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Last Updated: December 16, 2025

Profile for Russian Federation Patent: 2019124314


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2019124314

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
⤷  Get Started Free Aug 25, 2034 Astrazeneca Ab WAINUA (AUTOINJECTOR) eplontersen sodium
⤷  Get Started Free May 1, 2034 Ionis Pharms Inc DAWNZERA (AUTOINJECTOR) donidalorsen sodium
⤷  Get Started Free May 1, 2034 Ionis Pharms Inc TRYNGOLZA (AUTOINJECTOR) olezarsen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2019124314

Last updated: August 6, 2025

Introduction

Patent RU2019124314, granted by the Russian Federation, pertains to a chemical compound, formulation, or biotechnology invention within the pharmaceutical domain. A comprehensive understanding of this patent involves dissecting its scope, examining the claims, and evaluating its position within the existing patent landscape. This analysis aims to aid stakeholders — including pharmaceutical innovators, legal professionals, and market analysts — in assessing the patent's enforceability, freedom-to-operate, and strategic importance.

Patent Details Overview

  • Patent Number: RU2019124314
  • Application Filing Date: (Specific date not provided here; assumption based on typical timelines)
  • Grant Date: (Likewise, based on standard procedures)
  • Applicant: (Not specified without full database access; presumed to be a Russian pharmaceutical entity or research institute)
  • Publication Date: (Estimated from filing date)

The patent appears to relate to a novel pharmaceutical compound or composition designed for therapeutic purposes. It likely involves specific chemical structures, formulations, or methods of synthesis/administration.


Scope of the Patent

The scope of RU2019124314 encompasses the protected subject matter as defined within its claims. In Russian patent law, claims demarcate the legal boundaries of the patent. They determine what equivalents or variations infringe upon or avoid infringement of the patent.

A typical pharmaceutical patent claim, particularly in Russian practice, includes:

  • Compound Claim: Defines the chemical structure, including specific substituents or stereochemistry.
  • Method Claims: Describe methods of synthesis, purification, or administration.
  • Use Claims: Cover the use of the compound for specific therapeutic indications.
  • Formulation Claims: Encompass specific pharmaceutical compositions and dosage forms.

The precise scope depends on whether the patent claims are independent or dependent, and whether they are broad or narrow.

  • Broad claims aim to cover a wide range of chemical variants, offering extensive protection but are more susceptible to validity challenges.
  • Narrow claims focus on specific compounds or formulations, potentially limiting infringement but enhancing enforceability.

Analysis of the Patent Claims

1. Chemical Structure and Novelty

The core of the patent likely involves a chemical entity with therapeutic relevance. The claims presumably specify the molecular structure, including core scaffolds and substituents, aiming to establish novelty over prior art.

  • Novelty: Russian patent authorities emphasize demonstrating that the invention presents a new chemical entity or utilization not previously disclosed.
  • Inventive Step: The claimed compound must involve an inventive step over known medicines or synthetic methods.

2. Scope of Claims

  • Independent Chemical Claims: Likely define the compound’s structure with chemical specificity, including labels such as R-groups, stereochemistry, and specific substituents.
  • Method Claims: May cover synthesis steps, purification processes, or particular administration routes.
  • Use Claims: Could specify therapeutic use, e.g., treatment of certain diseases or conditions.
  • Formulation Claims: Possibly include pharmaceutical compositions incorporating the compound, including excipients and dosage forms.

3. Limitations and Potential Vulnerabilities

Given Russian patent practice, claims must balance breadth and specificity. Overly broad claims risk invalidation if prior art demonstrates overlapping compositions or methods. Conversely, overly narrow claims could undermine market exclusivity.


Patent Landscape Context

Evaluating RU2019124314 within the broader patent landscape involves assessing:

1. Prior Art and Patent Citations

  • Pre-existing Patents: Patentability depends on the prior art landscape, including previous Russian and international patents, scientific literature, and known chemical compounds.
  • Citations: The patent likely cites prior art to delineate novelty. A lack of relevant citations could signal broad claims or weak novelty.

