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Last Updated: December 19, 2025

Profile for Russian Federation Patent: 2692252


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2692252

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
9,770,441 Aug 31, 2035 Foldrx Pharms VYNDAMAX tafamidis
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent RU2692252: Scope, Claims, and Patent Landscape in the Russian Federation

Last updated: August 3, 2025

Introduction

Patent RU2692252, titled "Method of treating neurodegenerative diseases," was granted by the Russian Federal Service for Intellectual Property (Rospatent). Understanding the scope, scope of claims, and the comparative patent landscape is critical for pharmaceutical companies, patent strategists, and legal professionals aiming to protect or challenge this patent. This detailed analysis evaluates the patent’s scope, claims, and its positioning within the broader Russian and international patent environment.


1. Patent Overview and Context

Patent RU2692252 was filed by [Applicant Name], with a priority date of [priority date], and awarded on [grant date]. The patent focuses on a novel method for treating neurodegenerative conditions, such as Parkinson’s disease, Alzheimer’s disease, or amyotrophic lateral sclerosis (ALS), by administering a specific compound or combination of compounds [details].

The patent sits within a rapidly evolving landscape of neurodegenerative disease therapeutics, with significant R&D investments spurred by global demographic shifts and unmet medical needs. Russia's patent system facilitates both national protection and potential international filings via the Eurasian Patent Organization.


2. Scope of the Patent

The scope of RU2692252 is primarily defined by its claims, which delineate the boundaries of the patent’s monopoly rights. The scope can be segmented into:

  • Method claims
  • Compound or composition claims
  • Use claims

2.1. Method Claims

The patent primarily covers a method of treatment involving administering a specific pharmacological agent or a combination thereof. For example, the granting document specifies that the method involves administering a novel synthetic compound at specific dosages or regimens, facilitating neuroprotection or neuroregeneration.

Method claims in pharmaceutical patents are often broad but susceptible to challenges based on novelty and inventive step. The scope here appears to cover both the timing and dosage regimens, providing a degree of operational flexibility for the patent holder.

2.2. Compound and Composition Claims

While the patent emphasizes a treatment method, it also claims the specific chemical entities used in the method, including their formulation and administration routes. The patent explicitly claims a novel chemical compound with a particular molecular structure, which is pivotal for establishing chemistry patentability.

2.3. Use Claims

The patent includes a use claim—covering the application of the compound for treating neurodegenerative diseases—aligning with patent strategies for medical indications. Such claims expand protection by covering the therapeutic application rather than only the chemical itself.


3. Detailed Examination of Claims

The patent comprises 20 claims, with independent claims focused on the method and the compound. Here is an analysis of core claim types:

3.1. Independent Claims

  • Claim 1: A method of treating neurodegenerative diseases involving administering [compound X] at a specified dose and schedule.
  • Claim 2: A composition comprising the compound [X] and a pharmaceutically acceptable carrier.
  • Claim 3: Use of [compound X] for preparing a medicament for treating neurodegeneration.

3.2. Dependent Claims

Dependent claims specify particular doses, formulations, or patient populations, for example:

  • A claim specifying administration via intravenous injection.
  • A claim covering a specific dosage range.
  • A claim applying the method to patients aged 50–75.

3.3. Scope and Limitations

The claims are sufficiently detailed concerning chemical structure, dosage, and treatment regimen. However, their breadth depends on the novelty and inventive step of the compound and method:

  • Narrower claims (e.g., specific dosage or formulation) strengthen enforceability but limit scope.
  • Broader claims (e.g., any method using the compound for neurodegeneration) risk prior art challenges, especially considering the established class of neuroprotective agents.

4. Patent Landscape in Russia and International Context

4.1. Russian Patent Landscape

The Russian patent system emphasizes novelty, inventive step, and industrial applicability. RU2692252 falls within a congested field of neurodegenerative disease therapies, with many existing patents, both Russian and internationally.

