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: 2381023


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2381023

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
8,460,641 Nov 5, 2028 Pharmobedient OLUX E clobetasol propionate
8,460,641 Aug 13, 2027 Almirall VERDESO desonide
8,962,000 Aug 31, 2025 Pharmobedient OLUX E clobetasol propionate
8,962,000 Aug 31, 2025 Almirall VERDESO desonide
9,492,384 Aug 31, 2025 Almirall VERDESO desonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Drug Patent RU2381023

Last updated: July 30, 2025


Introduction

Patent RU2381023, filed and granted within the Russian Federation, pertains to a specific pharmaceutical invention. Analyzing such a patent involves detailing its legal scope, claim structure, technological novelty, and placement within the broader patent landscape. This report offers a comprehensive, business-oriented understanding tailored for stakeholders seeking insight into the patent’s enforceability, territorial relevance, and competitive implications.


Overview of RU2381023: Basic Patent Data

  • Patent Number: RU2381023
  • Grant Date: [Insert date, if known]
  • Filing Date: [Insert date]
  • Expiry Date: Typically 20 years from the filing date, subject to renewal and maintenance fees.
  • Applicants/Inventors: [Insert relevant applicants, assignees, or inventors, if available]
  • Priority: [Specify priority filing date, usually if based on PCT or other national filings]

(Note: Precise details should be sourced from the Russian Federal Service for Intellectual Property (ROSPATENT).)


Scope of the Patent

The scope of RU2381023 encompasses a specific pharmaceutical compound, formulation, or method of use designed for therapeutic application. Its scope is primarily defined by the patent’s claims, with additional boundaries set by the description and drawings.

Key features of the patent scope include:

  • Chemical Composition: If the patent claims a particular chemical entity, the scope covers that compound as claimed, including any structurally similar derivatives explicitly or implicitly encompassed by the description.
  • Method of Use: Claims may extend to specific therapeutic methods, such as administration protocols or treatment regimes.
  • Manufacturing Process: Some patents include claims concerning the process of synthesizing the active ingredient, further expanding the scope within manufacturing rights.

The patent’s restrictions depend on claim breadth—broad claims may cover a wide range of derivatives, while narrow claims focus on specific compounds or methods, affecting enforceability and potential for infringement.


Claims Analysis

Patent claims serve as the legal definition of the invention’s protective boundaries. Typical claims include independent claims, potentially supported by narrower dependent claims.

1. Independent Claims:

These establish the core invention—often a novel compound, formulation, or method. For RU2381023, the independent claims likely specify:

  • A chemical structure with particular substituents, e.g., a novel heterocyclic compound with therapeutic activity.
  • A formulation comprising the compound with specific excipients or carriers.
  • A method of treatment involving administering the compound under defined conditions.

2. Dependent Claims:

Supporting claims elaborate on specific embodiments, such as:

  • Particular dosages or administration routes.
  • Stabilization techniques or delivery systems.
  • Variations on the main compound with minor structural modifications.

The claims’ language directly impacts enforcement; broader claims can provide wider protection but may be more vulnerable to invalidation for lack of inventive step or novelty.

Claim Language and Clarity:

  • Clarity is crucial; overly broad or vague claims risk invalidation.
  • Specificity regarding chemical structures and methods enhances enforceability and reduces invalidity risks.

Technological and Patentability Aspects

  • Novelty: The invention must demonstrate a decisive difference from prior art. While prior art in the Russian pharmaceutical landscape is extensive, patenting of unique compounds with demonstrated therapeutic efficacy remains feasible.
  • Inventive Step: The patent must show an inventive step—i.e., non-obviousness over prior art. For RU2381023, this hinges on the structural uniqueness or unexpected therapeutic benefits.
  • Industrial Applicability: The invention's practical application in medicine must be demonstrated, aligning with Russian patent law requirements.

The patent’s claims should analyze overlapping prior art to identify their novelty and inventive step, ensuring robust enforceability against competitors.


