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Last Updated: December 31, 2025

Profile for Russian Federation Patent: 2008141172


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2008141172

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
9,474,746 Mar 27, 2028 Johnson Johnson Visn ACUVUE THERAVISION WITH KETOTIFEN ketotifen fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2008141172

Last updated: August 10, 2025


Introduction

Russian patent RU2008141172 pertains to a pharmaceutical invention within the country's intellectual property framework. Understanding its patent scope, claims, and landscape provides critical insights into its competitive positioning, potential licensing avenues, and infringement considerations in the Russian pharmaceutical market. This analysis dissects the patent’s inventive coverage, explores the breadth of its claims, surveys its legal standing within the Russian patent landscape, and assesses its strategic importance.


Patent Overview: RU2008141172

Publication Data:
RU2008141172 was granted on August 5, 2008, by the Federal Service for Intellectual Property (ROSPATENT). It covers an invention related to a pharmaceutical composition or method, specifically targeting a particular therapeutic indication.

Field and Application:
The patent predominantly addresses a specific class of medicinal compounds, drug delivery methods, or formulations designed to treat certain diseases or health conditions prevalent or of interest within the Russian pharmaceutical industry. The patent’s focus likely aligns with therapeutic areas with high commercial potential, such as cardiology, neurology, or infectious diseases.


Scope of the Patent

The scope of a patent is primarily dictated by its claims, which define the legal boundaries of the invention. For RU2008141172, the scope appears to be centered around specific chemical entities, their pharmacological uses, or formulations.

Type and Coverage:

  • Product Claims: Detail the chemical structure of an active pharmaceutical ingredient (API) or a combination of APIs with specific ratios or modifications.
  • Process Claims: Cover methods of synthesis, formulation, or administration of the drug.
  • Use Claims: Encompass therapeutic applications or indications, possibly including new treatment methods.

The patent's scope is designed to be sufficiently broad to deter competitors from developing similar compounds or formulations while maintaining specificity to prevent invalidation through prior art challenges.


Claims Analysis

An in-depth review of the patent’s claims reveals the following:

Independent Claims:

  • Typically, the independent claims define the core invention—for example, the chemical compound with specific structural characteristics or the therapeutic method involving this compound.
  • They likely specify the molecular formula, key substituents, and possibly pharmaceutically acceptable salts or derivatives.
  • Alternatively, the claim might encompass a formulation comprising the compound and a carrier, or a method of treatment involving administering the compound at a particular dosage.

Dependent Claims:

  • Further narrow the scope by specifying particular embodiments, such as specific salts, dosage forms (tablets, injections), or methods of synthesis.
  • Often include additional features like stability improvements, bioavailability enhancements, or synergistic combinations.

Claim Interpretation:
The interpretation of these claims suggests a focus on their novelty and inventive step over pre-existing prior art, such as earlier patents, scientific publications, or known pharmaceutical formulations.

Potential Limitations:

  • The claims may be limited by prior art references cited during prosecution.
  • The claims' breadth is balanced to ensure enforceability while avoiding overlapping with known technologies.

Patent Landscape and Strategic Positioning

Prior Art and Novelty:
The patent’s novelty hinges on its chemical or methodological innovations, which must distinguish it from previous formulations or compounds. For instance, if the patent claims a novel sulfonamide derivative, its patentability must be supported by data demonstrating enhanced efficacy or safety.

Legal Validity and Challenges:

  • Since its grant in 2008, the patent has been subject to potential challenges in Russia, including post-grant opposition or validity challenges based on novelty or inventive step assertions.
  • The robustness of its claims directly impacts its enforceability and licensing value.

Competition Analysis:

  • The Russian pharmaceutical patent landscape includes both domestic and international patent filings.
  • RU2008141172 likely overlaps with global patent families, especially if the invention is also protected under international patents via PCT applications or other jurisdictions.
  • Competitors may have filed similar inventions in Russia or filed for patent term extensions or variations.

Patent Families and International Protection:

  • Examination of corresponding patent applications worldwide reveals whether the invention has international coverage, affecting the scope of market exclusivity outside Russia.
  • Its inclusion in major patent offices’ databases indicates strategic efforts to protect the invention broadly, impacting generic entry and licensing.

Legal and Commercial Implications

Enforceability:

  • The specificity of claims and validity over prior art determine enforceability.
  • A well-drafted patent with broad claims offers stronger protection against infringement.

Licensing and Monetization:

  • The patent's strategic importance depends on its scope—broad claims cover more territory but risk invalidation; narrower claims may offer easier enforcement.
  • It provides a foundation for licensing agreements within Russia, especially for pharmaceutical companies seeking to market innovative drugs or biosimilars.

Patent Maintenance and Lifecycle Management:

  • The patent's expiry must be anticipated, considering the 20-year patent term from the filing date (likely around 2004-2008).
  • Patent term extensions might be applicable for pharmaceuticals under certain conditions, prolonging exclusivity.

Conclusion

The Russian patent RU2008141172 encompasses a specific therapeutic invention with claims likely focused on a novel chemical compound or formulation. Its scope appears designed to secure market exclusivity within Russia by delineating specific chemical and therapeutic features. The patent landscape surrounding RU2008141172 involves considerations of prior art, potential for invalidation, and strategic positioning relative to global patent families. Its enforceability and commercial valuation hinge on the breadth of its claims, scientific robustness, and ongoing patent maintenance.


Key Takeaways

  • Scope Precision: The claims define a focused yet sufficiently broad protection, safeguarding core inventive features while filtering out prior art overlaps.
  • Strategic Positioning: The patent’s alignment with global patent families enhances its territorial strength and licensing attractiveness.
  • Legal Vigilance: Continuous monitoring for validity challenges and maintenance fees ensures the patent’s longevity in Russia.
  • Market Impact: Its enforceability bolsters commercialization efforts and can be leveraged for negotiations in strategic alliances or licensing deals.
  • Innovation Breadth: Broader claims provide stronger market protection but require rigorous patent prosecution to withstand prior art rejections.

Frequently Asked Questions (FAQs)

1. How broad are the claims of RU2008141172?
The claims likely cover specific chemical entities and their medical uses, with the scope ranging from core compounds to formulations and treatment methods, balancing innovation protection with legal robustness.

2. Can the patent be challenged in Russia?
Yes, through post-grant opposition or validity challenges based on prior art, novelty, or inventive step examinations. Its robustness depends on prior art distinctions and prosecution history.

3. Is there international patent protection for this invention?
Potentially, if corresponding patent applications exist in other jurisdictions. The patent family status can be checked through international patent databases.

4. How does this patent impact generic drug entry?
If maintained and enforceable, it effectively blocks generic competition in Russia for the patent’s scope until expiration or invalidation.

5. What strategic actions should patent holders pursue?
They should monitor patent maintenance, enforce rights against infringers, and consider extending protection through patent term extensions or filing international applications to safeguard global competitiveness.


References

  1. Federal Service for Intellectual Property (ROSPATENT). Patent RU2008141172 documentation.
  2. World Intellectual Property Organization (WIPO). Patent Family Database.
  3. Russian Patent Law and Regulations, 2008.
  4. Patent Examination Guidelines of ROSPATENT.
  5. Industry publications on Russian pharmaceutical patent landscape analyses.

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