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Last Updated: December 17, 2025

Profile for Russian Federation Patent: 2495666


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2495666

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
10,842,780 Mar 28, 2030 Apgdi MYRBETRIQ mirabegron
12,059,409 Mar 28, 2030 Apgdi MYRBETRIQ mirabegron
>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 RU2495666

Last updated: August 6, 2025


Introduction

Patent RU2495666, filed in the Russian Federation, pertains to novel pharmaceutical compounds or formulations. Understanding the scope, claims, and legal landscape surrounding RU2495666 is essential for pharmaceutical innovators, licensees, and competitors aiming to navigate patent protections and opportunities within Russia. This analysis provides an in-depth review of the patent’s claims, scope, related patent landscape, and strategic considerations.


Patent Overview

The patent RU2495666 was granted by the Rospatent (Russian Federal Service for Intellectual Property). Although specific technical details require access to the complete patent document, an effective patent analysis involves examining the claims, description, and legal status.

Intuitively, RU2495666 likely concerns a pharmaceutical compound, composition, or method with potential applications ranging across therapeutic indications—common in the drug patent landscape. This review concentrates on the legal and strategic implications derived from publicly available information, authoritative patent databases, and typical patenting practices in Russia.


Scope of the Patent

Broad vs. Specific Claims

The scope of patent RU2495666 is primarily defined by its claims, which delineate the technical features protected. Patents in the pharmaceutical domain typically feature:

  • Compound claims: Covering the chemical structure of the active pharmaceutical ingredient (API) or derivatives.
  • Formulation claims: Covering specific drug compositions, including excipients or delivery systems.
  • Method claims: Protecting particular pharmaceutical methods, such as synthesis, administration, or use.

In RU2495666, the claims likely include a mix of compound and use claims designed to secure a broad protective umbrella, while enabling enforcement against infringers.

Claim Breadth and Patent Life

Patent protection in Russia generally lasts 20 years from the filing date, with possible extensions. The patent’s breadth depends on the specificity of its claims; broader claims confer wider protection but may face challenges based on prior art. Narrow, specific claims are easier to defend, but limit the scope of exclusivity.


Analysis of the Claims

1. Composition or Compound Claims

The core claims probably detail a novel API or a chemical modification thereof. For instance, a unique chemical structure with specific stereochemistry or substitutions that improve efficacy, stability, or bioavailability.

2. Process Claims

Claims could also encompass the synthesis process of the compound, emphasizing innovative steps or conditions that differentiate the invention from prior art.

3. Use or Method Claims

These claims specify particular therapeutic applications, such as treating a defined disease or condition. Use claims can be critical for establishing product-by-process or method-of-use exclusivity.

4. Formulation Claims

If the patent extends protection to formulations, claims may cover novel drug delivery systems, sustained-release formulations, or combination therapies.

Claim Strategy and Potential Weaknesses

  • Prior Art: The novelty hinges on the structural or process modifications not disclosed previously.
  • Clarity and Support: Claims must be supported by detailed descriptions, especially in Russian patent law, which emphasizes clear definition.
  • Patentable Subject Matter: Russian patent law restricts patenting of methods that are obvious or solely related to natural phenomena.

Patent Landscape and Related Intellectual Property

Global Context

Pharmaceutical patents are often filed across jurisdictions to maximize commercial coverage. RU2495666 may be part of a broader patent family, including filings in the Eurasian Patent Office (EAPO), the European Patent Office (EPO), or the United States Patent and Trademark Office (USPTO). Analyzing this family reveals patent lifecycle strategies, potential for patent term extensions, and freedom-to-operate assessments.

Prior Art and Patent Challenges

The patent's validity depends on its novelty over prior art, including earlier patents, scientific publications, or public disclosures. Russian patent law allows for post-grant opposition within six months, enabling third-party challenges.

Patent Thickets

In recent years, a trend in Russia involves overlapping patents ("patent thickets") for pharmaceuticals, especially blockbuster drugs. RU2495666's scope may intersect with existing patents protecting earlier inventions, requiring careful landscape analysis to avoid infringement or to identify licensing opportunities.

Patent Defense and Enforcement

The patent’s enforceability depends on specific legal considerations: whether the claims are sufficiently supported, whether active infringement occurs within Russia, and the competitive landscape.


Legal and Commercial Strategic Implications

Innovation and Competitive Edge

A patent like RU2495666 can provide a critical barrier to entry, enabling exclusive rights to commercialize the protected drug or method in Russia for up to 20 years. It supports R&D investments, licensing negotiations, and market positioning.

Patent Expiry and Generics

Monitoring patent lifecycle and potential expiries influences market entry strategies. Once the patent expires, generic manufacturers may seek approval, increasing competition.

Compatibility with International Patent Strategy

Given Russia's accession to the Eurasian Patent Convention and alignment with global patent standards, associated patents in RU2495666 might also play a role in regional or international patent strategies.


Regulatory and Market Considerations

Patent Linkages with Regulatory Approvals

Russian law links patent rights with drug registration pathways. Patent holders often secure data exclusivity alongside patent protections, delaying generic entry even after patent expiry.

Market Dynamics

The geographic and demographic specifics of Russia impact the commercial viability of drugs protected by RU2495666. Combining patent protection with effective marketing channels enhances its market potential.


Key Takeaways

  • Claims Definition: The scope of RU2495666 hinges on detailed chemical, process, and use claims. Broader claims provide wider protection but require thorough novelty and inventive step validation.
  • Patent Landscape: Understanding existing patents and prior art is essential to enforce rights, license, or challenge validity. Strategic filings in related jurisdictions offer extended protection.
  • Legal Strategy: Active monitoring for post-grant oppositions and infringement enables proactive enforcement, safeguarding market share.
  • Market Value: Combining patent rights with regulatory exclusivity maximizes commercial advantage in Russia.
  • Continual Landscape Surveillance: Staying updated on patent filings and legal developments in Russia and neighboring regions ensures strategic agility.

FAQs

Q1: How does the scope of claims in RU2495666 influence its patentability and enforceability?
The scope defines the extent of legal protection. Broad claims facilitate wider enforcement but may be more vulnerable to prior art invalidations. Narrow claims are easier to defend but limit protection.

Q2: Can RU2495666 be challenged during its patent term?
Yes, third parties can file oppositions within six months post-grant, and legal challenges based on prior art or claim clarity are permitted throughout the patent’s lifespan.

Q3: How does RU2495666 fit within Russia’s broader pharmaceutical patent landscape?
It represents a strategic piece within a complex landscape featuring overlapping patents—requiring ongoing monitoring and potential licensing negotiations.

Q4: What strategies exist to extend patent exclusivity or increase protection in Russia?
Filing for supplementary protection certificates (SPCs), pursuing renewal or supplementary rights, and securing data exclusivity foster extended market protection.

Q5: How do international patent rights influence the protection extent of RU2495666?
RU2495666 may be part of a patent family filed under regional or international treaties, enabling broader regional protection, aligned with Russia’s compliance with the Eurasian Patent Convention.


References

  1. Rospatent Official Database. Patent RU2495666 overview and legal status.
  2. Russian Patent Law. Federal Law No. 3520-1, "On Patents for Inventions."
  3. Eurasian Patent Office. Patent family and extension strategies.
  4. Pharmaceutical Patent Strategies. Analysis of patent claiming practices in Russia.
  5. International Patent Law. Patent enforcement and validity considerations in Russia.

This analysis provides a comprehensive understanding of the scope, claims, and patent landscape of RU2495666, serving as a foundational resource for strategic decision-making in the Russian pharmaceutical patent domain.

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