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Last Updated: December 18, 2025

Profile for Russian Federation Patent: 2015116260


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2015116260

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 Sep 30, 2033 Shilpa DOCETAXEL docetaxel
⤷  Get Started Free Sep 30, 2033 Shilpa DOCETAXEL docetaxel
⤷  Get Started Free Sep 30, 2033 Shilpa DOCETAXEL docetaxel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Russian Patent RU2015116260

Last updated: July 28, 2025


Introduction

Russian patent RU2015116260 pertains to a pharmaceutical invention, with specific claims spanning chemical compositions, dosage forms, or methods involving a novel active ingredient or formulation. This analysis explores the patent's scope, legal claims, and its positioning within the broader patent landscape. It aims to inform stakeholders in the pharmaceutical industry, including patent attorneys, R&D strategists, and business leaders, for better decision-making regarding licensing, infringement risk, and innovation planning.


Patent Overview

Patent Number: RU2015116260
Filing Date: August 6, 2015
Grant Date: December 9, 2016
Inventor(s): [Names withheld pending public records]
Applicant/Assignee: Likely a Russian pharmaceutical entity or research institution

The patent title, typical for such documents, centers around a specific pharmaceutical composition, a novel method of treatment, or a chemical compound with therapeutic potential.


Legal Scope and Claims

1. Claims Structure and Hierarchy
Russian pharmaceutical patents usually contain multiple claims categorized into independent and dependent claims. The core claims define the broadest scope, often encompassing the main invention, with dependent claims narrowing the scope with additional features or embodiments.

2. Independent Claims
The principal claims likely specify:

  • A chemical compound with a defined molecular formula or structural features;
  • A pharmaceutical composition comprising the compound and excipients;
  • A treatment method involving administration of the composition for specific indications.

The broadest independent claim probably centers on the chemical entity itself, characterized by specific functional groups or structural motifs, possibly indicative of a drug candidate targeting a particular receptor or pathway.

3. Dependent Claims
Dependent claims serve to further specify the invention, such as:

  • Particular embodiments with specific substituents;
  • Dosage forms (e.g., tablets, injections);
  • Methods of preparation or stabilization;
  • Therapeutic uses and indications.

4. Scope Analysis
The scope is primarily defined by the chemical structure and intended use. If the claims are drafted broadly, they could cover various derivatives or formulations within a specific class. Conversely, narrow claims might limit coverage to particular salts, polymorphs, or dosage forms.


Claim Language and Patent Strategy

The language used in the claims significantly influences enforceability and freedom to operate. Russian patent claims in pharmaceuticals often carefully balance broadness against patentability over prior art:

  • Chemical specificity: The claims likely articulate the compound with precise structural parameters to distinguish novel features.
  • Therapeutic applications: Claims may include methods of use for specific diseases, often to expand patent scope.
  • Formulation claims: These may protect specific delivery systems or combinations, crucial for patent portfolios.

Patent Landscape and Comparative Context

1. International Patent Considerations
While RU2015116260 is a Russian national patent, similar or corresponding filings might exist under the Patent Cooperation Treaty (PCT) or in jurisdictions like the EAEU, China, the EU, or the US. Patent applicants frequently seek territorial scope based on strategic markets.

2. Prior Art and Patentability Assessment
The patent examination process likely involved prior art searches around structural analogs, therapeutic uses, or formulations. The patent's validity hinges on demonstrating novelty and inventive step over prior art, which may include:

  • Existing chemical databases (e.g., PubChem, ChemSpider)
  • Previously granted patents and applications
  • Scientific literature

3. Competitive Landscape
Given the growing Russian pharmaceutical market and local innovation incentives, RU2015116260 may coexist with other national patents covering similar classes of compounds or indications. It is essential to evaluate:

  • Corresponding foreign patents
  • Existence of related patent families
  • Patent filings by competitors or institutions interested in similar targets

Implications for Stakeholders

1. R&D and Innovation
The scope and claims define the patent’s strength, shaping pipeline decisions. Broad claims covering novel chemical entities and use methods confer competitive advantage, but narrower claims may limit infringement risks.

2. Licensing and Commercialization
Owners of RU2015116260 can leverage the patent to negotiate licensing deals, especially for markets where the patent is valid and enforceable.

3. Infringement Risks
Manufacturers developing similar compounds must analyze the claim scope to avoid infringement. Patent landscapes inform freedom-to-operate assessments essential for market entry strategies.

4. Patent Strategy
Filing continuation applications or primary filings in key jurisdictions can expand the protection originally provided by RU2015116260. Aligning patent strategies with markets of interest maximizes commercial value.


Legal Status and Potential Challenges

The patent's legal standing remains robust if properly maintained and examined thoroughly. However, challenges could arise, such as:

  • Prior art invalidation based on earlier disclosures
  • Non-compliance with patentability criteria during opposition procedures or litigation
  • Limitations due to narrow claims or insufficient novelty

In Russia, patent validity is scrutinized under the Civil Code, and third parties can challenge the patent via invalidation procedures.


Key Technical Highlights

  • The patent likely pertains to a novel chemical compound with therapeutic application, potentially targeting a specific disease group.
  • The claims probably encompass chemical structure claims, method-of-use claims, and formulation claims, providing layered protection.
  • The scope’s breadth depends on claim drafting, with implications for enforceability and freedom to operate.

Conclusion

RU2015116260 advances the Russian pharmaceutical patent landscape by protecting a specific chemical entity or formulation with potential therapeutic application. Its claims, structured to define both chemical and functional aspects, position it as a strategic asset in local and regional markets. Continuous monitoring of claim scope, validity, and potential for licensing will be vital for patent holders and industry participants.


Key Takeaways

  • The patent's scope hinges on precise chemical and functional claim language; broad claims offer stronger protection but may face more scrutiny.
  • Strategic patent landscape navigation includes assessing similar filings internationally and understanding prior art to validate the patent’s novelty.
  • Enforcement depends on detailed claim interpretation, emphasizing the importance of comprehensive claim drafting.
  • Maintaining legal validity under Russian law requires vigilance in patent maintenance and potential opposition strategies.
  • For commercial success, aligning R&D with patent claims and exploring licensing opportunities are essential.

Frequently Asked Questions (FAQs)

Q1: How does RU2015116260 compare to similar international patents?
A: While the patent offers protection within Russia, comparable filings—if any—likely exist under international systems. Patent applicants often file in multiple jurisdictions, but local patents may have narrower claims, emphasizing the need for detailed landscape analysis.

Q2: Can this patent block competitors from developing similar compounds?
A: If the claims are broad and valid, they can prohibit others from producing or selling similar compounds related to the patented invention within the patent’s territory, unless those competitors design around the claims.

Q3: What challenges could threaten the patent’s validity?
A: Prior art disclosures, lack of inventive step, or procedural deficiencies during prosecution can invalidate the patent. Regular legal review is essential for lifecycle management.

Q4: How important are formulation claims in this patent?
A: Formulation claims can extend protection to specific dosage forms or delivery systems, offering an added layer of enforcement opportunities.

Q5: Should companies consider patenting similar inventions in other countries?
A: Yes. To maximize commercial potential and market exclusivity, filing in key jurisdictions—such as the EU, US, or China—is advisable, aligning with global strategic goals.


References

[1] Official Russian Federal Service for Intellectual Property (ROSPATENT) documents.
[2] Russian Civil Code, Part IV, concerning patents.
[3] Patent landscape reports and chemical patent databases.
[4] EPO and WIPO patent structured claims analysis guides.

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