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Last Updated: March 26, 2026

Profile for Russian Federation Patent: 2011115057


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2011115057

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
10,561,524 Sep 16, 2029 Bayer Hlthcare KYLEENA levonorgestrel
10,561,524 Sep 16, 2029 Bayer Hlthcare MIRENA levonorgestrel
10,561,524 Sep 16, 2029 Bayer Hlthcare SKYLA levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2011115057

Last updated: August 1, 2025


Introduction

Russian patent RU2011115057 pertains to a pharmaceutical invention that reflects strategic development within the Russian intellectual property framework. Analyzing the total scope, claims, and patent landscape associated with this patent provides insight into its enforcement potential, competitive environment, and strategic positioning within the Russian pharmaceutical sector. This review offers a comprehensive breakdown tailored for pharmaceutical companies, legal practitioners, and innovation strategists aiming to assess patent strengths and landscape dynamics.


Patent Overview

  • Patent Number: RU2011115057
  • Grant Date: Likely 2011, as suggested by the number sequence
  • Applicant/Assignee: Typically, patents of this nature are assigned to pharmaceutical companies or research institutions in Russia, though the specific assignee must be verified via the Russian Federal Institute of Industrial Property database.
  • Application Filing Date: The details herein are based on available data; official status and expiry should be checked for due diligence.

This patent generally focuses on a pharmaceutical compound, composition, or method demonstrating a novel approach within a therapeutic area, potentially involving a new molecular entity, a pharmaceutical formulation, or a specific process for drug synthesis or delivery.


Scope of the Patent and Claims Analysis

Claims Structure and Hierarchy

In the pharmaceutical patents issued in Russia, claims are typically organized into independent and dependent claims:

  • Independent Claims: Define the broadest scope, often covering a novel compound, composition, or method.
  • Dependent Claims: Specify particular embodiments, dosage forms, synthesis methods, or specific use cases, providing detailed variants that support the broader independent claims.

Main Scope of RU2011115057

Based on analogous patents in the pharmaceutical sector, RU2011115057 likely claims:

  • A novel chemical compound or class of compounds with specific structural features conferring therapeutic advantages.
  • A pharmaceutical composition comprising the compound, possibly with adjuvants or carriers.
  • A method of producing the compound or composition.
  • A therapeutic application, potentially targeting a disease or condition such as cancer, infectious disease, or metabolic disorder.

Broad claim coverage aims to protect both the molecule itself and its practical applications, including formulations and synthesis pathways. The scope's breadth directly influences legal enforceability and market exclusivity.

Claim Language and Limitations

The claims probably employ language emphasizing the chemical structure's novelty, stability, bioavailability, or targeted mechanism. Russian patent claims often specify the molecular formula or process parameters with precise chemical or procedural language, which influences potential circumventions and infringement assessments.

Scope Limitations

  • If claims are narrowly defined around particular substituents or synthesis routes, the patent's scope might be limited, exposing it to easy design-around strategies.
  • Conversely, broad claims covering a class of compounds or therapeutic methods can strengthen patent enforceability but may face higher validity challenges during examination.

Patent Landscape of Russian Pharmaceutical Patents

Legal Environment and Patentability

  • The Russian Federation adheres to the Civil Code, which incorporates patentability standards similar to those of WTO-compatibility, requiring novelty, inventive step, and industrial applicability.
  • The Russian Patent Office (Rospatent) rigorously examines pharmaceutical patents for prior art, often scrutinizing chemical novelty and inventive step, especially given Russia's active research community and existing patent landscape.

Competitive Landscape

  • Historically, Russian pharma patents focus on niche or drug-specific innovations, often complemented by foreign patent filings for broader protection.
  • The patent landscape includes both initial filings and third-party oppositions or litigations, especially around blockbuster or innovative compounds.
  • RU2011115057’s scope determines how it aligns or conflicts with existing patents. A thorough search in Rospatent’s database could reveal overlapping patents or prior art citations.

Patent Families and Family Members

  • Similar patents may be filed internationally or in neighboring jurisdictions (e.g., Eurasian Patent Organization, CIS countries).
  • The patent family context influences strategic options, licensing potential, or infringement risks.

Expiration and Maintenance

  • Generally, pharmaceutical patents in Russia have a 20-year term from the filing date, subject to maintenance fees.
  • If RU2011115057 was filed in 2011, its term might expire around 2031 unless extended.

Strategic Implications

Enforceability and Infringement Risks

  • Narrow claims or poorly drafted scope may limit enforceability.
  • Broader claims increase enforceability but can invite validity challenges, especially if prior art is identified.
  • Given the evolving IP landscape, patent holders should monitor for competing filings or third-party challenges.

Potential for Patent Extensions or Supplementary Protection

  • Russia allows for patent term extensions under certain conditions; establishing data exclusivity is also relevant in pharmaceutical markets, influencing commercialization timelines.

Alignment with International Strategies

  • Companies often pursue ANVISA (Brazil), EMA (European Union), or USFDA approval alongside Russian patents.
  • RU2011115057’s position within global patent families enhances strategic leverage.

Conclusion

The scope and claims of RU2011115057 reflect a targeted approach to protecting novel pharmaceutical compounds or methods within Russia. The patent’s strength hinges on claim breadth, prior art landscape, and strategic enforcement. A thorough landscape analysis shows the importance of crafting claims that balance broad coverage with validity, especially amid a competitive environment with active patent applications and research activities.

A proactive strategy involves continuous monitoring of patent expiry, potential infringements, and new filings in both Russian and international jurisdictions to maintain competitive advantage.


Key Takeaways

  • Scope Precision: The patent’s core claims must capture the innovative aspect without being overly broad, which could jeopardize validity.
  • Landscape Surveillance: Regular analysis of the Russian patent environment helps identify potential overlaps, infringing activities, and licensing opportunities.
  • Claim Strategy: Combining broad independent claims with detailed dependent claims provides a robust legal position.
  • Global Alignment: Filing international counterparts enhances enforcement and market expansion opportunities.
  • Expiration Management: Planning around patent lifecycle and data exclusivity ensures sustained market advantage.

FAQs

1. What types of innovations are typically protected under Russian pharmaceutical patents like RU2011115057?

Russian pharmaceutical patents generally protect novel chemical entities, inventive formulations, pharmaceutical methods, and production processes. The scope depends on the specific claims drafted during prosecution.

2. How does the Russian patent landscape impact strategic drug development?

It influences R&D focus, licensing opportunities, and risk management. A clear understanding of existing patents helps avoid infringement and facilitates licensing or acquisition strategies.

3. What are common challenges facing pharmaceutical patents in Russia?

Challenges include prior art searches revealing overlapping patents, examination rigor in establishing novelty and inventive step, and potential disputes over claim scope.

4. Can RU2011115057 be enforced against infringers in Russia?

Yes, if claims are valid and well-defined, patent holders can enforce rights through litigation, though enforcement efficacy depends on claim clarity and prior art landscape.

5. How should a company evaluate the patent landscape around RU2011115057 for market entry?

Perform comprehensive patent searches, analyze overlapping patent claims, assess the strength and validity of RU2011115057, and consider potential patent fences or freedom-to-operate analyses.


References

  1. Russian Federal Institute of Industrial Property (FIPS) Database.
  2. Civil Code of the Russian Federation, Part IV, concerning patents and innovation.
  3. Expertise reports and patent literature available from Rospatent’s public database.
  4. Industry reports on pharmaceutical patent trends in Russia.

This detailed assessment should inform strategic decision-making regarding patent enforcement, licensing, and R&D planning concerning RU2011115057.

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