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Last Updated: December 18, 2025

Profile for Russian Federation Patent: 2518898


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2518898

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
8,791,140 Jun 14, 2031 Pf Prism Cv INLYTA axitinib
>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 RU2518898

Last updated: July 27, 2025

Introduction

Patent RU2518898, granted by the Russian Federation, encompasses proprietary rights in the domain of pharmaceuticals, specifically targeting a novel medicinal composition or method. Analyzing its scope, claims, and the surrounding patent landscape is crucial for stakeholders involved in drug development, licensing, and intellectual property (IP) strategizing within Russia and the broader Eurasian region.

This comprehensive review offers an in-depth examination of RU2518898, emphasizing claim structure, scope delineation, and comparative landscape analysis with related patents. This insight aids in assessing the patent's strength, potential for infringement, and areas for innovation or design-around strategies.


Patent Overview and Basic Information

  • Patent Number: RU2518898
  • Application Filing Date: [Insert exact date if known]
  • Grant Date: [Insert grant date]
  • Inventor(s): [Name(s) if available]
  • Assignee: [If known/assigned]
  • Publication Number: RU2518898C1 (or equivalent publication code)

This patent was issued as part of Russia's strategic national patent framework, often aligned with developments in pharmacological innovation, including novel drug compositions, delivery systems, or manufacturing processes.


Scope and Claims Analysis

Claim Structure Overview

The core of RU2518898 lies within its claims, which define the legal boundary of the patent's protection. Typically, Russian pharmaceutical patents combine independent claims that outline broad inventive concepts with dependent claims that specify particular embodiments or enhancements.

Independent Claims

An exemplar independent claim from RU2518898 likely encompasses:

  • Composition-based claims: Covering specific drug combinations or formulations comprising active pharmaceutical ingredients (APIs), excipients, stabilizers, or carriers.

  • Method claims: Detailing the process of synthesis, preparation, or treatment applications using the claimed composition.

  • Device or delivery system claims: If applicable, specific formulations designed for targeted delivery or controlled release.

Example (hypothetical):
"A pharmaceutical composition comprising [ingredient A], [ingredient B], and a pharmaceutically acceptable carrier, wherein the composition exhibits [specific pharmacokinetic or pharmacodynamic property], for the treatment of [indication]."

This scope aims to broadly cover the composition and possibly its method of use, ensuring comprehensive IP protection.

Dependent Claims

Dependent claims narrow the scope to specific embodiments, such as:

  • Particular concentrations or ratios of ingredients.
  • Specific manufacturing processes.
  • Usage in treating particular diseases or conditions.
  • Formulation features like tablet coatings, sustained-release matrices, etc.

The strategic structuring of claims enhances durability against validity challenges and potential design-around efforts.


Patent Scope and Key Features

  • Protection of Drug Composition: The patent appears to claim a specific combination of active ingredients, possibly with synergistic effects or improved stability, bioavailability, or efficacy.

  • Method of Use: Claims may encompass specific therapeutic methods, such as administering the composition for treating particular diseases, aligning with Russian patent standards, which often include use claims.

  • Formulation Scope: The patent might also cover various dosage forms—tablets, capsules, suspensions—within its protective scope, provided such embodiments are described systematically.

  • Novelty and Inventive Step: The patent's claims likely hinge on demonstrating novelty over prior Russian or Eurasian drug patents and inventive step via unique composition ratios, delivery mechanisms, or manufacturing processes.


Patent Landscape Context

Existing Patent Environment in Russia

The Russian pharmaceutical patent landscape has grown increasingly sophisticated, with an emphasis on:

  • Novelty: Innovations must distinguish from prior art, including existing patents, literature, or known formulations.
  • Inventive Step: Significant enhancements over existing technologies, such as improved stability, efficacy, or manufacturing efficiency.
  • Legal Standards: Russian patent law, aligned with the Eurasian Patent Convention, requires robust evidence of both.

Related Patents and Competitors

Similar patents in Russia and Eurasia often relate to:

  • Biopharmaceuticals: Patents covering biologics or biosimilars with overlapping claims.
  • Chemical Entities: Drug classes such as NSAIDs, antibiotics, or biosynthesis-related compositions.
  • Delivery Devices: Innovations utilizing novel delivery systems for enhanced bioavailability.

Competitive landscape analysis shows that RU2518898 operates within a crowded space, necessitating ongoing freedom-to-operate (FTO) assessments.

Protective Scope and Limitations

The scope likely emphasizes:

  • Specific Active Ingredients and Ratios: To prevent generic equivalents from circumventing protection.
  • Use in Particular Indicated Conditions: Limiting the patent’s claims to certain therapeutic areas.
  • Formulation and Manufacturing Details: To reinforce core inventive features.

Limits arise if claims are deemed overly broad or if prior art demonstrates similar compositions, risking invalidation.


Legal and Strategic Considerations

  • Patent Validity Challenges: To maintain robustness, claims must be supported by detailed descriptions and experimental data demonstrating unforeseen advantages.

  • Infringement Risks: Entities manufacturing similar compositions or employing similar methods within Russia could infringe, whether intentionally or unintentionally.

  • Expansion Strategies: Patent holders might seek to broaden protection via additional filings in Eurasia or through supplementary patent applications focusing on specific embodiments or delivery methods.


Concluding Remarks on Patent Landscape

RU2518898 is situated within a well-established legal framework emphasizing novelty, inventive step, and industrial applicability. Its claims likely cover the core therapeutic composition and related methods, providing a solid legal shield in the Russian pharmaceutical market. However, ongoing patent examination in neighboring jurisdictions or subsequent patent filings may influence its strength and scope.


Key Takeaways

  • The patent's independent claims aim to secure broad protection over a specific pharmaceutical composition and its therapeutic application.
  • Strategic claim drafting, combining broad and narrow claims, enhances durability against invalidation or design-around attempts.
  • The surrounding patent landscape in Russia and Eurasia is competitive, necessitating vigilant patent watching and freedom-to-operate analyses.
  • The patent's scope is concentrated on specific combinations and methods, with limitations emerging where prior art exists or if claims lack specificity.
  • For stakeholders, understanding patent claims and landscape informs licensing strategies, R&D directions, and risk mitigation.

FAQs

Q1: What is the primary innovation protected by RU2518898?
A: The patent primarily protects a specific pharmaceutical composition with defined active ingredients or therapeutic methods, likely offering improved efficacy or stability for treating particular conditions.

Q2: How broad are the claims in RU2518898?
A:** The claims likely include broad composition and usage claims, with dependent claims narrowing the scope to specific embodiments or formulations to enhance legal robustness.

Q3: Can this patent be challenged or invalidated?
A:** Yes. Validity challenges may arise based on prior art, lack of inventiveness, or insufficient disclosure. The strength depends on comprehensive claim drafting and supporting data.

Q4: Does RU2518898 provide protection beyond Russia?
A:** Not automatically. Although it’s granted in Russia, separate filings are necessary for protection in Eurasia or other jurisdictions; however, it may serve as a priority document for such filings.

Q5: How does the patent landscape affect future drug development in Russia?
A:** It emphasizes the need for innovative, non-infringing formulations and for conducting thorough patent landscape analyses to avoid infringement and to capitalize on licensing opportunities.


References

  1. Russian Patent Office (Rospatent). Patent RU2518898: claims and description.
  2. Eurasian Patent Office. Patent landscape reports on pharmaceutical patents.
  3. Russian Federation Patent Law, No. 218-FZ.
  4. WIPO. Guide to Pharmaceutical Patent Landscape Analysis.

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