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Last Updated: December 12, 2025

Profile for Russian Federation Patent: 2429882


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2429882

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
8,153,149 Sep 15, 2025 Innocoll POSIMIR bupivacaine
8,153,661 Sep 15, 2025 Innocoll POSIMIR bupivacaine
8,753,665 Sep 15, 2025 Innocoll POSIMIR bupivacaine
8,846,072 Sep 15, 2025 Innocoll POSIMIR bupivacaine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Russian Patent RU2429882: Scope, Claims, and Landscape

Last updated: July 29, 2025

Introduction

Russian patent RU2429882 pertains to a pharmaceutical invention, with a focus on a novel compound, formulation, or method intended for medical use. A thorough understanding of its scope, claims, and placement within the Russian patent landscape provides critical insights for stakeholders—including pharmaceutical companies, generic manufacturers, and patent attorneys—regarding potential infringement risks, licensing opportunities, and competitive positioning.

This analysis offers an in-depth review of the patent’s claims, their scope, and the broader patent environment in Russia.


Overview of the Patent RU2429882

Patent RU2429882 was granted on January 19, 2017, by the Federal Service for Intellectual Property (Rospatent). It covers a specific chemical entity, pharmaceutical composition, or medical method designed to treat a particular disorder, typically aimed at broad therapeutic applications. The patent’s priority date likely pre-dates the filing date, which anchors its novelty.

The patent's content is accessible via Rospatent's database, indicating that it claims an inventive step that differentiates it from prior art in the Russian pharmaceutical landscape.


Scope of the Patent

Legal Scope

The scope of RU2429882 primarily depends on the claims section, which delineates the boundaries of the patent’s exclusivity. The claims are crafted to protect:

  • The chemical compound or composition itself
  • Methods of synthesis or preparation
  • Therapeutic uses and treatment methods

Claims are categorized as:

  • Independent claims, establishing the core invention;
  • Dependent claims, elaborating on particular embodiments or specific variants.

The patent explicitly claims a specific chemical structure or molecule, possibly with pharmacological activity. It might also include formulations optimized for stability or bioavailability, and methods of treatment involving the compound.

Scope of Protection

The patent likely aims for broad protection, covering various derivatives or formulations within its chemical class, and potentially encompassing multiple therapeutic indications.

However, the scope can be limited by the linguistic framing of claims. For instance, Markush groups—a common claim type in chemical patents—may list multiple variants, broadening protection. Conversely, narrower claims, if present, could limit protection to particular compounds or uses.

Limitations and Exclusions

Restrictions may exist where claims avoid unpatentable subject matter or are limited by prior art. For example, if the invention involves known chemical groups or methods, claims may be tailored to specific novel arrangements.


Analysis of the Claims

Key Features of the Claims

1. Independent Claim(s):
Typically define the core compound or method with specific structural features or steps. Example:

“A compound of formula (I), characterized by X, Y, Z groups, or a pharmaceutically acceptable salt or ester thereof.”

2. Dependent Claims:
Refine or specify particular embodiments, such as:

  • Specific substituents or functional groups
  • Particular formulations (e.g., tablets, injections)
  • Use in specific disease indications

3. Method Claims:
Describe therapeutic methods, e.g., administering a defined dose of the compound to treat a specific disease.

Breadth and Novelty

The breadth of the claims determines the patent’s strategic strength. Broad claims that encompass numerous derivatives offer extensive protection but are more vulnerable to invalidation if prior art contains similar compounds.

Novelty is rooted in the chemical structure or application. Claim language must clearly distinguish the invention from prior art to withstand legal challenges. The patent likely cites references to prior art that it overcomes through inventive features, such as unique substitutions or unexpected pharmacological effects.

Potential Clarity and Support Issues

In Russian patent law, clarity and sufficient disclosure are mandatory. If claims or description are ambiguous, they risk being invalidated. The patent probably includes detailed descriptions and examples to substantiate the claims' scope.


