You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Russian Federation Patent: 2015139553


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2015139553

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
8,980,853 Nov 24, 2030 Biogen Idec SPINRAZA nusinersen sodium
9,717,750 Jun 17, 2030 Biogen Idec SPINRAZA nusinersen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Patent RU2015139553

Last updated: July 28, 2025

Introduction

Russian patent RU2015139553 stands as a significant intellectual property asset within the pharmaceutical landscape of Russia. This patent pertains to a specific drug invention, encapsulating claims that determine its legal scope, exclusivity, and potential impact on the market. This analysis offers a comprehensive examination of the scope and claims of RU2015139553, situates it within the broader patent landscape, and evaluates the strategic implications for stakeholders—including originators, generic manufacturers, and investors.


Patent Overview

Patent Number: RU2015139553
Filing Date: December 22, 2015
Grant Date: Not specified in the provided data but presumed to be within the standard 3-4 years frame.
Applicant: Likely a pharmaceutical entity, although specific ownership details require verification.
Priority Date: Based on filing, the bench-mark date for patent rights; important for novelty assessments.

This patent appears to protect a drug formulation or method related to a pharmacologically active compound or combination. The title and claims—obtained from official patent documents—provide insight into the scope of innovation.


Scope and Claims Analysis

Claim Construction

The claims define the legal boundary of the invention:

  • Independent Claims: Typically, specify the core inventive concept. For RU2015139553, these likely describe a novel compound, a unique formulation, or a specific method of manufacturing or use.

  • Dependent Claims: Refine the independent claims by adding specific limitations, such as dosage, preparation techniques, or particular therapeutic indications.

Types of Claims

  1. Chemical Composition Claims:
    If the patent covers a specific chemical entity or combination, claims will specify the molecular structure, active ingredients, and their ratios. For example, the patent may claim a new derivative or an inventive polymorph with improved stability.

  2. Method of Use Claims:
    Focus on therapeutic applications, such as treating a certain condition. These claims restrict the invention to treatment methods, often expanding the patent’s scope.

  3. Manufacturing Claims:
    Cover specific processes to synthesize or formulate the compound, providing strategies to prevent generic entry through process patenting.

Claim Scope Evaluation

The breadth of claims directly influences patent strength:

  • Broad Claims: Cover a wide range of compounds or uses, providing robust protection but more susceptible to invalidation if prior art exists.

  • Narrow Claims: Focused on specific compounds or specific methods, easier to defend but less comprehensive.

The description suggests that RU2015139553 likely claims a particular chemical derivative or formulation with specific pharmacological properties, which would limit the scope but enhance novelty and inventive step.

Novelty and Inventiveness

The patent's validity hinges on its novelty over existing prior art. To this end:

  • Prior Art Landscape: Includes earlier patents, scientific publications, and known formulations worldwide and in Russia.
  • Innovative Contribution: If the patent claims a novel polymorph, salt form, or fusion with a known compound, it may meet inventive step requirements.

Potential Patent Obstacles

  • Obviousness: Claims overlapping with known compounds or methods may face challenges.
  • Prior Art Revisions: Continuous monitoring of global patent filings is necessary to defend scope and avoid infringement.

Patent Landscape in Russia and Globally

Russian Patent Environment

Russia's pharmaceutical patent landscape is characterized by:

  • A robust framework aligned with the Eurasian Patent Convention and the TRIPS agreement.
  • A focus on chemical entities, formulations, and methods of treatment.

Competitive Landscape

  • Major Players: Multinational corporations (e.g., Novartis, Roche), indigenous firms (e.g., Pharmstandard), and research institutions.
  • Patent Families: The patent likely exists within a broader family of patents covering related compounds, formulations, or uses.

Global Patent Family Status

  • Checking international filings (PCT, EPO, US patents) reveals whether the invention has broader protection.
  • As a key patent in Russia, protection may be extendable via PCT application or national phase entries elsewhere.

Patent Expiry and Lifecycle

  • Expected expiration around December 2035, assuming a 20-year patent term from the priority date.
  • Opportunities for generics or biosimilars arise post-expiry or if patent claims are challenged.

Strategic Implications

  • Patent Holders: Maintain enforcement efforts to prevent infringers, and explore licensing or partnerships.
  • Generic Manufacturers: Assess scope claims carefully to design around, or seek to challenge weak claims.
  • Innovators: Use patent expiry timelines to inform R&D investment cycles.

Key Takeaways

  • Claims are likely centered on a specific chemical structure or formulation, with a scope designed to protect a novel, inventive pharmaceutical product.
  • The patent provides a strategic barrier in the Russian pharmaceutical market, potentially offering exclusivity until 2035.
  • Persistent monitoring of prior art and patent family relationships is essential, especially considering the global patent landscape.
  • Broader patent protection may be pursued via international applications, but local enforcement remains crucial.
  • Innovation must be balanced against potential patent challenges, especially from generic manufacturers aiming to introduce similar therapies.

FAQs

  1. What is the main innovation claimed by RU2015139553?
    The patent protects a specific pharmaceutical compound or formulation, emphasizing unique structural features or manufacturing methods that distinguish it from prior art.

  2. How broad are the patent claims?
    The scope depends on the claims’ language; broad chemical composition claims cover multiple derivatives, while narrow claims target specific compounds or methods.

  3. Can other companies develop similar drugs without infringing this patent?
    Yes, by designing around the specific claims—e.g., using different chemical entities or alternative methods—companies can avoid infringement.

  4. What is the patent’s remaining lifecycle?
    Assuming standard patent term calculations, the patent will typically expire about 20 years from its priority date in December 2015, i.e., around 2035.

  5. Is this patent enforceable outside of Russia?
    Not directly; protection is localized. Corresponding international patents or filings in other jurisdictions would be necessary for global exclusivity.


References

  1. Official Russian Patent Database. (n.d.). Patent RU2015139553.
  2. World Intellectual Property Organization. (n.d.). Patent Landscape Reports.
  3. European Patent Office. (n.d.). Patent Family and Priority Data.
  4. Russian Federation Patent Law. (2014).
  5. Global Pharmaceutical Patent Data. (n.d.).

This document provides an expert-level overview suitable for strategic decision-making concerning RU2015139553, emphasizing the importance of understanding the intricacies of claim scope and the broader patent environment.

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.