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

Last Updated: December 15, 2025

Profile for Eurasian Patent Organization Patent: 027869


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 027869

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 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
⤷  Get Started Free May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
⤷  Get Started Free May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Eurasian Patent Organization Drug Patent EA027869

Last updated: July 28, 2025


Introduction

Patent EA027869, granted under the Eurasian Patent Organization (EAPO), represents a strategic element within the intellectual property landscape for pharmaceutical innovations in the Eurasian region. This detailed evaluation aims to dissect the scope, claims, and broader patent environment surrounding this patent, to assist stakeholders—pharmaceutical companies, legal practitioners, and R&D entities—in understanding its strategic implications.


Patent Overview: Basic Details and Filing Context

EA027869 was filed with the Eurasian Patent Office (EAPO), which consolidates patent rights across member states—including Russia, Belarus, Kazakhstan, Armenia, and Kyrgyzstan—forming a significant jurisdiction for pharmaceutical patent protection. Typically, such patents cover novel pharmaceutical compounds, formulations, methods of production, or therapeutic uses.

While precise bibliographic information (filing date, publication number, inventor, applicant) for EA027869 is not explicitly provided here, its classification likely pertains to the pharmacological domain, given the context.


Scope of the Patent: Functional and Material Boundaries

The scope of EA027869 is primarily encapsulated in its claims, which define the legal bounds of the patent’s exclusivity. In pharmaceutical patents, the scope often involves:

  • Compound Claims: Covering the specific chemical entity or derivatives thereof.
  • Method Claims: Outlining methods of synthesis or therapeutic application.
  • Formulation Claims: Encompassing specific compositions or drug delivery systems.
  • Use Claims: Covering novel therapeutic indications.

Key Point: The differentiation between independent and dependent claims in EA027869 determines the breadth of protection. Independent claims typically establish the core inventive concept, while dependent claims add further limitations or embodiments.


Analysis of Patent Claims:

  1. Core Chemical Compound or Structure:
    The primary claim in EA027869 likely identifies a unique chemical entity or class of compounds with specific structural features. Such claims aim for broad protection covering all variations within a certain structural framework, often using Markush groups, R-groups, or other generic descriptors.

  2. Therapeutic Application Claims:
    Possible inclusion of claims directed at methods of treating particular diseases or conditions, which substantiate inventive step and clinical relevance.

  3. Synthesis and Formulation Claims:
    Claims may detail novel synthetic routes or formulations that enhance bioavailability, stability, or patient compliance.

  4. Combination and Use Claims:
    Optional claims might specify synergistic combinations or novel therapeutic uses, expanding scope in follow-up embodiments.

Risk of Overbreadth:
In the EAPO context, claims that are overly broad—covering generic chemical classes without sufficient structural limitations—may face validity challenges, especially if prior art demonstrates earlier analogous compounds.


Patent Landscape: Strategic Positioning and Comparative Analysis

Regional Trends and Patent Filing Patterns

  • Major Players:
    Multinational pharmaceutical firms and regional biotech companies actively seek patent protection in Eurasia, targeting both core compounds and incremental innovations.

  • Patent Clusters:
    EA027869 fits within a landscape of patents covering therapeutics such as kinase inhibitors, monoclonal antibodies, or novel small molecules, depending on its chemical class.

Prior Art Considerations

Understanding the scope of EA027869 requires comparing its claims with prior art:

  • Existing Patents & Publications:
    Prior art searches in patent databases (e.g., World Intellectual Property Organization, Russian Patent Office) reveal similar compounds or methods, informing the novelty and inventive step assessments.

  • Potential Overlap:
    If similar compounds or methods are documented, EA027869’s claims may be narrowed during examination, or challenged via post-grant procedures.

Patent Family and International Strategy

  • Filing Strategy:
    Many applicants file in Eurasia to secure regional rights, followed by PCT international filings, to maximize global coverage.

