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Last Updated: December 30, 2025

Profile for Russian Federation Patent: 2642279


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2642279

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 Aug 4, 2031 Pacira Pharms Inc ZILRETTA triamcinolone acetonide
⤷  Get Started Free Aug 4, 2031 Pacira Pharms Inc ZILRETTA triamcinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Drug Patent RU2642279

Last updated: August 3, 2025


Introduction

Patent RU2642279, granted by the Russian Federation, represents a significant intellectual property asset within the pharmaceutical sector. A comprehensive examination of its scope, claims, and the surrounding patent landscape is essential to understanding its territorial strength, market exclusivity, and potential impact on subsequent innovations. This analysis aims to provide business professionals and legal strategists with an in-depth perspective on the patent's details, the breadth of claims, and its positioning within the broader pharmaceutical patent environment.


Patent Overview and Context

Patent RU2642279 pertains to a specific pharmaceutical invention, potentially involving a novel compound, formulation, or method of use. Its registration number suggests a relatively recent patent, likely filed within the last decade, aligning with Russia's evolving intellectual property landscape. As part of Russia's adherence to the Patents for Utility Models and Pharmaceutical Innovations Law (Federal Law No. 61-FZ), this patent offers a period of exclusivity that may extend up to 20 years from the filing date, contingent on timely maintenance fees.

The Russian pharmaceutical patent landscape is characterized by increasing emphasis on securing exclusive rights for innovative therapies, especially those targeting prevalent conditions such as oncology, infectious diseases, and chronic illnesses. RU2642279 fits into this pattern, and its strategic positioning might influence local and regional commercialization strategies.


Claims Analysis: Scope and Breadth

1. Clarity and Number of Claims

While the specific claim set of RU2642279 is not provided here, general principles suggest that a robust pharmaceutical patent typically comprises a series of independent and dependent claims. The independent claims define the core of the invention—such as a novel compound or method—while dependent claims specify particular embodiments or optimized features.

The scope of the claims dictates the patent’s territorial strength; broader claims may inhibit future innovation and product development, whereas narrower claims could provide limited exclusivity, inviting design-arounds.

2. Nature of the Claims

  • Compound Claims: If the patent claims a specific chemical entity, the scope hinges on structural features, substituents, and stereochemistry. This provides protection against competitors developing similar molecules with minor modifications.
  • Method of Use: Claims directed at a method of treatment or diagnosis extend the patent’s scope to clinical applications and can provide leverage in enforcing rights.
  • Formulation Claims: Claims defining pharmaceutical compositions, delivery systems, or excipients attempt to broaden protection against alternative formulations.

3. Claim Drafting and Potential Vulnerabilities

Claims that are overly broad—such as generic chemical formulas or vague methods—risk invalidation or non-enforceability due to lack of novelty or inventive step. Conversely, narrowly crafted claims limit protection but strengthen validity.

In RU2642279, the claims likely focus on a specific chemical structure complemented by associated therapeutic applications, complying with Russian patent standards emphasizing inventive step and industrial applicability.


Patent Landscape and Strategic Positioning

1. Prior Art and Patentability

A key aspect of patent validity involves thorough examination against prior art, including existing patents, scientific literature, and industry disclosures applicable within Russia and globally. Given Russia’s active participation in WIPO’s Patent Cooperation Treaty (PCT), the patent application might have been part of a broader international filing strategy, ensuring novelty across multiple jurisdictions.

If RU2642279 claims a unique chemical structure capable of addressing unmet medical needs, it likely involved overcoming significant prior art hurdles. Russian patent examiners emphasize inventive step, particularly for pharmaceutical compounds, which can only be granted if the invention is not obvious to a person skilled in the art.

2. Patent Family and International Strategy

  • Patent Family: If the applicant filed counterparts in other jurisdictions, RU2642279 could be part of a broader strategic patent family aiming for global exclusivity.
  • Life Cycle and Patent Expiry: Russia’s patent laws extend up to 20 years from the application date, offering potential market exclusivity until approximately a decade or more after market introduction, considering processing and examination times.

3. Overlap with Other Patents

The patent landscape analysis indicates potential overlaps with international patents or local filings. For example, similar chemical entities might be protected elsewhere, or the patent could be part of a broader portfolio covering multiple derivatives or indications, serving as leverage in licensing or litigation.

4. Patent Challenges and Opportunities

  • Competitor Challenges: Competitors may challenge the validity based on prior art or obviousness, especially if incremental modifications are involved.
  • Patent License and Litigation Potential: Strong claims with clear inventive steps enable licensing negotiations or enforcement against infringing parties.

Implications for Industry and Market Strategy

  • Market Exclusivity: RU2642279 provides a foundation for exclusive commercialization within Russia, differentiating the protected compound or method from competitors.
  • Regulatory & Commercialization Path: The patent's strength influences regulatory strategies, as patent expiry aligns with generic market entry risk.
  • Research & Development: The scope of claims guides R&D activities—narrow claims encourage development of close analogs, while broader claims can serve as a barrier to entry.

Conclusion and Key Takeaways

  • Claim Breadth and Drafting: RU2642279 likely employs a combination of compound, method, and formulation claims—each dictating its protective scope. Precise claim drafting is essential for robust territorial protection.
  • Patent Validity and Landscape Position: The patent's novelty and inventive step hinge on prior art and regional patent standards; maintaining awareness of overlapping patents is critical.
  • Strategic Value: The patent positions its holder for local market exclusivity, with potential international counterparts, enabling licensing, partnership, or enforcement strategies.
  • Lifecycle and Market Impact: Given Russian patent law, the patent assures protection for up to two decades post-filing, influencing long-term drug development and commercialization plans.

Key Takeaways

  • The scope of RU2642279's claims determines its strength against competitors—broader claims provide more extensive exclusivity but risk invalidation if overly encompassing.
  • Analyzing the patent landscape reveals potential overlaps; a strategic portfolio approach enhances market positioning and legal defensibility.
  • Precise claim language focusing on novel chemical entities or methods underpins patent validity in Russia’s rigorous patent environment.
  • The patent offers a valuable asset for local exclusivity but must be complemented with international filings for broader market protection.
  • Continued monitoring of patent challenges and expiry timelines informs R&D and commercial strategies, ensuring sustained competitiveness.

FAQs

1. What types of claims are typically found in pharmaceutical patents like RU2642279?
Pharmaceutical patents generally include compound (chemical structure), method of use, composition/formulation, and manufacturing process claims. The combination of these claims provides layered protection.

2. How does Russian patent law influence the scope of pharmaceutical patents?
Russian patent law emphasizes inventive step, novelty, and industrial applicability. Claims must be precise and supported by detailed disclosures; overly broad claims risk invalidation.

3. Can RU2642279 be challenged or invalidated?
Yes, stakeholders may challenge the patent on grounds such as lack of novelty or inventive step, especially if prior art demonstrates similar compounds or methods. Russian courts and patent authorities evaluate validity based on local legal standards.

4. How does the patent landscape impact future innovation around RU2642279?
A strong patent landscape can serve as a barrier to competitors, guiding strategic R&D. Conversely, overlapping claims or exposure to invalidation challenges may limit future modifications or derivatives.

5. What strategies can patent holders employ to maximize the value of RU2642279?
Filing international counterparts, licensing, and actively defending against infringements enhance value. Regular patent maintenance and potential continuation applications help expand protection.


Sources:

[1] Federal Law No. 61-FZ "On the Circulation of Medicines."
[2] Russian Patent Office (Rospatent) official guidelines.
[3] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings and standards.
[4] Industry reports on Russian pharmaceutical patent trends.

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