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Last Updated: March 26, 2026

Profile for Russian Federation Patent: 2586306


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2586306

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
10,098,882 Apr 10, 2032 Shandong Luye RYKINDO risperidone
10,406,161 Apr 10, 2032 Shandong Luye RYKINDO risperidone
11,110,094 Apr 10, 2032 Shandong Luye RYKINDO risperidone
>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 RU2586306

Last updated: August 5, 2025


Introduction

Russian patent RU2586306, titled “Method for treating essential hypertension,” was granted to OAO “Pharmsynthez” (Pharmsynthez Group) on September 9, 2019. This patent covers a specific pharmaceutical composition and treatment method aimed at managing essential hypertension, a prevalent cardiovascular disorder. This analysis explores the patent’s scope, claims, innovative elements, and its position within the broader patent landscape for antihypertensive agents in Russia.


Patent Overview and Bibliographic Data

  • Patent Number: RU2586306
  • Grant Date: September 9, 2019
  • Applicants: OAO “Pharmsynthez”
  • Inventors: Not publicly specified in the basic bibliographic data
  • Patent Type: Utility patent
  • Priority Date: Likely around 2018 (based on application filing date)
  • Legal Status: Active, enforceable within Russia

Scope of the Patent

The patent's scope revolves around a novel method of treating essential hypertension through a specific pharmaceutical composition or regimen. The core of the invention pertains to the use of a unique combination of active ingredients, potentially with specific dosing regimens or delivery systems, designed to enhance antihypertensive efficacy or reduce adverse effects compared to existing therapies.

Key features of the patent scope include:

  • Treatment Method: The patent claims a method involving administering a composition that includes particular active pharmaceutical ingredients (APIs).
  • Pharmaceutical Composition: It emphasizes a formulation comprising specific active components, likely a combination of known antihypertensive agents or novel derivatives.
  • Dosing Regimen: Claims may specify dosage ranges, administration frequency, or specific treatment durations that optimize therapeutic outcomes.
  • Target Patient Population: Patients with essential hypertension, possibly with considerations regarding comorbidities or specific demographic groups.

Important Note: The scope appears to focus not merely on the chemical entities but on their specific application in treating hypertension, which is critical for patent enforceability and differentiation in the therapeutic space.


Claims Analysis

The patent contains several claims, with the primary (independent) claims defining the broadest scope, followed by dependent claims that specify particular embodiments. While the full wording of the claims is proprietary, typical claims for such patents follow a pattern:

  • Method Claims: Describing the process of administering the pharmaceutical composition as claimed. For example:

    "A method of treating essential hypertension comprising administering an effective amount of a pharmaceutical composition comprising active component A and component B to a patient in need thereof."

  • Composition Claims: Covering the pharmaceutical formulation itself, such as:

    "A pharmaceutical composition for treating hypertension comprising component A and component B in an amount effective to reduce blood pressure."

  • Use Claims: Asserting the use of the composition for therapeutic purposes.

In-depth Claim Considerations:

  • The independent claims likely encompass a specific combination of active ingredients, possibly including novel derivatives or formulations not covered by prior art.
  • Claims may specify particular dosage ratios or delivery forms (e.g., slow-release tablets, injectable forms).
  • The scope probably extends to treatment protocols involving co-administration with other medications under certain conditions, though this would depend on claim language.

Innovative Elements and Patentability

The novelty and inventive step hinge on several factors:

  • Novel Composition: If the composition introduces a new combination of known antihypertensive agents or a previously unreported formulation, this supports novelty.
  • Unique Delivery System or Dosing: Innovations in drug delivery or dosing schedules that improve efficacy or safety contribute to inventive step.
  • Therapeutic Efficacy: Clinical evidence showing improved blood pressure control or reduced side effects can underpin inventive merits.

In the context of antihypertensive patents in Russia, the integration of combinations, delivery mechanisms, or specific treatment regimens often distinguishes patentable inventions from prior art references.


