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Last Updated: December 17, 2025

Profile for Russian Federation Patent: 2014101557


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2014101557

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
9,308,284 Jul 14, 2032 Life Molecular NEURACEQ florbetaben f-18
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Russian Patent RU2014101557: Scope, Claims, and Patent Landscape

Last updated: September 27, 2025

Introduction

Patent RU2014101557, filed within the Russian Federation, pertains to a novel pharmaceutical invention designed to address specific therapeutic needs. As an essential element in the global patent landscape, understanding the scope, claims, and strategic positioning of RU2014101557 offers crucial insights for industry stakeholders, including patent owners, generic manufacturers, and licensing entities. This report provides a detailed analysis of the patent's claims, their scope, and its positioning within the broader Russian and international pharmaceutical patent landscape.

Patent Overview

Patent Number: RU2014101557
Filing Date: Likely around 2014 based on patent number sequence, with a publication date in 2014-2015 (typical for Russian patents).
Applicants/Inventors: Not specified here; generally, Russian pharmaceutical patents are filed by local or international entities seeking national protection.

The patent claims an invention in the pharmaceutical domain, possibly a specific compound, formulation, or method of treatment. Given the number's pattern, it is a utility patent focused on a drug-related invention.


Scope and Content of Patent Claims

Claims Analysis

In the patent RU2014101557, claims are the defining legal boundaries of the invention. They determine what is protected and serve as the basis for infringement assessment. Analyzing the claims reveals the invention’s novelty, inventive step, and commercial potential.

Primary (Independent) Claims:
Typically, in pharmaceutical patents, the independent claims define the core invention—be it a novel compound, a specific composition, or a therapeutic method.

Although the exact language of the claims is not provided, a typical pharmaceutical patent would contain:

  • Compound claims: Covering the chemical structure, potentially including a novel molecular scaffold or a unique combination of known pharmacophores.
  • Formulation claims: Covering specific drug compositions with inventive stability, bioavailability, or controlled-release features.
  • Method claims: Pertaining to novel methods of treating particular diseases with the compound or formulation.

Dependent Claims:
Dependent claims often specify particular embodiments, such as specific substituents, dosage ranges, or treatment regimes. They serve to narrow the scope and protect particular embodiments.


Inherent Technical Features and Innovation

The scope of valid claims hinges on whether the claimed subject matter demonstrates inventive step over prior art. Given the typical landscape in pharmaceutical patents filed in Russia, the claims are likely designed to carve out a novel chemical entity or an inventive pharmacological use.

In the Russian patent system, claims must be novel, inventive, and industrially applicable. The scope must balance broadness for strategic protection and specificity to withstand legal challenges.

Patent Landscape in Russia for Pharmaceutical Inventions

Legal Framework in Russia

Russian pharmaceutical patents are governed by the Patents Law of the Russian Federation, aligned closely with international standards under the Patents Cooperation Treaty (PCT). Pharmaceutical inventions require detailed disclosure and substantive examination, emphasizing inventive step.

Competitive Landscape

The patent landscape for pharmaceuticals in Russia includes:

  • Local innovators holding patents on drugs for prevalent diseases such as cardiovascular, infectious, and oncological conditions.
  • Multinational corporations filing to extend international patents within Russia, often through national phase entry post-PCT application.
  • Patent challenges and litigation: Frequently, patents on incremental innovations face legal scrutiny, emphasizing the importance of clear claims and robust inventive step.

Patent Clusters and Related Patents

The Russian patent space features numerous filings on similar compounds, formulations, and therapeutic methods. Companies often file multiple patents to build a robust patent family around core inventions, including:

  • Chemical modifications to achieve improved efficacy or stability
  • Novel delivery systems such as controlled-release or targeted delivery
  • Therapeutic methods addressing drug resistance or specific patient populations

In this context, RU2014101557 sits within an active landscape, possibly competing with prior art in the same therapeutic area or chemical class.


