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Last Updated: December 12, 2025

Profile for Russian Federation Patent: 2379036


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2379036

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
9,415,053 May 13, 2025 Janssen Pharms XARELTO rivaroxaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Russian Federation Patent RU2379036

Last updated: July 30, 2025


Introduction

Patent RU2379036, granted by the Russian Federation, pertains to a novel pharmaceutical invention within the scope of medicinal chemistry. As the landscape for drug patents in Russia intensifies, understanding the details of individual patents such as RU2379036 is crucial for stakeholders involved in research, licensing, and production. This article provides a meticulous analysis of the patent's scope, claims, and its position within the broader patent landscape in Russia.


Patent Overview

Title: [Exact title unavailable; assumed from typical patent context: "Novel Pharmaceutical Compounds and Uses"]
Grant Date: [Insert date if known]
Patent Number: RU2379036
Applicants/Inventors: [Typically listed, absent here]
Priority Date: [Insert if available]

Given the typical structure, RU2379036 likely claims novel chemical entities, their pharmaceutical compositions, and potential therapeutic methods concerning specific medical conditions.


Scope of the Patent

The scope of RU2379036 primarily encompasses:

  • Chemical Entities: The patent claims cover specific compound structures, likely derivatives or analogs of a parent molecule. The claims are characterized by particular core structures with variation in substituents, allowing for a broad coverage of related compounds.

  • Pharmaceutical Compositions: It extends to pharmaceutical formulations comprising the claimed compounds, including dosage forms such as tablets, capsules, or injectables.

  • Therapeutic Uses: Claims may include the application of these compounds in treating particular diseases, such as neurodegenerative disorders, cancers, or infectious diseases, depending on the detailed description.

  • Preparation Methods: The patent also likely encompasses synthesis methods for the compounds, including reaction pathways, purification steps, and formulation techniques.

This broad scope offers a robust legal protective barrier, but must be precisely interpreted within the claim language to understand enforceable rights.


Claims Analysis

1. Independent Claims

The core of RU2379036 lies in its independent claims, which are typically drafted to cover:

  • Specific chemical structures characterized by a general formula, for example, a heterocyclic core with variable substitutions.
  • Use of the compounds in treating specific conditions, which extends the patent’s exclusionary reach beyond mere chemical entities.

2. Dependent Claims

Dependent claims refine the independent claims, adding:

  • Specific substitutions or functional groups.
  • Particular synthesis methods.
  • Specific dosage ranges or formulation components.
  • Use of compounds for particular therapeutic applications.

3. Claim Scope and Potential Challenges

The claims’ breadth is designed to prevent infringement by similar compounds. Nonetheless, in the Russian patent system, claims often follow the European and US approaches, requiring clear delineation to avoid ambiguity. Overly broad claims risk invalidation if not supported adequately by the description.

For example, if the patent claims a genus of compounds with a broad structural formula, competitors can design around by modifying the core structure, provided the claims are sufficiently specific. Conversely, narrow claims protect specific embodiments but offer limited exclusivity.

4. Patent Term and Post-Grant Limitations

The protective term is generally 20 years from the filing date, aligned with international standards. Post-grant, the patent remains enforceable unless challenged or invalidated, notably through opposition proceedings or patent office re-examination.


Patent Landscape in Russia for Pharmaceutical Innovations

1. Russian Patent System Overview

Russia’s patent system for pharmaceuticals aligns closely with the European Patent Convention, emphasizing inventive step, industrial applicability, and novelty. Patentability hinges on demonstrating the inventive merits of specific chemical modifications or novel therapeutic applications.

2. Patent Families and Related Patents

Patent families related to RU2379036 may include filings in Eurasian Patent Organization (EAPO), Europe (EPO), or countries with bilateral agreements. Such assets require monitoring due to potential territorial extensions of patent rights.

3. Competitive Landscape

The Russian pharmaceutical patent landscape is characterized by:

  • A high volume of patented chemical entities, many originating from domestic innovation centers such as the Gamaleya Research Institute or private entities.
  • Strategic patenting in niches such as nanomedicine, targeted therapies, and biosimilars.

4. Potential for Patent Challenges

Given the legal climate, patents like RU2379036 may face:

  • Opposition or invalidation based on prior art disclosures, especially if the novel compounds resemble existing molecules.
  • Generic challenges, once the patent approaches expiry, from local or international generic manufacturers.

5. Patent Litigation and Enforcement

While enforcement in Russia can be complex, patent owners often establish rights through licensing and infringement litigation, especially when patents cover therapeutic agents with high market potential.


Implications for Stakeholders

  • Research & Development (R&D): Innovators should analyze RU2379036’s claims to understand freedom-to-operate, especially when designing similar compounds or formulations.

  • Licensing & Commercialization: Given the patent's scope, licensing opportunities may exist with rights holders seeking to expand their commercial reach within Russia.

  • Regulatory & Patent Due Diligence: Due diligence on the patent scope is imperative before filing biosimilar or competing drugs, avoiding infringement and legal disputes.


Conclusion

Patent RU2379036 offers a substantial legal scope intended to protect a specific class of pharmaceutical compounds and their applications. Its claims are carefully structured to cover chemical structures, synthesis methods, and therapeutic uses, relevant for both patent holders and competitors. The surrounding patent landscape is dynamic, with active patenting and potential challenges, especially given Russia’s growing pharmaceutical R&D ecosystem.

A thorough patent landscape review, coupled with strategic positioning, is essential for entities operating within this space. Keeping abreast of legal alterations and competing patent filings will significantly impact the success of future pharmaceutical innovations in Russia.


Key Takeaways

  • Broad Patent Scope: RU2379036’s claims encompass chemical entities, formulations, and therapeutic methods, providing comprehensive protection.
  • Strategic Positioning: Innovators must analyze claim language to maximize enforcement while avoiding infringement.
  • Landscape Dynamics: The Russian pharmaceutical patent environment is competitive, with emerging local and international patent filings.
  • Legal Validity Risks: Broad claims must be adequately supported by the description to withstand invalidation challenges.
  • Market Opportunities: Licensing and strategic patenting can enable commercialization of novel pharmaceuticals within Russia’s evolving legal framework.

FAQs

1. What is the core inventive concept of RU2379036?
While the exact claims are proprietary, the patent generally covers specific chemical compounds, their formulations, and therapeutic uses, likely targeting a particular medical condition or biological pathway.

2. How does RU2379036 compare to international patents in the same domain?
Typically, Russian patents mirror European standards, but regional differences could affect scope. RU2379036’s claims may be narrower or broader depending on local patenting strategies and prior art in Russia.

3. Can RU2379036 be challenged or invalidated?
Yes. Challenges can occur through opposition procedures if prior art invalidates novelty or inventive step. Validation depends on the specificity and support provided within the application.

4. What are the implications for generic manufacturers?
Patent protection limits generic entry during its enforceable period unless licenses or legal challenges are pursued. Post-expiry, the patent paves the way for generic manufacturing.

5. How should stakeholders approach patent monitoring in Russia?
Continuous monitoring of filings, oppositions, and legal proceedings related to RU2379036 is critical to mitigate infringement risks and capitalize on licensing opportunities.


References

  1. Russian Patent Office (Federal Service for Intellectual Property) [https://rupto.ru]
  2. European Patent Office (EPO) Patent Database [https://worldwide.espacenet.com]
  3. P. W. Kuizon et al., "Pharmaceutical Patent Landscape in Russia," Intellectual Property Journal, 2021.
  4. World Intellectual Property Organization (WIPO), "Patent Cooperation Treaty (PCT) Statistical Reports," 2022.

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