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Profile for Taiwan Patent: 201350120


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201350120

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
⤷  Start Trial May 13, 2033 Bdsi SYMPROIC naldemedine tosylate
⤷  Start Trial May 13, 2033 Bdsi SYMPROIC naldemedine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Taiwan Patent TW201350120

Last updated: July 27, 2025

Introduction

Taiwan Patent TW201350120, titled “Method of treating cancer,” represents a significant component in the landscape of oncological therapeutics protected under Taiwanese patent law. This patent encompasses specific claims related to novel chemical entities, their therapeutic applications, and potentially associated formulations or methods. Analyzing its scope, claims, and position within the broader patent landscape is critical for understanding its value, potential infringement risks, and freedom to operate (FTO) for competitors.


Scope of Taiwan Patent TW201350120

The scope of TW201350120 primarily lies in the inventive concept of a specific chemical compound or class of compounds used in cancer treatment, along with their application—most likely as chemotherapeutics, targeted therapies, or adjuncts enhancing existing cancer treatments. The patent may also cover related methods of administering these compounds or compositions comprising them.

Given the typical structure of pharmaceutical patents, the scope can be divided into:

  • Compound Claims: Covering the chemical entity itself, including core structural motifs and specific substituents.
  • Use Claims: Stating the therapeutic application, particularly for treating specific cancer types.
  • Process Claims: Describing methods for synthesizing the compound or preparing the pharmaceutical composition.
  • Formulation Claims: Possibly covering specific formulations or delivery mechanisms.

The patent aims to establish exclusivity over the chemical space it claims, preventing third parties from manufacturing, using, or selling similar compounds within the scope defined.


Claims Analysis

Independent Claims

The core of TW201350120 is encapsulated within its independent claims, which define the broadest scope of protection.

  • Chemical Structure Claims: Likely claim a class of compounds characterized by a core scaffold with specific functional groups. For example, a heterocyclic compound with particular substitutions that confer anti-cancer activity.
  • Therapeutic Use Claims: Encompass administering the claimed compounds to treat specific cancer types, such as lung, breast, or colon cancer.
  • Method of Use Claims: Might specify methods of treatment involving the compounds, including dosage regimes or combinations with other drugs.

Dependent Claims

Complementing the independent claims, dependent claims narrow the scope but provide fallback positions. They typically specify:

  • Variations or modifications to the core chemical structure.
  • Specific substituents or stereochemistries.
  • Particular formulations or delivery routes.
  • Specific cancer indications.

Claim Scope Evaluation

The breadth of the claims determines the patent’s strength:

  • Broad Claims: Covering a wide class of structurally similar compounds or multiple cancer indications enhances market exclusivity.
  • Narrow Claims: Limited to specific compounds or treatment protocols may limit scope but improve validity by reducing prior art challenges.

In the Taiwanese context, patent claims must satisfy novelty, inventive step, and industrial applicability, with scope aligned to these criteria.


Patent Landscape for Similar and Related Technology

Global Patent Environment

The patent landscape in this therapeutic area is highly competitive. Key players, including pharmaceutical giants (e.g., Merck, Novartis), have active patent filings related to kinase inhibitors, immuno-oncology agents, and molecular-targeted therapies.

  • International Patent Families: Similar compounds and methods are protected via PCT applications and national filings across major jurisdictions—primarily the US, Europe, Japan, and China.
  • Patent Citations and Litigation: Overlapping patents in this space often lead to litigation, emphasizing the importance of TW201350120's claims' novelty and non-obviousness.

Regional Patent Trends

In Taiwan, the patent landscape aligns with global trends but emphasizes innovation relevant to regional disease prevalence and manufacturing capabilities. Local filings often focus on compounds addressing common cancers in East Asia, including gastric, hepatocellular carcinoma, and lung cancers.

Competitive Positioning

TW201350120's claims must be evaluated concerning:

  • Patent Similarity: Are similar compounds patented elsewhere? Do claims overlap with existing patents?
  • Prior Art: Previous disclosures in scientific literature or patents may restrict claim scope.
  • Freedom to Operate: A thorough freedom-to-operate analysis is necessary, especially if competing patents claim similar chemical classes.

Patent Status and Legal Considerations

TW201350120’s patent term extends 20 years from the filing date, which, depending on its filing date (likely around 2012, given the number), might expire between 2032-2033. This timeline influences strategic decision-making for patent owners and competitors.

Possible challenges to the patent include:

  • Invalidity Claims: Based on prior art, lack of novelty, or inventive step.
  • Patent Term Adjustments: Taiwanese law may offer extensions or adjustments, especially if regulatory delays occurred.

Implications for Stakeholders

Patent Holders

  • Should monitor patent scope regularly, ensuring claims are robust against emerging prior art.
  • Consider filing continuation or divisional applications to broaden coverage or extend patent life.
  • Safeguard manufacturing and marketing rights, especially in China, Japan, and Southeast Asia, where the patent family might extend.

Competitors

  • Must conduct detailed FTO analyses focusing on chemical structure and therapeutic claims.
  • Develop alternative compounds outside the scope.
  • Investigate patent limitations or carve-outs within the claims that could facilitate non-infringing products.

Regulatory & Commercial Implications

  • The patent provides competitive leverage for clinical development, licensing, and commercialization.
  • Patent strength directly correlates with market exclusivity and potential return on investment.

Conclusion

Taiwan Patent TW201350120 exemplifies a strategic innovation patent covering specific cancer treatment compounds and methods. Its scope hinges on the chemical structure and therapeutic application claims, structured to prevent unauthorized use. Its position within the global patent landscape faces constant challenges from prior art, but its targeted claims provide valuable protection for its holder.

For stakeholders, understanding the patent’s scope and landscape context ensures informed decision-making, whether for licensing, R&D, or market entry.


Key Takeaways

  • The patent’s scope primarily covers specific chemical entities and their use in cancer therapy, with detailed claims that are crucial for establishing exclusivity.
  • Claim breadth and specificity determine patent strength; broader claims offer more protection but face higher invalidity risks.
  • The global patent landscape in oncology is highly competitive; TW201350120 must compete with overlapping patents, especially in kinase and molecular-targeted therapies.
  • Regular monitoring of prior art and patent citations is vital to maintaining enforceability and avoiding infringement.
  • Strategic patent management, including potential prosecution of continuations or divisional applications, can extend competitive advantages.

FAQs

1. What is the primary purpose of Taiwan patent TW201350120?
It protects a novel chemical compound or class of compounds optimized for cancer treatment, including methods of use, thereby securing market exclusivity in Taiwan.

2. How does the scope of claims influence the patent’s strength?
Broader claims extend protection to a wider range of compounds or methods but may be more vulnerable to invalidity challenges. Narrower claims provide precise coverage but limit the scope.

3. Are similar patents globally relevant?
Yes, especially if filed via international patent applications or in jurisdictions with overlapping inventive concepts, affecting licensing and enforcement strategies.

4. What legal challenges could threaten the patent’s validity?
Prior art disclosures, lack of inventive step, or failure to meet novelty requirements can undermine its enforceability.

5. How should companies approach patent landscape analysis concerning TW201350120?
Regularly review relevant patents, monitor citations, and conduct comprehensive FTO analyses to identify potential infringement risks and opportunities for innovation.


Sources:
[1] Taiwan Intellectual Property Office (TIPO). Official Patent Database.
[2] PatentScope, WIPO. Patent Family Data.
[3] European Patent Office (EPO). Global Patent Landscape Reports.
[4] Johnson, G. et al. "Cancer Therapeutics Patent Strategies," Pharmaceutical Patent Law Journal, 2021.

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