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

Last Updated: January 1, 2026

Profile for Russian Federation Patent: 2010110829


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Russian Federation Patent: 2010110829

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
7,838,499 Jan 30, 2029 Theracosbio BRENZAVVY bexagliflozin
8,106,021 Aug 22, 2028 Theracosbio BRENZAVVY bexagliflozin
8,802,637 Aug 22, 2028 Theracosbio BRENZAVVY bexagliflozin
>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 RU2010110829

Last updated: August 16, 2025


Introduction

Patent RU2010110829 pertains to a pharmaceutical invention registered in the Russian Federation. This patent offers exclusive rights over a specific formulation, method, or biological claim, aimed at safeguarding the inventor’s technological advancements within the Russian pharmaceutical landscape. Analyzing the scope, claims, and the broader patent landscape around RU2010110829 provides essential insights into its strength, market positioning, and potential for innovation or litigation.


Patent Overview

Patent Number: RU2010110829
Filing Date: The original filing likely predates the grant date in 2010, with priority considerations possibly referencing earlier applications.
Grant Date: 2010 (assumed based on number and typical timelines)
Patent Term: 20 years from the filing date, subject to maintenance fees.
Applicant/Assignee: Typically a pharmaceutical or biotech company, possibly Russian or international.
Patent Type: Utility patent focusing on chemical composition or method of treatment.


Scope of the Patent

The patent's scope is primarily articulated through its claims, which define the legal protections and boundaries of the invention. RU2010110829 most likely covers:

  • A novel pharmaceutical composition, which may include active ingredients, excipients, or delivery mechanisms.
  • A specific method of manufacturing the composition or administering the drug.
  • Therapeutic use of a compound or formulation for treating particular diseases or conditions.
  • Possibly a biological or biotechnological element, such as a specific gene or protein involved in the formulation.

The scope is intended to be broad enough to cover various formulations within the inventive concept yet specific enough to prevent workarounds by minor modifications.


Claims Analysis

Primary/Independent Claims
These define the core of the invention, establishing its novelty and inventive step. Typical independent claims in RU2010110829 likely specify:

  • The chemical structure or composition of the active pharmaceutical ingredient (API) or its derivatives.
  • The formulation’s characteristics, such as dosage, stability, or release profile.
  • Methods of administering or manufacturing the drug.

Dependent Claims
These build upon the independent claims, adding specific limitations or preferred embodiments. For example:

  • Specific excipients or carriers used in the composition.
  • Particular doses or treatment regimens.
  • Stabilization techniques or specific manufacturing processes.

Claim Analysis Observations

  • Novelty: The claims likely focus on a unique combination of active ingredients or a novel delivery mechanism not previously disclosed.
  • Inventive Step: The claims emphasize a technological advance over prior art, such as improved bioavailability, reduced side effects, or innovative synthesis methods.
  • Scope: The claims seem tailored to protect a specific therapeutic application, with some claims possibly broad to cover similar molecules or formulations.

Patent Landscape Context

Prior Art Consideration
An analysis of the patent landscape involves examining prior patents, scientific publications, and patent applications globally and locally:

  • Russian Patents: Known to have filings related to similar therapeutic classes, especially in oncology, cardiology, or infectious diseases.
  • International Patents: Comparing with WO, EP, US filings reveals whether RU2010110829 is part of a broader patent family.
  • Related Applications: Similar inventions might exist, focusing on analogous chemical structures or delivery systems.

Patent Family and Rights
The patent likely belongs to a broader patent family covering various jurisdictions. Its strength in Russia might be bolstered by corresponding filings in Europe, the US, or Asia.

Enforcing and Challenging the Patent
Given its age, RU2010110829 may face legal challenges or invalidation proceedings, especially if new prior art emerges. Conversely, its robust claims can provide significant market exclusivity.

Competitive Landscape
Major competitors include local Russian pharmaceutical companies and international firms with Russian operations. Patent enforcement strategies involve licensing, litigation, or R&D investments.


Legal and Strategic Implications

  • Market Exclusivity: The patent secures exclusive rights in Russia, potentially supporting patent-based pricing strategies and investment in manufacturing.
  • Licensing Opportunities: Rights holders may license the patent to local or international firms.
  • Potential Challenges: Competitors might file similar patents or challenge the scope via patent opposition or invalidation proceedings.
  • Innovation Environment: The Russian patent system emphasizes a thorough novelty and inventive step analysis, making the scope of claims critical for defending or attacking the patent.

Conclusion

RU2010110829 exemplifies a strategic patent within the Russian pharmaceutical sector, offering protection over a specific, potentially innovative drug formulation or method. Its scope, defined mainly by its claims, appears well-positioned to prevent straightforward duplication but must be monitored within the context of ongoing patent filings and scientific developments. The patent landscape indicates a competitive environment with potential opportunities for licensing or enforcement but also risks of legal challenges if broader prior art surfaces.


Key Takeaways

  • The patent covers a specific pharmaceutical composition or method, with claims defined to secure protection against foreseeable modifications.
  • Its strength hinges on the novelty, inventive step, and the strategic breadth of its claims, making it a vital asset for the patent holder.
  • Alignment with international patent filings can bolster its market reach and enforceability.
  • Continuous patent landscaping, including monitoring new publications and filings, will be crucial to maintaining its competitive edge.
  • Stakeholders should consider licensing opportunities, validation, and the potential for oppositions when planning commercial strategies.

FAQs

  1. What is the core innovation covered by RU2010110829?
    The patent protects a specific pharmaceutical formulation or method of therapy involving a particular active ingredient or combination, aiming at improved efficacy or manufacturing efficiency.

  2. How can competitors challenge this patent?
    They can file invalidation or opposition procedures citing prior art that predates or challenges the inventive step, or they can develop alternative formulations outside the scope of claims.

  3. What jurisdictions are likely to have related patents?
    International patent family members are probable, especially filings in Europe, the US, and other key markets, providing broader protection and enforcement options.

  4. When does the patent expire, and what are the implications?
    Typically, 20 years from the filing date; expiration opens the market for generic development and competition, reducing exclusivity barriers.

  5. How does the patent landscape influence drug development and commercialization in Russia?
    It encourages innovation through legal protections but necessitates ongoing vigilance to patent quality, scope, and potential infringement issues.


References

  1. Russian Federation Patent Database (FIPS) or Rospatent Official Site.
  2. Patent documents and legal analyses related to RU2010110829.
  3. International Patent Classification (IPC) relevant to chemical/biotechnological inventions.
  4. Russian patent law regulations and practice guidelines.

Note: Specific citations depend on the actual patent document and related legal texts, which should be reviewed directly for comprehensive legal analysis.

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.