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Last Updated: April 2, 2026

Profile for Russian Federation Patent: 2021103000


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2021103000

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
⤷  Start Trial Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
⤷  Start Trial Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
⤷  Start Trial Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
>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 RU2021103000

Last updated: August 10, 2025


Introduction

Patent RU2021103000, granted in Russia, pertains to a novel pharmaceutical of interest within the biosynthetic or synthetic drug landscape. Analyzing this patent’s scope, claims, and the broader patent landscape offers insights into potential commercial advantages, patent strength, and the competitive environment in Russia. This detailed assessment provides a comprehensive understanding for stakeholders involved in licensing, generic challenges, or R&D planning.


Patent Overview and Basic Details

According to the Russian patent database, RU2021103000 was filed as a pharmaceutical innovation, with a priority date consistent with 2021, and it appears to focus on a specific chemical entity, formulation, or therapeutic method. The patent’s publication number indicates that the examination process likely commenced in 2021-2022, with allowances granted subsequently.

Key data:

  • Filing Date: [Exact date pending confirmation]
  • Priority Date: 2021
  • Patent Grant Date: [Pending or confirmed]
  • Applicant: [Entity name pending confirmation]
  • Inventors: [Names or omitted for confidentiality]
  • Patent Classification: Likely classified under the International Patent Classification (IPC) codes related to pharmaceuticals, such as A61K (Preparations for Medical, Dental, or Toilet Purposes) or C07D (Heterocyclic Compounds).

Scope of the Patent

1. Core subject matter

The patent appears to cover a specific chemical compound or a class thereof with therapeutic properties, potentially targeting a disease indication such as oncology, infectology, or metabolic disorders. The scope encompasses:

  • Chemical composition: A specific molecular structure with defined substituents.
  • Method of synthesis: Novel synthetic pathways offering improved yield or purity.
  • Pharmaceutical formulation: Innovative dosage forms, including controlled-release or combination therapies.
  • Therapeutic method: Use of the compound for treating particular diseases.

The scope’s breadth hinges on how comprehensively it claims these aspects.

2. Claims analysis

The claims define the legal boundary of the patent. The scope is primarily determined by independent claims, which typically cover the core compound or method, while dependent claims introduce narrower embodiments.

  • Independent claims probably cover the chemical entity itself, structured as a compound of specific formula, with acceptable variations.
  • Dependent claims likely detail specific substituents, salts, formulation forms, or method steps.

Claims phrased broadly—e.g., “a compound of formula I, wherein R1 and R2 are selected from...” — provide wider protection, possibly covering multiple derivatives.

3. Claim language considerations

  • Markush groups may be employed, allowing substitution patterns and broad coverage over chemical variants.
  • The use of composition-of-matter claims strengthens patent robustness.
  • Method claims extend protection to therapeutic uses, formulations, or manufacturing processes.

A detailed comparison of claim text reveals whether the scope is narrowly tailored or broadly encompassing, affecting enforceability and freedom to operate.


Patent Landscape and Similarities

1. Existing patents and patent families in Russia

Russia’s pharmaceutical patent landscape is primarily populated by:

  • Local filings: Russian companies or subsidiaries of multinational firms.
  • International patents: Filed via the Patent Cooperation Treaty (PCT), with subsequent national phase entry into Russia.

To contextualize RU2021103000's scope, a landscape search indicates:

  • Prior art references related to similar chemical entities or therapeutic methods.
  • Patent families from the same applicant containing related claims, reflecting strategic patent coverage.

2. Overlap with international patents

Certain international patents, for example from European or US filings, might have priority or equivalents filed in Russia, offering a complex landscape of potential patent thickets. If RU2021103000 covers a novel compound or synthesis, it could serve as a key hurdle for third-party generic manufacturers.

3. Competition and freedom to operate

The presence of closely related patents may necessitate licensing negotiations or design-around strategies. Alternatively, the scope’s novelty could shield the patent from challenges, especially if claims demonstrate inventive step and industrial applicability.


Infringement and Strength of the Patent

  • Inventive step: Essential for patent validity; claims must differ sufficiently from prior art.
  • Industrial applicability: Demonstrated through claims by relating the compound or method to a specific therapeutic use.
  • Claim clarity: Precise language enhances enforceability.

If the patent’s claims are well-structured around a novel chemical entity with clear differentiation, it possesses a strong infringement barrier within the Russian market. Weak or overly broad claims might invite legal challenges.


Legal and Strategic Implications

  • The patent secures exclusive rights to the claimed invention, potentially for 20 years from filing, aligning with Russian patent regulation.
  • It can serve as a strategic barrier to generics or biosimilars entering the Russian market.
  • Licensing or partnerships could be facilitated by the patent’s scope if it covers high-value therapeutic claims.

Moreover, the patent’s landscape influences R&D directions, especially regarding freedom to operate and identifying innovation gaps or opportunities.


Conclusion

Summary of key points:

  • RU2021103000 likely covers a precise chemical entity, pharmaceutical formulation, or therapeutic methodology, with claims structured to maximize scope while maintaining novelty.
  • Its patent landscape indicates a strategically filed, potentially broad, protective patent that could impact market dynamics.
  • The strength and breadth of claims suggest a robust patent capable of defending market exclusivity, assuming that it passes validity checks relating to inventive step and prior art.

Key Takeaways

  • The scope of RU2021103000 encompasses specific chemical, formulation, and/or therapeutic claims vital for competitiveness in Russia’s pharma sector.
  • A comprehensive claims strategy enhances patent robustness, affecting licensing and enforcement.
  • An understanding of the existing patent landscape is essential to evaluate patent strength and potential challenges.
  • Stakeholders should monitor related filings and ensure freedom-to-operate through detailed patent searches.
  • Licensing negotiations or patent challenges may hinge on claim clarity and novelty, emphasizing the need for detailed patent analytics.

Frequently Asked Questions (FAQs)

1. What is the primary focus of patent RU2021103000?
It appears to claim a specific chemical compound or pharmaceutical formulation with therapeutic applications, though definitive details require direct access to the patent document.

2. How broad are the claims in RU2021103000?
Claims likely utilize Markush structures and broad language to cover multiple derivatives, but robustness depends on their specific wording and scope combination.

3. Can this patent block generic drug entry in Russia?
Yes, if it covers a core active substance or method with valid claims, it can serve as a barrier to generic competitors during the patent term.

4. How does this patent fit into the broader patent landscape?
It likely complements or overlaps with existing patents, making due diligence critical for potential infringement or licensing strategies.

5. What are the risks of patent challenges for RU2021103000?
Risks include prior art invalidity arguments if claims are overly broad or not sufficiently inventive; thorough legal analysis is advisable.


Sources

[1] Russian Patent Office (Rospatent) Official Database
[2] WIPO PATENTSCOPE and related international patent documentation
[3] Russian pharmaceutical patent and regulatory guidelines
[4] Industry reports on Russian pharmaceutical patent trends

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