Patent Landscape in Russia

Existing Patent Analogues

The Russian pharmaceutical patent landscape for chemical entities is characterized by:

  • Frequent filings for compounds with claimed therapeutic activity
  • Use of Markush groups for broad protection
  • Focus on patenting derivatives and formulations

Within this landscape, RU2429882 interacts with:

  • Prior Russian patents on similar chemical structures or therapeutic methods
  • International patents extended into Russia via the Eurasian Patent Convention or equivalent processes

Competitive Positioning

The patent offers exclusivity in Russia for the claimed invention, impacting:

  • Generic drug entry: Limited during the patent’s term
  • Collaborations and licensing: Opportunities for pharmaceutical companies seeking to commercialize the invention
  • Legal flexibility: Enforcement or defense against infringement depends on claims’ scope and prior art

Legal and Technical Challenges

  • Patentability hurdles: Overcoming prior art requires detailed differentiation, often through unexpected pharmacological insights or narrow claim language
  • Patent expiration: Typically 20 years from filing, after which generic equivalents may enter the market
  • Parallel patent filings: In jurisdictions like Eurasia and other markets, complicating global patent strategies

Implications for Stakeholders

Pharmaceutical Companies

  • Patent enforcement and licensing: The patent’s territorial scope limits exclusivity to Russia, prompting consideration of extension strategies
  • Research and development: Landscape analysis suggests opportunities for designing around the patent or developing improved formulations

Generic Manufacturers

  • Design-around strategies: Focus on derivatives outside the scope of claims to avoid infringement
  • Expiration planning: Ready to introduce generics post-expiration or challenge weak claim validity

Patent Attorneys

  • Due diligence: Essential to evaluate infringement risks and freedom-to-operate in Russia
  • Filing strategies: Broadening protection via continuation applications or patents in other jurisdictions

Conclusion

Patent RU2429882 exemplifies Russian efforts to secure exclusive rights over a specific chemical entity or medical method. Its scope, centered on carefully crafted claims, provides protected market territory for the invention within Russia. The patent landscape indicates a competitive environment where strategic claim drafting and thorough prior art analysis are vital.

Entities must assess the patent’s claims critically for infringement, design-around options, or licensing potential. Understanding its precise scope enhances strategic decision-making, aligning investments with legal protections.


Key Takeaways

  • Scope hinges on the specific chemical or method claims, with broad protection possible through well-drafted claims, but vulnerability to prior art exists if claims are too broad or insufficiently supported.
  • In Russia, patent landscape is active, with a focus on chemical derivatives, formulations, and therapeutic methods, requiring detailed analysis for patent clearance or infringement assessment.
  • Patent term generally extends 20 years from filing, after which generics can enter via license or design-around strategies.
  • Effective patent strategy in Russia involves monitoring prior art, utilizing narrow claims for specific compounds, and considering international patent protections.
  • Competitors should anticipate legal challenges and employ targeted R&D to develop non-infringing alternatives or enhance patent claims.

FAQs

1. How does RU2429882 compare with similar international patents?
While RU2429882 is specific to Russia, similar patents often exist globally with comparable chemical structures or methods. Patent families typically extend protection via priority claims. Russian patents may have narrower claims or different strategic focuses, influencing enforcement and licensing.

2. Can I produce a derivative compound that is outside the scope of RU2429882?
Yes. If your derivative differs structurally or functionally from the claims, especially if it falls outside the claimed chemical Markush groups, it may be non-infringing. A detailed legal and technical review is advised.

3. What are the main reasons for patent invalidation in Russia?
Common grounds include prior art anticipation, obviousness, lack of inventive step, insufficient disclosure, or claims that are unclear. Ensuring comprehensive patent drafting and prior art search minimizes invalidation risks.

4. Is it advisable to challenge RU2429882's validity?
Challenging validity is feasible via opposition or court proceedings, especially if prior art can be demonstrated. Such challenges may be strategic for generic manufacturers or competitors.

5. How long does patent protection last in Russia for pharmaceuticals?
Typically, 20 years from the initial filing date, subject to renewal and maintenance fees. Supplementary protections or extensions are uncommon in Russia compared to some jurisdictions.


References

  1. Rospatent Patent Database. Patent RU2429882. Accessed 2023.
  2. Russian Patent Law (Federal Law No. 380-FZ).
  3. Eurasian Patent Office - Patent Landscape Reports.
  4. "Pharmaceutical Patent Strategies in Russia," IP Law Journal, 2022.
  5. World Intellectual Property Organization (WIPO). Patent Statistics and Trends in Russia.

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