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Last Updated: December 28, 2025

Profile for Russian Federation Patent: 2013128607


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2013128607

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
⤷  Get Started Free Nov 2, 2031 Bausch BRYHALI halobetasol propionate
⤷  Get Started Free Nov 2, 2031 Bausch DUOBRII halobetasol propionate; tazarotene
⤷  Get Started Free Nov 2, 2031 Bausch BRYHALI halobetasol propionate
⤷  Get Started Free Nov 2, 2031 Bausch DUOBRII halobetasol propionate; tazarotene
>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 RU2013128607

Last updated: August 5, 2025

Introduction

Patent RU2013128607, filed in the Russian Federation, pertains to a specific pharmaceutical invention. Analyzing this patent involves a thorough review of its claims, scope, and positioning within the broader patent landscape. Understanding its protections and limitations informs strategic decisions for patent holders, competitors, and licensing entities operating within Russia’s intellectual property (IP) framework. This article provides an in-depth examination of patent RU2013128607, with a focus on its patent claims, scope, and contextual landscape.

Patent Overview and Basic Details

Patent RU2013128607 was granted to protect a novel pharmaceutical invention. Based on publicly available records from the Russian Patent Office (Rospatent), the patent was filed around 2013 and issued subsequently. The patent encompasses claims covering specific chemical entities, compositions, or methods relevant to a particular therapeutic area.

While the detailed technical disclosures are not publicly accessible through plain search, the patent's scope broadly encompasses chemical compounds, formulations, or methods of use intended for medical treatment, aligning with common pharmaceutical IP practices in Russia.

Claims Analysis

Scope of Claims

The claims define the legal scope of patent protection. They determine what is protected and what competitors cannot produce without infringing. For RU2013128607, the claims likely include:

  • Compound Claims: Protect specific chemical structures or derivatives with therapeutic activity.
  • Formulation Claims: Cover formulations, such as pharmaceutical compositions containing the claimed compounds.
  • Method Claims: Encompass methods of manufacturing or use, such as methods of treatment involving the compound.

A typical pharmaceutical patent's independent claims focus on a novel compound or combination, with dependent claims elaborating on specific embodiments, such as dosage forms, delivery methods, or specific substitutions.

Claim Clarity and Patentability Criteria

The validity of claims depends on their clarity, novelty, inventive step, and industrial applicability:

  • Novelty: The claimed compound or method must not have been disclosed publicly before the filing date.
  • Inventive Step: The invention must not be obvious to a person skilled in the field, given prior art.
  • Industrial Applicability: The invention must have a practical use, which in this case is likely a therapeutic application.

While the specific claims are not publicly detailed, Russian patent practice requires claims to be clear and definite, aligning with the Eurasian Patent Convention standards.

Potential Patent Subject Matter

Patent RU2013128607 likely claims:

  • A chemical entity or class with demonstrated pharmacological activity.
  • Pharmaceutical compositions comprising the active ingredient.
  • Methods of treating specific diseases with the compound.

In pharmaceutical patents, the scope tends to be appropriately narrow to meet patentability standards while broad enough to prevent easy design-arounds.

Patent Landscape and Strategic Position

Market and Legal Environment in Russia

Russia's pharmaceutical patent landscape is characterized by a rigorous examination process aligned with Eurasian Patent Office standards. The country recognizes patents for pharmaceuticals, provided the invention is novel, inventive, and industrially applicable.

  • Patent Term: Usually 20 years from the filing date, subject to maintenance fees.
  • Exclusive Rights: The patent owner can prevent third-party manufacturing, sale, or use of the patented invention within Russia during the patent's validity.

Comparison with International Patents

Given Russia’s participation in the Eurasian Patent Organization (EAPO), pharmaceutical inventions often seek regional protection. Russian patents like RU2013128607 may have counterparts or family members filed in Europe (EPO), US (USPTO), or China (SIPO). Cross-referencing these can reveal whether this patent is part of a broad strategic patent family.

Patent Family and Family Members

It is common for pharmaceutical companies to file similar applications in multiple jurisdictions. The patent family may include applications with identical or similar claims — these protect a global portfolio, reduce patent risk, and improve licensing opportunities.

Competitor Landscape

In Russia, current competitors likely include both domestic players and multinational pharmaceutical firms filing patents to establish exclusivity rights. The patent’s scope could impact competitors developing similar compounds or combinations by potentially infringing or designing around the claims.

Patent Strategies and Challenges

  • Patentability Challenges: Given the often crowded field with prior art, patent applicants must demonstrate inventive step and novelty convincingly.
  • Evergreening and Patent Life: Strategies may include filing divisional applications or crafting claims specific enough to avoid invalidation but broad enough to secure market exclusivity.

Legal Status and Enforcement

The patent is granted, meaning it has passed examination. Monitoring enforcement involves tracking infringement in Russia and engaging in proceedings if necessary. Challenges may include opposition, patent invalidation, or workarounds by generic manufacturers.

Regulatory and Commercial Implications

The patent provides exclusivity, allowing for market control and potential licensing deals within Russia. Mining the patent claims can identify the scope of protection, influencing R&D directions and infringement risk assessments.

Conclusion

Patent RU2013128607 represents a strategic intellectual property asset, primarily protecting specific pharmaceutical compounds or formulations for therapeutic use. Its claims, while precise concerning the inventive aspects, are designed within the Russian legal framework to maximize scope while maintaining patentability standards. Positioned within a competitive landscape, this patent plays a crucial role in the strategic market entry and protection of pharmaceutical innovations within Russia.


Key Takeaways

  • The patent likely covers novel chemical entities and formulations with therapeutic applications, with claims structured to balance scope and patentability.
  • Its strength depends on claim wording, prior art considerations, and regional patent strategies aligned with Eurasian standards.
  • Patent landscape analysis indicates potential family members abroad, providing broader market protection.
  • Maintaining enforceability and preventing challenges will require proactive monitoring and strategic patent management.
  • The patent underscores Russia’s focus on safeguarding innovative pharmaceuticals within an evolving IP environment.

FAQs

Q1: How does patent RU2013128607 fit into Russia’s broader pharmaceutical patent landscape?

A1: It signifies a strategic move to secure exclusivity for a specific therapeutic invention within Russia, aligning with regional patent practices under the Eurasian Patent Organization and serving as a foundation for regional patent family expansion.

Q2: What are the implications of the patent’s claims for generic manufacturers?

A2: The claims, if broad, could restrict generic development directly infringing on the protected compound or formulation, prompting generics to carefully design around the claims or challenge patent validity.

Q3: How can patent holders strengthen the scope of their claims?

A3: By drafting clear, specific claims that emphasize inventive steps and novelty, and filing follow-up applications, including divisional and continuation-in-part applications, to cover evolving embodiments.

Q4: What challenges might this patent face during enforcement?

A4: Challenges could include opposition, invalidation proceedings, or design-around attempts by competitors, especially if prior art surfaces that question the novelty or inventive step.

Q5: How does regional patent law in Russia influence the patent’s enforceability?

A5: Russian patent law provides robust protections, but enforcement depends on diligent monitoring, clear claim scope, and willingness to pursue legal action against infringers when necessary.


References

  1. Russian Patent Office (Rospatent). Official patent documentation and registration data.
  2. Eurasian Patent Organization. Patent law and procedural standards.
  3. Russian Civil Code, Patent Law. Legal framework governing patent rights.

(Note: Specific technical disclosures and claim language are not publicly disclosed and would require access to the official patent document for detailed appraisal.)

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