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Profile for Russian Federation Patent: 2011149799


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2011149799

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
⤷  Start Trial Nov 28, 2032 Astellas XOSPATA gilteritinib fumarate
⤷  Start Trial Jul 28, 2030 Astellas XOSPATA gilteritinib fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Russian Patent RU2011149799

Last updated: August 8, 2025

Introduction

Russian Patent RU2011149799 pertains to a pharmaceutical invention filed within the Russian Federation, aimed at protecting specific drug formulations, methods, or compounds. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders such as pharmaceutical companies, generic manufacturers, and legal professionals engaged in IP strategy and market analysis within Russia. This analysis provides a comprehensive review of RU2011149799, focusing on its technical scope, claim structure, and positioning within the recent patent landscape.


Patent Overview

RU2011149799 was filed with the Russian Federal Service for Intellectual Property (ROSPATENT), with a patent grant date. The patent falls within the pharmaceutical and medicinal preparations domain, covering a specific composition or process intended for therapeutic applications.

Based on publicly available patent databases and patent documents, RU2011149799 primarily relates to a novel pharmaceutical composition or method for treatment (specifics depend on the actual document, but often involve active ingredient combinations, delivery systems, or manufacturing processes). Since the patent document is not directly accessible here, this analysis extrapolates from the standard structure and typical claim scopes related to Russian pharmaceutical patents.


Claims Analysis

Scope and Breadth of Claims

The core strength of the patent’s legal protection hinges on the scope of its claims, which clearly define the boundaries of the invention. The claims are usually categorized into:

  • Independent claims: These set the broadest protection, enumerating the main inventive features.
  • Dependent claims: These narrow down the scope, adding specific features or embodiments.

Typical Claim Features for RU2011149799

  1. Pharmaceutical Composition Claims: Often specify the active ingredients, their ratios, excipients, and the method of preparation. For example, claims may describe a composition comprising a specific active compound combined with certain carriers or stabilizers.

  2. Method Claims: Cover innovations in the synthesis, formulation, or therapeutic application of the drug. These may specify steps for manufacturing, dosing regimens, or administration methods.

  3. Use Claims: Claim focuses on the therapeutic use or indications, such as treatment of particular diseases or conditions.

  4. Device Claims (if applicable): If delivery systems or devices are involved, claims may specify apparatus features (e.g., inhalers, injectors).

Claim Language and Interpretive Scope

  • Broad Claims: If claims are drafted broadly, they protect a wide array of compositions or uses, potentially covering various embodiments.

  • Narrow Claims: More specific claims limit protection but reduce vulnerability to prior art.

Given Russian patent practice, claims are often detailed to withstand legal scrutiny but can vary in breadth depending on applicant strategy.

Legal and Strategic Considerations

  • The scope defines where potential infringers may operate without infringement.
  • Broader claims may offer greater market exclusivity but risk invalidation if prior art exists.
  • Narrower claims provide incremental protection but better withstand legal challenges.

Patent Landscape in Russia for Drug Patents

Legal and Regulatory Framework

Russia's patent system is based on the Patents Law (1992), aligned with the Eurasian Patent Convention and WTO standards. The landscape for pharmaceutical patents has evolved, especially post-TRIPS, emphasizing patentability criteria—novelty, inventive step, and industrial applicability.

Recent Trends

  • Increased patent filings for biologics and complex molecules.
  • Trend towards patenting formulations, combinations, and delivery methods.
  • Greater scrutiny on the inventive step, prompting applicants to strengthen claims' technical features.

Competitive Environment

Within Russia, a dynamic patent landscape exists, characterized by:

  • Domestic players: Large Russian pharmaceutical firms and R&D entities holding key patents.
  • International companies: Multinational pharma companies securing local patents to extend market exclusivity.
  • Patent litigation: Growing but still developing, with a tendency for disputes over patent validity and infringement.

Key Patent Classifications

RU2011149799 likely resides within classifications covering pharmaceuticals, medicinal preparations, or specific subclasses such as:

  • A61K: Preparations for medical, dental, or hygienic purposes.
  • A61P: Specific therapeutic activity classes.
  • C07D: Organic compounds with therapeutic activities.

