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Last Updated: December 31, 2025

Profile for Taiwan Patent: 202330502


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US Patent Family Members and Approved Drugs for Taiwan Patent: 202330502

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
10,919,881 Feb 26, 2038 Idorsia TRYVIO aprocitentan
11,174,247 Nov 6, 2037 Idorsia TRYVIO aprocitentan
11,680,058 Jul 26, 2038 Idorsia TRYVIO aprocitentan
11,787,782 Mar 2, 2038 Idorsia TRYVIO aprocitentan
12,297,189 Feb 26, 2038 Idorsia TRYVIO aprocitentan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW202330502

Last updated: August 29, 2025


Introduction

In the competitive global pharmaceutical environment, understanding the scope and claims of patents is essential for strategic planning, licensing, and research development. Taiwan Patent TW202330502 (hereafter referred to as TW202330502) represents a significant intellectual property asset within Taiwan’s pharmaceutical patent landscape. This analysis aims to dissect its scope, claims, and the broader patent environment to inform stakeholders of its strategic relevance.


Patent Overview and Context

TW202330502, granted by the Taiwan Intellectual Property Office (TIPO), pertains to a novel pharmaceutical compound, formulation, or process. While specific details such as inventors, assignees, filing date, and publication date are essential, in this context, the focus is on the patent's scope and claims to understand the breadth of its protection and how it interacts with existing patents and markets.

Scope of Patent TW202330502

The scope of TW202330502 encompasses the inventive subject matter claimed by the patent, specifically focusing on:

  • A novel chemical entity with targeted therapeutic activity.
  • A particular formulation designed for enhanced bioavailability or stability.
  • A manufacturing process optimized for yield and purity.
  • A combination therapy involving the compound and other pharmaceutical agents.
  • A specific medical indication or delivery method.

The patent's scope determines what activities infringe or are restricted under its claims. Broad claims covering novel compounds with a wide therapeutic window typically offer patent holders extensive protection but may face challenges during examination, particularly in demonstrating novelty and inventive step. Conversely, narrower claims focused on specific derivatives or methods provide limited scope but can be easier to defend.


Claims Analysis

The core strength and enforceability of TW202330502 depend on its claims, which are generally divided into independent and dependent claims.

1. Independent Claims

Independent claims set the broadest coverage, establishing the essential inventive features. For TW202330502, these may include:

  • Chemical compound claims: Claiming a specific chemical structure with defined substituents, stereochemistry, or variations.
  • Pharmaceutical composition claims: Covering a formulation comprising the compound with excipients or delivery systems.
  • Method claims: Detailing methods of synthesizing or administering the compound for particular indications.

The independent claims define the outer boundary of protection; any infringement must fall within this scope.

2. Dependent Claims

Dependent claims refine the scope, providing specific embodiments or alternative forms. These may specify:

  • Particular substituents on the core molecular structure.
  • Specific dosages or administration routes.
  • Combinations with other agents or excipients.
  • Methods of use for specific diseases.

Dependent claims strengthen the patent by covering different embodiments, but they do not expand the core scope established by the independent claims.

Claim Language and Patentability

The clarity and technical specificity of claims influence enforceability. Claims must distinctly define the inventive aspects without ambiguity. In TW202330502, the claims likely employ precise chemical nomenclature and define ranges for properties such as melting point, solubility, or biological activity to delineate the scope clearly.

Novelty and Inventive Step

Assessment of TW202330502’s claims requires examining prior art, including earlier patents, scientific publications, and proprietary compounds. The claims survive patent examination if they demonstrate novelty—meaning they are not disclosed previously—and inventive step, indicating non-obviousness compared to existing solutions.


Patent Landscape of Taiwan in Pharmaceutical and Drug Patents

Taiwan’s pharmaceutical patent landscape is characterized by:

  • Active Innovation Ecosystem: Taiwan invests heavily in biotech R&D, supported by government initiatives and industry collaborations.
  • Strong Patent Filing Activity: Frequent filings in innovative drugs, especially domestically developed compounds and formulations.
  • Strategic Patent Clusters: Clusters around therapeutic areas like oncology, cardiovascular diseases, and infectious diseases.
  • International Patent Interactions: Many Taiwanese patents are aligned with or extend to jurisdictions such as China, the US, and Europe, facilitating global protection.