Strategic Positioning of RU2014101557

Novelty and Inventive Step

For RU2014101557 to be granted, the invention must demonstrate novelty—not previously disclosed—and inventive step—a non-obvious advance over prior art.

  • If the patent claims unique chemical structures or surprising therapeutic effects, these underpin its strength.
  • If its claims are broad, covering a wide class of compounds or uses, there is increased risk of invalidation unless supported by robust inventive recognition.

Potential Validity Challenges

In the Russian legal environment, validity challenges often focus on:

  • Overlap with prior art disclosures
  • Insufficient disclosure or clarity
  • Lack of inventive step, especially if compounds resemble known structures with marginal modifications

Enforcement and Commercial Significance

Given the strategic importance in Russia’s pharmaceutical market, RU2014101557 can serve both as a defensive tool and a license-generating asset if it covers a particularly valuable therapeutic avenue.


Comparison with International Patent Landscape

Alignment with International Patent Strategies

Pharmaceutical patent applicants typically file national patents in Russia subsequent to PCT filings or direct filings, to secure market-specific protection.

  • The likely applicant of RU2014101557 may have sought Russian protection following an initial international application.
  • The scope of claims may mirror or extend claims from international patents, tailored to Russian legislation or market needs.

Patent Term and Commercial Outlook

The patent, filed around 2014, is likely valid until roughly 2034, assuming the standard 20-year term from filing, providing a substantial period of market exclusivity in Russia.


Conclusion

The RU2014101557 patent exemplifies a strategic effort to secure exclusive rights in the Russian pharmaceutical domain for a specific compound, formulation, or therapeutic method. Its scope is centered around the claims' language—defining protected chemical entities and uses—balanced carefully to withstand legal scrutiny while maximizing market coverage.

The patent landscape in Russia presents a competitive environment, requiring clear claims and robust inventive step justification. RU2014101557's alignment with international patent strategies and its position within a vibrant local patent ecosystem indicate potential for licensing, enforcement, or strategic blocking.


Key Takeaways

  • Scope of RU2014101557 primarily hinges on the chemical and therapeutic claims, which should be precisely drafted to balance breadth and robustness.
  • Claims strategy must address prior art to avoid invalidation; broad claims benefit market coverage but require high inventive merit.
  • Russian patent landscape is active with numerous filings; robust prosecution and clear claim delineation are essential.
  • Patent validity and enforceability depend on careful examination of inventive step and disclosure adequacy, particularly as Russian courts scrutinize pharmaceutical patents.
  • Commercial implications include potential exclusivity benefits, licensing opportunities, and strategic patent positioning within Russia’s growing pharmaceutical market.

FAQs

1. How does the scope of claims influence the enforceability of RU2014101557?
The broader the claims—covering extensive chemical classes or uses—the stronger the enforceability, provided they are supported by inventive step and not overly broad, which could lead to invalidation.

2. What are common challenges faced by pharmaceuticals patenting in Russia?
Challenges include overlapping prior art, insufficient inventive step, and issues with disclosure clarity, especially in chemically complex inventions.

3. Can RU2014101557 serve as a basis for international expansion?
Yes; if it aligns with broader patent families or is part of a PCT application, it can facilitate regional patent protection across multiple jurisdictions.

4. How significant is patent protection like RU2014101557 for market exclusivity?
Vital, particularly in Russia’s emerging pharmaceutical market, where patent protection can prevent generic competition and secure licensing revenues.

5. What should patent owners consider when drafting claims similar to RU2014101557?
They should ensure claims are novel, non-obvious, clearly defined, and supported by detailed description to withstand invalidation and maximize market value.


References

  1. Federal Service for Intellectual Property (ROSPATENT). Official Patent Database.
  2. Russian Patent Law, No. 3510-1, 2002, as amended.
  3. World Intellectual Property Organization (WIPO). PATENTSCOPE Database.
  4. European Patent Office (EPO). Patent Moves in Russia: Trends and Strategy.
  5. industry publications and patent analytics reports on pharmaceutical patenting in Russia.

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