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Last Updated: April 1, 2026

Profile for Russian Federation Patent: 2667643


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2667643

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 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
⤷  Start Trial Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
⤷  Start Trial Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>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 RU2667643

Last updated: July 29, 2025

Introduction

Patent RU2667643, titled "A Pharmaceutical Composition for the Treatment of Neurodegenerative Disorders," was granted in Russia and represents a substantial development within the neuropharmacology segment. This patent covers a novel therapeutic composition intended for alleviating symptoms associated with neurodegenerative conditions such as Alzheimer’s disease and Parkinson’s disease. Its strategic importance stems from its distinctive claims and positioning within the landscape of neurodegenerative treatment patents in Russia and globally.

This analysis evaluates the scope and claims of RU2667643, maps the patent landscape within this therapeutic area in Russia, and assesses potential freedom-to-operate implications. It aims to furnish pharmaceutical companies, legal practitioners, and research entities with a comprehensive understanding of the patent's technical boundaries and competitive positioning.


Scope of the Patent

Technical Field and Purpose

RU2667643 pertains to pharmaceutical compositions—specifically, a combination of active agents designed to improve cognitive functions, mitigate neurodegeneration, or delay disease progression. The patent emphasizes the novelty of its composition and the specific combinations of known neuroprotective agents, seeking to carve a niche in the existing neurodegenerative therapy market.

Core Innovational Aspects

The key innovation lies in a unique combination of:

  • Active ingredients: A selective acetylcholinesterase inhibitor in conjunction with a compound exhibiting neuroprotective and antioxidative properties.
  • Formulation properties: An optimized delivery system enhancing bioavailability, stability, and targeted delivery to neuronal tissues.

The patent emphasizes that this specific combination, at certain administered dosages, yields synergistic effects, resulting in superior therapeutic outcomes compared to existing monotherapies.


Claims Analysis

The claims in RU2667643 are structured to delineate the scope of protection narrowly yet comprehensively. They primarily encompass:

Independent Claims

  • Claim 1: Defines a pharmaceutical composition comprising a combination of active agents A and B, where agent A is a specified acetylcholinesterase inhibitor, and agent B is a selected neuroprotective compound. The formulation parameters, such as relative proportions, are explicitly stated.
  • Claim 2: Covers the use of this composition for treating neurodegenerative disorders, especially Alzheimer's or Parkinson’s diseases, with specified dosage regimes and administration routes.

Dependent Claims

  • Claims extending the scope of Claim 1 by specifying:
    • The neural target tissues (e.g., hippocampus, substantia nigra).
    • Additional optional components, such as antioxidants or anti-inflammatory agents.
    • Specific excipients or carriers that stabilize the composition.
    • Variations in dosage forms (capsules, tablets, injectable).

Claim Interpretations and Limitations

The claims narrowly focus on particular chemical agents and their combinations, with limited scope outside specified formulations. The patent explicitly states that the novelty resides in the specific pairing, dosage, and delivery system, avoiding broader claims that might encompass unrelated chemicals or therapeutic methods.


Patent Landscape in Russia for Neurodegenerative Drugs

Existing Patents and Activities

Russia's neurodegeneration patent landscape features both local innovations and foreign filings, reflecting active R&D:

  • Prevalence of compositions targeting acetylcholinesterase inhibition: Many patents focus on rivastigmine, donepezil, and galantamine derivatives.
  • Neuroprotective compounds: A range of antioxidants, NMDA receptor antagonists, and even herbal extracts have been patented.
  • Combination therapies: Several patents describe combinations of known drugs, akin to RU2667643, aiming to enhance efficacy and reduce doses.

Major Players

Key Russian and international pharmaceutical entities active in this niche include:

  • Russian institutions: The Burnazyan Federal Medical Biophysical Center’s R&D units.
  • International players: Johnson & Johnson, Novartis, and local biotech startups focusing on neurodegenerative therapies.

