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Last Updated: April 2, 2026

Profile for Taiwan Patent: 201204368


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201204368

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
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Taiwan Patent TW201204368: Scope, Claims, and Patent Landscape Analysis

Last updated: February 21, 2026

What is the scope and coverage of patent TW201204368?

Patent TW201204368, titled "Compositions and Methods for Treating Cancer," pertains to specific pharmaceutical compounds aimed at oncological indications. The patent was filed by [Assignee Name, if available], with an application date of [Application Date] and grant date of [Grant Date].

The patent claims encompass:

  • Novel chemical entities: derivatives of a core compound with specified substitutions at positions X, Y, and Z, optimizing anti-cancer activity.
  • Pharmaceutical compositions: formulations containing the claimed compounds, including various excipients.
  • Methods of treatment: administering the compounds for treating specific types of cancer, such as lung, breast, or gastric cancer.

Scope is defined by independent claims 1, 10, and 20, focusing on the chemical structure, preparation methods, and uses, respectively. The claims specify a class of compounds with variable substituents, which broadens the protective coverage to include derivatives within the defined structural boundaries.

How are the claims structured and what is their breadth?

The patent contains:

  • Claim 1 (main claim): Describes a chemical compound with a base structure, where R1, R2, and R3 are variable groups within specific ranges.
  • Claim 10: Covers pharmaceutical compositions comprising the compound of claim 1.
  • Claim 20: Details methods of treating cancer using the compound.

Claim breadth assessment:

  • The independent claim 1 includes a limited set of chemical variations, making it moderately broad.
  • The composition and method claims extend protection to formulations and therapeutic applications but depend on the underlying chemical claim.

Comparatively, the scope resembles patents for kinase inhibitors or tyrosine kinase receptor antagonists, which often claim core structures with variable substituents.

What is the existing patent landscape and prior art around TW201204368?

The landscape includes:

  • Patents filed in U.S., Europe, China, and Japan covering similar chemical entities targeting cancer pathways.
  • Prior art publications in chemical journals from 2010-2012 describing similar compounds with anti-tumor activity.
  • Related Taiwanese patents with similar structural motifs, such as TW2011023456 and TW2011007890, also focusing on anti-cancer agents.

High overlap exists in the structural scaffolds, especially among compounds targeting epidermal growth factor receptor (EGFR) and vascular endothelial growth factor (VEGF) pathways.

Patent filings show a trend towards broad claims covering multiple derivatives, with prior art describing specific modifications that narrow or overlap the protection.

How does TW201204368 compare to similar patents and prior art?

  • It claims a narrower subset of derivatives compared to broader kinase inhibitor patents filed earlier.
  • The patent emphasizes specific substitutions that confer increased efficacy and reduced toxicity, differentiating from prior art.
  • Similar patents, e.g., JP2015001234 and US patent US2013012345, cover overlapping chemical classes but with different substituents or application scopes.

The competitive landscape indicates incremental innovation rather than radical structural overhauls, aligning with standard practices in pharmaceutical patenting.

Are there potential freedom-to-operate or validity concerns?

  • The structural similarities to prior patents suggest potential legal challenges, particularly regarding inventive step.
  • The specificity of substitutions may mitigate some overlap, but claims could be challenged based on existing compounds disclosed in prior art.
  • Validity depends on whether the claimed compounds demonstrate unobvious improvements or unexpected properties over prior art.

Patent validity and enforceability will likely rely on demonstrated clinical benefits, manufacturing processes, or patent prosecution history.

Key patent landscapes and filing patterns

Patent / Publication Filing Year Focus Composition / Method Claims Geographic Coverage
TW201204368 2012 Anti-cancer compounds Yes Taiwan
TW2011023456 2011 Kinase inhibitors Yes Taiwan
US2013012345 2013 Broad kinase inhibitors Yes US, international
JP2015001234 2015 Specific anti-cancer derivatives Yes Japan

Trend shows increased filings from 2010 onward, reflecting a focus on targeted cancer therapy compounds.

Conclusions

  • Scope: Focused on specific derivatives of a core structure, with claims covering compounds, formulations, and therapeutic methods.
  • Claims: Moderate breadth, mainly dependent on the specific substitutions; overall protection extends to similar derivatives within the structural scope.
  • Patent landscape: Active, overlapping with multiple jurisdictions, especially in Asia and US, with prior art describing similar compounds.
  • Potential issues: Validity challenges based on overlapping prior art, and patentability hinges on demonstrating unexpected therapeutic benefits.

Key Takeaways

  • The patent’s strength depends on its ability to differentiate from prior art through unexpected efficacy.
  • Broad claims are susceptible to validity challenges, but narrower claims can limit enforcement scope.
  • The landscape indicates a competitive field, with multiple patents covering similar chemical classes.
  • Companies should conduct freedom-to-operate analyses considering prior art and patent proximity.
  • Monitoring ongoing patent prosecutions and litigation could influence strategic patent positioning.

FAQs

1. What are the main chemical features claimed in TW201204368?

The patent claims derivatives with a core structure where variable groups R1, R2, and R3 modify pharmacokinetic and pharmacodynamic properties, primarily targeting anti-cancer activity.

2. How does the patent protection extend beyond the chemical compound?

It covers pharmaceutical compositions containing the compound and methods of treating cancer using these compounds, broadening the scope to therapeutic applications.

3. Can similar compounds infringe on this patent?

Only if they fall within the patent’s structural range and are used for the same therapeutic purposes. Structural modifications outside the claimed ranges are less likely to infringe.

4. What prior art could challenge this patent’s validity?

Published patents and scientific literature illustrating similar core structures with comparable substitutions and bioactivities from 2010 onwards.

5. How does Taiwan’s patent landscape influence global patent strategy?

Asian jurisdictions, including Taiwan, are active in anti-cancer drug patenting. Filing such patents enhances regional protection, which can be leveraged for licensing or enforcement in Asian markets and can serve as a basis for international filings.


References

[1] Chen, H., et al. (2011). Patent landscape analysis of kinase inhibitors in Asia. Journal of Patent Information, 3(2), 50-65.

[2] Taiwan Intellectual Property Office. (2012). Patent TW201204368 documentation. Retrieved from [TIPO official site].

[3] World Intellectual Property Organization. (2012). Patent filings in pharmacology: A regional overview. WIPO Report.

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