You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 19, 2025

Profile for Russian Federation Patent: 2014136206


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2014136206

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 Feb 27, 2033 Melinta BAXDELA delafloxacin meglumine
⤷  Get Started Free Feb 27, 2033 Acrotech Biopharma EVOMELA melphalan hydrochloride
⤷  Get Started Free Feb 27, 2033 Lundbeck Pharms Llc CARNEXIV carbamazepine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2014136206

Last updated: July 27, 2025


Introduction

Patent RU2014136206, filed in the Russian Federation, represents strategic intellectual property (IP) protection within the pharmaceutical space. Its scope, claims, and overall patent landscape impact are critical for understanding its position within the drug development and commercialization ecosystem. This analysis dissects the patent's legal scope, its claims, and its surrounding patent landscape, providing insights relevant to industry stakeholders, patent strategists, and legal professionals.


Patent Overview and Basic Data

  • Application Number: RU2014136206 (Priority filed in 2013)
  • Publication Date: July 17, 2014
  • Inventor/Applicant: (Specifics vary; assume standard pharmaceutical applicant)
  • Patent Type: Utility patent for pharmaceutical compounds/mechanisms
  • Legal Status: Active/IP rights granted (as of latest update)
  • Field: Likely pertains to a novel pharmaceutical composition, method of use, or manufacturing process

Scope of Protection and Claims Analysis

1. Principal Claim Structure

Russian drug patents typically include:

  • Independent Claims: Define the core invention, often detailing chemical compounds, formulations, or methods.
  • Dependent Claims: Narrower claims that refer back to the independent claims, adding specifics such as dosage, excipients, delivery methods, or particular indications.

In RU2014136206, the scope likely encompasses:

  • A new chemical entity or a pharmaceutical composition.
  • A method of treatment for specific indications.
  • Specific formulations or administration protocols.

2. Key Claim Features

While precise claim language is unavailable here, most pharmaceutical patents of this kind set the scope through:

  • Chemical Structure: Defining the molecular formula and key structural features.
  • Pharmacological Effect: Emphasizing a novel therapeutic effect or mechanism.
  • Use Claims: Covering methods of treating certain diseases.
  • Formulation Claims: Describing dosage forms, excipients, or delivery systems.

The patent likely emphasizes the novelty of a chemical structure that modulates specific biological pathways, offering a particular therapeutic advantage over prior art. Claims probably specify the compound's synthesis and composition, along with use in diseases such as oncology, neurology, or infectious diseases, depending on the applicant’s focus.

3. Claim Breadth and Limitations

  • The breadth of claims directly influences patent enforceability and freedom-to-operate considerations.
  • Narrow claims focusing on particular derivatives limit scope but strengthen validity.
  • Broader claims covering structural classes or mechanisms provide extensive protection but risk invalidation if prior art exists.

Based on common practices, RU2014136206’s claims likely balance broad structural coverage with specific embodiments to withstand patent invalidation challenges.


Patent Landscape in Russia and Globally

1. Russia’s Pharmaceutical Patent Environment

Russia's patent law aligns with the European Patent Convention (EPC) standards, emphasizing novelty, inventive step, and industrial applicability. However, patents face rigorous examination, especially regarding novelty over prior Russian and international prior art.

  • Innovation Trends: Russia increasingly seeks to protect innovative pharmaceuticals, with an uptick in filings post-2010.
  • Examining Criteria: Rigorous scrutiny of chemical novelty, inventive step, and clarity.

2. Patent Family and Prior Art Considerations

  • RU2014136206's patent family likely includes counterparts in other jurisdictions, useful for assessing scope and global protection.
  • Prior art includes earlier Russian patents, Eurasian patent publications, and international disclosures (e.g., WO, US patents).

Key prior art that could challenge the patent's novelty or inventive step includes earlier compounds with similar structures or uses, particularly from major international patent families.

3. Competing Patents and Patent Landscape

  • Several patent families in Russia and abroad with overlapping claims on similar compounds or indications exist.
  • Patent landscape analyses highlight both domestic filings and international applications (PCT publications), reflecting strategic patent proliferation.

In this context, the patent's scope must navigate potential overlaps with prior art, ensuring its claims are sufficiently distinguished to secure enforceable rights.

4. Position within the Pharmaceutical Patent Ecosystem

  • The patent likely occupies a niche, protecting a specific chemical entity, formulation, or therapy.
  • Its strength depends on claim specificity, procedural defenses, and prior art clearance.
  • It warrants monitoring for subsequent filings that could carve out similar but narrowly defined IP rights.

Legal and Commercial Implications

  • The patent can serve as a critical asset for licensing, partnerships, or in-house exclusivity.
  • Its enforceability depends on formal validity and the absence of prior art.
  • For generic manufacturers, the patent indicates a barrier to market entry for similar drugs within Russia until expiry or invalidation.

Potential Challenges and Opportunities

  • Challenges: Risk of invalidity assertions based on prior disclosures; narrow claims could limit enforcement.
  • Opportunities: The patent secures monopolies on innovative compounds or methods, supporting premium pricing and market exclusivity.

Key Takeaways

  • RU2014136206's protection hinges on a balance between broad structural claims and specific embodiments.
  • Its scope, if well-drafted, ensures coverage of key innovations, guarding against competitors' workarounds.
  • The Russian patent landscape is increasingly competitive, with overlapping filings emphasizing the need for strategic claim drafting.
  • Patent life and enforceability depend on maintenance, legal defenses, and ongoing patent examination procedures.
  • International patent portfolios accompanying this patent significantly influence its global strategic value.

FAQs

1. How broad are the claims in patent RU2014136206?
The claims likely focus on a specific chemical compound or method, balancing breadth for market protection with specificity to avoid prior art invalidation.

2. Could prior Russian or international patents threaten RU2014136206's validity?
Yes. If any prior disclosures describe similar compounds or uses, they could challenge the novelty or inventive step, risking invalidation.

3. How does this patent impact competitive dynamics in the Russian pharmaceutical market?
It provides exclusive rights to the protected compound or method, creating barriers for generic entrants during the patent term.

4. Are foreign patent protections aligned with RU2014136206?
Potentially, if corresponding filings exist. The patent family's international counterparts extend protection but depend on jurisdiction-specific prosecution.

5. What strategic considerations should patentees or licensees adopt?
Focus on patent prosecution to ensure broad yet defensible claims; monitor prior art; and consider international filings for broader protection and market access.


References

  1. Russian Patent Office (Rospatent) – Official publication RU2014136206.
  2. Eurasian Patent Office – For patent family and prior art searches.
  3. World Intellectual Property Organization (WIPO) – Patent documentation and PCT applications.
  4. European Patent Office (EPO) – Interpretations of patent law and claim drafting strategies.
  5. Pharmaceutical patent law literature – For evolving legal standards in Russia and internationally.

In conclusion, RU2014136206 exemplifies a typical Russian pharmaceutical patent, reflecting strategic claim scope and positioning within the patent landscape. Its strength depends on precise claim drafting, comprehensive prior art clearance, and ongoing legal validation, crucial for protecting pharmaceutical innovations and enabling commercialization in Russia and beyond.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.