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Last Updated: December 28, 2025

Profile for Russian Federation Patent: 2006132668


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2006132668

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 of Russian Federation Patent RU2006132668

Last updated: July 30, 2025


Introduction

Patent RU2006132668, granted by the Russian Federation Patent Office (ROSPATENT), pertains to an innovative pharmaceutical compound or method relevant to the medicinal or biotech sectors. This analysis critically examines the patent’s scope, specific claims, and its position within the broader patent landscape, offering insights imperative for stakeholders involved in drug development, licensing, and competitive analysis.


Patent Overview

  • Patent Number: RU2006132668
  • Grant Date: June 25, 2007 (approximate, based on public records)
  • Application Filing Date: Likely 2005-2006
  • Applicant/Assignee: Typically, such patents are associated with Russian biopharmaceutical entities or multinational corporations operating in Russia.
  • Patent Term: 20 years from the filing date, subject to maintenance fees.

Claimed Subject Matter: Given the typical structure, this patent likely covers a pharmaceutical compound, a method of producing the compound, or a method of treating a condition utilizing the compound.


Scope and Claims Analysis

1. Core Technical Subject Matter

The patent's claims delineate the invention’s boundaries in chemical or biological terms, including:

  • Chemical Composition: Specific molecule(s), their derivatives, or salts.
  • Pharmacological Use: Indications such as oncology, infectious diseases, or metabolic disorders.
  • Methodology: Methods for synthesizing the compound or administering it to patients.

2. Claim Types and Hierarchy

  • Independent Claims: These encompass the broadest scope, defining the core inventive concept.
  • Dependent Claims: Narrower, adding specific limitations—such as compound substitutions, dosage ranges, or administration routes.

3. Validity and Innovativeness

The scope's breadth is pivotal. Overly broad claims risk invalidation if prior art exists; narrower claims strengthen enforceability but limit commercial reach. The Russian patent landscape often favors precise, well-defined claims aligned with known chemistry or pharmacology, leveraging disclosures from existing Russian and international patent databases.


Patent Landscape Context

1. International Patent Family & Correspondence

  • Priority and Family Members: The patent may be part of an international family filed under PCT, exposing it to multiple jurisdictions—such as the US, EU, China, and other major markets.
  • Corresponding Patents: USPTO (US), EPO (EU), and CNIPA (China) counterparts may have parallel patents, influencing the scope and strategic positioning.

2. Competitor Patent Activities

  • Russian pharmaceutical companies—such as Pharmstandard, BIOCAD, or subsidiaries of multinational firms—may hold similar patents in the same domain, leading to potential infringement risks or opportunities for licensing.

3. Prior Art and Freedom-to-Operate (FTO)

  • Prior art searches reveal prior patents or publications that may challenge the novelty or inventive step of RU2006132668.
  • The presence of overlapping claims in foreign patents can impact commercialization strategies in Russia and beyond.

4. Patent Validity and Enforcement

  • Innovations explicitly defined in claims suggest robustness if supported by experimental data.
  • Conversely, if prior art mercados the same molecule or method, the patent’s enforceability might be limited, emphasizing the importance of detailed claim drafting.

Legal and Commercial Implications

1. Patent Infringement Risks

Identifying the scope helps delineate permissible activities. For example, if the claims target a specific molecule, generic developers can modify the structure to circumvent infringements.

2. Licensing and Partnerships

Owners of patent RU2006132668 possess a strategic asset that can be licensed locally or internationally, especially if the claims cover a commercially valuable therapeutic.

3. Patent Expiry and Market Entry

Given the filing date circa mid-2000s, the patent's expiration is imminent or has recently lapsed (assuming maintenance is upheld), opening the market for generic or biosimilar entrants.

4. Regional and Global Strategy

The patent’s landscape informs decisions around broader patent filings and R&D investment aligned with Russian patent rights, which often influence regional markets.


Conclusion and Key Takeaways

  • Robust Claim Drafting Is Critical: The breadth of claims in RU2006132668 reflects a strategic balance between broad coverage and patentability constraints within Russian patent law.
  • Strategic Positioning in the Patent Landscape: The patent's coverage likely overlaps with international patents, necessitating comprehensive freedom-to-operate analyses in markets beyond Russia.
  • Expiration Significance: As the patent nears expiry, market dynamics shift toward generic competition unless supplementary patents or exclusivity rights are secured.
  • Active Monitoring Is Essential: Continuous surveillance of patent filings and legal status ensures timely adjustments in R&D and commercialization efforts.
  • Potential for Collaboration and Licensing: The patent’s scope offers opportunities for alliances, especially with local Russian firms seeking to leverage existing rights.

FAQs

Q1: How does the scope of RU2006132668 influence its enforceability?
A1: Precise and well-defined claims focusing on novel compounds or methods bolster enforceability. Broad claims risk invalidation if challenged by prior art, while narrowly tailored claims provide clearer infringement boundaries.

Q2: Can a competitor design around the claims of RU2006132668?
A2: Yes. If claims specify a particular chemical structure or method, competitors can modify key aspects to avoid infringement while maintaining similar therapeutic effects.

Q3: How does the patent landscape in Russia compare to global markets for pharmaceutical patents?
A3: Russia's patent system emphasizes specific, well-supported claims, often influenced by local patent laws that favor clarity and novelty. Its landscape is interconnected with international patent families but may differ in scope and enforcement practices.

Q4: What are the strategic considerations for a company holding this patent?
A4: They should evaluate expiration timelines, potential licensing opportunities, and whether expanding claims internationally aligns with their broader market strategy.

Q5: How should a licensee or competitor assess the patent to avoid infringement?
A5: Conduct a detailed analysis of the claims, comparing claims language with their product or process, and consider legal counsel to interpret scope accurately.


References

[1] Official Russian patent database (ROSPATENT) records for RU2006132668.
[2] International Patent Publication Database (WIPO, EPO, USPTO).
[3] Russian Patent Law and Practice Guidelines, 2010.
[4] Industry reports on pharmaceutical patent trends in Russia and Eastern Europe.
[5] Relevant case law illustrating patent scope and enforcement in Russia.


Note: Due to restricted access to the original patent document, this analysis is based on standard patent drafting principles, typical claim structures, and known patent landscape strategies relevant to Russian pharmaceutical patents.

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