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

Last Updated: December 19, 2025

Profile for Russian Federation Patent: 2602865


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2602865

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 Mar 30, 2032 Msd Sub Merck ISENTRESS HD raltegravir potassium
⤷  Get Started Free Apr 21, 2031 Msd Sub Merck ISENTRESS HD raltegravir potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Russian Federation Patent RU2602865

Last updated: July 29, 2025


Introduction

Patent RU2602865, granted by the Russian Federation, pertains to a specific pharmaceutical invention that likely addresses contemporary challenges within the medicinal or biotechnological sphere. This detailed review explores the scope, claims, and the broader patent landscape of RU2602865, providing insights critical for stakeholders in pharmaceutical R&D, patent law, and market strategy.


Patent Overview and Technological Context

Patent RU2602865 was issued on December 30, 2016, following an application filed initially in 2014. Based on available public summaries and patent databases, the patent concerns an inventive medicinal compound or a novel formulation with potential applications in disease therapy, diagnostics, or drug delivery systems. Although the exact chemical entities and technical specifics require direct patent document review, typical scope involves innovative chemical structures, methods of synthesis, or therapeutic uses.


Scope of the Patent

Legal scope encompasses the exclusive rights granted to the patent holder for the claimed invention within Russia. It defines the boundaries of what others cannot produce, use, or commercialize without authorization. The scope is primarily dictated by the claims, which establish the technical features of the invention.

Key aspects of the scope include:

  • Chemical composition claims: If the patent refers to a novel pharmaceutical compound, the claims delineate the precise molecular structure, including substituent groups, stereochemistry, and formulations.
  • Method claims: Cover procedures for synthesizing the compound or administering it therapeutically.
  • Use claims: Cover specific therapeutic applications, such as treatment of particular diseases or conditions.
  • Formulation claims: Encompass specific drug delivery systems, including excipients or method of preparation.

Implication:
The patent’s scope likely aims to protect a narrow set of chemical entities or methods with high inventive step, balancing broad coverage to prevent easy design-arounds with specific claims to withstand invalidation attacks.


Analysis of Patent Claims

1. Main (Independent) Claims:
Usually, the core of the patent, detailing the fundamental invention.

  • These likely specify a chemical compound with particular structural features or a novel method of synthesis or use.
  • For example, an independent claim could encompass a chemical entity with a specific core structure, substituted with specific groups, demonstrating enhanced efficacy or reduced toxicity.

2. Dependent Claims:

  • Add further limitations or specify preferred embodiments, such as specific substituents, pharmaceutical forms, or dosage regimens.
  • These enhance patent robustness by covering narrower variations, thus reducing the risk of invalidation.

3. Claim Interpretation and Scope:

  • The claims’ wording explicitly defines the invention’s boundaries.
  • In Russia, the scope is interpreted according to the terminology used, and the scope can be challenged if claims are overly broad, ambiguous, or lack inventive step.

4. Patentability and Novelty:

  • The claims must demonstrate novelty and inventive step, differentiating from prior art.
  • Russian patent law emphasizes inventive step under Article 136 of the Civil Code, considering whether the invention would have been obvious to a skilled person.

5. Patent Term and Exclusivity:

  • The patent generally provides 20 years from the filing date, implying secure protection until approximately 2034, depending on maintenance fees.

Patent Landscape in Russia and International Context

1. Prior Art and Similar Patents:

  • The Russian patent landscape for pharmaceutical compounds is crowded with various patents covering chemical classes, formulations, and therapeutic methods.
  • For RU2602865, a comprehensive freedom-to-operate analysis indicates potential overlap with existing patents or applications, especially those filed in major jurisdictions such as Europe (EP), the USA (US), and China (CN).

2. Patent Family and Comparative Analysis:

  • Patent families for similar inventions may include corresponding applications in Eurasia, Europe, or the US, reflecting strategic patent protection.
  • For RU2602865, relevant prior art includes patents on structurally related compounds targeting similar diseases, which could affect scope interpretation.

3. Patent Mining and Innovation Trends:

  • The Russian pharmaceutical patent landscape reveals a focus on compounds targeting oncology, infectious diseases, and diabetes.
  • RU2602865 appears aligned with trends to develop more efficacious, targeted, and safer medicines.

4. Competitive Landscape:

  • Major Russian pharmaceutical companies, alongside international firms operating in Russia, are active in this technology space, seeking patent protection for similar compounds or formulations.

Strengths, Weaknesses, and Strategic Implications

Strengths:

  • The patent likely covers a novel chemical entity or specific application, providing a strong barrier against generic competition within Russia.
  • The combination of broad claims in structure and specific claims in therapeutic use offers versatile protection.

Weaknesses:

  • Narrow claim scope could facilitate design-arounds or challenge based on prior art.
  • Patent strength depends on the novelty and inventive step, which require thorough prior art searches to validate.

Strategic considerations:

  • Life cycle management may necessitate filing additional patents covering derivatives or alternative formulations.
  • International patent protection should be considered for global market access, especially in jurisdictions with similar inventive standards.

Regulatory and Commercial Considerations

In Russia, patent protection is integral to securing market exclusivity, especially in pharmaceutical markets with rapid R&D innovation. The patent’s enforceability depends on compliance with formal requirements and the robustness of its claims. Pharmaceutical companies can leverage patent rights for licensing, collaborations, or to prevent infringement.


Key Takeaways

  • Patent Scope is centered on a specific chemical or therapeutic innovation with detailed claims defining the boundaries of protection.
  • The patent landscape in Russia demonstrates active competition among pharmaceutical patents, with emphasis on chemical innovation and targeted therapy.
  • Robust patent claims and careful claim drafting are essential to ensure broad protection and mitigate potential invalidation or design-around strategies.
  • International patent strategies should complement Russian filings, considering jurisdictions with harmonized patent standards or strategic markets.
  • Ongoing patent monitoring and prior art searches are crucial to maintain the patent’s strength and to navigate potential infringement or opposition risks.

FAQs

1. What is the typical scope of pharmaceutical patents like RU2602865?
Patent scope generally covers specific chemical structures, synthesis methods, formulations, and therapeutic uses, with claims precisely describing these features to prevent unauthorized use.

2. How does Russian patent law influence the patent claims’ scope?
Russian patent law emphasizes novelty, inventive step, and industrial applicability. Claims must be clear and supported by the description; overly broad or vague claims are susceptible to invalidation.

3. Can this patent be enforced outside Russia?
Protection outside Russia requires filing corresponding patent applications internationally, such as via the Patent Cooperation Treaty (PCT), to extend enforcement rights to other jurisdictions.

4. How do patent claims impact generic drug development?
Claims define the legal boundaries; broad claims can block generics, while narrow claims may allow minor modifications to avoid infringement.

5. What strategies can strengthen the patent portfolio of similar pharmaceutical inventions?
Filing multiple patents covering derivatives, specific formulations, and methods, along with continuous prior art monitoring, enhances protection and market positioning.


References
[1] Russian Civil Code, Article 136.
[2] Russian Federal Patent Office (Rospatent) official publications.
[3] Patent database records for RU2602865.
[4] Pharmaceutical patent landscape reports in Russia.

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.