  • Patent Family Size:
    A broad family signals an intent to defend combinations of compounds, formulations, or uses across key markets, potentially making EA027869 part of an active patent portfolio.


Legal Robustness and Enforcement Potential

  • Claim Validity:
    The strength of EA027869’s claims hinges on novelty, inventive step, and industrial applicability, confirmed through examination reports and opposition proceedings.

  • Enforceability:
    Given the Eurasian jurisdiction, enforcement involves national courts that recognize Eurasian patents; patent holders often face challenges from generic manufacturers, especially if claims are deemed overly broad or non-inventive.

  • Infringement Risks:
    Companies developing compounds similar to EA027869 must scrutinize claim language—particularly, whether their products encroach upon the patent’s scope.


Concluding Insights: Strategic Implications

EA027869 operates within a competitive and dynamic Eurasian patent landscape. Its scope appears to focus on specific chemical entities with supporting method claims, aligning with standard pharmaceutical patent strategies. Its strength depends upon the breadth of claims, prior art landscape, and ongoing patent prosecution or opposition proceedings.

For pharmaceutical entities, understanding the precise scope is essential for designing around strategies, licensing negotiations, or evaluating freedom-to-operate. The regional landscape underscores the importance of comprehensive patent landscaping and continued monitoring for similar or overlapping patents.


Key Takeaways

  • Claim Scope Defines Exclusivity:
    EA027869’s protection hinges on the specificity of its chemical and application claims. Broader claims can provide significant market barriers, but risk invalidation if overly ambitious.

  • Patent Landscape is Competitive:
    The Eurasian patent space is densely populated with similar innovations; thorough patent landscaping is essential for strategic decision-making.

  • Prior Art and Examination Outcomes Matter:
    Patent validity remains subject to prior art challenges. Ongoing legal challenges, opposition procedures, or reexaminations could influence enforceability.

  • Regional Strategy is Critical:
    EA027869 exemplifies a regional patent protection approach, emphasizing the importance of Eurasia’s emerging market status for pharmaceutical patent rights.

  • Continual Monitoring Ensures Competitive Edge:
    Regular surveillance of patent filings, litigations, and legal updates in Eurasia is vital for informed R&D and commercialization decisions.


FAQs

  1. What types of claims does EA027869 most likely include?
    It likely encompasses compound claims (covering specific chemical structures), method of use claims (therapeutic applications), and possibly formulation or synthesis claims.

  2. How does the Eurasian Patent Office assess the novelty of pharmaceutical claims?
    Based on the Eurasian Patent Convention, claims must be novel and inventive relative to prior art, which includes prior patents, scientific literature, and existing public knowledge.

  3. Can a patent like EA027869 be challenged after grant?
    Yes. Post-grant opposition or nullity proceedings can challenge validity if prior art is uncovered or if claims are found to lack novelty or inventive step.

  4. How does the patent landscape affect drug development in Eurasia?
    It influences strategic decisions on innovation focus, licensing, and FTO analyses; overlapping patents can hinder or delay entry into the market.

  5. What are the benefits of securing Eurasian patent rights through patents like EA027869?
    Regional protection in key Eurasian markets, deterrence against infringers, and leverage for licensing or partnership negotiations.


References

[1] Eurasian Patent Office (EAPO). "Patents in the Eurasian Patent Organization." Available at: https://www.eapo.org.
[2] WIPO. "Eurasian Patent Organization (EAPO) Patent Landscape." Accessible via WIPO Patent Landscape Reports.
[3] PatentScope. "Patent Data and Search Tools."
[4] Russian Federal Institute of Industrial Property (ROSPATENT). Patent examination and legal framework.
[5] Relevant legal texts: Eurasian Patent Convention (EAPC).


Disclaimer: This analysis is based on publicly available data and general patent practices within the Eurasian jurisdiction. For detailed legal advice or specific patent content interpretation, consultation with a patent attorney or direct access to patent application documents is recommended.

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.