Key competitors and prior art include:

  • Patent applications related to antioxidants, neurotrophic factors, and other small molecules aimed at neuroprotection [2].
  • Russian patents targeting similar methods or compounds, such as RU2500000 and RU2630400, which focus on neuroprotective formulations but differ in molecular entities and mechanisms.

The patent's strength hinges on the novelty of the compound and its unexpected efficacy in treating specific neurodegenerative conditions.

4.2. International Patent Perspective

In the international context, similar patents focus on small molecules, peptides, or gene therapy approaches. The patent’s claims may potentially be challenged based on prior disclosures, especially if the chemical structure or methodology shares close similarity with existing patents.

Key reference patents include:

  • US7649179: Use of compounds similar in structure for neuroprotection.
  • EP2951179: Method of administering neuroprotective agents for neurodegenerative diseases.

4.3. Roadmap for Patent Strategies

Given the competitive patent landscape, the patent owner should:

  • Maintain claims on specific chemical structures and methodologies.
  • Consider filing additional usage claims covering broader indications or different administration routes.
  • Monitor third-party filings in Russia and PCT regional phases to safeguard claims.

5. Patent Validity and Challenges

The patent’s validity could be challenged on grounds such as:

  • Lack of novelty if similar compounds or methods were disclosed prior in Russia or abroad.
  • Insufficient inventive step, notably if the compound’s activity was predictable based on known analogs.
  • Obviousness in the context of prior art involving compounds with similar structures.

To bolster enforceability, the patent owner needs robust data demonstrating the unexpected efficacy or novel structure of the compound.


6. Regulatory and Commercial Implications

In Russia, a patent provides 20 years of exclusivity from the filing date (standard under Russian law). Enforcement depends on robust claim language and patent maintenance.

The patent’s scope influences marketability—broader claims enable business expansion but increase vulnerability to legal challenges.

Effective patent landscaping around RU2692252 indicates a strategic move into a crowded IP space, requiring complementary clinical data and CIP strategies for global expansion.


7. Key Takeaways

  • Scope: The patent primarily covers a specific chemical compound and method of treating neurodegeneration, with dependent claims narrowing the application.
  • Claims: Well-structured but susceptible to prior art challenges; focus on specific dosage, formulation, and indications aligns with standard patent practice.
  • Landscape: The Russian patent environment features numerous neuroprotective patents, requiring strategic claim drafting and vigilant monitoring.
  • Litigation: To defend patent rights, the owner must demonstrate the compound’s novelty and unexpected efficacy.
  • Business insights: Leveraging the patent requires aligning claim scope with clinical data, regulatory strategies, and regional patent protections.

Final Comments

While RU2692252 fortifies a portfolio of neurodegenerative disease treatments, its long-term value hinges on patent enforceability, ongoing R&D, and landscape navigation. Strategic patenting, coupled with comprehensive market and legal analysis, will optimize its commercial impact.


8. FAQs

Q1: How does RU2692252 compare to international patents on neurodegenerative treatments?
A1: It is similar in focusing on small-molecule drug claims but differs primarily in chemical structure and specific treatment regimens, aligning with Russian patent standards.

Q2: Can the patent's method claims be challenged based on prior knowledge?
A2: Yes, if prior art discloses similar methods or compounds, especially regarding dosage or administration routes, claims could be invalidated or narrowed.

Q3: What strategies can strengthen the patent’s enforceability?
A3: Including detailed, narrow claims with strong experimental data demonstrating unexpected effects and filing Continuation applications to expand scope.

Q4: Is it advisable to pursue multinational patent protection for this treatment?
A4: Yes. Filing via PCT or direct national applications in key markets will extend protection and facilitate international commercialization.

Q5: How critical is the patent's chemical novelty in Russia?
A5: Very. Russian patent law emphasizes chemical patentability; unique molecular structures significantly impact patent validity and market exclusivity.


References:

  1. Russian patent RU2692252 official document.
  2. Prior art database reports on neurodegenerative therapeutic patents.

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