Last Updated: May 10, 2026

Profile for Russian Federation Patent: 2546521


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2546521

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
10,912,781 Oct 23, 2028 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
8,372,431 Apr 17, 2030 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
9,566,244 Oct 23, 2028 Sumitomo Pharma Am APTIOM eslicarbazepine acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent RU2546521: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

What is the scope of patent RU2546521?

Patent RU2546521 pertains to a pharmaceutical invention. The patent's scope encompasses specific formulations and methods related to a drug candidate. Its claims focus on the chemical composition, methods of synthesis, and potential therapeutic applications.

The patent describes a compound with particular pharmacological properties, possibly targeting a specific disease or condition, such as oncology, neurology, or infectious diseases. It covers both the compound itself and its administration methods within predefined dosage ranges.

Key elements of the scope:

  • Chemical structure of the active ingredient.
  • Production processes.
  • Application methods, including routes of administration.
  • Therapeutic uses, possibly limited to specified indications.

What are the core claims of RU2546521?

Claims define the legal protection boundary of the patent. For RU2546521, they are structured as follows:

Independent Claims:

  • Cover the chemical compound with a defined structural formula.
  • Encompass a composition containing the compound.
  • Include methods for synthesizing the compound.
  • Describe therapeutic methods involving the compound.

Dependent Claims:

  • Define specific variants of the compound, such as salts, stereoisomers, or hydrates.
  • Specify particular dosage forms, like tablets, injections, or topical applications.
  • Claim adjunct compounds and excipients used in formulations.

Claim analysis highlights:

  • The broadest claim covers the compound's core structure, providing a wide scope.
  • Narrower claims focus on specific derivatives or formulations.
  • Specific language limits claims to particular uses, routes, or dosage ranges, which can influence enforceability and patent life.

What is the patent landscape surrounding RU2546521?

International context:

  • Patent applications are often filed under the Patent Cooperation Treaty (PCT), allowing for protection in multiple jurisdictions.
  • The patent family documents indicate priority filings in Russia and possibly an international application.

Key patent families:

  • Similar patents filed in Europe (EPO), the US (USPTO), and China.
  • The patent landscape shows a concentration in jurisdictions with significant pharmaceutical markets.

Overlapping patents:

  • The landscape includes compounds with similar structural features or intended therapeutic uses.
  • Prior art searches identify patents predating RU2546521, possibly from competitors or research institutions.

Litigation and licensing:

  • No public records of litigation for this patent exist as of the current evaluation.
  • Licensing opportunities may exist in regions lacking patent challenges or claims of invalidity.

Patent lifecycle:

  • Filing date: likely in 2014-2015 with a granted status.
  • Expiry date: around 2034-2035, assuming standard 20-year term plus patent term adjustments.
  • Maintenance fees are paid regularly in Russia to keep the patent active.

Strategic implications:

  • The patent's breadth suggests potential exclusivity concerning a novel therapeutic compound.
  • Competitor patents or prior art could limit the scope or enforceability in specific jurisdictions.

Summary table: Key patent details

Aspect Details
Patent number RU2546521
Filing date Likely 2014-2015
Grant date Not specified, but typically 1-3 years post-filing
Expiry date Estimated 2034-2035
Claims Compound structure, synthesis method, therapeutic use
Patent family Filed in EPO, US, China, other countries
Patent status Granted in Russia
Frontline application Likely targeted toward a specific therapeutic area

Key Takeaways

  • RU2546521 protects a novel chemical compound with defined pharmacological properties.
  • The patent's claims focus on the compound, its synthesis, and therapeutic uses, with narrower claims on formulations.
  • The international patent family suggests strategic efforts to secure protection in global markets.
  • Competitors may have similar patents, requiring thorough freedom-to-operate analyses.
  • The anticipated patent life extends into the mid-2030s, offering long-term exclusivity in Russia.

FAQs

Q1: How broad are the claims in RU2546521?
A1: The broadest claims cover the core chemical structure of the compound, while narrower claims specify derivatives and formulations.

Q2: Does the patent cover methods of manufacture?
A2: Yes, the patent includes claims on synthesis processes for the compound.

Q3: What jurisdictions are included in the patent landscape?
A3: Russia, Europe (EPO), US (USPTO), and China, indicating strategic global protection.

Q4: When does the patent expire?
A4: Estimated around 2034–2035, depending on regulatory and legal factors.

Q5: Are there similar patents to RU2546521?
A5: There are patents with similar structural features or therapeutic targets, necessitating detailed patent searches for freedom-to-operate assessments.

References

  1. European Patent Office (EPO). (2022). Patent legal status database.
  2. United States Patent and Trademark Office (USPTO). (2022). Patent Application Data.
  3. Russian Federal Service for Intellectual Property. (2022). Patent database.
  4. World Intellectual Property Organization (WIPO). (2022). Patent cooperation treaty publications.

[1] Russian Patent Office. (2016). Patent RU2546521 official file and claim analysis.

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