2. Key Competitors and Patent Clusters

  • The patent universe centers around innovators developing similar chemical entities, therapeutic methods, or formulations.
  • Patent Thickets: Multiple overlapping patents on similar compounds can increase litigation risks and influence licensing strategies.

3. Patent Family and Geographic Coverage

  • RU2019124314's protection might be part of a broader patent family covering other jurisdictions, e.g., Eurasian Patent Organization (EAPO) countries, or international filings under PCT.

4. Legal and Regulatory Considerations

  • Russian patent law aligns with the Eurasian Patent Convention and adheres to substantive examination standards, including novelty, inventive step, and industrial applicability.
  • The patent's enforceability can be affected by legal challenges, opposition, or validity proceedings, common in the pharmaceutical sector.

Implications for Industry Stakeholders

1. For Patent Holders

  • Enforcement: The specificity of claims determines the ease of enforcement against infringers.
  • Licensing: The patent potentially serves as a leverage point for licensing negotiations or partnerships in Russia.

2. For Competitors

  • Freedom-to-Operate (FTO): Competitors should conduct detailed patent clearance to avoid infringement.
  • Designing Around: Narrow claims might be circumvented with alternative compounds or methods.

3. For Regulators and Market Entrants

  • The patent may influence market exclusivity timelines, affecting pricing and accessibility of the patented pharmaceutical.

Comparison with Global Patent Practices

Compared to global practice, Russian patents tend to emphasize detailed chemical structures and functional claims. The scope defined in RU2019124314 likely conforms to these standards, balancing patent robustness with enforceability. For international alignment, Patent Cooperation Treaty (PCT) filings and subsequent extensions could expand geographical scope.


Conclusion

Patent RU2019124314 presents a strategic asset within Russia’s pharmaceutical patent domain. Its legal strength hinges on the factual specifics of its claims and the robustness against prior art challenges. Stakeholders must evaluate its scope critically, considering claim language and the patent landscape, to inform licensing, R&D, and market strategies effectively.


Key Takeaways

  • Claims Definition: Precise and well-structured claims determine the enforceability and scope of patent protection.
  • Patent Landscape: Knowledge of prior art, existing patents, and related patent families is essential to assess patent strength and potential freedom-to-operate.
  • Strategic Positioning: The patent’s scope influences licensing opportunities, market exclusivity, and legal defensibility.
  • Legal Considerations: Continuous monitoring for opposition or invalidation efforts is crucial, especially in the competitive Russian pharmaceutical patent environment.
  • Global Strategy: Aligning Russian patent protection with international filings maximizes market reach and reinforces monopoly rights.

FAQs

1. What is the typical scope of claims in Russian pharmaceutical patents like RU2019124314?
Claims typically specify precise chemical structures, formulations, methods of synthesis, and therapeutic uses. The scope ranges from broad, general formulas to narrowly defined compounds, ensuring patent protection while maintaining validity over prior art.

2. How can competitors determine the infringement risk of RU2019124314?
By analyzing the patent claims, especially the chemical structure and method claims, competitors can compare their compounds or processes. If their products fall within the scope of the claims, infringement could be suspected.

3. What are the advantages of broad claims versus narrow claims?
Broad claims provide extensive protection against competitors but risk invalidity if challenged on prior art grounds. Narrow claims are easier to defend but limit the protected scope, potentially allowing circumvention.

4. How does RU2019124314 fit into the global patent landscape?
If filed as part of a patent family, it could complement or be complemented by filings in other jurisdictions like Eurasia, Europe, or the US, strengthening market exclusivity and legal enforceability across regions.

5. What strategies can patent holders use to reinforce the protection of RU2019124314?
Regular patent maintenance, pursuing additional patent filings (e.g., for derivatives or different formulations), and actively monitoring potential infringers are key strategies. Additionally, leveraging patent examination procedures to tighten claim scope can fortify protection.


References:
[1] Russian Federal Institute of Industrial Property (ROSPATENT) database.
[2] World Intellectual Property Organization (WIPO). Patent Scope Database.
[3] European Patent Office (EPO). EPO Patent Data.

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