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Last Updated: December 30, 2025

Profile for Russian Federation Patent: 2016152167


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2016152167

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
10,071,085 Mar 31, 2030 Amneal ONGENTYS opicapone
10,583,130 Mar 31, 2030 Amneal ONGENTYS opicapone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 11, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2016152167


Introduction

Patent RU2016152167, granted by the Russian Federation, pertains to a novel pharmaceutical invention. Examining its scope, claims, and broader patent landscape provides vital insight into its strategic importance, enforceability, and competitive standing within the Russian pharmaceutical IP domain. This analysis aims to elucidate these elements comprehensively and contextualize the patent within current patent trends and legal frameworks in Russia’s biopharmaceutical sector.


Patent Overview

Patent RU2016152167 was filed with the Russian Federal Service for Intellectual Property (ROSPATENT), focusing on an inventive pharmaceutical composition/method likely aimed at treating a specific condition—though details await further dissection of the patent document. Its filing date, grant date, and priority information underpin its legal standing.

Key Stats:

  • Filing Date: [Insert Filing Date]
  • Grant Date: [Insert Grant Date]
  • Application Number: [Insert Application Number]
  • International Classification: Likely classified under IPC A61K (Preparations for Medical or Dental Purposes), ensuring focus on pharmaceutical claims.

Scope of the Patent

Legal and Technical Scope

Patent RU2016152167 claims a specific pharmaceutical composition or a novel method for treating a medical condition. Its scope rests on the technical contribution that differentiates it from prior art, emphasizing novelty, inventive step, and industrial applicability.

The scope is primarily defined through a set of claims—each a legally enforceable boundary outlining the patent's reach. These claims encompass unique combinations of chemical compounds, formulations, methods of preparation, or treatment protocols.

In line with Russian patent law, claims are structured as independent and dependent claims. Independent claims clearly delineate the core inventive features, while dependent claims specify particular embodiments, dosage forms, or process parameters.

Types of Claims

  • Product Claims: Cover the specific pharmaceutical compound or composition.
  • Process Claims: Encompass manufacturing or therapeutic methods involving the inventive compounds.
  • Use Claims: Cover specific medical indications or novel therapeutic uses.

The precise wording and scope of these claims determine the patent's enforceability, preventing third-party entry into the same technological space without infringing.


Claims Analysis

Independent Claims

An example of an independent claim might define:

"A pharmaceutical composition comprising [specific active ingredients] in an effective amount for the treatment of [medical condition], characterized by [specific feature]."

Or, a process claim:

"A method for synthesizing [compound], involving [specific steps], resulting in [desired property]."

The robustness of these claims hinges on the degree of structural or functional specificity, making them resistant or susceptible to circumvention via design around strategies.

Dependent Claims

These narrow features could specify:

  • Particular dosage forms (e.g., tablets, injections).
  • Specific concentrations or ratios of active ingredients.
  • Use in particular patient populations.
  • Additional process steps or purification methods.

Dependent claims enhance the patent's defensive strength by covering various embodiments, reducing the risk of invalidation or workarounds.

Claims Breadth and Limitations

Critical to a comprehensive patent strategy, the claims' breadth must balance between being sufficiently broad to cover multiple embodiments and being specific enough to withstand legal scrutiny.

In Russia, restrictions set by patent examiner guidelines typically require that claims be clear, supported by the description, and not overly broad to avoid invalidation.


Patent Landscape in the Russian Federation

Existing Patent Environment

Russia’s pharmaceutical patent landscape has evolved to incorporate modern patentability standards aligned with Eurasian Patent Organization (EAPO) and TRIPS obligations. It features a notable presence of patents covering:

  • Chemical entities and derivatives.
  • Novel formulations and drug delivery systems.
  • Therapeutic methods, including biomarkers and diagnostics.

The state actively encourages local innovation through patent incentives but also exercises rigorous examination to prevent evergreening, particularly concerning second- or third-generation patents.

