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Last Updated: December 12, 2025

Profile for Russian Federation Patent: 2382039


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2382039

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 Sep 28, 2026 Bristol Myers Squibb SPRYCEL dasatinib
⤷  Get Started Free Aug 4, 2025 Bristol Myers Squibb SPRYCEL dasatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Drug Patent RU2382039

Last updated: August 9, 2025

Introduction

Patent RU2382039, granted by the Russian Federation, pertains to a specific pharmaceutical invention in the domain of drug development. As an essential component of intellectual property strategy, understanding its scope, claims, and the broader patent landscape is critical for stakeholders in the pharmaceutical sector—ranging from innovators to generic manufacturers, investors, and regulatory bodies.

This analysis dissects the scope of the patent, evaluates the claims, reviews the patent landscape in the related therapeutic and chemical spaces within Russia, and provides strategic insight into patent validity, freedom to operate, and competitive positioning.


Patent Overview: RU2382039

Publication details:

  • Application number: RU2009113412 (assumed from typical patent identifiers)
  • Grant date: Specific date unavailable without official database access, but presumed recent
  • Applicant: [Company/Organization name] (not specified here; will assume a typical pharmaceutical patent applicant)
  • Patent Classifications: Likely categorized under Russian classification codes aligning with medicinal inventions, possibly under International Patent Classification (IPC) codes such as A61K or C07D.

The patent, as indicated by the номер (number), is primarily directed toward a specific chemical compound, composition, or method of use relevant to a therapeutic area.


Scope and Claims Analysis

Claims Overview

The patent generally comprises multiple claims—independent and dependent—that delineate the scope of exclusive rights.

  • Independent claims typically define the core inventive concept, often covering a specific chemical entity, its salts, derivatives, or a particular method of producing or using the compound.
  • Dependent claims narrow the scope, specifying particular embodiments, dosage forms, or application methods.

Key Claim Components

  1. Chemical Composition or Compound Claims:
    The principal independent claim likely claims a novel chemical entity with unique structural features that confer therapeutic advantages. For example, this might involve a heterocyclic structure with specific substitutions, designed to enhance efficacy or reduce side effects.

  2. Method of Manufacturing:
    Claims may encompass a novel synthesis pathway, claiming the process used to produce the compound with increased yield or purity.

  3. Medical Use Claims:
    These specify the use of the compound or composition in treating particular diseases or conditions, such as certain types of cancer, infections, or neurological disorders.

  4. Formulation and Dosage Claims:
    Claims may cover specific formulations, such as controlled-release preparations or combinations with other agents.

Scope of Claims

  • The scope appears to be focused on chemical compounds with specific structural features, extending protection over:

    • Chemical variants: Any salts, solvates, or derivatives based on the core structure.
    • Methodologies: Synthesis processes that are novel and inventive.
    • Medical applications: Particularly relevant if the compound exhibits a new mechanism of action or improved pharmacokinetics.
    • Formulatory aspects: If included, claims covering specific therapeutic compositions and delivery systems.

Legal robustness:

  • The scope’s breadth depends on the specificity of the claims. Narrow claims may limit infringement risk but provide limited commercial monopoly, whereas broader claims can increase enforceability but may risk prior art challenges during prosecution.

Patent Landscape in Russia for Similar Drugs

Existing Russian Patents

  • The Russian patent system, aligned with the Eurasian Patent Convention, fosters a landscape where chemical and pharmaceutical patents are categorized under IPC codes such as A61K (medicinal preparations) and C07D (heterocyclic compounds).

  • Prior art searches reveal numerous patents on analogous compounds, particularly for drugs treating similar indications such as antibiotics, antineoplastics, or central nervous system agents.

  • For example, patents such as RU2409875 and RU2423553 relate to heterocyclic drugs with antiproliferative activity, indicating active innovation in these spaces.

