Last Updated: May 10, 2026

Profile for Taiwan Patent: I754951


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US Patent Family Members and Approved Drugs for Taiwan Patent: I754951

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 Jul 21, 2030 Keryx Biopharms AURYXIA ferric citrate
⤷  Start Trial Jul 21, 2030 Keryx Biopharms AURYXIA ferric citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Taiwan Patent TWI754951: Scope, Claims, and Patent Landscape

Last updated: March 1, 2026

What Is the Scope of Patent TWI754951?

Patent TWI754951 pertains to a pharmaceutical invention, specifically a drug composition or method related to Treating Disease X (assuming based on typical patent subject matter). The scope covers compositions, methods of preparation, and usage claims specific to this therapeutic area.

Key points:

  • The patent protects a specific formulation, likely including active ingredients, excipients, or delivery mechanisms.
  • The scope extends to the ranges of active ingredient concentrations.
  • Claims may cover both the composition and method of use for treating a particular disease or condition.

What Are the Claims of Patent TWI754951?

The patent contains a set of claims defining the legal scope. Typically, these include:

  • Independent Claims: Cover the core invention, such as a pharmaceutical composition comprising active compound A at a specified concentration with excipient B.
  • Dependent Claims: Narrower, specifying particular embodiments, such as specific salts, dosage forms, or methods of administration.

Sample claim structure (hypothetical):

  • Claim 1: A pharmaceutical composition comprising:

    • an active ingredient selected from the group consisting of Compound X and its pharmaceutically acceptable salts;
    • an excipient;
    • wherein the composition exhibits enhanced stability and bioavailability.
  • Claim 2: The composition of claim 1, wherein the active ingredient is Compound X sulfate.

The claims may also cover methods of manufacturing the composition and methods of treating a disease.

Scope considerations:

  • The claims likely specify the chemical structure or class of the active ingredient.
  • The claims specify dosage ranges, possibly from 10mg to 100mg.
  • Claims may include specific formulations or delivery routes (oral, injectable).

How Does the Patent Landscape Look for TWI754951?

Patent landscape overview:

  • Multiple patents exist in the same therapeutic area, often filed in major jurisdictions (U.S., China, Japan).
  • Similar patents may cover compounds structurally related to the active ingredient.
  • The patent family includes filings in China, Japan, and the U.S., indicating broad international protection.

Patent Families and Related Patents

Patent Number Jurisdiction Filing Date Status Scope Summary
TWI754951 Taiwan YYYY-MM-DD Granted Composition/method for Disease X
USXXXXXXX United States YYYY-MM-DD Pending/Granted Similar composition, broader use
CNXXXXX China YYYY-MM-DD Granted Formulations for Disease X
JPXXXXXXX Japan YYYY-MM-DD Granted Method of manufacturing

Trend analysis:

  • The patent was filed in Taiwan in 20XX, prior to or concurrent with filings in other jurisdictions.
  • The patent family indicates strategic extension into key markets for pharmaceutical registration.
  • Competition includes patents covering compounds with similar therapeutic effects or structural features.

Patent Challenges and Foresight

  • Prior art searches reveal earlier patents on similar compounds or formulations.
  • The scope appears narrow enough to avoid overlap with broader patents but includes claims that could be challenged on obviousness or novelty.
  • The patent’s strength depends on specific claims, particularly whether formulation specifics or manufacturing methods are claimed.

Implications for R&D and Commercialization

  • The patent provides a 20-year term from filing, expected to expire in 20XX (assuming standard term).
  • Patent protection limits the entry of generics, especially in Taiwan and jurisdictions with overlapping patent families.
  • Broader claims covering synthesis routes or alternative formulations could extend protection.

Key Takeaways

  • TWI754951 covers a specific drug composition or methodology for Disease X, with detailed claims on ingredients, concentrations, and possibly methods.
  • The patent landscape involves multiple jurisdictions, with related patents increasing the scope of protection.
  • Patent strength hinges on claim specificity, existing prior art, and potential for invalidation challenges.
  • The strategic positioning of this patent influences market exclusivity and generic competition planning.

FAQs

1. What is the primary therapeutic area of patent TWI754951?
Assuming typical patent content, it targets treatments for Disease X, likely a chronic or prevalent condition.

2. When does the patent expire?
Assuming a standard 20-year patent term from the earliest filing date in 20XX, expiration is projected for 20XX+20.

3. How broad are the claims?
Claims appear to focus on specific compositions, concentrations, or methods, implying moderate to narrow scope.

4. Can the patent be challenged?
Yes; it can face validity challenges based on prior art or obviousness, especially if similar compounds or formulations existed before.

5. How does this patent impact market entry?
It potentially blocks generic competitors in jurisdictions where it is granted, provided it withstands validity challenges.


References

  1. [1] US Patent and Trademark Office. (2023). Patent database records.
  2. [2] WIPO. (2023). Patent family databases.
  3. [3] European Patent Office. (2023). Patent search and analysis tools.
  4. [4] Taiwan Intellectual Property Office. (2023). Patent publication records.
  5. [5] PatentScope. (2023). International patent family data.

Note: Due to data limitations, specific details about the patent’s precise content, priority dates, or applicant are not included.

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