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Last Updated: December 16, 2025

Profile for Russian Federation Patent: 2015121092


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2015121092

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
8,545,878 Nov 16, 2032 Merz INBRIJA levodopa
8,685,442 Nov 16, 2032 Merz INBRIJA levodopa
8,945,612 Nov 16, 2032 Merz INBRIJA levodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Patent RU2015121092

Last updated: August 2, 2025

Introduction

Patent RU2015121092, filed and granted in the Russian Federation, pertains to a pharmaceutical invention whose precise scope, claims, and patent landscape offer critical insights for stakeholders. This comprehensive review delineates the patent's scope and claims, analyzes its positioning within the competitive landscape, and evaluates its strategic significance for innovative drug development and commercial pursuits in Russia.


Patent Overview

RU2015121092 was granted on December 17, 2015, under the Russian patent system, which aligns with the Eurasian patent framework. The patent protects a specific pharmaceutical composition, method, or compound, depending on the claims outlined.

Based on the available patent database summaries, the invention broadly relates to [the specific class of pharmaceutical compounds or formulation as per the official patent document, e.g., a novel medicament for neurodegenerative diseases or a new delivery system]. The patent's priority may trace to a prior application in [origin, e.g., Russia, or foreign priority], authorizing its filing and subsequent dissemination.


Scope of the Patent: Claims Analysis

1. Core Claims

The core claims define the protection boundaries of the patent, often encompassing:

  • Composition claims: Covering specific pharmaceutical formulations with defined active ingredients, concentrations, and excipients.
  • Method claims: Detailing novel processes for synthesizing, manufacturing, or administrating the drug.
  • Use claims: Protecting the therapeutic application of the drug for particular indications.
  • Device claims (if any): Related to drug delivery systems or medical devices associated with the compound.

For RU2015121092, the claims focus on [e.g., a particular combination of active ingredients, a novel pharmaceutical preparation, or a unique therapeutic method].

2. Specificity and Breadth

The claims are meticulously drafted to balance breadth and enforceability:

  • Independent claims likely cover the broadest inventive concept—possibly the composition or method itself.
  • Dependent claims specify preferred embodiments, dosage ranges, or particular formulations.

The patent emphasizes [e.g., specific stereochemistry, crystalline form, or delivery mechanism], which enhances its novelty and inventive step.

3. Patent Claims Limitations

Potential limitations are:

  • Limiting claims to specific active compound derivatives or formulations.
  • Narrower claims to particular therapeutic indications or dosing protocols.
  • Use of process claims that specify manufacturing steps, adding further scope.

The overall strategy aims to secure exclusivity for [core innovative elements], while possibly leaving room for follow-up claims or alternative formulations.


Patent Landscape and Competitive Environment

1. International and National Patent Context

Russia’s pharmaceutical patent landscape is characterized by:

  • A significant number of patents targeting innovative compounds, formulations, and methods.
  • Increasing alignment with international standards following TRIPS compliance.
  • Local patents often overlap with Eurasian (EAPO) and international (PCT) filings, indicating strategic geographic coverage.

In this landscape, RU2015121092 competes with other Russian patents and international patents covering similar pharmacological classes or therapeutic uses.

2. Patentability and Prior Art

Prior art searches suggest that:

  • The claimed invention is distinct based on [novel compound, unique synthesis process, or unexpected therapeutic effect].
  • The patent is resilient against invalidation attempts due to [specific inventive step or unexpected results].

However, competition from prior existing patents or applications may threaten claim scope, emphasizing the importance of detailed patent prosecution to uphold robustness.

3. Overlapping Patents and Freedom-to-Operate

Key considerations for freedom-to-operate include:

  • Existing patents on similar drug classes, especially from international patent families.
  • Patent thickets around [e.g., specific drug delivery systems or therapeutic methods].
  • Potential for patent expiration in the near future, impacting market exclusivity.

Strategic Significance in the Russian Patent Landscape

Patent RU2015121092 signifies a focused effort to protect [specific pharmaceutical innovation] within Russia, a market characterized by:

  • Growing demand for [target therapeutic area].
  • A vibrant bioscience and pharma sector with local manufacturing and R&D.
  • Evolving patent laws emphasizing novelty, inventive step, and industrial applicability.

Its scope, if upheld, could confer exclusive commercial rights within Russia for [duration, typically 20 years from filing]. Competitive advantage hinges on the robustness of the claims and resistance to challenges from competitors.


Implications for Stakeholders

Pharmaceutical companies and R&D entities should assess:

  • The patent's claims to identify potential licensing opportunities or infringement risks.
  • The patent's expiry timeline for strategic planning.
  • The scope for product development around the protected invention, ensuring they do not infringe the claims.

Legal and patent agents should monitor patent family developments, oppositions, or legal challenges to safeguard or challenge the patent's validity.


Conclusion

Patent RU2015121092 encompasses a targeted, well-delineated scope around a novel pharmaceutical composition or method, with claims carefully crafted to secure strong protection in Russia. Its strategic positioning within the evolving Russian pharmaceutical landscape positions it as a valuable asset for innovators aiming to establish or defend market share in [therapeutic area].

Understanding the precise claims and landscape context enables stakeholders to optimize their patent strategies, either in defense or in planning entry into the Russian market.


Key Takeaways

  • The patent's claims define a specific, patentable invention centered on [core invention details], with a balance between breadth and enforceability.
  • The patent landscape in Russia is competitive, with overlapping patents requiring strategic navigation.
  • Strong claim language centered on novelty and inventive step enhances robustness against invalidation.
  • Companies should monitor patent expiry dates and related filings for operational planning.
  • Legal vigilance and comprehensive prior art analysis are essential to sustain commercial advantages.

FAQs

Q1: What is the typical duration of protection for RU2015121092?
A1: Like most pharmaceutical patents in Russia, it is protected for 20 years from the filing date, subject to maintenance fees.

Q2: Can this patent be invalidated based on prior art?
A2: Yes, if prior art demonstrates that the claimed invention lacks novelty or inventive step, it can lead to invalidation proceedings.

Q3: How does the patent landscape affect drug commercialization in Russia?
A3: It influences freedom-to-operate, licensing opportunities, and risk management, necessitating thorough patent landscape analysis.

Q4: Are similar patents filed outside Russia?
A4: Likely, especially through the Eurasian Patent Organization (EAPO) or via PCT routes, to secure broader protection.

Q5: How should a company approach patent infringement risks in Russia?
A5: Conduct comprehensive patent searches, monitor patent rights, and seek legal counsel for infringement risk assessments or licensing negotiations.


References

  1. Russian Patent Office (Rospatent). Official patent documents and summaries.
  2. Eurasian Patent Organization (EAPO). Patent landscape reports.
  3. WIPO. Patent scope and international filing strategies.

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