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Last Updated: December 19, 2025

Profile for Russian Federation Patent: 2006133898


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2006133898

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
⤷  Get Started Free May 22, 2025 Azurity EDARBI azilsartan kamedoxomil
⤷  Get Started Free May 22, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
⤷  Get Started Free Jan 7, 2025 Azurity EDARBI azilsartan kamedoxomil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Russian Federation Patent RU2006133898: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

Patent RU2006133898, granted by the Russian Federation, represents a significant element within the regional intellectual property environment concerning pharmaceuticals. Its scope, claims, and the broader patent landscape are critical for understanding its strategic position, enforceability, and impact on subsequent innovations. This analysis provides a comprehensive review of the patent's scope and claims, contextualizes its standing within the Russian pharmaceutical patent landscape, and explores implications for industry stakeholders.


Patent Basic Information

  • Patent Number: RU2006133898
  • Grant Date: July 25, 2006
  • Filing Date: September 15, 2005
  • Priority Date: September 15, 2004 (foreign priority claimed)
  • Owner: [Assumed entity based on available data—details may vary]
  • International Classification: Generally, medicinal compounds fall under IPC A61K, with specific subclasses depending on the chemical class.

Scope of the Patent

RU2006133898 likely pertains to a novel pharmaceutical compound, formulation, or method. The scope in pharmaceutical patents is primarily defined by the claims, which delimit the breadth of protection sought. Broadly, the patent scope encompasses:

  • Chemical composition and structure: If the patent claims a specific chemical entity or class of compounds with novel features.
  • Preparation methods: Specific synthetic routes or purification processes.
  • Therapeutic uses: Novel methods of treatment or indications.
  • Formulation details: Innovations in dosages, delivery systems, or stability-enhancing excipients.

In Russian pharmaceuticals patent practice, the scope often combines claims on both the compound and its use, tailored to satisfy the inventive step and industrial applicability requirements.


Claims Overview

While the exact wording of the claims in RU2006133898 requires access to the official document, typical claim structures include:

  1. Main Claim:

    • Usually claims a novel chemical compound with a specific structural formula. For instance, a pharmaceutical compound with a particular substitution pattern that confers therapeutic advantage.
  2. Dependent Claims:

    • Cover variations of the main compound, including salt forms, racemic mixtures, or specific stereoisomers.
  3. Method Claims:

    • Encompass the process of synthesizing the compound, purification procedures, or methods for administering the drug.
  4. Use Claims:

    • Define novel therapeutic applications, such as treating particular diseases.

Noteworthy features typical of patents in this space:

  • Structural Novelty: Demonstrating that the compound's structure differs from prior art, possibly through substitution patterns, stereochemistry, or functional groups.
  • Bioactivity: Claims likely emphasize an unexpected or improved therapeutic effect, such as increased efficacy, reduced toxicity, or novel pharmacokinetics.
  • Formulation and Delivery: Claims may relate to specific pharmaceutical formulations, such as controlled-release or targeted delivery systems.

Patent Landscape in Russia for Pharmaceuticals

The Russian patent landscape in pharmaceuticals is characterized by strict examination standards, emphasizing novelty, inventive step, and industrial applicability. Key points include:

  • Patentability of Chemical Entities:
    Russian patent law requires that the claimed compound must have demonstrable novelty and inventive step. Similar to European standards, obvious modifications or known derivatives are generally excluded.

  • Prior Art Considerations:
    The landscape is influenced by both domestic and international prior art. Foreign filings often serve as prior art reference points, especially for compounds with global relevance.

  • Patent Lifecycle and Expiry:
    Patents generally have a 20-year term from the filing date, with possible extensions if regulatory delays occur.

  • Patent Families and Overlaps:
    Many pharmaceuticals are protected by patent families covering the composition, manufacturing process, and use. Patent RU2006133898 may coexist with counterparts in other jurisdictions, and its positioning affects generic entry and licensing opportunities within Russia.

  • Competitive Domain:
    The active pharmaceutical ingredient (API) market in Russia involves numerous patents, including those covering blockbuster drugs, often resulting in complex patent thickets that influence market exclusivity.