Mapping such classifications aids in understanding potential infringement or freedom-to-operate analyses.


Positioning of RU2011149799 within the Patent Landscape

Comparative Analysis

  • Similar patents exist within Russia and internationally that cover compositions with comparable active ingredients or methods.
  • Patent citations are critical; whether RU2011149799 cites prior Russian patents or international applications influences its legal strength.
  • Patents filed in major markets (e.g., EPO, USPTO) may influence or be referenced by Russia’s patent system, possibly affecting patent validity or enforcement strategies.

Innovation Level

  • The patent's novelty and inventive step depend on how it advances existing knowledge—whether via a new combination, improved stability, enhanced bioavailability, or novel manufacturing methods.
  • The scope of the claims must balance broad protection with defensibility against prior art.

Patent Term and Market Strategy

  • Russian patents generally provide 20 years of protection from the filing date.
  • Strategic patenting involves continuous innovation, filing divisional or continuation applications, and leveraging patent thickets to carve market niches.

Implications for Stakeholders

For Innovators

  • The patent likely provides robust protections if the claims are sufficiently broad and specific.
  • Understanding its scope aids in defining licensing, development, and enforcement strategies in Russia.

For Generic Manufacturers

  • The patent’s claims delineate the boundaries for potentially developing biosimilars or generics.
  • Narrow claims or patent expiration may open opportunities for entering the Russian market.

For Patent Attorneys and Strategists

  • Analyzing claim language and citation history informs validity assessments.
  • Recognizing the patent landscape aids in designing around strategies or preparing invalidation proceedings if necessary.

Key Takeaways

  • RU2011149799 likely covers specific pharmaceutical compositions or methods with claims tailored to ensure enforceability while offering significant market protection.
  • The scope varies from broad formulations to specific embodiments; its strength hinges on claim language and prior art analysis.
  • The current Russian patent landscape emphasizes innovation in biologics, delivery systems, and combination therapies, making the patent’s positioning critical.
  • Patent validity depends on ongoing examination, prior art citations, and potential challenges from competitors or patent offices.
  • Strategic patenting should consider international filings and alignment with market development and licensing plans.

FAQs

Q1: How does the scope of RU2011149799 compare to similar international patents?
A1: Russian patents often have narrower claims focusing on specific embodiments. To match broader international protection, applicants typically file corresponding applications with broader claims in jurisdictions like the EPO or USPTO.

Q2: Can RU2011149799 be challenged or invalidated?
A2: Yes, via legal proceedings in Russia that examine prior art, inventive step, or procedural compliance, especially if proof demonstrates lack of novelty or inventive activity.

Q3: How does patent expiration influence the Russian drug market?
A3: After 20 years from the filing date, patent protection expires, allowing generics to enter the market, potentially increasing competition and reducing prices.

Q4: What strategies can extend the patent life or strengthen protection?
A4: Filing divisional or continuation applications, patent term extensions (if applicable), or developing new formulations or delivery methods can help maintain market exclusivity.

Q5: Are there specific Russian regulations affecting pharmaceutical patent enforcement?
A5: Yes, Russian law provides mechanisms for patent infringement suits, compulsory licensing under certain conditions, and procedures for patent oppositions.


Conclusion

Russian Patent RU2011149799 exemplifies a strategic protection instrument within Russia’s pharmaceutical landscape, with its scope and claims shaping the competitive and legal environment. A thorough understanding of its claim language, scope, and position amid the evolving patent landscape empowers stakeholders to optimize IP portfolios, guide R&D efforts, and navigate market entry strategies effectively in Russia's dynamic pharmaceutical sector.


References

  1. Russian Federal Service for Intellectual Property (ROSPATENT) official database.
  2. WTO/TRIPS Agreement, 1994.
  3. Eurasian Patent Convention guidelines.
  4. Russian Civil Code, Patent Law, current edition.
  5. Patent landscape reports on pharmaceutical patents in Russia.

(Note: Specific patent claim details and exact filing/grant dates would require access to the official patent document.)

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