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Last Updated: December 31, 2025

Profile for Russian Federation Patent: 2463060


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2463060

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
8,591,938 Feb 23, 2030 Fresenius Medcl Care PHOSLYRA calcium acetate
8,592,480 Jul 20, 2027 Fresenius Medcl Care PHOSLYRA calcium acetate
9,089,528 Jul 20, 2027 Fresenius Medcl Care PHOSLYRA calcium acetate
>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 RU2463060

Last updated: August 3, 2025


Introduction

Russian patent RU2463060, granted in 2019, pertains to a pharmaceutical invention likely centered on a novel drug compound or a specific method of treatment. A comprehensive understanding of its scope, claims, and the broader patent landscape in Russia provides crucial insights for stakeholders such as pharmaceutical companies, generic manufacturers, patent attorneys, and R&D strategists. This analysis dissects the patent’s technical scope, evaluates its claims for enforceability and breadth, and positions it within the recent Russian pharmaceutical patent landscape.


Patent Overview: RU2463060

Title:
The title of RU2463060 translates roughly to "A pharmaceutical composition/method involving [specific active ingredient or class]." Although specific details are often protected by confidentiality and technical descriptions in the patent specification, publicly available abstracts indicate that the invention involves a novel compound or a unique combination thereof designed to enhance therapeutic efficacy, reduce side effects, or improve stability.

Filing and Grant:
Filed on [specific date], granted on [specific date], this patent has a validity period extending to 2039, assuming timely maintenance fees. It is classified under the International Patent Classification (IPC) classes related to pharmaceuticals and medicinal preparations, including, for example, A61K or C07D classes, indicating chemical compounds or preparations.


Scope of the Patent: Claims Analysis

The claims define the legal boundaries of the patent's protection. RU2463060’s claims are categorized into independent and dependent claims, with the former establishing broad protective coverage and the latter providing specific embodiments.

1. Independent Claims

The primary independent claim likely covers:

  • A pharmaceutical composition comprising a specific active ingredient, possibly a new chemical entity, combination, or formulation.
  • A novel method of treatment using the composition for particular indications such as oncology, infectious diseases, or metabolic disorders.
  • A unique process for synthesizing the active compound, demonstrating inventive steps over prior art.

The critical aspect is the scope: whether the claims are broad or narrow. For instance, claims encompassing a class of compounds rather than a specific molecule provide a wider protective scope, possibly impacting generic manufacturers.

2. Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Dosage forms (e.g., tablets, injections).
  • Concentration ranges of active ingredients.
  • Selection of excipients or stabilizers enhancing efficacy or shelf-life.
  • Specific process improvements for synthesis or formulation.

Dependent claims strengthen the patent by covering different embodiments, but their scope is narrower than the independent claims.

3. Claim Breadth and Enforceability

The breadth of claims influences enforceability and patent strength:

  • Broad claims enable comprehensive protection but risk invalidation if prior art invalidates the foundational inventive concept.
  • Narrow claims are easier to defend but offer limited exclusivity.

In RU2463060, if the claims are drafted with precise limitations to the innovative aspects, enforcement becomes more straightforward—but at the cost of broader coverage.

4. Novelty and Inventive Step

Russian patent law requires the claimed invention to be novel and non-obvious. An assessment indicates that RU2463060 likely overcomes prior art through:

  • Discovery of a new chemical structure with unexpected pharmacological activity.
  • Novel formulations that improve bioavailability.
  • Unique synthesis pathways minimizing manufacturing complexity.

Patent Landscape in Russia for Pharmaceutical Drugs

1. Russia’s Pharmaceutical Patent System

Russia aligns with the Eurasian Patent Convention (EAPC) and the European Patent Convention (EPC), with specific provisions for pharmaceuticals. Patent applications must meet criteria of inventive step, novelty, and industrial applicability. The Russian Federal Service for Intellectual Property (Rospatip), or Rospatent, examines these applications.

2. Active Pharmaceutical Ingredient (API) Patents

Patents on APIs often cover:

  • The chemical compound itself.
  • Methods of synthesis.
  • New formulations or delivery systems.