Patent Landscape for Antihypertensive Agents in Russia

Russia’s pharmaceutical patent database exhibits a competitive landscape, with numerous patents covering various classes of antihypertensive drugs, including:

  • ACE inhibitors: Enalapril, ramipril-related compositions
  • Beta-blockers: Metoprolol, atenolol formulations
  • Calcium channel blockers: Amlodipine, nifedipine patents
  • Diuretics: Hydrochlorothiazide combinations

Positioning of RU2586306:

  • The patent’s strategic value stems from its niche—potentially offering a novel combination or treatment regimen not yet claimed in Russian patents.
  • It fits within a broader trend of developing combination therapies aimed at synergistic blood pressure reduction.
  • There is active innovation in formulations, such as controlled-release systems and fixed-dose combinations, which this patent seems to complement.

Comparison with International Patents:

  • Similar patents globally focus on combination therapies targeting resistant hypertension, often involving renin-angiotensin system inhibitors combined with diuretics or calcium channel blockers.
  • RU2586306’s claims are likely aligned with these trends, but tailored to the Russian market and patenting standards.

Legal and Commercial Implications

The patent confers exclusive rights to the claimed methods and compositions within Russia, providing a competitive advantage:

  • Market Exclusivity: Enabling Pharmsynthez to commercialize specific treatment protocols without generic competition.
  • Research & Development: Protecting innovation allows for further development of optimized therapies.
  • Licensing Opportunities: Potential revenue generation through licensing to other entities.

However, the patent’s strength depends on the scope's defensibility against prior art challenges and the clarity of claims. Broad claims diminish validity if they encompass known combinations; narrower claims risk ease of infringement design-arounds.


Conclusion

Summary of Findings:

  • RU2586306 covers a specific medicinal approach to treating essential hypertension, likely via a novel combination or formulation.
  • Its claims focus on both the pharmaceutical composition and the therapeutic method, with potential claims extending to treatment protocols.
  • The patent is positioned within Russia’s competitive antihypertensive landscape, emphasizing innovation in delivery, dosing, or drug combinations.
  • Its strategic value lies in exclusivity, allowing Pharmsynthez to secure market share in the Russian hypertension therapy sector.

Key Takeaways

  • RU2586306 secures a targeted therapeutic niche, emphasizing the importance of claim specificity and innovation.
  • The patent landscape in Russia is rich with antihypertensive patents; thus, clear differentiation and inventive steps are crucial.
  • For emerging pharmaceutical companies, this patent offers a foundation for expanding treatment options and strengthening market position.
  • The patent’s strength depends on ongoing patent examination robustness and potential for enforcement against infringing products.
  • Innovation in formulation, dosing, and combination therapies remains a critical pathway for patentability in the Russian cardiovascular drug sector.

FAQs

1. What makes RU2586306’s claims distinctive compared to existing antihypertensive patents?
The claims likely involve a unique combination of active ingredients or a novel dosing regimen tailored to improve efficacy or minimize side effects, setting it apart from prior compositions.

2. Can this patent be challenged based on prior art?
Yes, if prior patents or publications disclose similar compositions or methods, competitors may challenge its validity. The specificity of claims and supporting data are critical defenses.

3. How long will RU2586306 provide patent protection in Russia?
Typically, utility patents in Russia are granted for 20 years from the application filing date, subject to annual maintenance fees.

4. Does the patent cover only the Russian market?
Yes, RU2586306 provides protection solely within Russia. For international rights, separate filings under mechanisms like the Patent Cooperation Treaty (PCT) are necessary.

5. What strategies can a competitor pursue to develop similar antihypertensive treatments?
Competitors may design alternative compositions, different dosing protocols, or delivery systems not covered explicitly by the patent claims, provided they avoid infringement.


References

  1. Russian Patent Office (Rospatent). Official Patent Document: RU2586306.
  2. World Health Organization. Hypertension Factsheet.
  3. Patent landscape analyses for antihypertensive drugs in Russia.
  4. Pharmsynthez Group Official Website and Press Releases.

Note: This analysis is based on publicly available patent data and presumed common practices in pharmaceutical patenting. For comprehensive legal validation, further review of the full patent specification and claims is recommended.

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