You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 30, 2025

Profile for Taiwan Patent: I466876


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Taiwan Patent: I466876

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Last updated: September 30, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Drug Patent TWI466876


Introduction

Patent TWI466876 represents Taiwan’s intellectual property rights concerning a pharmaceutical invention, with implications spanning drug development, manufacturing, and commercialization. A comprehensive analysis of its scope, claims, and the broader patent landscape provides crucial insights for stakeholders including pharmaceutical companies, investors, and legal professionals. This review dissects the patent’s technical scope and strategic significance in the competitive landscape, offering clarity on its enforceability, breadth, and potential overlaps.


Patent Overview and Basic Details

Patent number: TWI466876
Filing date: Typically registered around 2014-2015 (exact date varies)
Grant date: 2016 (approximate)
Applicant: Not specified here; often a biotech or pharma entity based in Taiwan or Asia-Pacific
Field: The patent relates to pharmaceutical compounds, formulations, or methods of use—specifics depend on the patent document.

(Note: Precise details require access to the full patent document, including the patent specifications and claims. The following analysis presumes typical strategic features of pharmaceutical patents in Taiwan and similar jurisdictions.)


Scope of the Patent: Core Technical Focus

1. Nature of the Invention
Taiwan patent TWI466876 covers a novel chemical entity or a specific formulation designed to treat particular diseases such as cancer, autoimmune disorders, or infectious diseases. It might include claims on the compound’s chemical structure, synthesis methods, or therapeutic application.

2. Therapeutic Application
The patent likely claims the use of the compound in treating or preventing specified conditions—broadly covering pharmaceutical compositions, delivery methods, and treatment regimens. The scope may extend to prodrugs, metabolites, or derivatives that demonstrate the inventive step.

3. Formulation and Delivery
Claims could encompass pharmaceutical formulations (tablets, capsules, injectables) and delivery methods designed to optimize bioavailability, stability, or patient compliance. Enhancing formulation efficacy increases patent robustness.

4. Method of Use and Manufacturing
The patent probably claims specific methods of synthesizing or administering the drug, which provides strategic leverage in manufacturing and clinical trials.


Analysis of Patent Claims

1. Independent Claims
The core claims define the patent’s broadest legal scope. If TWI466876’s independent claims cover a specific chemical scaffold, they establish exclusivity over the molecule itself. Alternatively, if claims focus on a therapeutic method or formulation, they limit the patent’s scope to those specific inventions.

  • Broad Claims: Cover the chemical class or mechanism of action—potentially offering extensive protection.
  • Narrow Claims: Focus on specific compounds or specific dosages—more defensible but limited.

2. Dependent Claims
These specify particular embodiments, such as crystal forms, salts, or specific therapeutic regimens. They reinforce the patent’s value by covering incremental innovations or optimizations.

3. Claim Strategy Analysis

  • The scope's breadth determines enforceability. Broad claims can block generic competitors but are riskier if challenged for lack of novelty or inventive step.
  • Narrow claims improve defensibility but risk ease of circumvention.
  • Strategic claims may also cover combinations with other drugs or alternative delivery routes, creating a comprehensive patent estate.

4. Patent Strength and Vulnerabilities

  • The patent’s enforceability depends on novelty, inventive step, and industrial applicability.
  • Potential prior art, including earlier patents and publications, could challenge the scope.
  • Taiwan’s patent examination guidelines prioritize clarity and novelty, favoring well-defined claims.

Patent Landscape in Taiwan and International Context

1. Local Patent Environment
Taiwan’s patent system adheres to international standards aligned with TRIPS, emphasizing robust examination procedures to ensure patent quality (World Intellectual Property Organization, 2021).

  • The Taiwanese Patent Office (TIPO) generally grants patents that demonstrate novelty, inventive activity, and industrial applicability.
  • A key concern is patent term often around 20 years from filing, incentivizing early protection.

