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Last Updated: March 26, 2026

Profile for Russian Federation Patent: 2006112589


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2006112589

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
8,182,838 Oct 20, 2028 Novartis SEEBRI NEOHALER glycopyrrolate
8,182,838 Oct 20, 2028 Novartis UTIBRON NEOHALER glycopyrrolate; indacaterol maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Patent RU2006112589

Last updated: August 8, 2025

Introduction

Patent RU2006112589, granted in Russia, pertains to an innovative pharmaceutical invention. Analyzing its scope, claims, and broader patent landscape provides insights into its commercial potential, legal robustness, and competitive environment within the Russian pharmaceutical sector. This detailed review highlights the patent’s claims’ breadth, overlaps with existing patents, and strategic positioning under Russian patent law, offering valuable guidance for stakeholders including patent holders, competitors, and legal analysts.


Patent Overview and Basic Data

  • Patent Number: RU2006112589
  • Title (as per official record): [Specific title not provided, typically related to an active pharmaceutical ingredient or formulation]
  • Filing Date: [Data not available; assume early 2000s based on number sequence]
  • Grant Date: 2006 (as suggested by the number format—"2006" in the application serial)
  • Patent Term: 20 years from filing, subject to maintenance fees and national law provisions.
  • Patent Office: Federal Service for Intellectual Property (ROSPATENT)

Note: A detailed patent document would ideally be sourced from the official dossier or database for precise claims and descriptions. For this analysis, assumptions based on typical pharmaceutical patents and patent classification are integrated.


Scope of the Patent

The scope of RU2006112589 is fundamentally defined by its claims. In pharmaceutical patents, these encompass novel chemical entities, compositions, processes, and uses. The scope can be categorized as:

  • Chemical Composition: Likely covers a specific active pharmaceutical ingredient (API), its derivatives, or formulations designed for therapeutic applications.
  • Method of Production: Claims may involve specific synthetic routes that confer advantages such as yield, purity, or stereochemistry specificity.
  • Use or Method of Treatment: Possible claims related to using the compound or formulation for particular medical indications.

The breadth of the patent scope determines its enforceability and commercial value. Broad claims, if valid, provide extensive protection against similar inventions, while narrow claims limit infringement scope but are easier to defend.


Analysis of the Claims

A typical pharmaceutical patent includes a hierarchy:

  1. Main Claim(s): Usually concerns the core invention, such as a specific chemical entity or formulation.
  2. Dependent Claims: Specify particular embodiments — e.g., lower doses, specific salts, formulations, or targeted therapeutic uses.
  3. Method Claims: Cover the process of manufacturing or use.

Potential Core Claims

Based on common pharmaceutical patents, the core claims of RU2006112589 probably involve:

  • A novel chemical compound or a class of compounds with specific structural features conferring enhanced efficacy or reduced side-effects.
  • A specific crystalline form or salt of the active compound, which improves stability or bioavailability.
  • A pharmaceutical composition comprising the active compound with a particular carrier or excipient.
  • A method of manufacturing the compound, emphasizing process advantages.
  • Clinical use claims, e.g., a method of treating a specific disease such as cancer, neurodegenerative disease, or infectious disease.

Claim Scope Evaluation

  • Novelty: Claims must specify features not anticipated by prior art, including previous patents, scientific literature, or common knowledge in the pharmaceutical field.
  • Inventive Step: The claims are non-obvious if they involve inventive modifications leading to unexpected benefits.
  • Industrial Applicability: The invention must be capable of being produced or used in industry, which is generally satisfied by pharmaceutical compositions.

Note: Without direct access to the claims text, this analysis remains hypothetical, aligning with common practice.


Patent Landscape and Competitive Environment

Prior Art and Patent Overlaps

  • Russian Pharmaceutical Patent Environment: Russia’s patent system aligns with the European Patent Convention (EPC), emphasizing novelty, inventive step, and industrial applicability.

  • Existing Patents: The patent landscape comprises prior Russian patents for similar molecules, salts, or formulations, often filed in the 1990s and early 2000s. A thorough patent search within the same IPC classification (e.g., A61K for medicinal preparations) reveals potential overlaps or prior art references.

  • Overlap Risks: If similar compounds or methods exist, the patent’s enforceability may face challenges, or it may be limited to narrow claims.

  • Freedom-to-operate (FTO) Considerations: Companies seeking to commercialize similar drugs should conduct comprehensive searches to identify infringements or opportunities for licensing.

Legal Status and Maintenance

  • The patent appears to be granted in 2006, with potential expiration around 2026 unless maintenance fees are paid.
  • Monitoring legal status is crucial to determine the current enforceability.

International Patent Landscape

  • Similar patents might exist in WIPO (WO patents), EPO (EP patents), and other jurisdictions.
  • The patent family likely includes applications in major markets, impacting global commercialization strategies.

Strategic Implications

  1. Scope as a Strength: Broad claims covering the core compound and its key derivatives confer significant commercial protection.
  2. Potential Vulnerabilities: Narrow claims or insufficient inventive step could allow competitors to design around the patent.
  3. Licensing and Partnerships: The patent’s claims could serve as a negotiation point for licensing partnerships or collaborations within the Russian pharmaceutical market.
  4. Legal Challenges: Competitors may challenge the patent’s validity based on prior art; hence, patent holders must maintain thorough documentation of inventive steps and claim support.

Conclusion

Patent RU2006112589 exemplifies a strategic Russian pharmaceutical patent with potentially broad claims covering specific chemical entities or formulations. Its scope aligns with typical pharmaceutical patent protection, emphasizing chemical innovation and therapeutic application. A comprehensive understanding of its claims and its position within the Russian and international patent landscape reveals both opportunities and challenges for commercialization and competitive positioning.


Key Takeaways

  • The patent’s strength largely hinges on the breadth and specificity of its claims; broad claims offer stronger protection but face higher scrutiny during examination.
  • Overlap with prior art and existing patents could limit the patent’s enforceability, emphasizing the importance of thorough patent landscape analysis.
  • The patent’s legal status, including renewal payments, is critical in evaluating current rights and potential infringing activities.
  • Companies should conduct detailed freedom-to-operate analyses before developing products related to the patent.
  • Monitoring international patent filings can reveal opportunities or risks related to global patent rights.

FAQs

Q1: How can I determine the exact scope of claims in RU2006112589?
A: Access the official patent document through the Federal Institute of Industrial Property (ROSPATENT) or authorized patent databases. Review the full set of claims, description, and drawings to understand scope.

Q2: What legal challenges could weaken the enforceability of this patent?
A: Prior art prior to the filing date, lack of inventive step, or insufficient disclosure can challenge validity. Frequent patentability validations and legal analyses are necessary.

Q3: Is this patent likely to block generic competitors in Russia?
A: If the claims are broad and valid, it can serve as a significant barrier; however, narrow claims or invalidation proceedings can reduce this effect.

Q4: Can this patent be extended or modified for new therapeutic uses?
A: Yes, new uses may warrant separate patent filings. Secondary patents can complement the original patent, extending protection.

Q5: How does the Russian patent landscape impact global drug development?
A: Russian patents can influence global strategies, especially in common jurisdictions or markets with similar patent standards, guiding licensing, manufacturing, and research activities.


References

  1. Federal Service for Intellectual Property (ROSPATENT) patent database.
  2. WHO International Patent Classification (IPC).
  3. Russian patent law and guidelines.

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