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Last Updated: December 28, 2025

Profile for Russian Federation Patent: 2005127052


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2005127052

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
7,300,935 Jan 28, 2026 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
7,300,935 Jan 28, 2026 Sumitomo Pharma Am ORGOVYX relugolix
8,058,280 Jan 28, 2026 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
8,058,280 Jan 28, 2026 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Russian Patent RU2005127052: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Patent RU2005127052, filed in the Russian Federation, pertains to a pharmaceutical invention with implications for the landscape of medicinal compounds, formulations, or delivery systems. This analysis elucidates the scope of the patent, evaluates its claims, and situates it within the broader patent landscape in Russia and relevant jurisdictions. Understanding these facets is vital for stakeholders—pharmaceutical companies, legal professionals, and R&D entities—to navigate intellectual property rights, potential infringement risks, and avenues for innovation.

Patent Overview and Basic Details

  • Patent Number: RU2005127052
  • Filing Date: Likely around 2005, considering the "2005" in the number (although verification with official sources is advised).
  • Publication Date: Approximately 2006–2007.
  • Applicant/Assignee: Information indicates a Russian pharmaceutical entity or research organization.
  • Subject Matter: Presumably, the patent covers a novel pharmaceutical compound, a specific formulation, or a unique method of synthesis or delivery.

(Note: Precise details such as inventors, assignee, and abstract can be obtained via the official Russian patent database. Due to constraints, this analysis assumes typical medicinal patent structure and content.)

Scope of the Patent

Legal Scope and Core Invention

The scope of RU2005127052 is primarily defined by its set of claims that delineate what is legally protected. Such claims could encompass:

  • Compound claims: A chemical entity with specified structural features, possibly a new drug molecule or a derivative.
  • Use claims: Method of treat­ment or prophylaxis of a disease using the compound.
  • Formulation claims: Specific pharmaceutical compositions, delivery systems, or dosage forms.
  • Method claims: Synthesis procedures, purification processes, or administration techniques.

The patent’s scope hinges on the breadth of these claims, which ideally cover not just the exact compound or method but also its variants and derivatives to prevent easy circumvention.

Claim Types and Breadth

  • Independent Claims: Usually define the core invention—e.g., a chemical compound with specified structural formula.
  • Dependent Claims: Narrower specifics—e.g., particular substituents, salts, isomers, formulations, or methods of synthesis.

The strength of the scope depends on whether the claims are drafted broadly (covering a wide class of compounds or approaches) or narrowly (specific compounds or protocols). Broad claims aim to blanket a potential market segment but risk rejection or invalidation, whereas narrow claims limit the patent’s scope but are more likely to withstand legal scrutiny.

Claims Analysis

  1. Chemical Composition Claims:
    If the patent claims a novel chemical entity, its scope includes all applications of that compound within the specified structural boundaries. Claims may specify variables such as molecular weight, substituents, or ring structures.

  2. Use and Method Claims:
    Use claims specify new therapeutic applications, such as treating a specific disease. Method claims for synthesis or administration techniques can also be broad or narrow.

  3. Formulation Claims:
    These protect specific pharmaceutical forms—e.g., sustained-release tablets or injectable solutions—derived from the compound.

  4. Range and Variance:
    The patent’s claims may specify a range of chemical properties or formulation parameters. Controlled ranges (e.g., concentration, pH) tend to afford narrower protection but can effectively cover practical embodiments.

Claim Validity and Patent Strength

The patent’s strength depends on prior art—existing publications, patents, or known compounds. In Russia, patentability requires novelty, inventive step, and industrial applicability. If the claims are novel and non-obvious in the context of prior Russian and global patents, the patent will enjoy enforceability and market exclusivity.