Patent Landscape and Market Context

1. Russian Patent Landscape for Pharmaceuticals:

Russia’s pharmaceutical patent landscape is characterized by:

  • A focus on chemical entities, especially those with novelty over prior Russian or international publications.
  • Increasing acceptance of biotech and peptide-based inventions.
  • Challenges concerning patent term adjustments and legal contestations, notably in the context of patentability criteria and prior art disclosures.

2. Competitor and Patent Busy Environment:

RU2381023’s placement within this landscape involves assessing:

  • Similar patents filed by domestic or foreign pharmaceutical companies.
  • Potential conflicts with prior Russian or international patents, especially if claiming similar compounds or methods.
  • The likelihood of patent infringement and freedom-to-operate considerations.

3. Patent Families and Related Rights:

  • The patent may be part of a broader international patent family, e.g., filed via PCT, extending protection to other jurisdictions.
  • Cross-licensing, patent validity challenges, and opposition proceedings could influence its strength.

4. Patent Strategies:

  • Filing continuation or divisional applications to expand coverage.
  • Licensing negotiations tied to RU2381023 and related patents.
  • Monitoring patent expiry timelines to evaluate market entry or generic competition.

Legal Status and Enforcement Prospects

The robustness of RU2381023’s claims under Russian patent law predicates its enforceability. Given the rigorous examination standards, including novelty and inventive step requirement, the patent’s claims are likely to be defensible if well drafted.

Potential issues include:

  • Invalidation Risks: Due to prior art, especially if similar compounds were disclosed publicly before grant.
  • Infringement Enforcement: Market actors producing similar drugs without license could be targeted, provided the patent’s scope covers their products.
  • Legal Challenges: Third parties may initiate opposition or invalidate claims, especially if the patent’s scope is broad or claims are perceived as obvious.

Concluding Perspective

Patent RU2381023 provides exclusive rights over a specific pharmaceutical compound, formulation, or therapeutic method within Russia, contingent on its claim scope and technological uniqueness. Its enforceability depends on clear, well-defined claims that withstand scrutiny against prior art, and its strategic value lies in its potential to block competitors and anchor licensing agreements.

Proactively, patent owners should monitor related patents, enforce rights against infringers, and consider extending protection through international filings.


Key Takeaways

  • Claim Clarity and Breadth: The patent’s enforceability hinges on clearly defined claims that balance breadth with novelty.
  • Strategic Positioning: RU2381023 forms a core asset in Russia’s pharmaceutical patent landscape, offering competitive leverage.
  • Landscape Awareness: Vigilant monitoring of prior art, similar patents, and ongoing legal challenges is essential to maintain patent robustness.
  • Territorial Focus: While strong within Russia, patent owners should explore international patent protection via PCT or direct filings for broader coverage.
  • Legal Vigilance: Regular legal audits and potential opposition proceedings are necessary to uphold patent validity.

FAQs

1. Does RU2381023 cover all derivatives of the claimed compound?
Not necessarily. The scope depends explicitly on how broad or narrow the independent claims are drafted. Protective coverage extends to derivatives explicitly included or implicitly encompassed within the claims.

2. How vulnerable is RU2381023 to challenges based on prior Russian or international patents?
Its strength depends on the novelty and inventive step over prior art. High-quality examination and specific claim language improve resilience against invalidation.

3. Can RU2381023 be extended or expanded?
Yes. Filing divisional, continuation, or international applications can broaden coverage, especially for related compounds, formulations, or methods.

4. What is the importance of claim language in enforcement?
Precise, specific claim language ensures clearer boundaries for infringement and defends against invalidation arguments.

5. How does RU2381023 interact with the global patent landscape?
While primarily territorial—limited to Russia—it can be part of a broader international patent strategy, especially through PCT filings, to secure protections in multiple jurisdictions.


References:
[1] Russian Federal Service for Intellectual Property (ROSPATENT). Patent database.
[2] Russian Patent Law, Federal Law No. 218-FZ, 2002.
[3] World Intellectual Property Organization (WIPO) Patent Scope Database.
[4] Business insights on Russian pharmaceutical patent landscape, [industry reports].

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.