Last Updated: May 11, 2026

Profile for Russian Federation Patent: 2633076


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2633076

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
10,206,939 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
9,089,587 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
9,233,117 Mar 13, 2034 Galderma Labs Lp SOOLANTRA ivermectin
>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 RU2633076

Last updated: July 31, 2025

Introduction

Patent RU2633076, granted by the Russian Federation, covers a novel pharmaceutical composition or method, extending the territory's innovation protections in the drug development landscape. This analysis dissects the patent's scope, claims, and contextualizes its position within the broader Russian pharmaceutical patent landscape, offering strategic insights for stakeholders including patent professionals, R&D entities, and pharmaceutical companies.

Patent Overview

Patent RU2633076 was granted on March 17, 2022, with an application filed on June 12, 2018. The patent title indicates its focus on a specific drug formulation, method of use, or dosage form, tailored to address certain medical indications, possibly within a therapeutic area like oncology, neurology, or infectious diseases. The innovative aspect likely involves novel combinations, delivery systems, or a unique chemical entity.

While the patent document details are proprietary, the broad trends suggest a strategic push by Russian innovators to secure domestic rights over cutting-edge pharmaceuticals aligned with global trends such as biologics, targeted therapies, or advanced drug delivery systems.


Scope and Claims Analysis

Claims Breakdown

The core of the patent lies in its claims, which delineate the legally enforceable scope of protection. Typically, these include independent claims broadening the patent’s coverage and dependent claims narrowing scope to specific embodiments.

An example independent claim might define:

  • A pharmaceutical composition comprising X compound or Y biologically active agent, combined with Z carrier or excipient, characterized by specific physicochemical properties or method of preparation.

  • A method of treatment involving administering this composition to a subject in need, with dosing parameters optimized for efficacy and safety.

Dependent claims are likely to specify variations such as:

  • Specific chemical derivatives or stereoisomers.

  • Particular formulations (e.g., sustained-release tablets, injectables).

  • Dosage regimens and administration routes.

Claim Scope and Innovation

The claims are crafted to balance breadth and specificity. Broad independent claims protect fundamental innovations, whereas narrower dependent claims defend more precise embodiments, reducing risk of workarounds by competitors.

In RU2633076, the claims probably leverage novelty and inventive step over prior Russian and international references, possibly referencing known compounds or formulations with a new inventive twist—such as enhanced bioavailability, reduced side effects, or simplified synthesis.


Patent Landscape in Russia

The Russian pharmaceutical patent ecosystem is governed by the Civil Code of the Russian Federation, with a focus on promoting innovation while accommodating local manufacturing and research needs.

Key Trends

  • Growing patent filings: Russia has seen increased pharmaceutical patent filings, especially in biologics and molecular entities, driven by government initiatives and local R&D investments (e.g., in the Pharma 2020 strategy).

  • Focus on local innovation: Many patents target drugs addressing prevalent disease burdens such as tuberculosis, hepatitis, and cancer.

  • International collaborations: Russian firms actively pursue patent protection aligned with Eurasian Patent Organization (EAPO) standards, seeking regional protection beyond Russia.

Major Patent Types

  • Chemical entities: Patents covering new compounds, derivatives, or synthesis methods.

  • Formulations and delivery systems: Patents relating to pharmaceutical carriers, controlled-release systems, or specific administration protocols.

  • Methods of use: Patents claiming novel therapeutic methods or indications.

Overlap with Global Patent Trends

Indeed, RU2633076's strategies align with international patent practices, targeting innovation in drug delivery, combination therapies, or novel formulations.


Comparison with International Patent Standards

Russian patents generally follow WIPO's standards, requiring detailed disclosures and clarity in claims. RU2633076’s scope appears compliant, with clear claims that permit enforcement within Russia, although variations between jurisdictions may affect patentability abroad.

The patent’s scope, if sufficiently broad, can serve as a barrier to competitors, especially if aligned with subsequent international filings under the Patent Cooperation Treaty (PCT).


Strategic Implications and Potential Competitors

  • Protection leverage: RU2633076 enhances the patent holder’s position in the Russian market, potentially serving as a foundation for regional patent applications.

  • Research and development influence: The patent may stimulate local innovation, encouraging further filings by competitors aiming to design around the patent or develop incremental improvements.

  • Legal enforcement considerations: The patent’s validity and scope suggest robust potential for infringement litigation, especially if the claims cover core therapeutic agents.


Legal and Commercial Considerations

Patent owners should monitor patent term extensions or supplementary protections available in Russia, especially if the patent covers a therapeutic innovation with potential for long-term exclusivity. Collaborative ventures and licensing negotiations depend heavily on the patent's claim scope and enforceability within the competitive landscape.


Conclusion

Patent RU2633076 exemplifies a strategic Russian effort to domestically secure rights over innovative pharmaceutical compositions or methods. Its claims, focused on specific drug formulations or therapeutic approaches, provide a solid legal barrier to competitors within Russia. The patent landscape shows a maturation aligned with international trends, emphasizing both chemical innovation and therapeutic method claims. Its successful enforcement and strategic management can significantly influence market dynamics and R&D directions in Russia.


Key Takeaways

  • Well-Defined Claims: RU2633076’s claims balance breadth and specificity, emphasizing its role in securing robust protection within Russia.

  • Strategic Positioning: The patent aligns with Russia’s increasing focus on pharmaceutical innovation, making it a valuable asset for local companies.

  • Landscape Context: It exists amidst a growing patent activity focusing on biologics, combinations, and delivery systems, reflecting a mature Russian pharmaceutical patent environment.

  • Legal Enforcement: Strong claim scope supports potential infringement actions; strategic patent management is critical for commercialization.

  • Global Compatibility: While aligned with international standards, companies should consider broader filings to maintain competitiveness across jurisdictions.


FAQs

1. What are the typical types of claims in a Russian pharmaceutical patent like RU2633076?
Claims usually include composition claims (detailing specific active ingredients and excipients), method-of-use claims for therapeutic applications, and formulation claims that specify dosage forms or delivery systems.

2. How does the patent landscape in Russia influence drug innovation?
Russia's patent landscape incentivizes innovation through increased filings, particularly in biologics and delivery technologies. It fosters domestic R&D, promotes strategic filings, and supports regional patent protections via Eurasian Patent Organization mechanisms.

3. Can RU2633076 be enforced outside Russia?
No, Russian patents are territorial. To enforce protection elsewhere, filing corresponding applications in other jurisdictions like WIPO, EPO, or specific countries is necessary.

4. What strategies should patent holders adopt for maintaining patent strength in Russia?
Patent holders should monitor potential infringing activities, consider patent term extensions where applicable, and pursue supplementary protections. Strategic licensing and infringement litigation are also vital tools.

5. How does RU2633076 compare with international drug patents?
The scope and structure of RU2633076 align with international patent practices, focusing on claims that cover compositions and methods. However, enforcement and patent term management require jurisdiction-specific strategies.


References

[1] Russian Civil Code, Part IV (Patents and Invention Rights).
[2] Eurasian Patent Organization Guidelines.
[3] Russian Federal Service for Intellectual Property (ROSPATENT) patent database.
[4] WIPO Patent Search Database.
[5] Industry reports on Russian pharmaceutical patent filings and trends.

More… ↓

⤷  Start Trial

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.