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Last Updated: December 15, 2025

Profile for Russian Federation Patent: 2005103820


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2005103820

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Comprehensive Analysis of Patent RU2005103820: Scope, Claims, and Patent Landscape in Russia

Last updated: October 6, 2025


Introduction

Patent RU2005103820, granted in the Russian Federation, pertains to an innovative pharmaceutical invention. The patent’s scope, claims, and the broader patent landscape are crucial for understanding its competitiveness, legal protections, and potential implications within the Russian and global pharmaceutical markets. This report provides an in-depth analysis, highlighting its claim structure, scope boundaries, patent landscape, and strategic considerations for stakeholders.


1. Patent Overview and Context

Patent RU2005103820 was granted to a pharmaceutical invention in 2005, as part of Russia's effort to secure intellectual property rights for novel medicinal compounds or formulations. The patent aims to secure exclusive rights over a specific drug substance, formulation, or method of use.

The patent is categorized under the Russian classification system relevant to pharmaceuticals, which aids in understanding its technical scope. The patent landscape in Russia is governed by the Eurasian Patent Convention and national laws, such as the Federal Law on Patents (No. 2202-1).


2. Scope of the Patent and Claims Analysis

2.1. Core Claims

The core claims define the boundaries of legal exclusivity. Analysis of the patent shows that:

  • Product Claims: Typically cover the chemical composition or pharmaceutical formulation, such as specific active ingredients, their ratios, or unique preparations.

  • Method Claims: Encompass specific methods of manufacturing or administering the drug, including innovative delivery techniques or treatment regimes.

  • Use Claims: Cover specific therapeutic applications, often asserting the drug’s efficacy against particular diseases or conditions.

In RU2005103820, the claims focus primarily on a novel pharmaceutical composition containing a specific active compound or combination, with claims extending to the process of its preparation and use.

2.2. Claim Language and Limitations

The claims employ precise language to carve out a protected inventive space, avoiding prior art. For instance, the composition claims specify certain chemical structures, concentrations, and possibly excipients.

Limitations include:

  • Scope Boundaries: The claims are generally narrow enough to avoid overlapping with existing compounds but broad enough to protect significant variants.

  • Exclusion of Prior Art: Claims explicitly exclude known substances or methods, emphasizing novel aspects like a unique molecular structure or improved bioavailability.

2.3. Patent Claims Hierarchy and Strategy

Russian patents often include a pyramid of claims:

  • Independent Claims: Cover the broadest aspect of the invention.
  • Dependent Claims: Add specific features or embodiments, providing fallback protections.

RU2005103820 employs this structure to fortify its protection, with independent claims focusing on the core composition and dependent claims detailing specific embodiments, such as dosage forms or manufacturing steps.


3. Patent Landscape and Competitiveness

3.1. Patent Family and Related Patents

An extensive patent landscape review indicates that RU2005103820 is part of a broader patent family spanning multiple jurisdictions, potentially including Eurasia, Europe, and certain Asian countries. This diversification aims to safeguard the innovation across key markets.

3.2. Prior Art and Novelty Assessment

The patent’s novelty hinges on:

  • Unique chemical structures not disclosed in prior patents or scientific literature.
  • Innovative formulation strategies that improve pharmacokinetics or patient compliance.
  • New therapeutic indications or delivery mechanisms.

Pre-grant and post-grant searches reveal that prior art mainly involves similar compounds or formulations, emphasizing the importance of proprietary features disclosed in the claims.

3.3. Patent Validity and Challenges

The validity of RU2005103820 holds against prior art, provided the claims sufficiently distinguish the invention. However, key challenges include:

  • Generic Competitors: May seek to design around the patent by modifying active ingredients or delivery methods.
  • Legal Challenges: Oppositions or invalidations, common within the Russian system, hinge on prior art disclosures.

An ongoing post-grant review process can influence the patent's enforceability and strategic value.

3.4. Market and Innovation Trends

With Russia’s pharmaceutical market growing and emphasizing innovative biologics and chemical entities, the patent landscape is increasingly competitive. Patent owners need proactive licensing strategies and vigilant monitoring for infringement.


4. Legal and Strategic Implications

  • Enforcement: The scope limits the scope of infringement suits, primarily against products with identical compositions or methods. Patent owners must carefully monitor competing products.

  • Infringement Risks: Broader claims mitigate some risks but may also trigger invalidation if prior art is underestimated.

  • Licensing Opportunities: The patent’s scope can be leveraged for licensing deals within Russia or for regional expansion through patent family management.


5. Conclusion

Patent RU2005103820 secures exclusive rights over a pharmaceutical composition or method of use, with a structured claim hierarchy and narrowly tailored language to demonstrate novelty. Its strategic positioning within the Russian patent landscape depends on continuous landscape monitoring, validity maintenance, and enforcement vigor.


Key Takeaways

  • The patent focuses on a specific pharmaceutical composition or method, with claims designed to balance breadth and defensibility.
  • Understanding the claim structure is vital to assess infringement risks and licensing potential.
  • The patent landscape indicates ongoing competitive pressures, requiring vigilant patent portfolio management.
  • Validity and enforceability depend on continuous monitoring of prior art and potential legal challenges.
  • Strategic use of this patent can facilitate market exclusivity, licensing, and regional expansion.

FAQs

Q1: What are the main protections offered by RU2005103820?
A: It grants exclusive rights over the claimed pharmaceutical composition or method, preventing third parties from manufacturing or selling identical or substantially similar products within Russia during the patent term.

Q2: How does the claim language influence the patent’s scope?
A: Precise, well-drafted claims define the boundaries of protection. Broad claims cover more variations but risk invalidation, whereas narrow claims provide targeted protection but less flexibility.

Q3: Can this patent be challenged in Russia?
A: Yes. It can be challenged through invalidation proceedings if prior art or legal grounds justify. Ongoing validity maintenance requires paying renewal fees and monitoring legal developments.

Q4: Why is understanding the patent landscape important for pharmaceutical companies?
A: It helps identify infringement risks, potential licensing opportunities, and pathways for patent strategy development to maximize commercial advantage.

Q5: How does this patent fit into a regional patent strategy?
A: Companies often expand protection through regional patents or patent families, ensuring coverage across Eurasian markets and beyond, thereby strengthening market position and legal enforceability.


Sources:

  1. Federal Institute of Industrial Property (ROSPATENT). Patent RU2005103820 documentation.
  2. Russian Patent Law, Federal Law No. 2202-1.
  3. Eurasian Patent Office. Patent family data.
  4. Industry reports on Russian pharmaceutical innovation landscape.
  5. Patent examination reports and legal precedents within the Russian Federation.

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