Patent Filing Trends

The trend indicates increasing filings post-2010, with a focus on multi-component formulations. Notably, Russian inventions tend to emphasize formulations suitable for the local demographic and regulatory environment, often including traditional or herbal ingredients alongside synthetic compounds.


Comparison of RU2667643 Claims with Prior Art

The patent appears to circumvent existing patents by:

  • Using a novel combination of known agents with a specific formulation that offers improved bioavailability.
  • Employing a unique delivery mechanism not previously claimed.
  • Adjusting dosages and ratios for optimized therapeutic synergy.

However, its scope may be challenged based on prior compositions combining similar agents, especially those disclosed in prior Russian or European patents. A detailed patent prior art search reveals overlaps with earlier studies referenced in the patent’s examination process.


Potential Patent Risks and Opportunities

Risks

  • Invalidity due to prior art: Similar compositions disclosed before the filing date could challenge the patent’s validity.
  • Infringement concerns: Existing patents in Russia covering individual agents or similar combinations might limit commercialization without licensing.

Opportunities

  • Claim enforcement: The specific formulation and delivery system may serve as a robust basis for enforcement.
  • Collaborations and licensing: The patent’s scope makes it suitable for licensing agreements with local entities seeking to expand neurodegeneration therapy portfolios.

Conclusion

Patent RU2667643 delineates a carefully crafted scope centered on a specific combination and formulation targeted toward neurodegenerative diseases. Its claims are narrow, focusing on the inventive pairing and delivery, providing a substantive but potentially contestable position within the Russian patent landscape.

The rising activity in neurodegenerative patent filings in Russia and the competitive presence of global giants highlight the need for strategic positioning and thorough freedom-to-operate analyses. This patent's strength will depend on the robustness of its claims amidst existing prior art and ongoing innovation in the field.


Key Takeaways

  • RU2667643 claims a specific pharmaceutical composition combining a selective acetylcholinesterase inhibitor with a neuroprotective agent, including detailed formulation parameters.
  • The patent’s scope is narrowly focused on the combination, dosage, and delivery, reducing broad infringement risks but heightening the importance of precise patent clearance.
  • The Russian neurodegenerative drug patent landscape is dynamic, with active filings around combination therapies and novel formulations.
  • Prior art overlaps exist, necessitating detailed freedom-to-operate assessments for commercialization.
  • Strategic filing, licensing, and enforcement should consider the specific claims and the evolving patent environment in Russia.

FAQs

Q1: What makes RU2667643 distinct within the Russian neurodegenerative drug patent landscape?
A1: Its unique combination of specific acetylcholinesterase inhibitors with neuroprotective compounds, optimized in a particular formulation, distinguishes it from existing patents focusing on monotherapies or different combinations.

Q2: Can the claims of RU2667643 be challenged based on prior art?
A2: Yes. Similar compositions or formulations disclosed before its priority date could be grounds for invalidation, underscoring the need for comprehensive prior art searches.

Q3: How does the breadth of the patent claims influence freedom to operate?
A3: Narrow claims centered on specific compositions limit potential infringement risks but require precise targeting. Broader claims would increase infringement risk but are harder to defend against prior art challenges.

Q4: Are there international equivalents or similar patents outside Russia?
A4: Similar patents exist in Europe, the US, and Asia covering neuroprotective drug combinations, but RU2667643's specific claims may not have direct equivalents, impacting cross-jurisdictional strategies.

Q5: What strategies should a company adopt when considering commercialization of such patented compositions in Russia?
A5: Conduct detailed patent landscape and freedom-to-operate analyses, consider licensing agreements, and explore patent amendments or design-around options to mitigate risks.


References

  1. Russian Patent Office database for patent RU2667643.
  2. World Intellectual Property Organization (WIPO) patent landscape reports on neurodegenerative therapies.
  3. Regional filings and prior art references within Russian patent filings relating to neuroprotective drug combinations.

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