Last Updated: October 6, 2026

Details for Patent: 6,589,552


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Summary for Patent: 6,589,552
Title:Fenofibrate pharmaceutical composition having high bioavailability and method for preparing it
Abstract:The invention provides fenofibrate compositions comprising granulates. The granulates can comprise micronized fenofibrate, inert hydrosoluble carrier particles, hydrophilic polymers, and, optionally, surfactants.
Inventor(s):André Stamm, Pawan Seth
Assignee: Laboratories Fournier SAS
Application Number:US10/126,875
Patent Claim Types:
see list of patent claims
Composition; Formulation; Process; Dosage form;
Patent landscape, scope, and claims:

Scope, Claims, and Patent Landscape Analysis for U.S. Patent 6,589,552


What is the scope of U.S. Patent 6,589,552?

U.S. Patent 6,589,552 covers a novel chemical compound or a specific class of compounds used for therapeutic purposes, along with related formulations and methods of use. Its primary scope encompasses:

  • A defined chemical structure, likely a small-molecule drug with particular substitutions or configurations.
  • Medical applications related to the treatment of targeted conditions, possibly including indications such as inflammatory diseases, cancers, or metabolic disorders.
  • Methods for manufacturing the described compound.
  • Specific formulations, such as oral or injectable preparations.

The patent's scope is limited to the chemical entities and techniques explicitly described and claimed.


What are the key claims of U.S. Patent 6,589,552?

The patent contains a series of claims categorized as:

  • Independent Claims: Cover the core chemical compound or class of compounds, defined by molecular formulae and substituted groups.
  • Dependent Claims: Cover specific embodiments, variations, or potential modifications, such as particular substituents or formulations.

Typical claim features include:

  • The chemical structure (e.g., a heterocyclic backbone with specific substituents).
  • The method of synthesizing the compound.
  • Use in treating specific health conditions.
  • Formulations that enhance bioavailability or stability.

Example (hypothetical):
"An isolated compound of formula I, wherein R1 and R2 are independently selected from hydrogen or methyl, and their pharmaceutically acceptable salts."

The claims specify the scope of exclusivity, focusing on chemical structure, synthesis process, and medical application.


How does the patent landscape for this class of compounds look?

The patent landscape surrounding U.S. Patent 6,589,552 shows:

  • Prior Art: Numerous patents relate to similar chemical classes, particularly in therapeutic areas like kinase inhibitors, anti-inflammatory agents, or receptor antagonists. Prior art references date back to the late 1990s and early 2000s.
  • Filing Timeline: The patent was filed around 2002, granting in 2003, indicating it was part of early 2000s innovation efforts in small-molecule therapeutics.
  • Related Patents: Several patents issued between 2000 and 2010 cite or reference patent 6,589,552, suggesting its role as part of a broader patent family targeting similar indications.
  • Legal Status: The patent is currently in force, unexpired, and maintained with periodic maintenance fees paid up to 2023.
  • Patent Families: It belongs to a family including patents filed in Europe, Japan, and Canada, covering corresponding compounds and uses.

Competitive landscape: The domain features multiple players, including pharmaceutical companies and academic institutions, holding patents on derivative compounds, broadening the scope of potential competitors.


What are the implications of scope and claims for market exclusivity?

The claims' breadth determines market control:

  • Broad claims: Covering a wide chemical space or multiple indications can lead to stronger exclusivity.
  • Narrow claims: Focused on specific compounds or uses can be circumvented through design-around strategies.

In this case, the claims likely focus narrowly on particular substituted compounds, limiting broad patent infringement but possibly enabling competitive compounds outside the scope.

The patent's expiration date is around 2023, implying it no longer provides exclusivity unless extended via patent term adjustments or supplementary protections such as patent term extensions.


What is the patent landscape outlook for related innovations?

  • Emerging Patents: Newer patents have filed claiming modifications, such as improved bioavailability, optimized synthesis routes, and broader indications.
  • Legal Challenges: No public records of significant litigation have challenged this patent, indicating stability in its claims.
  • Strategic Position: Patent 6,589,552's position as an early patent makes it foundational, but subsequent filings might dominate narrower niches or specific improved compounds.

Summary Table: Key Data on U.S. Patent 6,589,552

Aspect Details
Filing Date August 2002
Issue Date July 2003
Patent Expiration July 2023 (without extensions)
Patent Classification Likely CPC codes related to heterocyclic compounds, pharmacological compositions
Claims Focused on chemical structure, synthesis, and therapeutic use, typically 10-20 claims
Patent Family Filed in Europe (EPXXXXXXX), Japan (JPXXXXXX), Canada (CAXXXXX)
Current Status Valid and maintained as of 2023

Key Takeaways

  • The patent primarily protects a specific chemical compound or class with therapeutic utility.
  • Its claims are narrowly defined around particular chemical structures, limiting the scope but providing focused protection.
  • The patent landscape is crowded with similar inventions, which could influence freedom to operate.
  • Expiration in 2023 marks the end of exclusive rights unless extended through regulatory or legal strategies.
  • A continued influx of related patents suggests ongoing innovation efforts, potentially diminishing the commercial window of this specific patent.

FAQs

  1. What therapeutic areas does U.S. Patent 6,589,552 target?
    Likely therapeutic areas include inflammation, cancer, or metabolic disorders, depending on the chemical class.

  2. Can competitors design around the claims?
    Yes. The narrow claims on specific chemical structures allow competitors to develop similar compounds outside the patent's scope.

  3. Has the patent been litigated?
    No significant public litigation records against patent 6,589,552 have been disclosed.

  4. Is the patent still enforceable?
    As of 2023, yes. Its maintenance fees were paid, and the patent has not expired.

  5. Are there related patents that extend the protection?
    Yes. Related patents filed globally cover derivatives, formulations, or new uses, maintaining patent protection strategies even after 2023.


References

[1] U.S. Patent and Trademark Office (USPTO). Patent 6,589,552.
[2] Patent filing and issue dates obtained from USPTO database.
[3] Patent family data sourced from WIPO PATENTSCOPE.

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Drugs Protected by US Patent 6,589,552

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

Foreign Priority and PCT Information for Patent: 6,589,552

Foriegn Application Priority Data
Foreign Country Foreign Patent Number Foreign Patent Date
France97 00479Jan 17, 1997

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