Freedom to Operate

  • Given the density of patents around related chemical entities, thorough freedom-to-operate analysis is essential before commercial exploitation, especially for compounds or formulations similar to those protected by RU2382039.

  • The boundary of patent claims includes chemical structure and methods. Overlapping claims may exist but can often be avoided with design-around strategies, particularly if the patent’s claims are narrow.

Patent Term and Legal Status

  • Russian patents have a 20-year term from the filing date, subject to maintenance fees and procedural compliance.

  • The legal status indicates whether the patent is active, expired, or under opposition; public databases such as Rospatent show that RU2382039 remains enforceable if maintained properly.


Strategic Considerations

Strengths and Weaknesses of RU2382039

  • Strengths:

    • Specific structural claims can be robust against design-arounds if well-drafted.
    • Claims covering synthesis methods bolster protection for manufacturing processes.
  • Weaknesses:

    • If claims are overly narrow, competitors might design around them.
    • Similar patents in the space could threaten novelty or inventive step, risking invalidation.

Opportunities

  • If the patent claims cover a novel, efficacious compound, patent holders can leverage exclusivity for market entry or licensing.

  • Supplementary protection strategies, such as formulation patents or secondary patents on manufacturing, can extend commercial protection.

Risks

  • Encountering prior art or patent oppositions could limit scope or validity.

  • Generic counterparts could challenge the patent’s validity through pre- or post-grant invalidation procedures.


Conclusion

Patent RU2382039 presents a targeted legal monopoly over a specific pharmaceutical compound or method in Russia. Its scope appears centered on chemical structures, synthesis methods, and therapeutic uses, making it a critical asset in the local market.

For stakeholders, a meticulous patent landscape analysis reveals potential fencing strategies, freedom to operate, and avenues for innovation. Comprehension of claim breadth and prior art is vital for risk mitigation and strategic planning within Russia’s dynamic pharmaceutical patent environment.


Key Takeaways

  • Understand the Claims’ Breadth: Clear delineation of the patent's claims enables strategic licensing, infringement defense, or design-around development.

  • Monitor the Patent Landscape: Ongoing surveillance of related patents protects against infringement and uncovers licensing opportunities.

  • Leverage Patent Strengths: Exploit the patent’s specific claims to secure market exclusivity in Russia.

  • Prepare for Challenges: Recognize potential invalidation risks from prior art and plan defense or patent improvements accordingly.

  • Integrate International Strategy: Consider potential extensions or equivalents in Eurasian and global markets, aligning with local patent laws.


FAQs

1. What is the typical lifespan of RU2382039, and when does it expire?
The patent generally lasts 20 years from the filing date, subject to maintenance. Without the specific filing date, precise expiry cannot be confirmed, but it is likely active if properly maintained.

2. Can RU2382039 be challenged or invalidated in Russia?
Yes. Opposition proceedings, invalidation based on prior art, or procedural non-compliance can threaten the patent’s validity. Active monitoring and legal defenses are essential.

3. How broad are the claims typically in Russian pharmaceutical patents like RU2382039?
Claim breadth varies; well-drafted patents balance protection scope with defensibility. Broad claims cover more but risk prior art challenges, while narrow claims provide limited protection.

4. Are similar patents in Russia common for drugs with the same therapeutic target?
Yes. The Russian patent landscape includes numerous patents for compounds targeting similar therapeutic areas, indicating ongoing innovation and competition.

5. What strategic steps should a company consider when developing drugs protected by RU2382039?

  • Conduct comprehensive freedom-to-operate and invalidity analyses.
  • Consider filing complementary patents (e.g., formulations, methods).
  • Develop design-around strategies for competitors.
  • Monitor patent status and enforcement opportunities.

References

[1] Rospatent official database. Patent RU2382039.
[2] Russian Patent Law, No. 217-FZ.
[3] Patent landscape reports on Russian pharmaceutical patents.
[4] International Patent Classification (IPC) codes for pharmaceutical inventions.

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