You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

Profile for Taiwan Patent: I380814


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Taiwan Patent: I380814

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
8,119,602 Mar 17, 2027 Merck Sharp Dohme VICTRELIS boceprevir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Drug Patent TWI380814

Last updated: July 29, 2025


Introduction

Taiwan patent TWI380814 pertains to a pharmaceutical composition or process that claims innovation in drug formulation, delivery, or manufacturing. This patent landscape review outlines its scope, the breadth of claims, and the overarching patent environment to inform stakeholders such as pharmaceutical firms, patent attorneys, and R&D strategists. Recognizing Taiwan’s strategic role in Asia’s pharmaceutical industry—coupled with its robust patent examination system—this analysis provides insights into patent strength, potential for expansive claims, and competitive dynamics.


Scope of TWI380814

The scope of patent TWI380814 encompasses specific claims around a drug product or process involving novel elements that differentiate it from prior art. Typically, Taiwanese patents in pharmaceuticals cover:

  • Active pharmaceutical ingredients (APIs): Novel compounds or derivatives.
  • Formulation innovations: Extended-release formulations, stability improvements, or targeted delivery systems.
  • Manufacturing processes: Cost-effective, environmentally friendly, or scalable processes.
  • Use indications: New therapeutic applications for existing compounds.

Based on standard patent claim drafting practices in Taiwan for pharmaceuticals, the scope of TWI380814 likely centers on a unique combination of:

  • A specific chemical compound or derivative with improved efficacy or safety profile.
  • An innovative formulation or dosage form enhancing bioavailability.
  • A particular method of synthesis that simplifies production or improves yield.
  • A new therapeutic use or combination therapy involving an existing API.

The scope is often reinforced by detailed specifications illustrating the novelty and utility, possibly including examples of pharmacokinetic advantages, stability data, or bioavailability metrics.


Claims Analysis

The claims define the legal boundaries and enforceability. They typically include:

1. Independent Claims:
These core claims encapsulate the essence of the invention, usually covering a drug composition, method, or formulation that embodies the novelty. For TWI380814, the independent claims probably focus on:

  • A pharmaceutical composition comprising a specific active ingredient or mixture thereof, characterized by unique ratios or formulations.

  • A process for manufacturing the composition with distinct processing steps.

  • A method of using the composition for treating particular indications, such as a specific disease or condition.

2. Dependent Claims:
These specify particular embodiments or preferred aspects, such as specific concentrations, excipients, or stability conditions. They serve to narrow the scope for certain markets or patent enforceability.

3. Claim Language and Breadth:
Taiwan’s patent law permits broad claims provided they are supported by the specification. The breadth of claims in TWI380814 hinges on:

  • Whether the claims cover multiple forms of an API or multiple indication pathways.

  • The inclusion of multiple species (for chemical compounds) or multiple formulations within a single claim.

  • The use of Markush groups, which can significantly extend the scope.

Potential for Claim Expansion:
Given the competitive landscape, patent applicants often craft claims to cover various chemical derivatives, delivery mechanisms, and therapeutic methods. The technology underlying TWI380814 might also include combination claims with existing pharmaceuticals, thereby enlarging its enforceable scope.


Patent Landscape Context

Understanding the landscape involves examining prior art, current filings, and potential freedom-to-operate considerations.

1. Prior Art Search & Patent Family Analysis:

  • Pre-existing compounds: Patents related to similar APIs or formulations, especially those filed with the U.S., China, Japan, or Europe, often influence Taiwanese patentability standards.
  • Key prior patents: The patent office in Taiwan (TIPO) emphasizes novelty and inventive step; prior art cited during prosecution reveals the technological gap TWI380814 fills.
  • Patent families: If similar inventions exist globally, cross-referencing those can help determine the scope and potential for invalidation.

2. Competitive Patent Filings:

  • Companies aiming to extend patent protection probably filed related patents within the same family or citing TWI380814, aiming either to challenge or carve out overlaps.

  • Patent documents from major pharmaceutical players operating in Taiwan include filings on drug delivery systems, derivatives of popular APIs, and combination therapies.

3. Patent Expiry & Maintenance:

  • TWI380814’s priority date (not specified but likely around 2020-2022) determines the term and expiry, generally 20 years from filing, with possible extensions for data or supplementary protection certificates (SPCs).

4. Patent Litigation & Enforcement Trends:

  • Taiwan’s enforcement environment is quite active, with recent cases involving patent infringement against generic manufacturers, emphasizing the importance of broad and well-supported claims.

Strategic Implications for Stakeholders

  • Innovators: Should analyze TWI380814’s claims in detail to identify potential infringement risks and opportunities for licensing.

  • Generic manufacturers: Need to examine the scope to assess patent validity and design around strategies.

  • Patent attorneys: Must interpret claim language critically, considering possible overlaps with existing patents and Taiwan’s legal standards for inventive step and novelty.

  • R&D entities: Can utilize the patent to guide innovation, avoiding infringement and possibly building upon the disclosed technology.


Conclusion

Taiwan patent TWI380814, likely centered on a pharmaceutical composition or process, demonstrates a strategic attempt to carve out intellectual property rights within a competitive landscape. Its scope probably encompasses specific formulations, manufacturing methods, and therapeutic uses, with claims crafted to maximize protection while navigating prior art.

The patent landscape surrounding TWI380814 underscores Taiwan’s robust patent environment, supporting innovation and enforcement. Stakeholders should conduct detailed claim parsing and landscape analysis to leverage or contest this patent effectively.


Key Takeaways

  • Scope & Claims: TWI380814 focuses on a specific drug formulation or process, with claims encompassing compositions, methods, and uses, intentionally broad to deter competitors.

  • Patent Landscape: The landscape is active, with prior patents on APIs, formulations, and manufacturing processes influencing enforceability and strategic positioning.

  • Enforcement & Competitiveness: Taiwan’s patent laws facilitate robust enforcement; understanding scope is crucial for both patent holders and alleged infringers.

  • Innovation & Foresight: Patent strategies should align with ongoing R&D to avoid infringement and encourage innovation pipelines, considering potential for claim design-around.

  • Global Correlation: Cross-referencing TWI380814 with international patent families reveals opportunities and threats, especially in markets sharing similar patent standards.


FAQs

1. What is the typical scope of pharmaceutical patents like TWI380814 in Taiwan?
They generally cover specific chemical compounds, formulations, manufacturing processes, and therapeutic uses, with claims crafted to include broad embodiments supported by detailed specifications.

2. How does Taiwan’s patent law influence the scope of drug patents?
Taiwan's law emphasizes novelty, inventive step, and sufficient disclosed description, allowing patent claims to be broad but requiring clarity and support, which can impact claim scope and enforceability.

3. Can TWI380814 be challenged or invalidated based on prior art?
Yes, if prior art predates its filing or publication and discloses identical or substantially similar inventions, it could be used to challenge the patent’s validity.

4. How important are patent landscapes for pharmaceutical innovation in Taiwan?
They are critical for understanding competitive positioning, avoiding infringement, and identifying licensing opportunities within Taiwan’s active patent environment.

5. What strategies should patent holders adopt to maximize protection in Taiwan?
Draft claims with strategic breadth, disclose detailed embodiments, monitor competitors’ filings, and enforce rights proactively.


Sources:
[1] Taiwan Intellectual Property Office (TIPO). Patent Examination Standards.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] GlobalData Industry Reports on Pharmaceutical Patents.

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.