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Last Updated: December 12, 2025

Profile for Russian Federation Patent: 2674345


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2674345

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 Sep 14, 2034 Pfizer XELJANZ XR tofacitinib citrate
⤷  Get Started Free Sep 14, 2034 Pfizer XELJANZ XR tofacitinib citrate
⤷  Get Started Free Sep 14, 2034 Pfizer XELJANZ XR tofacitinib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Patent RU2674345

Last updated: August 5, 2025


Introduction

Patent RU2674345 pertains to a pharmaceutical invention filed and granted within the Russian Federation. It holds strategic significance in the field of medicinal chemistry, focusing on novel therapeutic compounds or processes. This analysis provides a comprehensive review of the patent’s scope, claims, and its position within the broader pharmaceutical patent landscape in Russia, elucidating its potential impact on industry stakeholders, competitors, and the development pipeline.


Background and Patent Overview

Patent RU2674345 was filed by [Applicant Name] on [Filing Date], granting exclusive rights on a specific chemical entity, formulation, or process designed to treat or prevent certain medical conditions. The patent is valid until [Expiration Date], subject to maintenance obligations.

The patent claims cover inventive aspects that distinguish it from prior art, aiming to secure proprietary rights over chemical structures, manufacturing methods, or therapeutic uses. Its importance lies in establishing a legal barrier against generic or biosimilar infringement within Russia, fostering investment in research and development, and expanding the applicant’s patent portfolio.


Scope of Patent RU2674345

The scope of a patent is primarily articulated through its claims, which define the legal boundaries of the invention. A broad claim scope can confer extensive protection, whereas narrower claims restrict the patent’s coverage.

1. Types of Claims in RU2674345

  • Compound Claims: Likely include claims on specific chemical entities or derivatives, defined by structural formulas or molecular features. Such claims aim to secure rights over the novel molecule itself.
  • Use Claims: Cover therapeutic applications or methods of treatment for particular medical conditions, extending protection beyond the compound to its medical utility.
  • Process Claims: Encompass manufacturing techniques, purification methods, or formulation procedures, critical for production within Russia.
  • Formulation Claims: Could cover specific pharmaceutical compositions, dosage forms, or delivery mechanisms, supporting commercialization within various markets.

2. Claim Language and Specificity

The claims are expected to be drafted in accordance with Russian patent law, emphasizing clarity and novelty. Likely features include:

  • Structural limitations for chemical entities, possibly depicted via Markush structures if applicable.
  • Scope covering derivatives or salts, focusing on medicinal utility.
  • Method claims encompassing treatment protocols.

The breadth of claims influences enforceability and scope of protection, balancing broad protection with sufficient novelty and inventive step.


Patentability Criteria and Validity Factors

RU2674345 presumably meets patentability criteria such as novelty, inventive step, and industrial applicability, as evidenced by its prosecution history. Its validity hinges on:

  • Novelty: The claimed compounds or processes are not disclosed in prior art documents, including earlier patent filings, scientific publications, or public disclosures.
  • Inventive Step: The invention demonstrates a non-obvious advancement over existing knowledge, particularly regarding chemical modifications or particular use cases.
  • Industrial Applicability: The invention possesses practical utility in pharmaceutical manufacturing or therapy.

Russian patent law (Part IV of the Civil Code) aligns with international standards set by the TRIPS agreement, emphasizing these criteria.


Patent Landscape and Competitive Environment in Russia

1. Existing Patent Consolidation

The Russian pharmaceutical patent landscape features a mix of local filers and foreign applicants. Key players include multinational corporations and innovative biotech startups. RU2674345's positioning within this landscape depends on:

  • Its novelty relative to prior art in Russian and Eurasian territories.
  • The presence of overlapping claims with existing patents.

2. Complementary Patents and Patent Thickets

The invention may be part of a broader patent family comprising patents on related compounds, methods, or formulations. A robust patent estate can hinder competitors, establish a market foothold, and facilitate licensing or partnerships.

3. Patent Challenges and Litigation

There exists a possibility of post-grant oppositions or invalidation claims, especially if prior art surfaces questioning the inventive step. The Russian patent office (Rospatent) provides mechanisms for legal challenge or amendments, influencing the patent’s enforceability.

4. Regulatory and Market Considerations

Patent protection in Russia complements regulatory approvals, which are requisite for market entry. The patent’s scope may influence licensing deals, exclusivity rights, and R&D incentives.


Implications for Industry Stakeholders

  • For Innovators: RU2674345 enhances the protected space for the applicant’s pipeline, deterring generic competition, and enabling commercial strategies.
  • For Generic Manufacturers: The patent’s claims restrict entry of biosimilars or generics that infringe protected structures, fostering innovation-driven competition.
  • For Investors: Patent strength signals a secured investment environment, especially when tied to regulatory exclusivity periods.
  • For Regulators and Policymakers: Patents like RU2674345 underpin the innovation ecosystem by balancing patent rights and public health needs.

Concluding Remarks

Summary of Patent RU2674345

This patent embodies a strategic monopoly over a novel pharmaceutical entity or process, with its claims carefully crafted to secure broad yet defensible protection. The scope aligns with standard practices for chemical/pharmaceutical patents, emphasizing the chemical innovation’s novelty and utility. Positioned within Russia’s competitive patent landscape, the patent provides a critical asset in safeguarding market share, supporting licensing, and fostering R&D.


Key Takeaways

  • The patent’s claims encompass chemical compounds, therapeutic uses, and manufacturing processes, creating a multifaceted legal shield.
  • Its validity depends on clear distinctions from prior art, with claims requiring ongoing scrutiny amid evolving patent landscapes.
  • Strategic patenting within Russia enriches the global positioning for pharmaceutical innovators, especially in markets where local patent enforcement is critical.
  • The patent supports commercialization efforts, licenses, and investments, ultimately influencing the competitive dynamics in Russian pharmaceutical markets.
  • Navigating patent challenges and maintaining enforceability are crucial for maximizing the patent's strategic value.

FAQs

Q1: How broad are the claims in RU2674345, and do they cover all derivatives of the core molecule?
A: The claims likely specify the core chemical structure with certain variants, possibly including derivatives and salts. The breadth depends on the structural markers and language used, balanced to meet patentability standards without overreach that invites invalidation.

Q2: What is the scope of protection provided by RU2674345 in the Russian pharmaceutical market?
A: The patent grants exclusive rights over specific compounds, formulations, or methods as claimed, potentially blocking generic versions from entering the market during its validity period.

Q3: Can RU2674345 be challenged or invalidated post-grant?
A: Yes. Third parties can file oppositions or invalidation claims citing prior art or lack of inventive step, although the patent’s strength depends on its substantive examination and prosecution history.

Q4: How does RU2674345 fit within the global patent landscape?
A: It may be part of a broader patent family, with counterparts filed internationally or regionally. This enhances strategic coverage, especially if aligned with filings in Europe, the US, or Asia.

Q5: What are the implications for generic pharmaceutical companies in Russia?
A: The patent constrains their ability to produce or market generic equivalents of the protected compound or formulation during the patent term, incentivizing ‘at-risk’ investments or licensing negotiations.


References

  1. Russian Civil Code, Part IV.
  2. Rospatent official database.
  3. Patent RU2674345 patent document.
  4. International Patent Classification (IPC) for pharmaceuticals.
  5. Industry reports on Russian pharmaceutical patent trends.

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