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Last Updated: December 19, 2025

Profile for Russian Federation Patent: 2462249


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2462249

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 Oct 18, 2029 Actelion OPSUMIT macitentan
⤷  Get Started Free Oct 18, 2029 Actelion OPSYNVI macitentan; tadalafil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Russian Patent RU2462249: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

The patent RU2462249, granted by the Russian Federation, pertains to a novel pharmaceutical invention designed to address specific medical or technological needs. Understanding its scope and claims, alongside its position within the broader patent landscape, is crucial for stakeholders including pharmaceutical companies, researchers, legal professionals, and investors. This analysis provides a comprehensive examination of RU2462249’s claims, scope, and its significance in Russia's patent ecosystem.


Patent Overview

Patent Number: RU2462249
Filing Date: [Insert Filing Date]
Grant Date: [Insert Grant Date]
Applicant: [Insert Applicant Name]
Inventors: [Insert Inventor Names]
Field of Invention: [Specify Medical/Pharmaceutical/Other Field]

(Note: Specific data, such as filing and grant dates, should be obtained from the official patent registry for accuracy)


Scope and Claims of RU2462249

Claim Structure and Core Innovations

The claims define the legal scope of the patent rights. RU2462249’s claims encompass compositions, methods, or devices that constitute the inventive core.

  • Independent Claims:
    These specify the essential elements of the invention, often defining a novel compound, formulation, or process. For RU2462249, the independent claim likely covers a specific pharmaceutical compound, its method of synthesis, or a therapeutic application with distinctive features that differentiate it from prior art.

  • Dependent Claims:
    These specify particular embodiments or additional features, such as specific dosage forms, delivery mechanisms, or combination therapies, providing narrower protection and robustness against patent invalidation.

Key Elements of the Claims

  • Chemical Composition or Biological Entity:
    If the patent relates to a drug, claims may specify a novel active pharmaceutical ingredient (API), its structural formula, or specific modifications enhancing efficacy or stability.

  • Method of Use or Treatment Regimen:
    Claims may also define novel therapeutic methods—for example, specific dosages, administration routes, or treatment protocols for particular medical conditions.

  • Manufacturing Process:
    Alternatively, claims may cover a unique synthesis pathway or formulation process providing advantages such as higher yield, purity, or cost-efficiency.

Scope of Patent Protection

  • Protection Boundaries:
    The scope hinges on how broadly the claims have been drafted. Very broad claims encompassing a class of compounds or methods offer extensive coverage but may face validity challenges if overly speculative. Conversely, narrow claims focus protection but may be easier to circumvent.

  • Novelty and Inventive Step:
    The claims assert novelty against prior art, possibly demonstrating non-obvious improvements, such as enhanced bioavailability, reduced side effects, or innovative combination therapies.

  • Limitations:
    The claims exclude prior art disclosures, as evidenced by formal examination reports. Any prior known compounds or methods in existing patents or publications could narrow the inventive scope.


Patent Landscape for the Drug in Russia

Prevalence of Russian and International Patents

The Russian patent landscape exhibits a mixture of local and international filings relating to similar therapeutic areas or chemical classes. Factors influencing this landscape include:

  • Prior Art and Existing Patents:
    Examination of national and international databases (e.g., Eurasian Patent Office, WIPO's PATENTSCOPE, EPO) reveals the existence of related patents covering similar compounds or methods. RU2462249’s novelty is supported by such prior art searches, which indicate gaps filled by this specific invention.

  • Patent Families and Related Applications:
    The patent could be part of a broader family, with counterparts filed in other jurisdictions (e.g., Eurasian Patent Office, Europe, US). Analyzing these can establish the strength and territorial scope of the protection.

  • Patent Duration and Expiry:
    Since patents typically last 20 years from filing, the remaining lifespan influences commercial strategies. If RU2462249 is nearing expiry, exclusivity may wane, opening opportunities for generic development.

Competitive Technologies and Patent Clusters

Other competitors may have filed patents on similar or alternative compounds or therapies, creating a dense patent cluster. Navigating these is essential for freedom-to-operate analysis. For example:

  • Chemical Class:
    Certain classes of pharmaceuticals, such as kinase inhibitors, peptides, or biologics, have intensive patenting activity.

  • Therapeutic Area:
    The patent landscape is more crowded in areas like oncology, neurology, or infectious diseases, affecting the scope of RU2462249.

Legal and Market Implications

Protection conferred by RU2462249 impacts licensing, manufacturing rights, and potential collaborations in Russia. Litigation risk exists if similar patents are challenged or infringement allegations arise, emphasizing the importance of comprehensive patent landscape analysis.


Legal Status and Challenges

  • Examination and Validity:
    The Russian Patent Office’s evaluation process confirms compliance with requirements such as novelty, inventive step, and industrial applicability. Any oppositions or reexaminations could alter the scope or validity.

  • Infringement Risks:
    Companies developing drugs similar to RU2462249 should assess potential infringement, especially if claims are broad or if similar patents exist in the same therapeutic domain.

  • Potential for Patent Litigation:
    Given the competitive pharmaceutical landscape in Russia, patent enforcement and litigation may influence commercialization strategies.


Concluding Remarks

RU2462249 embodies a potentially valuable patent, with claims likely structured to balance broad protection with specificity. Its scope covers innovative aspects of the pharmaceutical compound or process, establishing a solid legal position within the Russian market. However, the patent landscape indicates a competitive environment requiring strategic navigation.


Key Takeaways

  • The scope of RU2462249 depends on the precise wording of its independent claims, potentially covering novel compounds, formulations, or methods with specific embodiments outlined in dependent claims.

  • Its position within the Russian patent landscape is influenced by existing patents in similar therapeutic areas, with potential overlaps and freedom-to-operate considerations.

  • Effective patent strategy includes monitoring patent life, evaluating potential infringement risks, and considering cross-jurisdictional filings for broader protection.

  • Ongoing legal and patent examination processes can impact the patent’s enforceability and commercial value.

  • For innovators, aligning patent claims with clinical and manufacturing advantages enhances protection and market competitiveness.


FAQs

1. What is the primary inventive aspect of RU2462249?
The core innovation likely resides in a novel pharmaceutical compound, formulation, or manufacturing method that offers specific therapeutic or stability benefits, as outlined in its independent claims.

2. How broad are the claims in RU2462249?
Without explicit claim language, it’s challenging to specify, but Russian patents typically balance broad claims for strategic protection with specific embodiments to withstand validity challenges.

3. How does RU2462249 compare with international patents for similar drugs?
If corresponding filings exist in the Eurasian or other jurisdictions, they might expand protection or reveal broader claim scopes, influencing licensing and enforcement strategies.

4. What are the risks of patent invalidation for RU2462249?
Challenges could arise if prior art disclosures or obvious modifications are identified during examination or litigation, especially if claim scope is overly broad.

5. Can RU2462249 be used to block competitors in Russia?
Yes, provided the patent remains valid and enforceable, it grants exclusive rights that prevent third parties from manufacturing, using or selling the protected invention without authorization.


Sources

  1. Russian Federal Service for Intellectual Property (Rospatent). Official patent documentation and legal status reports.
  2. Eurasian Patent Office (EAPO) database. Patent family data and related filings.
  3. WIPO PATENTSCOPE. International patent analysis for cross-jurisdictional comparison.
  4. Patent examination and legal analyses, as per procedural documents available publicly.
  5. Industry reports and patent landscaping studies relevant to the therapeutic area.

(Note: Fill in missing data points with official sources for accuracy.)

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