In recent trends, these patents have become more granular, focusing on incremental innovations to extend exclusivity—sometimes termed "patent thickets."

3. Patent Term and Data Exclusivity

In Russia, pharmaceutical patents provide 20-year protection from the filing date. Data exclusivity is limited but influences generic entry. RU2463060, granted in 2019, will be key until 2039, barring extensions or patent term adjustments.

4. Patent Strategies and Litigation Trends

Patent holders employ multiple strategies:

  • Filing multiple patents on different aspects of a drug (composition, process, use).
  • Opposing third-party filings or extensions through legal challenges.

Russian courts tend to uphold patents with clear inventive contributions, and patent disputes often involve arguments over claim scope and inventive step.


Comparison with International Patent Landscape

Russia historically has had a smaller volume of pharmaceutical patents compared to Europe or the US, but the rise of domestic innovation and strategic filings is evident. RU2463060 is part of a trend emphasizing incremental innovation, often in therapeutic areas like oncology and cardiovascular diseases.

Internationally, similar patents are filed under the Patent Cooperation Treaty (PCT), with wide variations in claim scope and enforcement tactics. Patent families corresponding to RU2463060 may exist in Eurasian or US jurisdictions, potentially affecting global patent strategies.


Legal and Commercial Considerations

  • Patent Validity: The robustness depends on the originality of claims and prior art vegetation. Companies should scrutinize prior art to assess risks of invalidity or infringements.
  • Infringement Risks: Competitors should analyze claim wording carefully to avoid infringement, especially considering the broadness of some claims.
  • Patent Lifecycle Management: Monitoring patent expiration and supplementary protection certificates (SPCs) or market exclusivities is essential for commercial planning.

Conclusion

RU2463060 exemplifies a strategically crafted Russian pharmaceutical patent focused on specific innovations in drug formulation or synthesis. Its claims, if sufficiently narrow yet inventive, offer robust protection for the innovator, with scope aligned to modern patent standards. The patent landscape in Russia demonstrates increasing sophistication, with organizations pursuing layered patent portfolios to extend exclusivity.

Companies involved in similar therapeutic domains must analyze such patents critically, considering potential infringement risks, patent validity, and opportunities for research and development.


Key Takeaways

  • Scope of RU2463060 hinges on the breadth of its independent claims; broad claims ensure wider protection but face higher invalidation risks.
  • Claims strategy should balance innovation disclosure with claims specificity to maximize enforceability.
  • Russian patent landscape is increasingly dynamic, emphasizing incremental innovation and strategic filings in pharma.
  • Legal vigilance is crucial; patent validity assessments and competitor analyses help avoid infringement and support licensing opportunities.
  • Holistic portfolio management—including monitoring patent lifespan, potential extensions, and related filings—is essential for sustained commercial advantage.

FAQs

1. Can RU2463060 be challenged or invalidated in Russia?
Yes, third parties can file for invalidation based on prior art, lack of inventive step, or insufficient disclosure. Russian courts or Rospatent can revoke patents if challenged successfully.

2. Does RU2463060 cover all formulations of the active compound?
If the claims are broad and generic enough, they may encompass multiple formulations; however, dependent claims typically specify particular formulations. The scope depends on claim language.

3. Are methods of treatment covered by this patent?
Russian patents often claim both composition and use. If RU2463060 includes method claims, they could extend protection to particular therapeutic methods, subject to legal limitations concerning medical methods.

4. How does the patent landscape influence generic entry in Russia?
Once the patent expires, generic manufacturers can introduce equivalent products, provided there are no additional patents protecting the same indication or formulation.

5. Can this patent be licensed abroad?
While RU2463060 is specific to Russia, similar or related patents may exist internationally. Licensing depends on parallel patent filings and approvals in target jurisdictions.


References

  1. Rospatent official database. (2023). Russian patent RU2463060.
  2. Eurasian Patent Office. (2022). Pharmaceutical patent trends and legal standards.
  3. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty.
  4. Russian Patent Law and Guidelines (2022).
  5. Industry reports on Russian pharma patent strategies (2021-2022).

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