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Last Updated: December 13, 2025

Profile for Russian Federation Patent: 2666367


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2666367

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
10,005,783 Oct 21, 2029 Bayer Hlthcare VITRAKVI larotrectinib sulfate
10,005,783 Oct 21, 2029 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,047,097 Oct 21, 2029 Bayer Hlthcare VITRAKVI larotrectinib sulfate
10,047,097 Oct 21, 2029 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,774,085 Oct 21, 2029 Bayer Hlthcare VITRAKVI larotrectinib sulfate
10,774,085 Oct 21, 2029 Bayer Healthcare VITRAKVI larotrectinib sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Russian Patent RU2666367: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent RU2666367, granted by the Russian Federation, pertains to a novel pharmaceutical invention. As part of strategic intellectual property (IP) management, understanding its scope, claims, and position within the patent landscape is vital for stakeholders, including pharmaceutical companies, researchers, and legal professionals. This analysis delineates the patent's scope, interprets claims, explores relevant prior art, and situates RU2666367 within the broader patent environment in Russia and globally.


Patent Overview

Patent Number: RU2666367
Filing Date: [Insert filing date]
Grant Date: [Insert grant date]
Applicants/Inventors: [Insert applicant/inventor details if available]
Field: Pharmaceutical compositions, potentially involving new chemical entities, formulations, or methods of use.

(Note: Since specific details such as filing or grant date are not provided here, this should be supplemented with the official patent document for a precise timeline.)


Scope of RU2666367

The scope of a patent fundamentally encompasses the technical aspects protected by its claims. It defines the legal boundaries of exclusive rights granted to the patent holder.

Type of Patent Protection

RU2666367 appears to be a standard utility patent, protecting a particular composition, method, or use of a pharmaceutical agent. Its scope hinges primarily on claims, which specify the precise features deemed inventive.

Claims Analysis

The core of the patent resides in its claims, which articulate the technical features the patent holder seeks to protect. Claims are generally categorized as:

  • Independent Claims: Broadly outline the essential invention.
  • Dependent Claims: Narrower, specify particular embodiments or applications.

Note: Exact wording of claims is required for precise interpretation, but in absence of the text, a typical analysis follows.


Detailed Claims Examination

1. Composition Claims

If the patent claims a pharmaceutical composition, it likely specifies:

  • The active ingredient(s), including chemical structure or class.
  • Concentration ranges.
  • Auxiliary components such as stabilizers, carriers, or excipients.
  • Formulation characteristics (e.g., oral, injectable, topical).

Implication: Such claims safeguard proprietary formulations with specific combinations or characteristics, preventing competitors from producing similar compositions within the defined parameters.

2. Method Claims

If the patent includes method claims, these could pertain to:

  • Production processes for the active compound.
  • Administration protocols (dosing regimen, delivery method).
  • Treatment methods for particular conditions or patient groups.

Implication: Method claims extend protection to novel processes or therapeutic protocols, potentially covering ethical, surgical, or manufacturing procedures.

3. Use Claims

Use claims may specify:

  • Therapeutic indications.
  • Specific patient populations.
  • Novel methods of treatment.

Implication: Use claims tighten the scope, protecting specific therapeutic uses, which can impact patentability and licensing strategies.


Patent Landscape in Russian Federation

National Patent Policies and Pharmaceutical IP

Russia's patent regime aligns with international standards, governed primarily by the Civil Code of the Russian Federation and the Patents Law. The country actively participates in the World Intellectual Property Organization (WIPO) and adheres to TRIPS agreements.

Pharmaceutical Patent Trends in Russia

  • Increasing number of pharmaceutical patents since the 2010s, driven by local innovation and foreign investment.
  • Emphasis on second-generation formulations, biosimilars, and method of use patents.
  • Patent term: Typically 20 years from filing, with possibilities for extensions under certain circumstances (e.g., data exclusivity).

Key Players and Patent Clusters

Major Russian pharmaceutical companies, alongside international operators with local presence, pursue patenting strategies aligned with global trends. The patent landscape features clusters of overlapping patents on similar molecules, formulations, or methods, leading to a competitive environment.

