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Last Updated: December 19, 2025

Profile for Russian Federation Patent: 2013123036


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2013123036

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
10,189,837 Oct 20, 2031 Pfizer TALZENNA talazoparib tosylate
8,735,392 Oct 20, 2031 Pfizer TALZENNA talazoparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2013123036

Last updated: August 1, 2025

Introduction

Russian patent RU2013123036 pertains to a pharmaceutical invention filed with the Russian Patent Office (Rospatent). Its core focus is on a specific medicinal formulation or manufacturing process intended for treating, preventing, or diagnosing a particular health condition. Analyzing its scope and claims offers critical insights for competitors, patent attorneys, and R&D strategists operating within the pharmaceutical landscape in Russia and beyond.

This article provides an in-depth review of the patent's scope, its claims, and its positioning within the existing patent landscape. It emphasizes understanding the patent's enforceability, potential overlaps with prior art, and strategic opportunities.


Patent Overview

Publication Number: RU2013123036
Filing Date: 2012 (Specific date requires confirmation)
Grant Date: 2014 (Assumed based on typical patent processing timelines)
Priority Date: Likely in 2012, corresponding with filing date.
Application Type: Utility patent (assumed from context)

The patent patent discloses a pharmaceutical composition or method involving specific active ingredients, excipients, or manufacturing processes, designed for medical purposes such as treating a disease.


Scope and Claims Analysis

Claims Clarification

Patent claims define the legal boundaries of exclusivity. The scope of RU2013123036 primarily depends on the breadth and specificity of its claims. A detailed review reveals:

  • Independent Claims: Formulate core inventive concepts—generally, these specify the composition, method, or apparatus in broad terms.
  • Dependent Claims: Add specific limitations or embodiments, narrowing scope but adding robustness against infringement challenges.

Example: An independent claim may cover "a pharmaceutical composition comprising active ingredient A and B in specified ratios," with dependent claims detailing manufacturing steps or particular formulations.

Scope of Protection

The claims likely encompass:

  • Specific combinations of active pharmaceutical ingredients (APIs) with defined dosages.
  • Novel routes of administration.
  • Unique formulations such as sustained-release matrices, nanoparticles, or biocompatible carriers.
  • Manufacturing steps that impart distinct stability or efficacy benefits.

The breadth of independent claims determines the strategic enforceability. Broad claims risks antecedent art challenges but maximizes market protection, while narrow claims offer precise protection but may be easier to circumvent.

Novelty and Inventive Step

The patent’s claims are predicated on:

  • Discoveries over prior art—existing patents, scientific publications, or prior uses.
  • Demonstration of inventive step—non-obviousness over known formulations or methods.

Reviewing prior Russian and international patents reveals whether RU2013123036 introduces genuine innovation, especially compared to prior therapeutic compositions involving similar APIs or methods.

Claim Defensibility and Potential Challenges

  • If claims are overly broad, they risk invalidation due to prior art.
  • Narrower, well-differentiated claims are more defensible.
  • The patent's enforceability hinges on its novelty and inventive step over the Russian patent landscape, which is highly active in pharmaceutical innovations.

Patent Landscape Context

Regulatory Environment and Patent Strategy in Russia

Russia’s patent system aligns with the Eurasian Patent Convention (EAPC) and is influenced by both Russian law and international agreements. The patent landscape for pharmaceuticals in Russia is characterized by:

  • High patent activity around APIs, formulations, and delivery systems.
  • Strategic filings aimed at blocking competitors or expanding market exclusivity.
  • Use of patent families and divisional applications to maximize protection.

Key Competitors and Existing Patents

Reviewing the top competitors in Russia’s pharmaceutical patent landscape, notably local and international players like Pfizer, Novartis, Sanofi, and Russian firms like Pharmstandard, reveals:

  • Parallel patents targeting similar APIs or diseases.
  • A substantial portfolio of formulations and delivery systems.
  • Potential patent thickets that could impact freedom-to-operate analyses.

In particular, prior patents may cover formulations involving the same APIs, specific manufacturing techniques, or indication-specific treatments, thus imposing limitations on new entrants.

Patent Litigation and Infringement Risks

While patent litigation in Russia remains less prevalent than in the U.S. or Europe, the risk for infringement claims or oppositions exists, especially during patent examination or market entry phases. The strength of RU2013123036’s claims will influence its robustness during such proceedings.


Strategic Implications

For Innovators:
The patent's scope determines how effectively it can serve as a blocking patent or as part of an expansion of a patent portfolio. A well-drafted patent can deter competitors and enable licensing strategies.

For Competitors:
Identifying overlaps with existing patents is crucial to avoid infringement and to explore possible design-around options. Requires meticulous patent landscape analysis and prior art searches.

For Investors and R&D Managers:
Understanding patent strength and scope informs investment decisions, licensing negotiations, and R&D directions within Russia and in subsequent markets.


Key Technical and Legal Considerations

  • Scope of Claims vs. Prior Art: Confirm whether the patent claims are sufficiently broad to cover emerging formulations.
  • Patent Term and Exclusivity: The patent filed in 2012 likely has 20-year term, expiring around 2032, providing substantial market exclusivity.
  • Potential for Patent Opposition: Actions for revocation or opposition in Russia, particularly based on lack of novelty or inventive step, could diminish patent value.
  • Patent Family and International Filing: Checking if similar patents exist in Eurasia, EPO, or PCT applications can reveal strategy for broader protection.

Conclusion

Russian patent RU2013123036 offers a significant strategic tool, contingent upon its claims' scope and robustness within the existing patent landscape. Its broadness, targeted technology, and legal enforceability will shape its role in defending or challenging market positions. Companies operating in Russia must analyze this patent alongside other regional patents to optimize their R&D and commercialization strategies.


Key Takeaways

  • Effective assessment of RU2013123036’s scope depends on detailed claim analysis, especially the independent claims’ breadth.
  • The patent landscape in Russia for pharmaceuticals is highly active; particularly, prior art and existing patents pose potential challenges.
  • A proactive patent landscape analysis enables strategic positioning, licensing potential, or designing around existing patents.
  • Ensuring claims are well-differentiated from prior art maximizes enforceability and market exclusivity.
  • Continuous monitoring for oppositions or legal challenges in Russia is vital to sustain patent value.

FAQs

  1. What is the primary inventive contribution of RU2013123036?
    The patent claims a specific pharmaceutical composition or method, potentially involving unique active ingredient combinations or novel manufacturing processes, designed for targeted medical applications.

  2. How broad are the claims typically in this type of pharmaceutical patent?
    Actually, the scope varies; independent claims tend to be broad enough to cover key formulations but are carefully crafted to pass novelty and inventive step criteria. Narrower dependent claims specify particular embodiments.

  3. Can this patent be challenged or invalidated?
    Yes, if prior art predates its filing date or if it can be demonstrated that the claims lack novelty or inventive step, the patent may be challenged through opposition procedures or legal actions.

  4. How does this patent fit within the wider Russian pharmaceutical patent landscape?
    It likely complements a portfolio of patents around similar APIs or therapeutic areas. Its strength depends on claim specificity and prior art considerations within Russia and Eurasia.

  5. What are the strategic considerations for a competitor given this patent?
    Competitors should conduct extensive prior art searches to identify potential design-arounds, assess infringement risks, and evaluate opportunities for licensing or patent licensing negotiations.


Sources:
[1] Rospatent official database.
[2] Russian Federation Patent Law.
[3] Eurasian Patent Office guidelines.
[4] Industry analysis reports on Russian pharmaceutical patents.

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