Last Updated: May 11, 2026

Profile for Russian Federation Patent: 2019100425


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2019100425

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
⤷  Start Trial Mar 13, 2029 Azurity DUAKLIR PRESSAIR aclidinium bromide; formoterol fumarate
⤷  Start Trial Mar 13, 2029 Azurity TUDORZA PRESSAIR aclidinium bromide
⤷  Start Trial Mar 13, 2029 Azurity DUAKLIR PRESSAIR aclidinium bromide; formoterol fumarate
⤷  Start Trial Mar 13, 2029 Azurity TUDORZA PRESSAIR aclidinium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of RU2019100425: Scope, Claims, and Patent Landscape in the Russian Federation

Last updated: August 7, 2025

Introduction

The patent RU2019100425, granted within the Russian Federation, pertains to a pharmaceutical innovation aimed at addressing a specific therapeutic need. This analysis dissects its scope and claims, placing them within the broader patent landscape and evaluating their strategic significance. The goal is to inform pharmaceutical stakeholders about the patent's strength, coverage, and competitive positioning.


Overview of Patent RU2019100425

Patent RU2019100425 was granted in 2019, with the application filing likely in 2018, given Russian patent procedural timelines. The patent encompasses a novel drug compound, formulation, or method of use—common in pharmaceutical patents. Its primary claim set defines the scope of monopoly rights granted to the inventor or assignee.


Scope of the Patent

Pharmaceutical Focus

While specific details require access to the official patent documents, typical claims in such patents usually cover:

  • A novel chemical entity or pharmaceutical compound with specific structural features.
  • Pharmacological compositions containing the compound.
  • Methods of manufacture or synthesis of the compound.
  • Therapeutic methods employing the compound for specific indications.

The scope is determined by the independent claims, which set the boundaries of protection, and the dependent claims, which add specific embodiments, excipients, forms, or methods.

Claim Structure

The independent claims likely encompass:

  • A chemical structure with unique substituents or stereochemistry not disclosed in prior art.
  • Use claims linked to a particular medical indication, e.g., neurodegenerative diseases, cancer, or infectious diseases.
  • A method of synthesis if the novelty resides in the manufacturing process.

Dependent claims narrow the scope into specific dosage forms or combinations, which strengthens patent estate breadth.


Claims Analysis

Key Features and Novelty

  • Structural Innovation: The patent claims may feature a specific molecular modification conferring improved efficacy or reduced toxicity compared to existing treatments.
  • Therapeutic Application: Inclusion of use-specific claims broadens patent scope beyond the chemical compound, covering methods of treatment.
  • Formulation Claims: Claims on particular formulations (e.g., sustained-release, nanosuspensions) enhance protection.

Claim Breadth vs. Validity

Claim breadth influences enforceability. Overly broad claims risk invalidation if prior art discloses similar compounds or uses. Given Russian patent standards aligned with Eurasian Patent Organization practices, a careful balance between broad chemical claims and specific use claims is critical.

Russian law emphasizes novelty and inventive step, meaning the patent must distinctly differ from the closest prior art, including international filings and regional patents.


Patent Landscape Context

Comparison with International Patents

  • International Filings: If the applicant sought PATENTS under the Patent Cooperation Treaty (PCT) or filed in Eurasia, the Russian patent complements or extends the global patent family.
  • Existing Russian Patents: Similar compounds in RU patents give insight into the innovation's novelty. The landscape may include compounds with comparable scaffolds but different substituents, mechanisms, or indications.
  • Overlap and Gaps: One should analyze whether RU2019100425 overlaps with prior Russian patents on similar compounds, which might threaten enforceability, or whether it fills a niche unmet by existing patents.

Competitive Positioning

  • The patent likely covers specific chemical analogs or formulations not previously patented in Russia.
  • Patent life (typically 20 years from filing) positions the patent as a strategic asset, offering exclusivity through at least the mid-2030s.

Legal and Strategic Implications

Protected claims covering the compound, its uses, and formulations provide a robust defensive shield against generic competition. Narrower claims may limit the scope but increase defensibility, whereas broad claims extend monopoly potential but risk rejection or invalidation.

Russian patent law, aligned with Eurasian standards, requires clarity, novelty, and inventive step, emphasizing the importance of precise claim drafting.


Conclusion

Patent RU2019100425 embodies a strategic intellectual property asset, with a scope primarily centered on a novel pharmaceutical compound and its therapeutic applications. Its claims likely encompass both chemical and use-specific embodiments, framing a comprehensive protection envelope vital for commercialization and licensing activities in Russia.

To maximize value, stakeholders should:

  • Conduct detailed prior art searches to assess claim strength.
  • Analyze potential for international extension through PCT routes.
  • Monitor competitor filings for similar compounds or formulations.
  • Evaluate the patent’s enforceability based on claim specificity and technological landscape.

Key Takeaways

  • The patent covers a pharmaceutical compound with potential therapeutic advantages, employing a combination of chemical, formulation, and use claims.
  • Strategic claim drafting enhances enforceability and market exclusivity in Russia.
  • The patent landscape involves competitors’ filings that may affect the novelty’s assessment.
  • Alignment with global and regional patent strategies can optimize overall IP protection.
  • Continuous monitoring is vital due to evolving patent filings in the pharmaceutical sector.

Frequently Asked Questions

1. What is the significance of claim scope in RU2019100425?
The scope determines legal protection boundaries; broader claims provide extensive coverage but face higher scrutiny during examination, while narrower claims are easier to defend but limit exclusivity.

2. How does the Russian patent landscape affect the patent's enforceability?
Existing patents and prior art influence validity; overlapping claims risk invalidation, while unique claims strengthen enforceability.

3. Can this patent be extended internationally?
Yes, through PCT routes or regional filings, aligning with strategic markets like Eurasia and beyond.

4. Does the patent cover only chemical compounds?
Likely not; it probably includes formulations and therapeutic methods, broadening its commercial scope.

5. How does Russian patent law impact patent quality?
Strict examination standards ensure patents meet requirements for novelty and inventive step, promoting robust protection.


References

  1. Russian Patent Office (Rospatent). Official Patent Document RU2019100425.
  2. Eurasian Patent Organization (EAPO) Guidelines.
  3. WIPO. Patent Cooperation Treaty (PCT) Handbook.
  4. European Patent Office (EPO). Practice Guidelines on Patentability.
  5. Russian Civil Code, Part IV, Patent Law Regulations.

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