Relevant Prior Art and Similar Patents

  • Similar active compounds: Patents involving analogous chemical structures or classes.
  • Formulation patents: Covering specific drug delivery systems.
  • Use patents: Targeted at particular indications, often overlapping but distinguishable.

The positioning of RU2666367 revolves around its novelty against these existing patents identified through patent searches, such as those in the Russian patent database (FIPS) or international databases like EPO and WIPO.


Analysis of Patent Validity and Novelty

Novelty and Inventive Step

To assess patent strength, the following factors are considered:

  • Distinctiveness from prior art: RU2666367’s claims must demonstrate an inventive step, i.e., non-obviousness over prior art.
  • Identification of closest prior art: Existing patents or publications presenting similar compositions or methods.
  • Unique features: Any specific chemical modification, formulation, or method that distinguishes RU2666367.

Potential Challenges

  • Existing similar patents: Could challenge the novelty.
  • Obviousness: If the claimed invention results as an obvious modification to prior art, its validity may be questioned.
  • Claims scope reduction: During patent examination or litigation, claims scope might be narrowed.

Patent Landscape Analysis

Global Context

While RU2666367 is Russian-specific, pharmaceutical patents often seek international protection via Patent Cooperation Treaty (PCT) applications and regional filings (EPO, USPTO).

Russian vs. International Protection

  • Russian patent: Primarily provides rights within Russia.
  • International filings: Broader protection; pending or granted patents in multiple jurisdictions might resemble RU2666367.
  • Patent family analysis: Identifies whether similar patents are filed elsewhere.

Legal and Commercial Implications

  • The patent affects generic entry, licensing negotiations, and research investments.
  • In Russia, patent infringement actions enforce rights and can lead to injunctions and damages.

Strategic Considerations

  • Patent strength: Well-drafted claims focusing on inventive features are critical.
  • Freedom-to-operate (FTO): Screening for overlapping patents is essential before commercialization.
  • Lifecycle management: Considering patent extensions and supplementary protection certificates (SPC) potential.

Key Takeaways

  • RU2666367’s scope is primarily defined by its claims covering specific pharmaceutical compositions or methods.
  • The patent’s strength depends on its novelty, inventive step, and claim clarity, established through comprehensive prior art analysis.
  • The Russian patent landscape exhibits an active environment, with ongoing development in pharmaceutical IP strategies.
  • Protecting the unique features of RU2666367 requires vigilant monitoring of similar patents, both domestically and internationally.
  • Strategic patent management benefits from aligning claims with strong inventive features while ensuring a clear landscape to defend against challenges.

FAQs

1. What is the core inventive concept of RU2666367?
Without access to the specific claims, it is likely centered on a novel pharmaceutical formulation or method, with unique active ingredients, concentrations, or delivery techniques that differentiate from prior art.

2. How does RU2666367 compare to similar patents in Russia?
It potentially distinguishes itself through specific chemical modifications, unique use indications, or formulation features, but a detailed comparison requires access to the claim set and prior art database.

3. Can RU2666367 be extended beyond 20 years?
In Russia, extensions are generally limited; however, certain supplemental protections like SPCs may be applicable, subject to national regulations.

4. What are the risks of patent invalidation for RU2666367?
The main risks include prior art invalidating the novelty or inventive step, or claim language being too broad or vague leading to legal challenges.

5. How should patent owners leverage RU2666367?
By enforcing the claims against infringers, licensing to third parties, and integrating the patent into broader IP strategies to maximize commercial value.


References

  1. Federal Institute of Industrial Property (FIPS) Russia Patent Database.
  2. "Russian Patent Law," Civil Code of the Russian Federation.
  3. WIPO Patent Cooperation Treaty Database.
  4. European Patent Office (EPO) Patent Database.
  5. World Intellectual Property Organization (WIPO) Publications on pharmaceuticals patenting.

(Note: For precise legal or technical analysis, access to the full patent document and prior art references is essential.)

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