profile for Taiwan Patent: 201444590


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201444590

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
10,188,632 Mar 14, 2033 Abbvie VIBERZI eluxadoline
11,007,179 Mar 14, 2033 Abbvie VIBERZI eluxadoline
11,090,291 Mar 14, 2033 Abbvie VIBERZI eluxadoline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Taiwan Patent TW201444590

Last updated: July 29, 2025

Introduction

Taiwan Patent TW201444590 pertains to innovative developments in pharmaceutical compositions, specifically targeting improvements in drug efficacy, stability, or delivery mechanisms. As part of a comprehensive patent landscape assessment, this analysis dissects the scope of the patent claims, their legal breadth, and the broader innovation environment in Taiwan’s pharmaceutical patent ecosystem.

Patent Overview

TW201444590 was granted in Taiwan, with an effective filing and publication date reflective of a strategic move by the patent holder to safeguard innovation in a competitive pharmaceutical space. Although the detailed patent specification is not provided here, typical patent documents encompass claims, description, and drawings that delineate the scope of the invention.

Based on the standard structure, this patent likely covers a novel pharmaceutical composition, potentially involving active pharmaceutical ingredients (APIs), excipients, or delivery systems designed to enhance therapeutic profiles.

Scope of the Patent Claims

Claims Analysis

The core of the patent’s enforceability lies in its claims, which define the legal boundary. For TW201444590, the claims can be categorized into primary types:

  • Composition Claims: Cover specific formulations, ratios, or combinations of APIs and excipients. These claims often seek protection over the unique blend shown to improve drug stability or bioavailability.

  • Method Claims: Describe particular methods of manufacturing or administering the drug, possibly including novel processes or delivery cycles.

  • Use Claims: Specify the therapeutic uses or indications enabled by the invention—such as treatment for certain diseases or conditions.

Claim Breadth and Specificity: Given the patent’s strategic value, the claims likely aim for broad coverage to prevent easy design-around. However, Taiwanese patent practice emphasizes clarity and specific inventive steps, which may result in narrower claims compared to U.S. or European patents.

Legal and Technical Breadth

  • Independent Claims: Usually encompass the core invention—effective in establishing a broad scope if well-drafted. Their language should specify essential components, ranges, or steps.

  • Dependent Claims: Add further detail and limitations, narrowing scope but reinforcing protection. They often specify alternative embodiments or particular parameter ranges.

Potential for Claim Overlap or Challenges

Given the competitive pharmaceutical landscape in Taiwan and nearby markets, TW201444590’s claims could face challenges based on prior art, especially if similar formulations or methods exist. Patent examiners in Taiwan rigorously assess novelty, inventive step, and industrial applicability, which determines the strength of the patent’s scope.

Patent Landscape Context

Taiwan's Pharmaceutical Patent Environment

Taiwan maintains a robust patent system aligned with international standards, notably the TRIPs Agreement, providing a secure environment for pharmaceutical innovations. The Taiwan Intellectual Property Office (TIPO) carefully examines new patent applications, balancing innovation incentives with public health considerations.

The patent landscape for pharmaceuticals in Taiwan features:

  • High competition among domestic and international pharmaceutical firms.
  • Evergreening strategies, where companies file multiple patents over a drug’s lifecycle.
  • Challenges from generic manufacturers, especially post-patent expiry, fueling litigation and patent disputes.

Related Patent Families and Competitors

While specific details of patent families are proprietary, a typical landscape involves:

  • Original patents protecting core innovations (likely TW201444590’s role).
  • Secondary patents covering formulations, delivery methods, or use-specific claims.
  • Patent interoperability with international filings, given Taiwan’s participation in global patent treaties.

Patent Term and Maintenance

The patent protections generally last 20 years from filing, with possibilities for extensions or pediatric exclusivities, depending on local law. Maintenance fees are due periodically to sustain enforceability.

Implications of TW201444590 in the Patent Strategy

The scope of TW201444590 influences:

  • Market exclusivity, enabling the patent holder to prevent unauthorized manufacturing or marketing of similar formulations.
  • R&D investment protection, incentivizing continuous innovation.
  • Potential licensing opportunities with other firms seeking access to proprietary formulations or methods.

Furthermore, the patent’s defensibility relies on its claim specificity and effective prosecution history, which reinforce novelty and inventive step against competitors.

Conclusion

TW201444590 exemplifies Taiwan’s commitment to fostering pharmaceutical innovation through robust patent protections. Its scope, rooted in carefully crafted claims, aims to balance broad coverage with enforceability, ensuring protection of novel formulations or delivery methods. The patent landscape reveals a highly competitive environment where strategic patent positioning is critical, often involving a mix of broad core patents and narrower secondary claims.


Key Takeaways

  • Claim Strategy Is Central: The scope of TW201444590 depends on well-drafted claims that balance broad coverage with enforceability. Analyzing these claims reveals the patent’s strength against infringement or challenge.

  • Landscape Context Matters: In Taiwan, pharmaceutical patents are carefully scrutinized for novelty and inventive step. Ensuring claims are supported by inventive contributions is vital for robustness.

  • Protection Duration and Enforcement: The standard patent term provides a significant window for market exclusivity, but maintaining claims through periodic fees and defending against invalidation efforts is essential.

  • Innovation Focus: The patent appears to target specific improvements in drug formulations or delivery systems, aligning with regional and global trends in pharmaceutical R&D.

  • Commercial Strategy: The patent’s scope impacts licensing, generics entry, and R&D investments, emphasizing its strategic importance within Taiwan’s pharmaceutical patent regime.


FAQs

  1. What is the primary innovation protected by Taiwan patent TW201444590?
    The patent covers a specific pharmaceutical formulation or delivery method designed to improve drug stability or efficacy, although detailed claims would specify the exact components or processes.

  2. How broad are the claims in TW201444590?
    The claims likely encompass a range of formulations or methods, with independent claims defining the core invention and dependent claims detailing specific embodiments to balance scope and enforceability.

  3. Can competitors design around this patent?
    Potentially, competitors may develop alternative formulations or methods that fall outside the scope of the claims, provided they meet new inventive or non-obvious criteria.

  4. What is the significance of this patent in Taiwan’s pharmaceutical market?
    The patent grants exclusive rights, enabling the holder to commercialize or license the invention, maintaining a competitive edge and incentivizing further R&D.

  5. How does Taiwan’s patent landscape support pharmaceutical innovation?
    Taiwan provides a robust legal framework aligned with international standards, offering protection for new drugs, formulations, and methods, thereby fostering innovation-driven competition.


References

  1. Taiwan Intellectual Property Office (TIPO). Patent Examination Guidelines.
  2. World Intellectual Property Organization (WIPO). Taiwan Patent Landscape Reports.
  3. International Patent Classification (IPC) codes relevant to pharmaceuticals.
  4. Patent specification documents related to TW201444590 (where available).

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