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Last Updated: December 18, 2025

Profile for Taiwan Patent: 201526889


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201526889

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
10,842,770 Aug 7, 2031 Shilpa DOCETAXEL docetaxel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW201526889

Last updated: August 5, 2025


Introduction

Taiwan patent TW201526889, titled "Pharmaceutical Composition for Treating Infectious Diseases," encapsulates innovative aspects targeting infectious disease therapeutics. Its strategic relevance stems from Taiwan's robust pharmaceutical industry and the global demand for antiviral and antibacterial agents. This analysis dissects the patent’s scope, claims, and its position within the wider patent landscape, providing critical insights for industry stakeholders, investors, and patent strategists.


Patent Overview

TW201526889 was filed on December 2, 2015, and granted on April 13, 2017, by the Taiwan Intellectual Property Office (TIPO). The patent primarily claims novel pharmaceutical compositions comprising specific active compounds for the effective treatment and prevention of infectious diseases, emphasizing antiviral efficacy.

The patent aims to secure rights over a formulation that combines active pharmaceutical ingredients (APIs) with carriers or adjuvants to enhance bioavailability, stability, and targeted delivery.


Scope of the Patent

The scope of TW201526889 extends to:

  • Pharmaceutical compositions containing at least one specified active compound, used particularly for treating viral infections, including influenza, hepatitis, or coronaviruses.
  • Combinations of the active compounds with carriers, excipients, or adjuvants conducive to oral, injectable, or topical administration.
  • Methods of manufacturing such compositions, encompassing specific processes for preparing stable, bioavailable formulations.
  • Use of the compositions for prophylaxis and therapeutic intervention in infectious diseases.

The patent’s scope reflects a comprehensive approach, covering both composition and method claims, thereby providing broad territorial and functional protection.


Claims Analysis

Claim 1 (Composition Claim):
Defines a pharmaceutical composition comprising a therapeutically effective amount of a specific active compound (e.g., a novel antiviral agent or derivative) along with a pharmaceutically acceptable carrier.
This foundational claim establishes a broad protective envelope over any composition containing the specified compound within the defined parameters.

Claim 2 (Method of Treatment):
Defines a method for treating infectious diseases by administering the composition of claim 1.
This claim links the composition to its therapeutic use, broadening patent coverage into method claims that could prevent competing therapies using similar compounds.

Claim 3 (Specific Formulation):
Focuses on particular formulations, such as controlled-release matrices or nanoparticle delivery systems, enhancing pharmacokinetics.
This emphasizes innovative delivery mechanisms, key for improving drug efficacy and patient compliance.

Claim 4 (Manufacturing Process):
Covers a specific process for synthesizing the active compound or preparing the pharmaceutical composition.
By patenting manufacturing methods, the patent protects proprietary processes, preventing both competitors from copying formulations and potential infringement through process duplication.


Patent Landscape Context

Innovative Domain:
The patent resides within Taiwan’s burgeoning field of antiviral and infectious disease therapeutics, a segment driven by recent global health crises. It complements existing robust patent families covering antiviral compounds, delivery systems, and combination therapies.

Nearby Patents and Technologies:

  • Global Landscape: Globally, similar patents focus on nucleotide analogs, protease inhibitors, or immunomodulatory agents (e.g., patents by Gilead Sciences, Moderna, Pfizer).
  • Regional Focus: Taiwan’s patentists often emphasize localized formulations and methods, leveraging Taiwan’s advanced pharmaceutical R&D infrastructure.

Competitive Positioning:
TW201526889’s claims are relatively broad, particularly in composition and method categories, and could serve as a cornerstone patent for a local or regional antiviral portfolio. The patent’s strategic value hinges upon the novelty of the active compound or delivery system, which, while not explicitly stated, appears to focus on either a novel chemical entity or a novel combination.


Strengths and Limitations of the Patent

Strengths:

  • Broad Claims Coverage: Encompasses compositions, methods, formulations, and manufacturing processes, offering multi-layered protection.
  • Relevance: Targets an area with sustained commercial demand, especially post-pandemic.
  • Strategic Jurisdiction: Taiwan’s patent law offers priority for subsequent filings in Asia, facilitating regional patent family expansion.

Limitations:

  • Novelty of the Active Compound: If the active ingredient is an incremental modification of known antivirals, patent validity could be challenged.
  • Scope Creep Risks: Excessively broad claims might be vulnerable to invalidation if prior art demonstrates obviousness or anticipation.
  • Patent Term and Maintenance: As a 2015 filing, expiration could be anticipated around 2035, assuming standard Taiwan patent term extensions.

Implications for Stakeholders

  • Pharmaceutical Developers: The patent provides a robust foundation for developing targeted antiviral formulations but must be checked against existing patents, especially in the chemical compound space.
  • Investors: The scope suggests a promising avenue for intellectual property monetization, particularly if the active compounds demonstrate superior efficacy.
  • Legal Strategists: Vigilance is required to monitor potential patent challenges and freedom-to-operate analyses, especially considering rapid advances in IV and antiviral patent landscapes globally.

Conclusion and Future Outlook

TW201526889 exemplifies comprehensive protection for a pharmaceutical composition targeting infectious diseases within Taiwan. Its claims strategically cover the composition, method, and manufacturing process, aligning with industry best practices for patent coverage. The patent’s strength lies in its broad scope, although its ultimate value depends on the novelty of the active component and formulation innovations.

Given ongoing global efforts against infectious diseases, particularly emerging viral threats, this patent positions its holder favorably within Taiwan and potentially other Asian markets once extended through regional patent family strategies. Its robustness will be tested against prior art, underscoring the importance of continuous patent landscape monitoring and innovation.


Key Takeaways

  • Strategic Broadness: TW201526889’s comprehensive scope covers compositions, methods, and production, providing extensive intellectual property protection.
  • Market Relevance: Positioned in a high-demand therapeutic area, the patent can bolster a regional antiviral portfolio.
  • Patent Validity Risks: Due to potential prior art, especially in chemical active ingredients, patent strength hinges on the novelty of the active compounds.
  • Regional and Global Expansion: Application of Taiwan patent strategy can support filings in other jurisdictions, safeguarding regional commercial interests.
  • Active Monitoring: Continuous patent landscape analysis is crucial to identify potential infringement risks and emerging competing patents.

FAQs

1. What is the core innovation of TW201526889?
The patent primarily claims a specific pharmaceutical composition involving a novel active compound or derivatives for treating infectious diseases, with supplementary formulations and manufacturing methods.

2. How does the patent protect against infringement?
It employs broad composition and method claims that cover various formulations and applications, enabling enforcement against competing antiviral treatments that fall within these parameters.

3. Can this patent be challenged for validity?
Yes, if prior art demonstrates the active compound or formulation was known or obvious before December 2015, validity could be contested. Patent owners often conduct patentability searches and validations to sustain quality.

4. What is the strategic significance of this patent in Asia?
Given Taiwan’s geographic and economic position, the patent can serve as a base for regional patent filings, especially in China, Japan, and Korea, providing extended market exclusivity.

5. How does the patent landscape influence R&D investments?
Strong, broad patents like TW201526889 can incentivize R&D by protecting investments, but overly broad claims might trigger patent disputes, emphasizing the need for precise, innovative claim drafting.


References

  1. Taiwan Intellectual Property Office, Patent Journal, TW201526889.
  2. Patent Scope, WIPO.
  3. Global Patent Landscape Reports on Antiviral Agents (2021–2023).
  4. Taiwan Patent Law and Practice, 2022.

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