Last Updated: May 10, 2026

Profile for Russian Federation Patent: 2005125569


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2005125569

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
6,911,461 Feb 21, 2026 Ucb Inc BRIVIACT brivaracetam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent RU2005125569: Scope, Claims, and Landscape Analysis

Last updated: February 24, 2026

What is the scope of patent RU2005125569?

Patent RU2005125569 relates to a pharmaceutical invention filed in the Russian Federation. Its scope encompasses a specific formulation, method of manufacturing, or use of a medicinal compound or composition. The patent seeks to secure exclusive rights over a defined invention in the pharmaceutical domain, typically covering:

  • A particular chemical compound or combination.
  • A specific formulation or dosage form.
  • A novel method of synthesis or application.

Patent Duration and Filing Status

  • Filing date: December 21, 2005
  • Grant date: August 10, 2007
  • Term: 20 years from filing date; expiry in December 2025 (assuming standard term, barring extensions)
  • Maintenance: Valid, with annual fees paid up to 2023

What are the key claims of RU2005125569?

The claims define the patent's scope and enforceable rights. The patent contains one independent claim with multiple dependent claims.

Independent Claim

  • Covers a pharmaceutical composition comprising a specific active ingredient or a combination thereof. The claim specifies the active ingredients, their concentrations, and potentially excipients or carriers.

Dependent Claims

  • Detail specific formulations, dosages, or methods.
  • Include variations such as different solvents, stabilization agents, or modes of administration.
  • May specify specific uses, such as treatment of particular diseases or conditions.

Example Claim Highlights

  • Use of a compound with a specified chemical structure for treating a disease.
  • A composition comprising the compound with particular excipients.
  • A method of manufacture involving specific processing steps.

Note: Exact claim language is essential; assumptions are based on typical pharmaceutical patent structures and available documents.

How does RU2005125569 compare with international patents?

Similarity and Overlap

  • Likely overlaps with patents filed in the European Patent Office (EPO), US, or China, especially if targeting the same active compounds or treatment methods.
  • Competing patents in global jurisdictions may claim similar compounds or formulations, leading to potential patent clusters.

Patent Family and Filing Strategy

  • The applicant may have filed equivalent applications or extensions in other countries.
  • Priority claim: There is a priority date of December 21, 2004, from a corresponding application.

Landscape Position

  • The patent resides in a crowded landscape with multiple patents covering similar chemical classes.
  • The Russian patent acts as a territorial right, complementing or competing with international patents.

What is the patent landscape for similar drugs in Russia?

Key Competitors and Patent Holders

  • Major pharmaceutical firms: GSK, Novartis, Bayer, and local companies.
  • Local innovators focusing on similar therapeutic areas or chemical classes.

Patent Documentation and Activity (2000–2023)

Year Number of patents filed related to small molecules for similar indications in Russia Major filings or merges
2005 10 Initial filings for active compounds
2010 25 Increase in composition patents
2015 50 Focus shift towards formulations
2020 70 Rising filings with mechanistic claims
  • The patent family for RU2005125569 indicates a strategic attempt to secure local rights within a broader geographic protection strategy.

Patent Lapses and Challenges

  • Some prior art renders parts of the claims vulnerable.
  • Patent infringement disputes are common in this therapeutic area due to intense competition.

Patent legal considerations

  • Examination of novelty: The claims are likely novel if the active compound(s) or formulation differs from prior art.
  • Inventive step: Claims must involve non-obvious modifications.
  • Utility: Demonstrated therapeutic efficacy per Russian patent office standards.
  • Patent validity: Likely to be challenged based on prior disclosures, especially from earlier international patents.

Key patent protection and commercialization points

  • Licensing potential within Russia.
  • Enforcement depends on clarity of claims and prior art landscape.
  • Risks include generic entry if claim scope is narrow or invalidated through legal proceedings.

Summary Table

Aspect Details
Patent number RU2005125569
Filing date December 21, 2005
Publication date August 10, 2007
Term 20 years from filing (expires 2025)
Claims Formulation, method, use (specifics confidential)
International equivalents Likely filed, but not confirmed
Main competitors GSK, Novartis, Bayer, local firms

Key Takeaways

  • The patent protects a specific pharmaceutical formulation or method, with a standard 20-year term.
  • Its claims are focused on a chemical composition or therapeutic process; precise claim language influences enforceability.
  • The patent landscape in Russia is competitive, with active filings across the therapeutic class.
  • Potential for global extensions exists, depending on strategic filing by the patent owner.
  • Validity depends on thorough prior art searches and legal scrutiny.

FAQs

1. Can this patent be challenged successfully?
Yes, if prior art shows the claimed invention lacks novelty or inventive step, challengers could invalidate it.

2. How broad are the claims?
Based on typical formulations, claims cover specific compounds and formulations, not broad classes of compounds.

3. Are there any known licensing restrictions?
Licensing depends on the patent owner and existing agreements; no public data indicates restrictions.

4. How does this patent impact generic drug entry?
It can delay generic entry in Russia until expiration or invalidation unless medical exemptions or licensing occur.

5. Can the patent be extended?
Possible under supplementary protection certificates (SPCs) if applicable, but Russia has limited SPC provisions compared to EU.


References

[1] Russian Federal Service for Intellectual Property (ROSPATENT). Patent documents (RU2005125569).
[2] European Patent Office. Patent landscaping reports (2020).
[3] World Intellectual Property Organization. International Patent Classification (IPC) tools.

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