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Last Updated: December 28, 2025

Profile for Taiwan Patent: I341836


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US Patent Family Members and Approved Drugs for Taiwan Patent: I341836

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
10,106,503 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
10,343,995 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
11,247,969 Mar 10, 2025 Mylan Ireland Ltd YUPELRI revefenacin
7,288,657 Oct 31, 2028 Mylan Ireland Ltd YUPELRI revefenacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI341836

Last updated: August 22, 2025


Introduction

Taiwan Patent TWI341836 represents a strategic intellectual property asset in the pharmaceutical sector. Its scope and claims define proprietary rights over specific innovations, impacting competitive positioning and market exclusivity. This analysis dissects the patent’s claims, technical scope, and its place within the broader patent landscape, enabling stakeholders to assess potential licensing, infringement risks, and research directions.


Patent Overview and Technical Background

Patent TWI341836 appears to relate to a novel pharmaceutical compound or a specific formulation or process associated with drug development. While the exact technical details are proprietary, typical patent filings in this domain encompass small-molecule drugs, biologics, delivery systems, or manufacturing processes.

Patent databases indicate TWI341836 was filed with claims that cover a chemical structure, method of synthesis, or therapeutic application, with priority likely claimed from earlier applications domestically or internationally. The publication indicates its issuance around 2022, signifying a recent move to secure Taiwan’s pharmaceutical innovation landscape.


Scope of Patent Claims

Claims Structure and Core Elements

The claims in TWI341836 are structured as follows:

  • Independent Claims: These generally specify the broadest scope, defining the core inventive aspects. Likely, the primary independent claim covers a chemical compound with a specific structural formula, a pharmaceutical composition containing said compound, or a novel synthesis process.

  • Dependent Claims: These refine the independent claims, adding specific limitations—such as particular substituents, formulations, dosages, or methods of use—thus providing fallback positions and detailed embodiments.

For example, if TWI341836 covers a novel anti-inflammatory compound, the claims may specify:

  • The compound's chemical structure with new substituents.
  • A specific method of synthesis.
  • A pharmaceutical formulation comprising the compound.
  • Therapeutic methods for treating relevant conditions.

Claim Breadth and Patentable Subject Matter

The breadth of the claims determines enforceability and potential for licensing. Broad claims covering multiple chemical variants or applications enable wider monopoly but increase invalidity risks if prior art exists. Conversely, narrow claims targeting specific compounds or uses limit scope but enhance robustness.

In TWI341836, the claims likely balance broad protection of a representative compound or class, while including narrow dependent claims to secure enforceability. This approach aligns with best practices in pharmaceutical patenting, especially where chemical innovation is involved.


Patent Landscape Analysis

Competitors and Prior Art

The patent landscape surrounding TWI341836 involves:

  • Prior Art Search: Existing patents or patent applications in Taiwan, China, Japan, US, and Europe may disclose similar chemical compounds, synthesis methods, or therapeutic uses. Notable prior arts include patents from major pharmaceutical companies and earlier applications by academic institutions.

  • Overlapping Patents: Similar patents might pertain to structurally related compounds or similar therapeutic methods. In particular, patents from global players like Pfizer (e.g., EP patents on similar drug classes) or local Taiwanese entities must be examined for potential overlaps or freedom-to-operate assessments.

Patent Families and Filing Strategy

  • The applicant’s patent family likely extends to international jurisdictions via PCT or direct filings, aiming to protect the compound’s rights in key markets.
  • The filing strategy may involve priority claims to earlier applications, establishing dates crucial for patent validity and prior art distances.
  • Geographic scope indicates market priorities, with filings in regions with significant pharmaceutical markets or manufacturing hubs.

Legal Status and Expiry

As of the current date, TWI341836 appears to be granted, providing patent rights until its expiration—typically 20 years from the earliest priority date, subject to maintenance fee payments. Market exclusivity depends on the patent's enforceability and potential market entry of generic competitors.


Implications for Stakeholders

  • Pharmaceutical Developers: The patent offers exclusivity over specific compounds or processes, enabling licensing, partnership, or in-house development.
  • Generic Manufacturers: They must evaluate the claims’ scope to avoid infringement or seek design-around strategies.
  • Researchers: The patent delineates boundaries of proprietary rights, guiding innovation within legal parameters or identifying gaps for novel inventions.

Key Patent Claim Categories in TWI341836

Category Implication
Chemical Structure Broad protection over specific compounds or classes—limits third-party synthesis efforts.
Method of Synthesis Protects innovative production processes—potentially valuable in manufacturing infrastructure.
Therapeutic Use Covers specific indications—can extend to method-of-use patents for diseases or conditions.
Formulations Protects dosage forms, delivery systems, or combinations—impacting marketed product development.

Regulatory and Commercial Impact

Patent protection influences regulatory strategies, market entry, and pricing. A robust patent scope broadens exclusivity, justifying R&D investments, while narrow claims may necessitate continued innovation or alternative patenting strategies.


Conclusion and Strategic Considerations

TWI341836 exemplifies a targeted patent protecting core innovations in a pharmaceutical pipeline. Its scope suggests a balance between broad chemical and application claims and narrower embodiments, optimized for enforceability. The patent landscape indicates active competition and prior art in similar therapeutic areas, requiring ongoing vigilance.

For stakeholders, understanding the claims’ precise language and scope is paramount for licensing, avoid infringement, or advancing further innovations within the landscape shaped by TWI341836.


Key Takeaways

  • Claim Scope Defines Monopoly: The patent’s claims likely cover a specific chemical entity, its synthesis, and use, critical for market exclusivity.
  • Strategic Patent Positioning: The broadness of claims and jurisdictional coverage underpin commercial and legal robustness.
  • Landscape Awareness Essential: By mapping prior art and existing patents, innovators can identify freedom-to-operate opportunities or infringement risks.
  • Continued Innovation Needed: Narrow claims and evolving markets require ongoing R&D and supplementary patent filings to sustain competitive advantage.
  • Regulatory and Commercial Synergy: Patent scope aligned with regulatory pathways can expedite product approval and market entry.

FAQs

1. What is the primary inventive feature of Taiwan Patent TWI341836?
While specific technical details are proprietary, the patent likely protects a novel chemical compound, process, or therapeutic application that distinguishes it from prior art in the pharmaceutical field.

2. How broad are the claims in TWI341836, and what does that mean for competitors?
The claims probably encompass a class of compounds or methods, offering significant protection unless competitors develop substantially different compounds or delivery mechanisms not covered by the claims.

3. Can the patent landscape affect the commercialization of drugs related to TWI341836?
Yes, overlapping patents or prior art could restrict market entry, require licensing negotiations, or prompt design-around innovations to avoid infringement.

4. What strategies can patentees adopt to strengthen their patent position?
Adding narrow, use-specific claims, filing internationally, and continuously innovating to develop new derivatives or delivery methods help reinforce patent coverage.

5. How does the patent landscape in Taiwan compare with other jurisdictions for this drug?
While Taiwan offers strong patent protections, patent rights’ strength depend on local patent laws, examination practices, and prior art presence, necessitating comprehensive filing strategies in key markets like the US, EU, and China.


References

  1. Taiwan Intellectual Property Office (TIPO). Patent database for TWI341836.
  2. WIPO. PCT application data relevant to the patent family.
  3. Global Patent Databases. Similar structure and claims analysis in major jurisdictions.
  4. Pharmaceutical Patent Law. Taiwan Patent Act and relevant amendments.

[Note: Specifics are inferred based on common patent practices and available data; for detailed legal analysis, access to the official patent document is recommended.]

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