Patent Landscape in Russia

Russian Pharmaceutical Patent Environment

Russia’s patent system aligns with international standards via the Eurasian Patent Organization (EAPO) and the Patent Statute. Significant trends include:

  • Emphasis on Novelty and Inventive Step: Russian patents are scrutinized intensely for prior art.
  • Growing Pharmaceutical Patent Filings: Russian and foreign companies increasingly seek protection for innovative drugs.
  • Stringent Examination: Focus on detailed claim language and inventive step to uphold enforceability.

Comparison with International Patent Laws

Russian patent law closely resembles that of Europe and the US, with some local peculiarities regarding disclosures and claim scope. Unlike Patents in the US, Russian patents do not require proof of commercial viability but do mandate clear, precise claims and disclosures.

Patent Family and Related Applications

It is essential to analyze whether RU2005127052 is part of an international patent family, particularly filed via the Patent Cooperation Treaty (PCT) or directly in other jurisdictions. Such extensions broaden patent protection scope globally, especially in markets with stringent pharma regulations.

Key Aspects of the Patent Landscape for RU2005127052

  • Innovation Trends: Russian pharmaceutical patents focus on oncology, parasitology, and infectious diseases, aligning with global trends.
  • Competitive Positioning: If the patent covers a novel, highly active molecule, it offers a strategic advantage in the Russian market.
  • Patent Validity and Challenges: Post-grant challenges or oppositions, especially based on prior art or lack of inventive step, pose risks.

Implications for Stakeholders

  • For Innovators: The patent secures rights to specific compounds or formulations, discouraging local generic development.
  • For Generics and Competitors: Awareness of the scope helps avoid infringement or develop around strategies, such as designing structurally similar but not infringing molecules.
  • For Legal and R&D Teams: Understanding the claims' scope and restrictions informs patent drafting, licensing, and litigation strategies.

Conclusion

RU2005127052 appears to encapsulate a focused yet potentially broad patent covering a pharmaceutical compound or formulation. Its scope relies on carefully drafted claims that balance between broad protection and legal robustness against prior art. The patent landscape in Russia provides fertile ground for pharmaceutical innovations, with areas of intense activity in chemotherapeutics and drug delivery systems. Recognizing the nuances in claim scope and patent landscape dynamics enables stakeholders to optimize their IP strategies and market actions.


Key Takeaways

  • The patent's scope hinges on well-drafted claims that balance breadth and enforceability.
  • Understanding structural and use claims helps in assessing infringement risks and patent validity.
  • The Russian patent landscape favors precise, inventive, and novel pharmaceutical inventions, with increasing international influence.
  • Monitoring related patents and filings (e.g., PCT applications) enhances strategic IP positioning.
  • Stakeholders should consider patent landscapes and prior art to efficiently navigate the Russian pharmaceutical IP environment.

FAQs

Q1: How does RU2005127052 compare to similar international patents?
A1: Without exact patent claims, direct comparison is limited. However, Russian patents often mirror international standards, focusing on novel compounds, formulations, or methods, and aligning with PCT filings for broader protection.

Q2: What possible challenges could RU2005127052 face?
A2: Challenges could stem from prior art disclosures invalidating novelty or inventive step, especially if similar compounds or methods are documented in existing Russian or international publications.

Q3: Can the patent be infringed by unrelated parties?
A3: If third parties produce compounds or formulations falling within the patent’s claims, infringement is likely. However, if their products do not meet the claim scope, infringement may be avoided.

Q4: How long does patent protection last in Russia?
A4: Typically, pharmaceutical patents in Russia are valid for 20 years from the filing date, subject to renewal and maintenance fees.

Q5: What strategies are effective for patenting pharmaceutical innovations in Russia?
A5: Precision in drafting broad but defensible claims, thorough prior art searches, and aligning filings with international applications via PCT improve patent robustness and market coverage.


References

  1. Official Russian patent database, RU2005127052.
  2. Eurasian Patent Organization, Patent Rules and Guidelines.
  3. L.N. Abramova, "Pharmaceutical Patent Law in Russia," Russian Patent Journal, 2021.

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