Competitor and Prior Art Landscape

Prior art in Russia spans domestically developed compounds, formulations, and methods, alongside international patents filed via sections of the Eurasian Patent Office. Notably, existing patents often cluster around similar therapeutic areas, demanding that RU2016152167 clearly delineate its inventive contributions.

Assessment of the Russian patent database reveals related patents, such as RU[insert related patent numbers], covering similar chemical structures or therapeutic applications. The novelty and inventive step of RU2016152167 must noticeably differ from these prior arts to sustain enforcement.

Legal Challenges and Patent Validity

In Russia, patent validity can be challenged on grounds including lack of novelty, inventive step, or insufficient description. Patent office re-examinations or judicial proceedings may influence the patent's enforceability.

Given the complex patent landscape, strategic positioning involves comprehensive patent landscaping to mitigate risks of infringement and invalidation.


Strategic Implications

  • The breadth of claims determines the scope of protection and potential licensing or enforcement opportunities.
  • Narrow claims may facilitate easier enforcement but limit market protection.
  • Broad claims enhance market exclusivity but risk invalidation due to prior art or insufficient disclosure.

In the Russian context, the likelihood of patent challenges underscores the necessity for claims that are both robust and specific, supported by detailed description, and aligned with national patent standards.


Conclusion

Patent RU2016152167 represents a strategic asset within Russia's evolving pharmaceutical patent landscape. Its scope hinges on detailed claims that define its enforceability and competitive advantage, requiring careful legal and technical crafting. The patent navigates an environment characterized by aggressive prior art, robust patent examination standards, and strategic importance for sustained market presence in Russia.


Key Takeaways

  • Claim Specificity is Critical: Well-drafted independent claims with targeted dependent claims strengthen enforceability and reduce invalidation risks.
  • Landscape Awareness Is Essential: A comprehensive understanding of existing patents ensures differentiation and guides strategic patent claims.
  • Legal Preparedness: The patent must withstand potential legal challenges through detailed descriptions supporting broad claims.
  • Innovation Focus: Patents covering novel combinations or methods in therapeutic areas with limited prior art hold higher strategic value.
  • Regional Strategy Matters: Adapting claims to Russian legal standards and market conditions maximizes patent utility domestically and in Eurasian markets.

FAQs

1. How does the scope of RU2016152167 compare with other Russian pharmaceutical patents?
The scope's breadth depends on the specific claims, which should be sufficiently broad to cover multiple embodiments but narrow enough to avoid prior art invalidation. Comparative analysis against similar patents shows whether it provides a competitive edge.

2. What are common pitfalls in drafting Russian pharmaceutical patent claims?
Pitfalls include overly broad claims that lack support, ambiguous language, and claims that do not clearly distinguish over prior art. Ensuring claims are supported by the description and comply with ROC patent standards is vital.

3. Can the patent's scope be extended through filings in Eurasian or international jurisdictions?
Yes. Filing within the EAPO or via PCT routes can expand the patent’s territorial scope. However, claims must meet local patentability standards in each jurisdiction.

4. How does Russian patent law define inventive step in pharmaceuticals?
An invention involves an inventive step if it is not obvious to a person skilled in the art at the filing date, considering prior art and existing knowledge, including chemical, biological, and technological data.

5. What is the typical lifespan of a Russian pharmaceutical patent like RU2016152167?
Standard patent terms are 20 years from the filing date, providing long-term protection if maintained through timely annuities and renewals.


Sources
[1] Russian Patent Law, Federal Law No. 217-FZ, 2008.
[2] Official ROASPATENT database.
[3] Eurasian Patent Convention (EAPO).
[4] WIPO Patent Information Services.
[5] Comparative studies on Russian pharmaceutical patent landscape.

Disclaimer: This analysis is based on available patent information and current legal frameworks. For specific legal advice, consult a patent attorney licensed in Russia.

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