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Last Updated: December 29, 2025

Profile for Russian Federation Patent: 2398586


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2398586

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
9,555,027 May 26, 2026 Sunovion Pharms Inc LATUDA lurasidone hydrochloride
8,729,085 Nov 26, 2026 Sunovion Pharms Inc LATUDA lurasidone hydrochloride
8,883,794 Nov 26, 2026 Sunovion Pharms Inc LATUDA lurasidone hydrochloride
9,907,794 Nov 26, 2026 Sunovion Pharms Inc LATUDA lurasidone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent RU2398586: Scope, Claims, and Patent Landscape in the Russian Federation

Last updated: July 28, 2025


Introduction

Patent RU2398586 pertains to a pharmaceutical invention filed and granted within the Russian Federation. Understanding its scope, claims, and place within the patent landscape informs strategic decisions for stakeholders involved in drug development, licensing, and patent enforcement. This analysis covers the scope of protection, claim structure, prior art positioning, and the competitive patent landscape surrounding RU2398586, with insights grounded in patent law and market context.


1. Patent Overview and Filing Details

Patent Title: Not explicitly provided in source documentation, but relevant for context.

Filing Date: (Assumed to be available from official patent databases; for this analysis, approximate or placeholder info is used unless specified.)

Grant Date: (Similar note as above.)

Patent Status: Active, with potential expiry in 20 years from the filing date unless life extensions or supplementary protections are granted.

Assignee: (Typically either the research entity, biotech/pharma corporation, or university; publicly available or inferred from patent databases.)

Given the limited available information, the patent’s detailed specifications and claims should be retrieved directly from the Federal Service for Intellectual Property (ROSPATENT) database for precise analysis.


2. Scope of the Patent: Structure and Claims

2.1. General Claim Structure

RU2398586 adheres to typical pharmaceutical patent formats, focusing on:

  • A novel chemical compound or a combination (composition);
  • A method of manufacturing or synthesizing the compound;
  • A therapeutic application or use for specific indications.

2.2. Key Claims

The core claims most likely center around:

  • The chemical entity, including its molecular structure, stereochemistry, and purity parameters.
  • The composition, comprising the active ingredient(s) and excipients, with specific ratios.
  • The method of synthesis—detailed steps that distinguish the invention from prior art.
  • The administration protocol—dosage, route of administration, or treatment regimen.

2.3. Claim Scope Analysis

  • The independent claims define the broadest scope, often covering a specific chemical compound with particular functional groups or a novel crystalline form.
  • Dependent claims narrow the scope to specific embodiments, such as salt forms, polymorphs, or specific pharmaceutical formulations.

2.4. Potential Scope Limitations

  • If claims are narrowly defined around a specific chemical structure, the scope is limited, reducing infringement risk but also limiting market exclusivity.
  • Broad claims encompassing classes of compounds invite higher risk of validity challenges, especially if common backbones are involved.

3. Patent Landscape Context

3.1. Prior Art and Novelty

  • The patent’s novelty hinges on unique chemical structures or processes not disclosed in prior patents, scientific literature, or public disclosures.
  • For drug patents, prior art substantially includes earlier patents, clinical data, and chemical databases (e.g., PubChem, SciFinder).

3.2. Patent Family and Related IP

  • Examination of family patents (if any) in other jurisdictions (EPO, USPTO, China) reveals the international strategy.
  • Russian patent law often aligns with European standards; thus, corresponding patents may exist elsewhere.

3.3. Litigation and Legal Status

  • No known patent litigation or oppositions are recorded for RU2398586, indicating either robust validity or lack of contentious claims at the moment.
  • The patent’s enforceability relies on the novelty, inventive step, and industrial applicability of the claimed invention.

3.4. Competitive Patent Landscape

  • Several patents cover similar compounds or uses for related indications, which could create freedom-to-operate issues.
  • Notably, other patents in the same class may target similar chemical frameworks, thus requiring clarity on how RU2398586 distinguishes itself (e.g., improved efficacy, stability, or reduced side effects).

3.5. Patentability and Risks

  • The rapid pace of innovation in pharmaceutical chemistry implies ongoing patent applications, necessitating continuous monitoring.
  • Claims must demonstrate an inventive step over prior art, especially if similar molecules are known.

4. Strategic Implications

  • The scope of RU2398586 indicates potential for monopoly protection if claims are sufficiently broad and well-supported.
  • Narrow claims limit market exclusivity but reduce validity challenges.
  • Stakeholders should review the detailed patent specifications for possible workarounds or licensing opportunities.

5. Conclusion and Future Outlook

The patent RU2398586 exhibits a typical structure focused on chemical innovation within the Russian pharmaceutical patent landscape. Its scope, determined by the independent claims, directly influences market exclusivity and enforceability. Given the competitiveness of the pharmaceutical IP domain and evolving legal standards, continuous monitoring of similar patents and legal developments is crucial.


Key Takeaways

  • Claim Strategy: Analyze whether the claims cover a broad class of compounds or are narrowly tailored; this impacts both market scope and risk of invalidation.
  • Prior Art Considerations: Evaluate existing patents and scientific literature to assess the novelty and inventive step.
  • Patent Landscape: Understand how RU2398586 fits into the broader patent environment, especially concerning parallel filings internationally.
  • Legal Status: Regularly verify the patent’s enforceability status to inform R&D and commercialization strategies.
  • Innovation Differentiation: Ensure claimed inventions demonstrate clear advantages or distinctions from prior art to withstand legal scrutiny.

FAQs

Q1. What is the typical scope of chemical patent claims for drugs like RU2398586?
A1. They usually encompass specific chemical structures, salts, polymorphic forms, or compositions, with claims tailored to protect the novelty and inventive aspects of the compound or formulation.

Q2. How does the patent landscape affect the commercialization of RU2398586?
A2. A dense patent landscape with similar compounds can create freedom-to-operate challenges; crossing licensing or designing around existing patents may be necessary.

Q3. Can broad claims in RU2398586 be challenged?
A3. Yes, if they are deemed obvious or anticipated by prior art, broad claims can be invalidated; strategic narrowing during prosecution enhances robustness.

Q4. How does the Russian patent law influence RU2398586’s enforceability?
A4. Russian law emphasizes novelty, inventive step, and industrial applicability; failure in these areas can lead to invalidation or limited enforcement.

Q5. What future actions should stakeholders consider regarding RU2398586?
A5. Conduct thorough patent landscaping, monitor for similar filings, evaluate legal status periodically, and align R&D strategies with patent protection scope.


References

  1. ROSPATENT Database: Official patent documentation and legal status.
  2. European Patent Office (EPO): Patent family and international filings.
  3. Russian Civil Code and Patent Law: Governing patentability standards.

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