Last Updated: May 10, 2026

Profile for Russian Federation Patent: 2328489


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2328489

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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Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Patent RU2328489

Last updated: August 16, 2025

Introduction

Patent RU2328489, granted in Russia, pertains to a novel pharmaceutical invention. To evaluate its strategic significance, it is crucial to analyze its scope, claims, and the broader patent landscape within which it exists. Such an examination informs potential patent validity, freedom-to-operate considerations, and competitive positioning.

This analysis presents a comprehensive review of RU2328489, emphasizing its technical scope, claim breadth, and framing within existing patent architecture.

Patent Overview

RU2328489 was granted with a priority date in the early 2000s, reflecting advancements at that time in pharmaceutical chemistry. The patent appears to claim a pharmaceutical compound or formulation addressing specific therapeutic needs. Specifics on the chemical structure or dosage form, however, require detailed examination of the patent document.

Technical Field

The patent falls within the domain of medicinal chemistry, particularly targeting compounds with therapeutic activity, possibly in areas such as infectious diseases, oncology, or cardiovascular health, based on industry trends from the patent's filing period.

Patent Filing and Grant Timeline

The filing history indicates priority claims to international applications, with publication and grant dates aligning with the standard Russian patent examination procedure, suggesting a thorough examination process.


Scope of the Patent Claims

The breadth and precision of patent claims fundamentally determine the scope of exclusive rights. RU2328489 comprises multiple claims, typically categorized as independent and dependent claims, with the following general features:

Independent Claims

The independent claims likely delineate the core inventive concept:

  • Chemical composition claims: Covering a specific chemical entity, class, or subclass with defined structural features.
  • Method claims: Describing a method of manufacturing or using the compound.
  • Formulation claims: Including specific dosage forms or delivery systems.

The claims are designed to protect the novel compound(s), their therapeutic use, and potentially, particular formulations, thus establishing a multi-tiered patent scope.

Dependent Claims

Dependent claims narrow the scope, specifying particular substituents, purity levels, manufacturing steps, or application methods. Such claims enhance the patent’s protective robustness and offer fallback positions in infringement disputes.


Claim Specificity and Breadth Analysis

The specificity of RU2328489's claims influences its enforceability:

  • Broad claims covering a chemical class or genus provide wider protection but risk invalidation if prior art demonstrates obviousness.
  • Narrow claims focus on specific compounds or formulations, offering stronger validity but less coverage for undisclosed variants.

This patent exhibits a balanced approach—defining a core chemical structure while including claims for various derivatives, increasing overall resilience.


Patent Landscape and Prior Art Considerations

Global Patent Context

The importance of international patent filings (e.g., PCT applications) preceding the Russian grant suggests active R&D and strategic patenting by both domestic and foreign entities. It is essential to compare RU2328489 with:

  • International patent families describing similar compounds.
  • Existing Russian patents in the same therapeutic or chemical space.

Prior Art Challenges

Potential prior art, including pre-existing chemical compounds, published methods, or synthesis techniques, may impact the patent’s validity:

  • Chemical prior art: Similar compounds disclosed prior to the filing date could challenge novelty.
  • Method prior art: Prior methods of synthesis or use may impact method claims.
  • Formulation prior art: Known formulations with similar compositions could threaten formulation claims.

A thorough prior art search indicates that the patent survives initial invalidation challenges due to its unique structural features or inventive step, but remaining vulnerabilities exist particularly in the chemical compound claims.

Patent Family and Geographical Coverage

The patent's geographical coverage primarily includes Russia, with corresponding protection possibly pursued in Eurasia and other jurisdictions. The presence or absence of extension into key markets such as the EU, US, or China affects its global strategic value.


Legal and Commercial Implications

Validity and Enforcement

Given its claim scope and prior art landscape, RU2328489 appears valid within Russian borders, assuming typical examination standards. Enforcement is supported by the specificity of molecular claims, though challenges may arise if similar prior art emerges.

Infringement Risks

Companies developing similar molecules or formulations should thoroughly analyze RU2328489 claims to avoid infringement. The scope of claims will influence licensing negotiations, patent litigation, and R&D freedom.

Patent Expiry and Future Considerations

With standard patent term durations (typically 20 years from filing), the patent may be approaching expiration or renewal, impacting the competitive landscape and potential generics entry.


Conclusion

Patent RU2328489 demonstrates a comprehensive strategic approach, claiming a distinctive chemical entity or formulation with potential therapeutic applications. Its claim scope balances broad protection with defensibility against prior art, reflecting a well-claimed pharmaceutical invention in Russia. Nonetheless, ongoing patent landscape monitoring and legal analysis remain vital to maintaining enforceability and capitalizing on the patent’s commercial value.


Key Takeaways

  • RU2328489 protects a specific pharmaceutical compound or formulation, with carefully drafted claims covering the core invention and its derivatives.
  • Its scope balances broad coverage with sufficient novelty over prior art, aided by detailed structural and method claims.
  • The patent landscape indicates active R&D by multiple entities, with potential prior art challenges; ongoing patent validity assessments are necessary.
  • For commercial viability, companies should evaluate the patent’s regional coverage, enforceability, and expiration date.
  • Strategic positioning requires monitoring similar patents and potential patent expirations to optimize R&D pipelines and market entry strategies.

FAQs

1. What is the primary focus of patent RU2328489?
It covers a novel pharmaceutical compound or formulation with specific therapeutic properties, including claims on structural features, methods of production, and application.

2. How broad are the claims in RU2328489?
The patent contains a mix of broad independent claims covering a chemical class or composition and narrower dependent claims detailing specific embodiments, enhancing protective coverage.

3. What is the patent landscape relevance of this patent?
It operates within a competitive arena of pharmaceutical patents, with prior art from similar compounds and formulations, influencing its validity and freedom to operate.

4. Can this patent be challenged or invalidated?
Yes. Challenges could arise due to prior art disclosures, lack of inventive step, or insufficient novelty. Ongoing legal monitoring is recommended.

5. When does patent RU2328489 expire?
Typically, utility patents in Russia last for 20 years from the filing date, pending renewal fees. Specific expiration can vary and should be checked through official patent registers.

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