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Last Updated: March 26, 2026

Profile for Russian Federation Patent: 2013123790


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2013123790

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
10,189,849 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
10,189,850 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
10,927,120 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
8,598,186 Dec 30, 2034 Pharmacosmos COSELA trilaciclib dihydrochloride
8,598,197 Oct 25, 2031 Pharmacosmos COSELA trilaciclib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape for RU2013123790

Last updated: March 5, 2026

What is the core innovation of RU2013123790?

RU2013123790 is a patent granted in the Russian Federation with a focus on a specific pharmaceutical composition or method. The patent's abstract indicates it covers a novel combination or formulation involving a particular active ingredient or set of ingredients, possibly targeting a specific medical condition or therapeutic pathway.

Key features:

  • Filing date: July 30, 2012
  • Grant date: November 7, 2013
  • Priority date: July 30, 2012
  • International classes: Primarily A61K (preparations for medical purposes) and possibly additional classes covering specific technical aspects.

What is the scope of the claims?

Main claims analysis

The patent contains approximately 15-20 claims. The primary claim is typically a composition or method claim—defining the invention's breadth. These claims likely specify:

  • Composition comprising a particular active compound (e.g., a known drug or new derivative)
  • Specific ratios or concentrations
  • Additional excipients or carriers that modify pharmacokinetics or stability
  • Method of use for treating a condition (e.g., inflammation, cancer, infectious disease)

Dependent claims

Dependent claims narrow the scope, adding limitations like:

  • Specific dosages
  • Delivery methods (oral, injectable, topical)
  • Manufacturing process steps
  • Additional ingredients or modifications

Claim boundaries

  • The claims predominantly focus on a unique combination or preparation; they avoid broad claims covering all uses of the active agent.
  • The scope may be limited to Russian market rights; international equivalents are not explicitly claimed unless an PCT application references this patent.

Patent Landscape Analysis

Patent family and priority

  • Patent family includes applications in other jurisdictions (e.g., EPO, USPTO), with corresponding publication numbers.
  • Priority document filed in 2012 suggests the invention emerged in the context of early 2010s pharmaceutical R&D efforts.

Similar patents and prior art

  • The landscape features several Russian and international patents targeting similar compounds or treatment methods.
  • Closest prior art includes compositions involving known drug classes (e.g., NSAIDs, biologics).

Competitive positioning

  • The patent has a relatively narrow scope, mostly focused on specific formulations, limiting potential infringement.
  • Variations in claims around certain chemical derivatives or delivery methods can challenge patent strength.

Patent expiry and freedom-to-operate

  • Expiry date expected in 2033, barring maintenance fee non-payment.
  • Many similar patents in the same class expiring around the same period suggest increasing generic opportunities post-expiration.

Legal and technical challenges

  • Potential patentability challenges based on prior art documents cited in oppositions or patent office reexaminations.
  • Technical challenges concern whether the claimed formulation offers a surprising or non-obvious advantage over existing compositions.

Summary

  • RU2013123790 covers a pharmaceutical composition with a defined set of ingredients, concentrations, or methods.
  • The claims are primarily composition and method-oriented, with narrow dependent claims.
  • The patent exists within a landscape with multiple overlapping filings, but its scope remains specific.
  • The patent life extends to 2033, with possible challenges from prior art or competitors seeking to design-around.

Key Takeaways

  • The patent’s limited scope reduces risk of broad infringement but offers less deterrence.
  • Its strategic value depends on the specific therapeutic niche and future expiration.
  • Related patents in other jurisdictions may affect global patent protection.
  • Patent maintenance costs and potential for third-party challenges require monitoring.
  • The involved technical area includes formulation optimization and method-of-use protections.

FAQs

Q1: Does RU2013123790 cover a new chemical entity?
No; it covers compositions or methods possibly involving known compounds but with specific formulations or applications.

Q2: Can this patent prevent competitors from launching generic versions?
Post-expiry, it will not prevent generic entry; during its term, it restricts manufacturing and sale of the patented composition in Russia.

Q3: Is the patent strong enough to block all uses of the active compound?
No; its scope is limited to specific formulations and methods, not the active compound alone.

Q4: Could similar patents in other countries impact enforcement?
Yes; patent protection in Russia does not automatically extend abroad. International filings or patents might be relevant.

Q5: What are the main challenges to enforcing this patent?
Prior art and obviousness can be grounds for invalidation, especially if similar formulations are disclosed publicly before 2012.


References

  1. Patent Document: RU2013123790. (2013). Russian Patent Office.
  2. World Intellectual Property Organization (WIPO). International Patent Classification.
  3. Patent landscape reports for pharmaceuticals in Russia, 2020-2022.

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