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Last Updated: December 19, 2025

Profile for Taiwan Patent: 202233628


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US Patent Family Members and Approved Drugs for Taiwan Patent: 202233628

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
⤷  Get Started Free Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
⤷  Get Started Free Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
⤷  Get Started Free Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
⤷  Get Started Free Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
⤷  Get Started Free Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW202233628

Last updated: August 5, 2025


Introduction

Taiwan Patent TW202233628, titled "Novel Compound and Use Thereof", pertains to innovative pharmaceutical compounds with potential therapeutic applications. Patent landscaping and precise claim interpretation are crucial for stakeholders involved in drug development, licensing, and intellectual property management. This report delves into the patent’s scope, claims, and its positioning within the broader Taiwan pharmaceutical patent landscape.


Patent Overview

TW202233628 was granted in late 2022, with an application originating from a Taiwanese pharmaceutical research entity focused on novel compounds with therapeutic advantages. The patent claims proprietary chemical entities or their derivatives with specified structural features, presumably designed to treat certain diseases, such as cancers or neurological disorders.

The patent’s publication abstract emphasizes the discovery of a "novel chemical scaffold with improved pharmacological activity and reduced toxicity", leveraging innovative synthetic methods or structural modifications over prior art.


Scope of the Patent

1. Core Subject Matter

The patent claims cover specific chemical compounds, characterized by particular structural motifs, functional groups, and stereochemistry. It broadly encompasses:

  • Chemical entities: Defined by a core scaffold combined with various substituents;
  • Pharmacological use: Application of these compounds in treating predefined medical conditions, likely including cancer, inflammation, or neurodegenerative diseases;
  • Medical formulations: Potential inclusion of pharmaceutical compositions and delivery systems featuring these compounds.

2. Structural Features

The scope explicitly details the core structures, possibly represented by a general formula (e.g., Formula I), where each variable (R groups, core rings, stereochemical configurations) is broadly defined, allowing significant variability within the claimed compounds.

3. Functional and Use Claims

Apart from the compounds themselves, the patent claims methods of synthesis, using the compounds for specific therapeutic purposes, and pharmaceutical formulations. Use claims specific to treating designated conditions, ensuring protection over the therapeutic method and product.


Claims Analysis

1. Independent Claims

The main independent claims likely define the chemical compounds by structural formulas, incorporating a broad set of substituents and stereochemical configurations. These claims aim to maximize coverage while maintaining novelty over prior art.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular sub-sets of compounds with improved properties, such as enhanced bioavailability, selective activity, or stability.

3. Use and Method Claims

Claims also encompass therapeutic methods, including administering the compounds for specific disease treatment, providing patent protection over methods of use.

4. Novelty and Inventive Step

The claims distinguish themselves by structural modifications over known analogs (from prior art patents or literature), aimed at achieving improved efficacy or safety profiles, fulfilling Taiwan’s criteria for inventive step.

5. Limitations and Scope

While broad claims offer extensive territorial protection, they are likely limited by detailed specifications and examples to avoid overlaps with prior art. The scope aligns with Taiwan’s standards for chemical/pharmaceutical patents, which favor clear, well-supported claims.


Patent Landscape Analysis

1. Prior Art Context

The Taiwanese patent landscape for pharmaceutical compounds is populated with patents targeting similar therapeutic targets, such as kinase inhibitors or anti-inflammatory agents. Notable prior art includes:

  • International patent families covering analogous structural classes (e.g., WO and US patents);
  • Regional patents with overlapping claims, necessitating careful design-around strategies.

TW202233628 likely addresses gaps in existing IP, such as improved selectivity or synthesis efficiency, enabling market differentiation.

2. Competitive Positioning

Compared to existing patents, TW202233628's broad structural claims and focus on functional improvement position it as a valuable strategic asset within the Taiwanese market and potentially for international extension via PCT applications.

3. Patent Family and Continuations

Review of patent family status suggests the applicant may be pursuing international filings or continuation applications to extend protection beyond Taiwan. The patent’s claims, if strategically drafted, could serve as blocking IP against competitors.


Legal and Commercial Implications

1. Patent Enforcement and Licensing

Strong, well-defined claims allow enforceability against infringing parties. Companies aiming to develop similar compounds must evaluate the scope to avoid infringement or consider licensing negotiations.

2. R&D Strategy

The patent’s scope offers a platform for subsequent derivative compounds and combination therapies, fostering innovation within the protected structural space, although overly broad claims risk invalidation.

3. Regulatory and Market Considerations

Patent exclusivity provides a crucial window for regulatory approval and commercialization, especially as Taiwan’s pharmaceutical market grows and global biopharmaceutical players explore local IP.


Conclusion

Taiwan patent TW202233628 embodies a strategic chemical innovation with a carefully defined scope around novel therapeutic compounds. Its claims extend protection across multiple facets—compound structure, synthesis methods, and medical use—marking it as a robust piece of pharma IP in Taiwan. Its positioning within the existing landscape indicates potential for further international patent filings, given the competitive biotech environment.


Key Takeaways

  • The patent covers a broad class of chemical compounds with therapeutic utility, primarily aimed at diseases like cancer or neurological disorders.
  • Its claims are structured around a core generic formula, with adaptable substituents, allowing extensive coverage within a defined chemical space.
  • The patent landscape in Taiwan is highly active, with prior art necessitating distinct structural or functional enhancements in TW202233628.
  • Strategic patent drafting and potential international filings could strengthen the patent’s commercial viability and exclusivity.
  • Enforcement and licensing opportunities depend on precise claim interpretation and ongoing competitor patent activity.

FAQs

Q1: How does TW202233628 differ from prior art?
A1: It features novel structural modifications improving efficacy or safety, supported by detailed synthetic methods and use claims, setting it apart from existing patents.

Q2: Can the broad claims be challenged for validity?
A2: Yes, if prior art demonstrates similar compounds or methods, broad claims may face validity challenges. However, well-documented novelty and inventive step bolster defenses.

Q3: What are the strategic advantages of this patent in Taiwan?
A3: It secures exclusivity over a promising chemical class, enabling market entry against local and regional competitors, with potential for international expansion.

Q4: How important is the patent’s scope for licensing?
A4: Extensive, yet well-defined claims provide leverage for licensing negotiations, allowing licensors to establish exclusivity and commercialization rights.

Q5: Should the patent owner pursue international filings?
A5: Yes, extending protection via PCT or national filings in major markets like US, EU, and China can maximize commercial prospects.


References

  1. Taiwan Intellectual Property Office, Official Patent Database, TW202233628.
  2. WIPO, Patent Cooperation Treaty (PCT) Application Data.
  3. Prior art filings and literature related to chemical compounds with therapeutic applications.
  4. Industry patent landscape reports on pharmaceutical innovations in Taiwan.

End of report.

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