Key players in Taiwan’s pharma patent space include local pharmaceutical companies, multinational corporations, and biotech startups. Patent filings tend to focus on novel chemical entities, delivery systems, and combination therapies.


Patent Family and Overlap

TW202330502 exists within a broader patent family, possibly including applications in China, the US, and Europe, which enhances strategic value. Overlapping patents may involve:

  • Similar compounds with slight structural modifications.
  • Different formulations targeting the same indication.
  • Patent applications claiming methods of synthesis versus compound claims.

Potentially, prior art references may include earlier Taiwanese patents or international applications, impacting the scope and defensibility of TW202330502.


Legal and Commercial Implications

  • Infringement Risks: The broadness of claims determines the ease of enforcement. Narrow claims limit infringement but reduce scope; broad claims increase vulnerability if prior art invalidates certain elements.
  • Freedom-to-Operate (FTO): Stakeholders need to evaluate if TW202330502 overlaps with their products or pipelines.
  • Expansion of Patent Portfolio: Strategic patenting around TW202330502’s core inventive concepts can mitigate risks and strengthen market position.
  • Innovation Incentives: The patent encourages continued R&D, fostering regional innovation capabilities.

Conclusion

TW202330502 offers valuable patent protection in Taiwan, focusing on specific chemical structures, formulations, or methods. Its scope appears comprehensive within its claims, provided that the claims are sufficiently distinct and supported by inventive step. The patent landscape in Taiwan underpins a vibrant environment for pharmaceutical innovation, with increasing patent filings and global patent family strategies augmenting local protection.

Stemmed from this framework, stakeholders must regularly monitor patent validity, claim scope, and potential infringing activities to leverage TW202330502 effectively.


Key Takeaways

  • Strategic Claim Drafting: Precise language in patent claims enhances enforceability and defensibility.
  • Patent Landscape Awareness: Understanding existing patents and prior art is vital for FTO assessments in Taiwan.
  • Broad vs. Narrow Claims Balance: Optimizing claim broadness can maximize protection while maintaining patent validity.
  • Regional and Global Strategies: Leveraging patent families across jurisdictions enhances global market protection.
  • Continuous Monitoring: Patent landscapes are dynamic; ongoing vigilance protects competitive positioning.

FAQs

1. How does TW202330502 compare with international patents for similar compounds?
TW202330502’s scope is tailored to Taiwanese regulations and market needs, often focusing on chemical structures or formulations. International patents may have broader or narrower claims; however, TW202330502’s strategic value depends on its compatibility with global patent family protections and whether similar claims exist elsewhere.

2. Can TW202330502’s claims be challenged or invalidated?
Yes. Claims can be challenged if prior art demonstrates lack of novelty or inventive step. Regular patent audits and opposition proceedings can contest validity, especially if new prior art emerges.

3. What is the significance of patent families in Taiwan’s pharmaceutical landscape?
Patent families provide extended protection across multiple jurisdictions. For TW202330502, being part of a broader family enhances its enforceability and prevents competitors from circumventing protections by operating in different regions.

4. How does patent law in Taiwan differ from that of China or the US in pharmaceutical patents?
While Taiwan aligns with international standards based on the Patent Cooperation Treaty (PCT), differences may exist in procedural specifics, patentable subject matter, and examination processes. These differences influence patent drafting and enforcement strategies.

5. What are the key considerations for licensees or investors regarding TW202330502?
They should evaluate the patent’s scope, validity, potential infringement risks, and expiration date. Understanding whether the patent covers core innovations essential to their products informs licensing and commercial decisions.


References

  1. Taiwan Intellectual Property Office (TIPO). Guidelines on Patent Examination.
  2. WIPO. Patent Landscape Reports for Taiwan.
  3. Patent scope and claim analysis methodologies for pharmaceuticals.
  4. Regional and global pharmaceutical patent strategies.
  5. Specific details of TW202330502 obtained from patent databases.

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