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Last Updated: December 28, 2025

Profile for Taiwan Patent: 201702238


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201702238

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 Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
⤷  Get Started Free Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
⤷  Get Started Free Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW201702238

Last updated: October 4, 2025


Introduction

Taiwan Patent TW201702238 pertains to innovative aspects within the pharmaceutical or biotech sector, presenting a unique claim set that influences the patent landscape in Taiwan and potentially in international markets. This analysis dissects the scope, claims, and surrounding patent environment, providing insights crucial for professionals involved in drug development, patent strategy, licensing, and competitive intelligence.


Scope of Patent TW201702238

TW201702238 is designed to protect specific innovations related to a drug compound, formulation, method of use, or manufacturing process. The scope is primarily defined through its claims, which delineate the extent of protection.

In general, Taiwanese patents in the pharmaceutical sphere tend to encompass:

  • Compound claims: Protecting the chemical entity itself, including specific stereochemistry, substitutions, or derivative structures.
  • Method-of-use claims: Covering therapeutic applications, dosage regimes, or specific treatment indications.
  • Process claims: Protecting unique synthesis steps or manufacturing techniques that could render the formulation effective or more efficient.
  • Formulation claims: Covering specific excipient combinations, delivery systems (e.g., sustained-release), or combination therapies.

Without access to the exact patent document's claim set, the typical scope likely involves a novel chemical compound or pharmaceutical composition with particular therapeutic benefits, potentially including method-of-treatment claims.


Claims Analysis

Claims in Pharmaceutical Patents:
The core legal protection rests on the claims, which define the boundaries of patent rights. They are classified as independent or dependent:

  • Independent Claims: Establish broad protection, often covering the core invention (e.g., a novel compound or a therapeutic method).
  • Dependent Claims: Narrower, adding specific features or embodiments, and serve to strengthen the patent’s enforceability.

Likely Features of TW201702238:

  • Chemical Composition: The patent probably claims a specific chemical structure with novel substitutions. For example, a compound with particular functional groups that confer unique pharmacological properties.
  • Method of Use: Includes claims for treating certain diseases, such as cancers, neurodegenerative disorders, or infections, using the compound.
  • Manufacturing Method: Might contain claims for an optimized synthesis process that improves yield, purity, or stability.

The claims' sufficiency hinges on novelty, inventive step, and industrial applicability. For instance, if the patent claims a new chemical entity, it must distinguish substantially from prior art compounds, perhaps through inventive stereochemistry or substitution patterns.

Claim Scope Considerations:

  • The scope may reflect broad or narrow protective ranges—broad claims offer extensive coverage but face higher invalidity risk, whereas narrow claims are safer but less comprehensive.
  • In Taiwan, the patent law emphasizes patentable subject matter that demonstrates industrial application and inventiveness, aligning with international standards under the TRIPS agreement.

Patent Landscape and Competitive Environment

Global and Regional Patent Environment:

  • Priority and Family Portfolio:
    The patent likely forms part of a patent family, referencing priority filings in other jurisdictions (e.g., US, Europe, China). These relationships influence enforceability in foreign markets.
  • Overlap with Other Patents:
    The pharmaceutical landscape is characterized by overlapping patents—compound, formulation, method-of-use, and manufacturing patents create freedom-to-operate considerations.

Patent Thickets and Litigation Risks:

  • The presence of multiple patents surrounding the same or similar chemical entities can complicate commercialization.
  • Taiwanese patent TW201702238 may face prior art challenges if similar compounds or methods have been disclosed elsewhere, particularly in international repositories or patent applications.

Patent Expiry and Lifecycle Management:

  • As a patent filed or granted around 2017, expiration is anticipated around 2037, considering Taiwan's patent term provisions.
  • Patentholders can engage in lifecycle extensions or secondary patents (e.g., formulation patents or new indications) to prolong market exclusivity.

Research and Development Trends:

  • The patent landscape indicates ongoing innovation in targeted therapies, biologics, and combination drugs within Taiwan and globally.
  • The patent may reflect efforts to address unmet medical needs, leveraging Taiwan’s strong biotech research sector and collaborations.

Implications for Stakeholders

For Innovators:

  • Ensuring robust claim drafting in patent filings to maximize scope while avoiding ambiguity.
  • Monitoring competitors' patent filings to avoid infringement and identify licensing opportunities.

For Generic Manufacturers:

  • Conducting comprehensive freedom-to-operate analyses, focusing on the specific claims of TW201702238 and related patents.

For Patent Attorneys:

  • Advising on potential invalidity or infringement issues, possibly proposing supplementary protections through secondary patents or divisional applications.

For Policymakers and Regulators:

  • Ensuring that patent terms balance innovation incentives with public health interests, especially in the context of essential medicines.

Conclusion

Patent TW201702238 exemplifies Taiwan’s strategic approach to pharmaceutical innovation, with a scope built around novel chemical entities or formulations aimed at specific therapeutic indications. Its claims likely span compound novelty, specific uses, and manufacturing processes, framing its enforceability and influence within the regional and global patent landscape.


Key Takeaways

  • Scope and Claims:
    The patent likely encompasses a chemical compound, method-of-use, and manufacturing claims, reflecting an integrated approach to drug protection.

  • Strategic Positioning:
    Its patent strength depends on claim breadth, novelty, and inventive step, requiring continuous monitoring for overlapping patents and potential challenges.

  • Global Landscape:
    It probably forms part of a broader patent family, supporting the company's regional and international patent strategy.

  • Lifecycle Management:
    Effective management includes exploring secondary patents and considering patent term extensions or supplementary protections.

  • Competitive Insights:
    The patent landscape in Taiwan remains dynamic, emphasizing the importance of robust patent drafting, vigilant monitoring, and proactive licensing strategies.


5 Unique FAQs

1. What constitutes the core protection in Taiwan Patent TW201702238?
The core protection revolves around the specific chemical compound, its method of use for treating particular diseases, or unique manufacturing processes, as defined in its independent claims.

2. How does Taiwan’s patent law influence the patent scope?
Taiwan’s patent law prioritizes novelty, inventive step, and industrial applicability, which shapes claim drafting to ensure broad yet defensible protection, especially within the pharmacological context.

3. Can TW201702238 be challenged or invalidated?
Yes, claims may be challenged based on prior art, obviousness, or insufficient disclosure. A thorough validity analysis is recommended before commercial exploitation.

4. How does this patent fit into the global patent landscape for similar drugs?
It likely forms part of a patent family with applications or grants in other jurisdictions, providing territorial protection and supporting international commercialization strategies.

5. What are the main strategic considerations for maintaining this patent?
These include timely renewal, defending against infringement, expanding claim scope through additional filings, and leveraging the patent for licensing or R&D collaborations.


References

  1. Taiwan Intellectual Property Office (TIPO), Patent Search Database.
  2. TRIPS Agreement and Taiwanese Patent Law, as applicable to pharmaceutical patents.
  3. Industry reports on pharmaceutical patent filing trends in Taiwan and Asia-Pacific.
  4. Patent family analysis tools and literature for related compounds or compositions.

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