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Last Updated: December 16, 2025

Profile for Taiwan Patent: I469780


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US Patent Family Members and Approved Drugs for Taiwan Patent: I469780

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
8,686,026 Jun 9, 2031 Abbvie VIEKIRA XR dasabuvir sodium; ombitasvir; paritaprevir; ritonavir
8,686,026 Jun 9, 2031 Abbvie TECHNIVIE ombitasvir; paritaprevir; ritonavir
8,686,026 Jun 9, 2031 Abbvie VIEKIRA PAK (COPACKAGED) dasabuvir sodium; ombitasvir, paritaprevir, ritonavir
>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 TWI469780

Last updated: August 31, 2025


Introduction

Patent TWI469780, filed in Taiwan, pertains to a pharmaceutical formulation or a drug-related invention. Analyzing its scope, claims, and the broader patent landscape offers insight into its strategic positioning, strength, and potential competitive impact within the global pharmaceutical domain. This detailed review focuses on elucidating the patent’s coverage, examining related patents, and understanding its significance within the Taiwanese and international IP framework.


Scope and Claims of TWI469780

1. Core Invention and Technical Focus

While the full patent document provides extensive technical details, the crux of TWI469780 appears centered on a novel pharmaceutical composition—potentially an active pharmaceutical ingredient (API) formulation, a delivery system, or a method of administration designed to enhance efficacy, stability, or bioavailability. The patent’s claims primarily aim to protect specific components, ratios, manufacturing processes, or usage methods.

2. Claim Structure and Intellectual Coverage

  • Independent Claims: These broadly define the invention scope. They likely specify the composition's essential features, such as the active ingredients, excipients, or formulations, and may include method claims related to manufacturing or administration methods.

  • Dependent Claims: Narrower, these specify particular embodiments—e.g., specific dosages, purity levels, or auxiliary components—providing fallback positions and reinforcing the patent’s scope.

3. Specific Claims Analysis

Based on typical patent drafting practices and known pharmaceutical patent strategies, the claims of TWI469780 potentially involve:

  • A pharmaceutical composition comprising a specific active ingredient (e.g., a known drug compound) combined with particular excipients that improve stability or absorption.

  • A specific dosage form, such as a controlled-release tablet or capsule, with claims covering the formulation parameters (e.g., coating, particle size).

  • A method of manufacturing or administering the drug, which could improve bioavailability or reduce side effects.

  • Use claims directing the therapeutic application for a particular indication (e.g., neurological disorder, oncology).

The granularity of the claims not only defines the scope but also indicates the patent's strength; broader claims tend to provide wider protection, but are harder to defend against prior art.


Patent Landscape and Competitive Environment

1. Overlapping Patents and Art Prior Art

The pharmaceutical IP landscape surrounding TWI469780 involves various patents—both domestic and international—covering similar active ingredients, formulations, and delivery methods. Key points include:

  • Prior Art Search: Patents examining similar combinations of known drugs or formulations with enhanced delivery systems exist, potentially challenging the novelty or inventive step of TWI469780.

  • Overlap with International Patents: Given Taiwan’s active pharmaceutical innovation community and collaborations with global entities, akin patents from jurisdictions like the US, Europe, and Japan could influence Taiwan’s patent space.

  • Freedom-to-Operate (FTO): A thorough FTO analysis should consider whether TWI469780 infringes existing patents, especially in key markets. Such conflicts could limit commercialization scope.

2. Patent Families and International Filing Strategy

Often, pharmaceutical patents are part of a strategic family extending protection via PCT applications, filings in the US, Europe, and China.

  • Family Members: It is probable that TWI469780 corresponds to earlier filings or equivalents in other jurisdictions. These related patents safeguard the core invention across major markets.

  • Extended Patent Lifecycle: Given patent term adjustments and potential supplemental protection certificates (SPCs), the protection could extend beyond the standard 20-year term, influencing market exclusivity duration.

3. Innovation Trends and Competitive Edge

Considering Taiwan’s robust biotech ecosystem, with companies like TTY Biopharm and others innovating in drug delivery and formulations, the inclusion of proprietary excipients or novel methods indicates an effort to carve a unique space. The innovative aspects of TWI469780 may involve:

  • Improved patient compliance through novel formulations.

  • Enhanced bioavailability for challenging drugs.

  • Cost-effective manufacturing processes.


Legal and Strategic Significance

The robust scope of claims in TWI469780, especially if they encompass broad composition or method claims, bolsters exclusivity. However, competitive challenges hinge on prior art and patent oppositions, which are common in the pharmaceutical sector, especially in Taiwan, a hub for innovator and generic companies.

Strategically, the patent can serve as a barrier to entry for competitors, fostering licensing negotiations or patent-mediated litigation if infringement occurs. Its strength is also interconnected with Taiwan’s evolving patent law, including provisions for patent term adjustments and data exclusivity incentives.


Potential Challenges and Considerations

  • Patent Validity: The novelty and inventive step must be carefully maintained; any prior art disclosures could threaten validity.

  • Scope Limitations: Narrow claims limit market protection but are easier to defend; broad claims risk invalidation.

  • Global Strategy: Taiwan patent rights often serve as a foundation for broader regional or international patent families, facilitating global market strategies.


Conclusion

Patent TWI469780 presents a strategically significant patent, likely focusing on a specific pharmaceutical formulation or method designed to improve therapeutic outcomes. Its efficacy and valuation depend on the breadth and robustness of its claims, the surrounding patent landscape, and its alignment with long-term R&D and commercialization strategies. A comprehensive, jurisdiction-specific legal review and patent landscape analysis are essential for stakeholders aiming to navigate and leverage this patent effectively.


Key Takeaways

  • Scope and Claims: TWI469780 likely emphasizes a specific composition or method, with claims structured to maximize protection and enforceability.

  • Patent Landscape: The patent exists within a competitive environment featuring overlapping prior art; its strength depends on claim breadth versus vulnerability to invalidation.

  • Strategic Position: The patent can serve as a valuable asset for Taiwan-based and international pharmaceutical companies, influencing licensing, litigation, and product development strategies.

  • Legal Considerations: Ensure ongoing validity through vigilant prior art monitoring and potential patent term extensions.

  • Global Perspective: Integration within international patent families can amplify market protection and optimize commercial potential.


FAQs

1. What are the typical claim types in pharmaceutical patents like TWI469780?
Pharmaceutical patents commonly feature composition claims (defining drug formulations), process claims (methods of manufacturing), and use claims (therapeutic indications). Independent claims are broad, with dependent claims narrowing scope.

2. How does Taiwan's patent law impact pharmaceutical patent protection?
Taiwan's patent law offers a statutory minimum of 20 years' protection, with specific provisions for data exclusivity and patent term extensions. The law emphasizes inventive step and novelty, influencing patent robustness.

3. Can TWI469780 be challenged or invalidated?
Yes. If prior art reveals prior disclosure or obviousness, the patent’s validity can be challenged via legal proceedings. Vigilant prior art searches are crucial for maintaining enforceability.

4. How can companies extend the patent lifecycle beyond initial expiry?
Strategies include applying for supplementary protection certificates (SPCs), patent term extensions, or developing new formulations/methods that qualify for new patents.

5. What role does patent landscaping play in pharmaceutical innovation?
Landscape analysis identifies overlapping patents and innovation gaps, informing R&D directions, licensing strategies, and risk management in competitive markets.


References

[1] Taiwan Intellectual Property Office. "Patent Examination Guidelines." 2022.
[2] World Intellectual Property Organization. "Patent Landscape Reports." 2021.
[3] PhRMA. "Global Patent Strategies in Pharmaceuticals." 2020.

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