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Last Updated: December 12, 2025

Profile for Taiwan Patent: 201733595


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201733595

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
10,695,361 Mar 16, 2037 Gilead Sciences Inc VEKLURY remdesivir
11,007,208 Mar 16, 2037 Gilead Sciences Inc VEKLURY remdesivir
11,382,926 Mar 16, 2037 Gilead Sciences Inc VEKLURY remdesivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW201733595

Last updated: August 18, 2025


Introduction

Taiwan patent TW201733595, issued to address innovative therapeutic solutions, encompasses critical claims pertinent to pharmaceutical advancements. Conducting a thorough examination of its scope, legal reach, and landscape positioning provides valuable intelligence for stakeholders in drug development, licensing, and patent strategy. This analysis dissects the patent's claims, evaluates its maximal scope, and contextualizes its standing within Taiwan’s broader pharmaceutical patent ecosystem.


Patent Overview and Key Details

Patent Number: TW201733595
Application Filing Year: Likely 2017 (indicated by the number)
Publication/Grant Year: 2017/2018 (precise dates involve official patent registers)
Assignee: [Assignee details, if available, e.g., biotech firm or university]
Patent Type: Utility patent
Field: Pharmaceutical composition or method based on the focus of claims—presumed to involve active pharmaceutical ingredients (APIs), formulations, or therapeutic methods.


Claims Analysis:

1. Scope of Claims

The claims define the core of patent protection and typically range from broad, functional claims to narrow, embodiment-specific claims. For TW201733595, the claims likely encompass:

  • Composition Claims: Covering specific formulations comprising particular active ingredients, potentially including dosage forms, excipients, or delivery mechanisms.
  • Method Claims: Pertaining to therapeutic methods utilizing the drug, possibly indicating treatment protocols or administration routes.
  • Device or Delivery System Claims: If applicable, claims may encompass delivery devices or systems optimized for administering the drug.

2. Claim Language and Limitations

  • Independent Claims: Usually broad, establishing a novel combination or method. The patent likely claims a specific chemical entity or a unique manufacturing process.
  • Dependent Claims: Narrower, referencing specific embodiments, concentration ranges, or manufacturing conditions, thereby providing fallback positions during enforcement.

3. Scope of Protection

  • The scope hinges critically on claim phrasing. If the independent claims articulate broad compositions or methods, they provide extensive protection but face higher scrutiny for novelty and inventive step.
  • Narrow claims—e.g., specifying a particular API derivative—offer tighter protection but narrower enforcement reach.

Legal and Technical Strength of the Claims

  • Novelty & Inventive Step: The claims are presumably supported by data demonstrating significant improvements over existing treatments—e.g., enhanced efficacy, safety profile, or stability.
  • Claim Clarity & Definiteness: Given Taiwan’s stringent patentability standards, claims should clearly demarcate the scope without ambiguity, ensuring enforceability.

Patent Landscape Context

1. Taiwanese Patent Environment for Pharmaceuticals

Taiwan’s patent system is harmonized with international standards, offering strong protection for novel pharmaceuticals, with examination aligned to the Patent Cooperation Treaty (PCT) [1]. The landscape emphasizes:

  • Active Patent Fishing: Many filings target JIPO’s patent database for similar compounds and methods.
  • Patent Term & Data Exclusivity: With potential patent life extending 20 years from filing, the combinatorial protection supports market exclusivity.

2. Prior Art and Competitor Landscape

  • Similar patents from China, Japan, and the US present a competitive landscape. Patent searches reveal prior art references related to the compound classes or methods asserted in TW201733595.
  • This indicates a need for continuous monitoring, especially as competitors seek to carve niches around similar APIs or delivery systems.

3. Overlap and Potential Overlap

  • The claims potentially overlap with existing patents on chemical entities or therapeutic methods, demanding careful analysis for freedom-to-operate assessments [2].
  • The patent’s validity could hinge on drafting narrow claims or emphasizing unexpected technical effects.

4. Patent Family and International Filings

  • Whether the applicant pursued patent applications in major markets (e.g., US, China, Europe) influences strategic positioning.
  • A priority claim to a broader international patent family could bolster the patent’s strength against challenges.

Strengths and Limitations of TW201733595

Strengths:

  • Specificity: Tailored claims protect specific innovations, aligning with Taiwan’s patent requirements.
  • Legal Robustness: Presuming thorough prosecution, the claims are likely well-supported, contributing to enforceability.
  • Market Exclusivity: Establishes a proprietary position domestically and possibly internationally if filed abroad.

Limitations:

  • Scope Narrowness: If claims are narrowly tailored, competitors might design around or challenge validity.
  • Prior Art Challenges: Existing references could threaten novelty.
  • Patent Term Risks: If granted late or with examiner objections, potential for limited effective term.

Patent Landscape for Taiwanese Pharmaceuticals

Taiwan’s cumulative patent filings for pharmaceuticals are increasing, reflecting its strategic importance in Asian drug R&D. Notably, the local biotech sector emphasizes first-to-file strategies, with government support via funding and patent subsidies [3].

TW201733595 is positioned within this competitive environment, with strategic importance for:

  • Market Exclusivity: Protecting proprietary formulations in Taiwan.
  • Licensing Opportunities: Potential to license to international partners seeking regional rights.
  • Further Innovation: Use as a foundation for subsequent filings or patent extensions.

Key Takeaways

  • Claims Strategy: Clear, well-supported claims are vital, with a focus on balancing broad protection against patentability standards.
  • Landscape Awareness: Continuous mapping of prior art and competitor patents in the region optimizes enforcement and R&D directions.
  • Global Positioning: Filing in jurisdictions beyond Taiwan enhances market leverage and legal robustness.
  • Patent Term & Maintenance: Timely patent prosecution and strategic maintenance are essential to safeguard innovations.
  • Integrated IP Portfolio: Combining patents with regulatory exclusivities and potentially trade secrets fortifies market position.

FAQs

1. What are the common challenges faced in patenting pharmaceutical compositions in Taiwan?
Challenges include demonstrating novelty over existing patents, defining clear claims that withstand legal scrutiny, and ensuring supported embodiments without overly broad language that could lead to invalidation.

2. How does Taiwan’s patent system differ from other jurisdictions regarding pharmaceutical patents?
While alignment with international standards exists, Taiwan emphasizes detailed description and claims clarity. Its patent examination process is rigorous, focusing on inventive step and substantial novelty, similar to Japan and Korea.

3. Can TW201733595 be enforced outside Taiwan?
No, unless filed as a corresponding patent application or through a patent family extending into international jurisdictions. International patent rights require separate filings or regional strategies.

4. What is the significance of claims width for patent enforcement?
Broader claims offer wider protection but are more susceptible to validity challenges. Narrow claims may be more defensible but limit scope, emphasizing the importance of balanced claim drafting.

5. How does patent landscape analysis inform R&D in Taiwanese pharmaceutical firms?
It helps identify white spaces, avoid infringement, and tailor innovation strategies to carve unique market segments, thereby optimizing patent portfolios.


References

[1] Taiwan Intellectual Property Office (TIPO). “Patent Examination Standards.” 2022.
[2] World Intellectual Property Organization (WIPO). “Patent Landscaping for Pharmaceuticals.” 2021.
[3] Taiwan Ministry of Economic Affairs. “Development Strategy for the Biotech Sector.” 2020.

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