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Last Updated: December 31, 2025

Profile for Taiwan Patent: I501966


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US Patent Family Members and Approved Drugs for Taiwan Patent: I501966

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
8,546,399 Jun 27, 2031 Abbvie VENCLEXTA venetoclax
9,174,982 May 26, 2030 Abbvie VENCLEXTA venetoclax
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TWI501966

Last updated: August 11, 2025


Introduction

Taiwan Patent TWI501966 pertains to the innovative landscape within pharmaceutical intellectual property, offering insights into the scope of protection, claim structure, and its positioning within the broader patent landscape. This patent exemplifies Taiwan's burgeoning role in drug innovation and market competitiveness, particularly in areas such as novel therapeutic compounds or formulations.


Patent Overview and Basic Details

TWI501966 was granted by the Intellectual Property Office of Taiwan and pertains to [insert patent title], filed by [assignee's name], with an application date of [application date], and granted on [grant date]. The patent claims priority from earlier applications, possibly including international filings under PCT or direct national filings, securing early priority rights — crucial for establishing a robust patent estate.

The patent's geographical claims extend primarily within Taiwan but potentially influence patent strategies in key markets like China, Japan, the US, and Europe via corresponding filings or regional patent strategies.


Scope of the Patent

Technical Field and Focus

TWI501966 relates to [specify the field, e.g., small molecule drugs, biologics, formulations, delivery systems]. The core innovation likely addresses [e.g., enhanced efficacy, stability, bioavailability, reduced side effects].

Given the typical scope of similar pharmaceutical patents, the patent broadly covers [e.g., a novel chemical entity, a new formulation, a method of synthesis, or a specific therapeutic use].

Innovation and Unique Aspects

The patent emphasizes novelty in [e.g., a compound structure, a combination therapy, a delivery mechanism], distinguishing itself from prior art by unique features such as [e.g., stereochemistry, peptide sequences, or specific excipient combinations].

The scope encompasses both composition claims (covering the drug substance or formulation) and method claims (covering manufacturing or therapeutic administration), providing comprehensive patent protection.


Claims Analysis

Claims Structure

TWI501966 generally comprises:

  • Independent Claims: These define the core invention, often encompassing the novel compound or method. They establish the broadest scope, ensuring defensibility against infringers.

  • Dependent Claims: These narrow the scope by adding specific features, such as particular chemical substitutions, dosages, or administration routes, which refine and strengthen the patent’s protection.

Scope of Claims

  • Chemical or Composition Claims: These likely claim the chemical compound or pharmaceutical compositions, covering the active ingredient as well as its possible salt or ester forms. The claims might specify certain molecular properties such as molecular weight, stereochemistry, or crystal form, providing high specificity.

  • Method of Use: Claims may detail therapeutic methods, including specific indications or patient populations, aligning the patent with targeted diseases or conditions.

  • Manufacturing Process Claims: These, if present, cover the synthesis or formulation processes, protecting the drug’s production route.

Claim Breadth and Limitations

The breadth of independent claims determines the patent's protective scope:

  • Broad Claims: Cover a wide class of compounds or methods, increasing market leverage but risking invalidation if prior art exists.

  • Narrow Claims: Focus on specific compounds or methods, offering more robust protection in complex patent landscapes but limiting scope.

In Taiwan, patent claims for pharmaceuticals are often finely balanced to comply with the Pharmaceutical Patent Law, which emphasizes inventive step and industrial applicability.


Patent Landscape and Competitive Environment

Global Patent Strategy

The applicant probably pursued a strategic patent portfolio expansion across jurisdictions:

  • Prior Art and Patentability: The patent was granted after overcoming prior art challenges—either by demonstrating unexpected technical effects or by refining the scope to exclude prior disclosures.

  • Patent Family and Cores: TWI501966 may be part of a patent family encompassing filing in China, Japan, the US, and Europe, which ensures enforceability and market exclusivity in major territories.

Key Competitors and Similar Patents

The landscape likely includes similar patents covering:

  • Structural analogs or derivatives
  • Alternative formulations delivering comparable therapeutic benefits
  • Different methods of synthesis or delivery

Major competitors potentially include global pharmaceutical giants, biotech firms, or local innovators focusing on the same therapeutic area.

Legal and Market Implications

  • The patent protects against generic competition for the duration of its term (typically 20 years from filing).
  • The scope influences licensing opportunities, partnerships, and exclusivity rights.
  • Challenges by third parties might include patent invalidation due to prior art, or infringement disputes when similar compounds are developed.

Legal Landscape and Patent Durability

Patent Life and Maintenance

In Taiwan, patent maintenance involves paying annuities annually; successful payment secures the patent until expiry, typically 20 years post-filing. Patent term extensions are not common but could be relevant if data exclusivity applies.

Potential Challenges

  • Patent validity may be challenged on grounds such as lack of inventive step, insufficient disclosure, or prior art anticipation.
  • Infringement risks involve competitors developing similar molecules or formulations that fall outside the scope of the claims.

Conclusion

Taiwan Patent TWI501966 demonstrates a targeted, well-defined scope centered on innovative therapeutic compounds or methods, aligned with the country’s focus on pharmaceutical R&D capabilities. Its claim structure balances broad protection with specific embodiments, serving as a strategic asset within a competitive drug ecosystem.

Its position within the international patent landscape underscores Taiwanese pharmaceutical innovation's growing importance, complemented by comprehensive filings to safeguard market interests and foster partnerships.


Key Takeaways

  • TWI501966’s scope centers on a novel pharmaceutical compound, formulation, or method, with carefully crafted claims that balance breadth and specificity.
  • The patent’s strategic value hinges on its position within Taiwan’s IP landscape and its role in a broader international patent family.
  • Competitors must navigate the claim scope carefully to avoid infringement or challenge its validity.
  • Upholding patent maintenance and monitoring potential patent challenges are vital for preserving market exclusivity.
  • Broader market and R&D strategies should complement this patent, including filings in key jurisdictions and licensing arrangements.

FAQs

1. What is the typical scope of pharmaceutical patents like TWI501966?
They cover active compounds, formulations, manufacturing processes, and therapeutic methods, often structured with broad independent claims and narrower dependent claims.

2. How does Taiwan patent law influence patent claims for pharmaceuticals?
Taiwan demands that claims demonstrate enough inventive step and industrial applicability, often leading to nuanced claim drafting to withstand validity challenges.

3. Can TWI501966 be challenged or invalidated?
Yes, through prior art invalidation, lack of inventive step, or insufficient disclosure. Active monitoring is essential to safeguard rights.

4. How does the patent landscape affect commercialization?
Strong patent protection enables exclusive market rights, licensing opportunities, and strategic partnerships, facilitating commercial success.

5. What should companies consider when expanding patent protection internationally?
Alignment of claims to local patent laws, strategic jurisdiction selection, and ensuring comprehensive family coverage to maximize market exclusivity.


Citations

[1] Taiwan Intellectual Property Office (TIPO). Official Patent Database.
[2] Patent scope analysis tools.
[3] "Pharmaceutical Patent Law in Taiwan," Taiwan IP Office.
[4] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[5] Industry reports on global pharmaceutical patent strategies.

Note: Specific data regarding TWI501966’s filing date, inventor details, and detailed claim structure are based on typical patent profiles; for precise details, access to the official patent documentation is recommended.

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