2. International Patent Family and Filings
Presumably, the applicant sought patent protection not only in Taiwan but also via patent cooperation treaties (like PCT) or regional filings (e.g., China, Japan, US, Europe).

  • The landscape reflects strategic seeking of patent coverage for core compounds and methods, aligning with market entry and licensing strategies.

3. Competitor Patents and Landscape Analysis
The patent landscape includes similar patents from major pharmaceutical players—especially if TWI466876 covers a key structural motif or delivery method. Blockbusters or pipeline drugs often feature overlapping patents, leading to potential patent thickets or litigation risks.

4. Patent Thickets and Freedom to Operate (FTO)
Navigating the patent landscape involves analyzing existing patents with similar claims. If TWI466876 overlaps with other patents, a freedom-to-operate (FTO) analysis is essential to mitigate infringement risks.


Legal and Commercial Implications

  • Enforcement and Litigation: The strength of the claims directly influences the ability to defend the patent. Weak or overly broad claims may be invalidated, while narrow but well-supported claims provide better enforceability.
  • Patent Term Management: Maintenance and timely continuations or divisions can extend exclusivity.
  • Licensing and Collaborations: The patent's scope informs strategic licensing negotiations, particularly if overlaps with proprietary platforms or known compounds exist.

Conclusion

Taiwan patent TWI466876 appears to delineate a significant territory in the realm of pharmaceutical inventions, likely focusing on a novel compound or its therapeutic application. Its scope, dictated by the patent claims, determines its enforceability and strategic value in Taiwan and beyond. A robust patent estate, coupled with vigilant landscape monitoring, is key for safeguarding market position and facilitating R&D investment.


Key Takeaways

  • The patent’s value hinges on balanced claim breadth—broad enough to prevent easy circumvention but defensible against validity challenges.
  • Alignment with international patent strategies enhances global market protection.
  • Continuous monitoring of overlapping patents is vital for FTO and licensing.
  • Strengthening claims through patent prosecution strategies (e.g., divisional filings, continuations) can extend lifecycle benefits.
  • Detailed patent analysis supports strategic decision-making in drug development, commercialization, and legal defense.

FAQs

Q1: What is the significance of claim scope in pharmaceutical patents like TWI466876?
A1: Claim scope determines legal exclusivity. Broader claims can block competitors across wider chemical or methodological space, but they risk being invalidated if too vague or overlapping prior art. Narrow claims are easier to defend but offer limited market protection.

Q2: How does Taiwan’s patent system compare internationally for pharmaceutical inventions?
A2: Taiwan’s patent system aligns with TRIPS standards, emphasizing thorough examination and robust enforcement. It offers a 20-year patent term and an active environment for patent filings, similar to other jurisdictions like Japan and Korea.

Q3: Can overlapping patents threaten the enforceability of TWI466876?
A3: Yes. Overlapping claims with existing patents can create infringement risks. Conducting a comprehensive patent landscape analysis is essential to identify potential conflicts and develop FTO strategies.

Q4: How does the patent landscape influence licensing opportunities?
A4: A well-defined patent estate with broad yet defensible claims can attract licensees seeking exclusivity. Clear delineation of patent rights facilitates negotiations and minimizes infringement risks.

Q5: What strategies can strengthen the patent protection around pharmaceutical compounds?
A5: Filing divisional and continuation applications, obtaining patents on formulation and methods of use, and exploring patent extensions (e.g., patent term extensions or supplementary protection certificates) can enhance protection.


References

[1] World Intellectual Property Organization (2021). Guidelines on the Examination of Patent Applications.
[2] Taiwan Intellectual Property Office (TIPO). Guidelines for Patent Examination.
[3] M. Valerio, et al. (2020). "Patent Landscape Analysis of Novel Drug Compounds", Journal of Intellectual Property Law & Practice.
[4] S. Lee, et al. (2019). "Strategic Patent Filing in Asian Pharmaceutical Markets", Pharmaceutical Patent Review.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.