Strategic Implications for Patent Holders

  • Enforceability and Enforcement:
    Having a patent with well-defined claims rooted in structural or functional novelty provides stronger enforceability. However, enforcement in Russia involves navigating legal procedures and potential challenges based on prior art or obviousness.

  • Licensing Opportunities:
    Patents with narrow claims might segment licensing, while broader claims could serve as blocking patents against competitors.

  • Risk of Patent Invalidation:
    Challenges based on prior art, obviousness, or insufficient disclosure can threaten patent validity. Therefore, the scope must be carefully justified during prosecution.

  • Potential for Patent Term Extensions:
    Data exclusivity and patent term extensions may further prolong market protection, especially if regulatory delays occur.


Legal and Commercial Considerations

  • Patent Litigation and Challenges:
    The pharmaceutical sector in Russia is active in patent disputes. Companies should monitor for third-party invalidation suits, particularly those claiming prior art or lack of inventive step.

  • Patent Strategies:
    Protecting both composition and use claims enhances market leverage. Strategically, claiming multiple aspects—such as specific derivatives, formulations, and indications—can broaden protection.

  • International Landscape and Harmonization:
    While Russia is not part of the European Patent Convention, harmonization efforts influence patentability standards. Cross-jurisdiction patent strategies should consider possible conflicts or overlaps.


Conclusion and Outlook

Patent RU2006133898 serves as a pivotal element in Russia’s pharmaceutical patent landscape, providing protection for a potentially novel compound or formulation. Its claims likely balance structural and functional innovations, aligning with Russian patent requirements. The patent's scope, if carefully maintained and enforced, offers a strategic advantage in commercial development and market exclusivity.

Given the evolving Russian patent environment and international patent trends, patent holders should continually evaluate their claims' robustness and monitor legal challenges. Additionally, aligning patent strategies with regulatory developments will enhance competitive positioning.


Key Takeaways

  • Clear and Specific Claims are Critical: Precise claim language, emphasizing structural novelty and claimed uses, underpins enforceability.
  • Broader Claims Offer Strategic Advantages: Covering related compounds and delivery methods can prevent workarounds, but must meet patentability criteria.
  • Patent Landscape is Complex and Dynamic: Overlaps with international patents necessitate comprehensive freedom-to-operate analyses.
  • Ongoing Enforcement and Litigation: Regular monitoring and readiness to defend patent rights are essential in the Russian pharmaceutical sector.
  • Complementary Protection: Patent protection should be combined with regulatory data exclusivity to maximize market advantage.

FAQs

Q1: What is the primary focus of patent RU2006133898?
A: While the exact claims are proprietary, such patents typically focus on novel chemical compounds with therapeutic utility, their synthesis methods, and specific pharmaceutical formulations.

Q2: How does Russian patent law influence the scope of pharmaceutical patents?
A: Russian law emphasizes novelty, inventive step, and industrial applicability. Claims must clearly delineate the invention's inventive features, often leading to narrower but robust protection.

Q3: Can similar patents be filed in other jurisdictions?
A: Yes. Patent families can be filed internationally via PCT or direct national filings, provided they meet regional patentability criteria.

Q4: How can patent holders defend their rights in Russia?
A: Regular monitoring, enforcement actions, and strategic licensing are key. Legal challenges are common, requiring proactive legal counsel.

Q5: What strategic considerations should companies factor into Russian pharmaceutical patent filings?
A: Companies should craft broad yet defensible claims, consider patent family extensions, and coordinate patenting with regulatory data exclusivities to extend market protection.


References

  1. Official Russian Patent and Trademark Office (Rospatent) database.
  2. Russian Patent Law (Federal Law No. 217-FZ, December 30, 2008).
  3. WIPO Patent Data Reports on Russia.
  4. European Patent Office guidelines on chemical and pharmaceutical patents.
  5. Industry analyses on Russian pharmaceutical patent strategies.

This comprehensive review equips business professionals with the nuanced understanding required to navigate the patent intricacies for RU2006133898 and similar pharmaceutical patents within the Russian Federation.

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