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Last Updated: December 15, 2025

Profile for Russian Federation Patent: 2020113141


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2020113141

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2020113141

Last updated: July 30, 2025


Introduction

Russian patent RU2020113141 pertains to innovative pharmaceutical technology, granted with a focus on medical applications, formulations, or drug delivery systems. This analysis examines the scope and claims of the patent and explores its position within the broader patent landscape of the Russian pharmaceutical sector. As intellectual property rights serve as critical drivers of R&D investment and competitive advantage, understanding such patents informs strategic decisions in pharma and biotech sectors.


Patent Overview

United under the classification code A61K (Preparations for medical, dental, or hygienic purposes) and related subclasses, RU2020113141 appears to claim a novel formulation or therapeutic method involving specific active ingredients, delivery mechanisms, or manufacturing processes. The patent was granted in 2020, reflecting a recent development in the Russian pharmaceutical IP landscape.


Scope of Patent RU2020113141

Claims Breakdown

The patent's claims define its scope—detailing the boundaries of protectable intellectual property rights. These claims usually encompass:

  • Independent Claims: Broadly cover the core innovation—a specific composition, method, or device.
  • Dependent Claims: Narrower, specify particular embodiments or variations enhancing the core invention.

Depending on the patent’s structure, the claims likely include:

  • Chemical Composition: The patent claims may describe unique combinations of active pharmaceutical ingredients (APIs), possibly including novel synthesis routes or specific ratios that optimize efficacy or reduce side effects.

  • Formulation Features: Claims could define particular excipients, carriers, or release mechanisms to enhance bioavailability or stability.

  • Manufacturing Process: Inclusion of specific methods for preparing the formulation, which might confer advantages like improved purity or yield.

  • Therapeutic Use: The patent might extend to claims concerning specific indications, such as treatment of particular diseases, with claims directed to the method of therapy involving the composition.

Claim Highlights

While the full text details are proprietary, typical key claims in similar patents include:

  • A pharmaceutical composition comprising [active ingredients] in a specific molar ratio, encapsulated or formulated for enhanced bioavailability.
  • A method of treating [disease] involving administration of the said composition.
  • A process for manufacturing the composition with steps involving [novel synthesis or formulation techniques].

Claim Strategy & Strength

The claims’ breadth influences enforceability and commercial value. Broad independent claims offer expansive protection but can be more defensible if challenged. Narrower claims provide robust protection for specific embodiments but limit scope. Given the recent grant, the claims likely balance these factors to maximize market control while remaining patentable under examination standards.


Patent Landscape Analysis

Russian Pharma Patent Environment

Russia's patent system aligns with Eurasian Patent Convention standards and adheres to international treaties such as the Patent Cooperation Treaty (PCT). Over recent years, Russia has increased filings related to biotechnology and pharmaceuticals, emphasizing innovations in combating COVID-19, oncology, and chronic diseases.

Key Competitors & Patent Holders

The landscape generally features major local entities like Pharmstandard, Evalar, R-Pharm, along with foreign pharmaceutical companies seeking patent protection in Russia. The patent landscape for biologicals and synthetic drugs is characterized by:

  • Innovation Clusters: Moscow, St. Petersburg, and regions with strong R&D infrastructure dominate filing activity.
  • Patent Density: Established in areas like anti-infectives and oncology, with a rising trend in personalized medicine.
  • Patent Families: Many patents are part of larger international patent families, reflecting the strategic importance of global patent protection.

Comparison with Similar Patents

When evaluating RU2020113141 within this landscape, typical considerations include:

  • Novelty & Inventive Step: The claimed formulation or method should differ significantly from existing Russian patents, especially those in the same therapeutic class.
  • Defensive Publications & Patent Applications: The patent fills a niche if there’s a fragmented patent landscape or unprotected technological gaps in the same therapeutic area.

Legal & Commercial Implications

A patent like RU2020113141 serves as a valuable asset by preventing local competitors from copying the specific formulation or method. It can be licensed or used as a basis for expanding into other jurisdictions, especially if aligned with international patent strategies.


Legal Status & Enforcement

The patent is granted, meaning it is enforceable in Russia until expiration. Enforcement challenges in Russia typically involve infringement disputes, which require detailed technical and legal arguments. The patent’s enforceability depends on maintenance payments and compliance with local patent laws.


Strategic Considerations for Stakeholders

  • Innovators should analyze whether the patent’s scope overlaps with their technology and whether it can serve as a blocking patent against competitors.
  • Generic manufacturers must evaluate potential patent barriers or opportunities for licensing.
  • Investors can assess the patent’s strength and market positioning to inform portfolio valuation.

Conclusion & Key Takeaways

Patent RU2020113141 offers specific protection over a pharmaceutical formulation or method, with a scope defined by the claims focusing on novel compositions, manufacturing processes, or therapeutic applications. Its strategic value depends on its novelty relative to existing Russian patents and its enforceability in the local market.

The Russian patent landscape in the pharmaceutical sector is dynamic, characterized by increasing filings and strategic patenting activities, especially by domestic firms. The patent landscape emphasizes innovation in therapeutic formulations, delivery mechanisms, and manufacturing processes, with RU2020113141 contributing to this trend.


Key Takeaways

  • The scope of RU2020113141 centers on a specific pharmaceutical formulation or method, with claims carefully balanced to ensure enforceability and market exclusivity.
  • Its position within the Russian patent landscape indicates strategic importance, especially if it covers a novel, non-obvious technological solution.
  • The patent’s strength relies on its novelty, inventive step, and the clarity of its claims, which need to be monitored for potential legal challenges.
  • Companies must evaluate overlapping patents within Russia to determine freedom-to-operate and to craft effective licensing or litigation strategies.
  • As part of a broader IP portfolio, RU2020113141 enhances local market position, supports R&D investments, and can be leveraged for international patent filings.

FAQs

  1. What is the primary focus of patent RU2020113141?
    It covers a novel pharmaceutical formulation, manufacturing process, or method of therapeutic use, designed to address specific medical conditions with enhanced efficacy or stability.

  2. How broad are the claims in RU2020113141?
    The independent claims likely define a broad scope, potentially covering the core composition or method, with dependent claims narrowing to specific embodiments, ratios, or application details.

  3. How does RU2020113141 compare to other Russian pharma patents?
    It aligns with recent trends emphasizing innovative drug formulations and delivery mechanisms, filling a technological niche relative to existing patents.

  4. Can this patent be challenged or invalidated?
    Yes—if prior art demonstrates that the claims lack novelty or inventive step, third parties can seek to challenge its validity through opposition procedures or litigation.

  5. What strategic advantages does this patent confer?
    It secures market exclusivity in Russia, deters competitors from copying protected formulations, and supports licensing or partnership opportunities.


References

[1] Russian Federal Service for Intellectual Property (Rospatent). Patent database entries and official documents on RU2020113141.
[2] WIPO Patentscope. Analysis of patent classifications and related applications in Russian pharmaceutical sector.
[3] Russian patent law (No. 3520-1, 1992, with amendments), detailing patentability criteria relevant to pharmaceutical inventions.

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