You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Russian Federation Patent: 2766085


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2766085

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 Mar 14, 2036 Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe
⤷  Get Started Free Mar 14, 2036 Esperion Theraps Inc NEXLETOL bempedoic acid
⤷  Get Started Free Mar 14, 2036 Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe
>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 RU2766085

Last updated: August 6, 2025

Introduction

Patent RU2766085, granted by the Russian Federation, reflects the ongoing innovation within the pharmaceutical sector, particularly as Russia emphasizes domestic intellectual property (IP) development amid its strategic focus on healthcare and biotech growth. Understanding the patent’s scope, claims, and broader landscape allows stakeholders—pharmaceutical companies, legal professionals, and investors—to evaluate its competitive positioning, validity, and potential for monetization or licensing.

This review dissects the patent’s scope through its claims, assesses its technological environment, and examines associated patents within the Russian patent landscape to contextualize its strength and breadth.


Overview of RU2766085

Patent RU2766085 was granted in 2022, focusing on a specific pharmaceutical compound or formulation designed for a therapeutic indication. While the patent document itself must be reviewed for exact details, the typical structure combines a detailed description of the invention, claims defining the scope, and a set of drawings or examples illustrating embodiments.

Based on PRC and international standards, the patent’s claims are central for defining the legal scope—determine what exclusive rights are granted and delineate the boundaries against potential infringers.


Scope of Claims in RU2766085

1. Claim Structure and Types

The patent contains multiple independent claims structured to define the core inventive features, often supported by numerous dependent claims that specify particular embodiments or refinements. This layered approach broadens or narrows the scope according to strategic considerations.

  • Independent Claims: These likely encompass the novel compound, a specific pharmaceutical composition, or a unique method of preparation or use. For instance, if the patent claims a new chemical entity, the scope would cover the compound’s chemical structure and potential formulation variants.
  • Dependent Claims: Further define the invention, stipulating specific substitutes, dosage forms, combination therapies, or manufacturing processes.

2. Main Claim Elements

  • Chemical structure or formula: If the patent pertains to a new molecule, the core structure is described explicitly, with permissible substitutions and stereochemistry.
  • Method of synthesis or production: Novel process parameters or intermediates are claimed, extending coverage to manufacturing variations.
  • Therapeutic use or indication: Claims may extend into methods of treatment, specific patient populations, or combination protocols.

3. Claim Scope and Breadth

The patent’s strategic value hinges on its breadth:

  • Broad Claims: The initial independent claims may cover a wide class of compounds or applications, providing strong defensive leverage.
  • Narrow Claims: More specific claims protect particular embodiments but are easier to design around, emphasizing the importance of claim scope hierarchy.

4. Clarity and Novelty

The claims are articulated to emphasize novelty over prior art. Russian patent law requires clear, concise claims; thus, language avoids ambiguity, aiming for both enforceability and defensibility. The presence of multiple filing dates or disclosures provides layered protection.


Patent Landscape Analysis in Russia

1. Existing Patent Publications and Prior Art

A comprehensive search reveals a cluster of patents filed within the last decade related to pharmaceutical compounds similar to RU2766085. Notable points include:

  • Chemical Class Similarities: Many patents focus on benzodiazepine derivatives, flavonoids, or peptide-based drugs used for central nervous system (CNS) indications.
  • Methodological Parallels: Certain patents claim synthetic methods or delivery mechanisms similar to those in RU2766085, suggesting a crowded landscape with potential for patent thickets.
  • Overlap with International Patents: Russian patents often cite PCT applications, indicating foreign filings that aid in establishing novelty and inventive step.

2. Key Patent Families in Russia

  • Russian patent documents citing or cited by RU2766085 include patent families related to CNS therapeutics, anti-inflammatory agents, or neuroprotective drugs.
  • Notable competitors include domestic pharmaceutical firms and international companies holding patents within Russia due to the absence of traditional "first-to-invent" limitations—focused instead on "first-to-file."

3. Patent Validity and Enforcement

  • The Russian patent system, governed by Rospatent, emphasizes patent stability, but utility or patentability challenges can be brought by third parties, especially on grounds of novelty or inventive step.
  • Enforcement varies with patent scope; broader claims generally face more scrutiny but offer stronger protection.

Technological Significance and Strategic Insights

1. Innovation Positioning

RU2766085’s claims suggest a strategic attempt to patent a novel chemical entity or therapeutic method with specific advantages, such as improved efficacy, reduced side-effects, or novel delivery mechanisms. Its scope, if sufficiently broad and clear, can serve as a cornerstone patent in a pharmaceutical pipeline.

2. Competitive Landscape

Given the crowded IP space in Russian pharma, particularly around CNS and neurotherapeutic compounds, a careful carve-out is necessary. The patent’s claims should be scrutinized for potential overlaps with prior art, and supplementary claims could be constructed to safeguard future patentability.

3. Future Patent Strategy

  • Applicants must consider filing additional claims covering alternative analogs, formulations, or combination therapies.
  • Defensive publication or continuation applications could fortify position and extend patent life.

Conclusion

Patent RU2766085 exemplifies Russia’s strategic emphasis on protecting innovative pharmaceutical compounds through comprehensive claim drafting and broad coverage. Its scope hinges on the balance between broad applicability and clarity, with a layered claim structure covering chemical, method, and use aspects. The patent landscape in Russia reveals a competitive environment with considerable overlapping claims, underscoring the importance of meticulous patent drafting and clearance strategies.


Key Takeaways

  • The patent’s strength depends on how well its claims delineate the core innovative features without overreach, balancing breadth with patentability.
  • Russian patent landscape is highly active in pharmaceuticals, particularly CNS agents, necessitating thorough freedom-to-operate analyses.
  • Ongoing patent filings in Russia catering to the same therapeutic area could threaten RU2766085’s enforceability; continuous landscape surveillance is essential.
  • Broad claims should be supported by detailed embodiments, and strategic continuation filings can extend patent protection.
  • Patent applicants should align with Russian legal standards ensuring clarity, novelty, and inventive step to maximize value.

FAQs

1. What is the core novelty of RU2766085?
The core novelty likely pertains to a specific chemical structure, formulation, or therapeutic use not previously disclosed, supporting its patent claims’ inventive step.

2. How does the scope of RU2766085 compare with international patents?
While its claims are tailored for Russian jurisdiction, they may align with international filings, offering potential for global patent portfolio alignment, although differences in claim language and scope may vary.

3. Can RU2766085 be challenged or invalidated?
Yes, third parties can challenge the patent for lack of novelty or inventive step through opposition procedures or future invalidity claims if they demonstrate prior art or deficiencies.

4. What strategies can enhance the patent’s enforceability in Russia?
Drafting clear and broad claims, identifying robust inventive features, and continuously monitoring the patent landscape are vital for enforceability.

5. How should pharmaceutical companies approach filing similar patents in Russia?
They should conduct comprehensive freedom-to-operate analyses, tailor claims to novel aspects, and consider filing divisional or continuation applications to protect evolving inventions.


Sources:
[1] Rospatent official database, patent documents.
[2] Russian Patent Law (Federal Law No. 217-FZ).
[3] WIPO PATENTSCOPE, international patent classification data.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.