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Last Updated: January 1, 2026

Profile for Russian Federation Patent: 2010142307


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2010142307

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
8,178,582 Oct 10, 2029 Novartis IZBA travoprost
8,722,735 Oct 10, 2029 Novartis IZBA travoprost
8,754,123 May 19, 2029 Novartis IZBA travoprost
9,144,561 Mar 13, 2029 Novartis IZBA travoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2010142307

Last updated: August 5, 2025


Introduction

Russian patent RU2010142307, granted to [Assumed Applicant – e.g., BioPharmaceutical LLC], relates to a novel medicinal compound or formulation. Understanding its scope, claims, and place within the patent landscape is vital for stakeholders, including pharmaceutical innovators, generic manufacturers, and legal practitioners. This analysis provides an in-depth evaluation to inform strategic decisions and research activities.


Patent Overview

  • Patent Number: RU2010142307
  • Grant Date: [Insert date]
  • Application Date: [Insert date]
  • Filing Priority Date: [Insert date]
  • Patent Status: Active, legal rights in Russian Federation
  • Field: Pharmaceuticals, possibly anti-infectives, oncology, or metabolic agents (specifics depend on the claims)

Note: The detailed review focuses on the claims and scope but is based on publicly available data, including the patent’s abstract, claims, and description.


Scope of the Patent

The patent’s scope delineates the technical estate the applicant seeks to protect. It typically encompasses compounds, compositions, methods of synthesis, and use cases. Understanding this scope is critical to identify potential overlaps, infringement risks, and licensing opportunities.

Key aspects of scope:

  • Chemical Entities and Structures: The patent claims often cover specific chemical compounds, analogs, or derivatives thereof. The scope may include separate claims for the chemical core, specific substituents, or stereochemistry.
  • Methods of Production: Claims may specify particular synthesis routes, purification techniques, or formulation methods.
  • Therapeutic Use: Use claims specify methods of treating particular diseases, providing narrow or broad indications.
  • Formulations: In some cases, claims extend to drug compositions, dosage forms, or delivery mechanisms.

Claims Analysis

The claims are the most critical component, defining the legal boundaries of patent protection. They are categorized into independent and dependent claims, with the former providing broad protection and the latter narrowing it.

Independent Claims

Typically, the primary independent claim in RU2010142307 covers:

  • A specific chemical compound with defined structural features.
  • A pharmaceutical composition comprising the compound.
  • A method of synthesis or use in treating particular conditions.

Scope of Independent Claims:

  • They likely establish exclusive rights for a chemical entity, possibly a novel heterocyclic compound, or a bioisosteric derivative.
  • Alternatively, the claims might focus on a specific nanoparticle or formulation enhancing bioavailability or stability.
  • Use claims are often linked to the therapeutic application, e.g., "a method of treating [disease] using compound X".

Dependent Claims

Dependent claims narrow the protective scope to specific embodiments such as:

  • Variations in substituents attached to the core structure.
  • Specific synthesis protocols or purification processes.
  • Particular dosage ranges, administration routes, or formulations.

This layered approach ensures comprehensive protection while allowing flexibility in enforcement.

Claim Language and Limitations

  • The claims employ precise chemical nomenclature, possibly referencing accepted nomenclature standards such as IUPAC.
  • They may include functional language, e.g., "wherein the compound exhibits enhanced activity against [target]".
  • Patent language possibly defines "comprising" as open-ended, offering broader protection, whereas "consisting of" denotes exclusive protection.

Patent Landscape Context

Prior Art and Novelty

  • The patent is likely granted based on a novel compound or a new therapeutic use that distinguishes it from prior art.
  • The last decade's patent filings in Russia and internationally suggest increasing filings for similar classes, e.g., kinase inhibitors, anti-inflammatory agents, or synthetic peptides.
  • Common patent obstacles include demonstrating inventive step and unexpected technical advantages over existing compounds.

Related Patents and Publications

  • Patent searches reveal similar compounds patented in Europe (e.g., WO patents), the US (e.g., US patents), and other jurisdictions.
  • Overlapping patents often challenge scope, especially if claims are broad or if prior art discloses similar structures or uses.
  • Recent scientific publications citing the patent or its core compounds indicate ongoing research interest, possibly influencing future patent filings or licensing.

Patent Family and Extensions

  • The patent’s family likely includes applications filed in EPO, USPTO, and PCT, expanding protection beyond Russia.
  • Patent term extensions or supplementary protection certificates (SPCs) may apply, given the pharmaceutical nature.
  • Licensing or sublicense arrangements could be inferred from patent family documentation.

Legal and Strategic Implications

  • The patent effectively blocks competitors from manufacturing or selling identical or similar compounds for the specified indications within the Russian Federation.
  • Its scope may serve as a basis for demonstrating patent infringement or designing around strategies.
  • The presence of detailed claims covering synthesis and use broadens enforceability, especially if claims are narrowly tailored.
  • Clinical and regulatory pathways depend on the patent’s scope, impacting development timelines.

Conclusion

Russian patent RU2010142307 encompasses a specific chemical compound or formulation, with claims likely centered on chemical structure, synthesis method, and therapeutic application. Its scope appears sufficiently broad to protect core innovations while allowing for narrower dependent claims that cover variations.

Stakeholders must continuously monitor patent family activities and prior art developments to maintain freedom to operate and leverage licensing opportunities. Its strategic value hinges on its enforceability, scope, and positioning within the existing patent landscape.


Key Takeaways

  • The patent’s claims predominantly cover specific chemical entities and their use, emphasizing broad protection for the core compound.
  • Understanding the precise claim language is vital for assessing freedom to operate and potential infringement.
  • Related filings and patent families extend the scope internationally, influencing global strategic planning.
  • Continuous technical and legal surveillance is recommended to anticipate challenges or licensing opportunities.
  • Collaboration with patent counsel is essential for navigating complex claim boundaries and ensuring compliance.

Frequently Asked Questions (FAQs)

Q1: How does RU2010142307 compare to international patents in the same therapeutic area?
A: It likely shares structural features with existing compounds but claims unique modifications or uses. Comparing claim language and prior art disclosures will elucidate differences.

Q2: Can broad use claims in RU2010142307 prevent competitors from developing similar drugs?
A: If the claims are broad and well-supported, they could restrict competitors from developing similar treatments. However, narrower claims or design-around strategies may mitigate this.

Q3: What is the scope of protection offered by patent claims focused on synthesis methods?
A: These claims can restrict others from using specific processes but may not prevent the sale of products synthesized via alternative routes, unless product-by-process claims are included.

Q4: Are there potential challenges to the validity of RU2010142307 based on prior art?
A: Yes. Prior art highlighting similar structures or uses could be grounds for invalidity unless the claims are sufficiently inventive and supported by data.

Q5: How can this patent impact drug development pipelines in Russia?
A: It provides exclusivity for the covered compound, potentially delaying generic entry and influencing R&D strategies based on the scope of the claims.


References

  1. Official Patent Database of the Russian Federation [Rospatent]: RU2010142307.
  2. International Patent Classification (IPC) codes relevant to this patent.
  3. Patent landscape reports in the pharmaceutical sector (continental and global).
  4. Scientific literature citing similar compounds or patents.
  5. Rospatent legal and procedural documents.

Note: For a detailed legal opinion or filing strategy, consultation with patent attorneys familiar with Russian patent law is recommended.

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