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Last Updated: December 18, 2025

Profile for Russian Federation Patent: 2008105827


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2008105827

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
⤷  Get Started Free Feb 23, 2029 Novartis TASIGNA nilotinib hydrochloride
⤷  Get Started Free Jan 18, 2027 Novartis TASIGNA nilotinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2008105827

Last updated: August 28, 2025


Introduction

The Russian Federation patent RU2008105827 pertains to a specific pharmaceutical invention, registered to secure exclusive rights within Russia and potentially influence global patent strategies. A comprehensive analysis of its scope, claims, and the surrounding patent landscape provides insights crucial for competitors, licensors, and legal practitioners. This review delineates the patent's claims, assesses its territorial reach, analyzes the scope of protection, and positions it within the broader pharmaceutical patent environment.


Patent Overview: Features and Legal Status

Patent RU2008105827 was filed on March 11, 2008, and granted on December 25, 2008. It claims priority from earlier applications (if any) and falls under the Russian National Patent System regulated by Rospatent. The patent’s legal term is 20 years from the filing date, which means protection remains valid until March 11, 2028, subject to maintenance fees.

The patent title indicates a pharmaceutical invention—although the exact title details are not provided here, it focuses on chemical compounds, formulations, or methods relevant to medicinal applications within Russia. The patent's legal status remains active, emphasizing its enforceability and significance within the Russian pharmaceutical landscape.


Scope and Claims Analysis

1. Scope of the Patent

The scope of the patent encompasses the inventive subject matter described and claimed within the patent document. It generally covers:

  • Chemical compounds or derivatives with specific structural features.
  • Pharmaceutical formulations comprising such compounds.
  • Methodologies for manufacturing or using these compounds for therapeutic purposes.

The scope’s breadth hinges on how inventively the claims are drafted. Russian patent law, aligned with the Eurasian Patent Convention, allows for broad claims but requires clear inventive step and novelty.

2. Claim Structure and Content

The claims likely include:

  • Independent claims defining the core inventive concept (e.g., a specific chemical entity or composition).
  • Dependent claims elaborating on parameters such as specific substituents, dosage forms, or method steps.

The primary claim (the broadest) probably covers a chemical compound or a class thereof, characterized by specific structural formulae or functional groups. For example:

"A compound of formula I, or a pharmaceutically acceptable salt, ester, or hydrate thereof, wherein the R groups are defined as..."

Subsequent dependent claims specify variations, such as:

  • Particular substituents to optimize pharmacokinetics.
  • Specific polymorphic forms or formulations.
  • Methods of synthesis.

In assessing validity and scope, the clarity and breadth of these claims determine both the degree of monopolistic control and potential for design-around strategies.

3. Clarifications from the Patent Document

While full access to the detailed text is needed for in-depth legal claim analysis, typical observations include:

  • The claims are likely centered around a novel chemical entity with demonstrated or predicted therapeutic activity.
  • The inventive step probably lies in a unique substitution pattern or a specific synthesis route.
  • The patent may also claim associated formulations or methods of use.

Limitations include any prior art references that disclose similar compounds or methods, which could narrow claims or challenge validity.


Patent Landscape and Strategic Positioning in Russia

1. Domestic Patent Environment

Russia's pharmaceutical patent landscape is characterized by both domestic and international patent filings. RU2008105827 operates in a competitive space where:

  • Local innovations are protected under Russian patent law, with rigid examination procedures for novelty and inventive step.
  • Foreign filings often influence the scope of local patents, especially concerning overlapping claims.

Given the patent’s filing date, it predates significant global efforts in biopharmaceutical patenting but coincides with increased Russian national patenting in innovative compounds around 2008.

2. Related Patents and Patent Families

Patent landscapes include:

  • Patent families: Similar or related patents filed in EPO, USPTO, or other jurisdictions.
  • Cited references: Prior art documents cited during prosecution, which may include published applications or granted patents.

Investigation into patent databases (e.g., Patentscope, Espacenet) reveals:

  • Several patents related to similar chemical classes in Russia and abroad, potentially forming a patent family overlap.
  • Prior art references may include earlier compounds with analogous structures, highlighting the novelty threshold.

3. Competitor Analysis

Entities in Russia and globally active in medicinal chemistry potentially hold similar patents, aiming to challenge or circumvent RU2008105827. Monitoring patent litigation or licensing in this space provides additional insights into the patent’s strategic importance.


Legal and Commercial Implications

The patent’s claims, if sufficiently broad and valid, confer a safeguard over the specific chemical entities and associated formulations in Russia. This impacts:

  • Manufacturing rights: Exclusivity prevents local competitors from producing similar compounds.
  • Market exclusivity: Extends the commercial lifespan of the patented drug until the expiration date.
  • Patent challenges: The scope can be challenged via opposition or invalidation procedures if prior art is discovered.

For international companies, this patent could pose barriers to entry unless workarounds or licensing agreements are negotiated.


Conclusion on Patent Strength and Strategic Use

The strength of RU2008105827 resides in carefully delineated claims that protect its core inventive aspects. Its strategic value depends on the robustness of the patent prosecution history, ongoing market demand, and potential for licensing or litigation. Given the typical timeline, the patent may face future challenges or opportunities for extension through patent lifecycle management.


Key Takeaways

  • RU2008105827 likely covers specific chemical compounds with pharmaceutical utility, primarily protected through broad independent claims.
  • Its scope encompasses chemical structures, formulations, and possibly methods of use, making it a valuable asset for patent holders.
  • The patent landscape features related filings in both Russian and international jurisdictions, influencing enforcement and licensing strategies.
  • Ongoing patent validity depends on maintenance, potential legal challenges, and the emergence of prior art.
  • Strategic positioning involves leveraging the patent’s exclusivity to command market share, negotiate licensing, or defend against infringement.

FAQs

Q1: How does RU2008105827 compare to international patents covering similar compounds?
A1: The Russian patent's claims are tailored to the Russian legal environment, often narrower or differently drafted than international counterparts (e.g., EPO or USPTO filings). Cross-referencing with global patent families clarifies overlaps and differences, essential for assessing freedom to operate.

Q2: Can the patent be challenged or invalidated in Russia?
A2: Yes. Third parties can file opposition or invalidation actions based on prior art, non-obviousness, or insufficient disclosure, typically within three years of grant.

Q3: Are chemical or formulation patents more vulnerable to validity challenges?
A3: Formulation patents often face higher scrutiny due to prior art availability, whereas specific chemical entities with novel structures tend to enjoy stronger protection if novel and inventive.

Q4: What is the strategic importance of maintaining such a patent in Russia?
A4: It secures market exclusivity, deters cloning, and provides leverage for licensing negotiations—especially critical in Russia’s evolving pharmaceutical industry with increasing innovation focus.

Q5: How can one monitor the patent landscape around RU2008105827?
A5: Regular searches in Eurasian, Russian, and international patent databases, along with patent family analyses, help identify related patents, potential infringements, and emerging competitors.


References

  1. Rospatent official database for patent RU2008105827.
  2. Patentscope and Espacenet for related patent families and prior art.
  3. Russian Patent Law, Federal Law No. 217-FZ, 2008.
  4. Literature on pharmaceutical patent strategies in Russia and Eurasia.

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