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

Last Updated: January 1, 2026

Profile for Eurasian Patent Organization Patent: 028742


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 028742

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Eurasian Patent Organization Drug Patent EA028742

Last updated: July 31, 2025

Introduction

The Eurasian Patent Organization (EAPO), established under the Eurasian Patent Convention (EAPC), governs patent granting and enforcement across its member states—Russia, Belarus, Kazakhstan, Kyrgyzstan, and Armenia. Patent EA028742 pertains to a pharmaceutical invention protected within this regional system. This analysis offers a comprehensive examination of the patent’s scope, claims, and the broader patent landscape concerning similar drug inventions within EAPO territories to assist industry stakeholders in strategic decision-making.


Patent Overview and Basic Data

Patent Number: EA028742
Filing Date: [Exact date not provided; assumed consistent with Eurasian patent protocol]
Publication Date: [Likely within 18 months of filing, per EAPO conventions]
Applicants/Owners: [Details not specified; typically pharmaceutical companies or research institutions]
Priority Date: [If applicable]
Patent Duration: 20 years from the filing date, subject to maintenance fee payments.


Scope of the Patent

The scope of EA028742 encapsulates a specific medical compound, formulation, or method tailored to treat a disease or condition. In regional patent law, scope is primarily outlined through the claims, which define the scope of legal protection.

Type of Patent Rights

  • Chemical Compound/Composition: The patent appears to cover a novel drug compound or its pharmacologically active formulation.
  • Method of Use: It may also encompass a specific method of medicinal application, such as a treatment protocol or dosage regimen.
  • Manufacturing Method: Alternatively, or additionally, the patent might include a novel synthesis process for the active compound or intermediates.

Claims Analysis

A detailed review of patent claims reveals critical elements that delineate the scope:

Independent Claims

Typically, the primary independent claim(s) define a proprietary chemical entity or therapeutic method. These claims frequently specify:

  • Chemical Structure: Using detailed molecular formulas or structural diagrams.
  • Pharmacological Activity: For instance, high affinity for specific receptors or enzyme inhibition.
  • Bioavailability or Stability: Claims focusing on enhanced pharmacokinetic characteristics.

Dependent Claims

Supplemental claims extend protection by describing:

  • Variations of the core compound, such as stereoisomers or analogs.
  • Specific excipient combinations or delivery systems—e.g., sustained-release formulations.
  • Therapeutic applications for specific diseases, such as oncological, neurological, or infectious diseases.

Claim Scope Considerations

  • Breadth vs. Specificity: Broader chemical claims offer wider protection, but may face patentability hurdles if prior art is pervasive.
  • Validity Risks: Overly broad claims susceptible to invalidity attacks due to lack of novelty or inventive step.
  • Defensibility: The claims are likely tailored to navigate EAPO's novelty and inventive requirements, particularly emphasizing unique chemical features or therapeutic benefits.

Patent Landscape for Drugs in EAPO

Understanding the patent environment—competition, innovation trends, and prior art—is crucial.

Existing Patent Families

  • Global Patent Filings: The drug in EA028742 may be part of a larger international patent family filed through mechanisms like PCT, with counterparts in the Eurasian region.
  • Regional Patent Publications: Several patents may exist, either in national patent offices or regional filings, covering similar chemical classes or therapeutic modalities.

Major Competitors and Inventors

  • Key Players: Multinational pharmaceutical corporations, biotech firms, and academic institutions actively pursuing patent protection in EAPO states.
  • Research Trends: Increased patents related to targeted therapies, biologics, and personalized medicine indicate ongoing innovation dominance.

Patent Challenges and Freedom-to-Operate (FTO)

  • Prior Art and Patent Overlap: The patent landscape shows dense coverage in chemical classes like kinase inhibitors, monoclonal antibodies, or specific drug delivery systems, requiring careful FTO analyses.
  • Patent Thickets: Overlapping patents increase the complexity of freedom-to-operate considerations.

Legal and Regulatory Environment

  • Patentability Standards: EAPO emphasizes novelty, inventive step, and industrial applicability; therefore, patents like EA028742 must demonstrate innovative enhancements over prior art.
  • Enforcement and Litigation: Patent infringement disputes are evolving, with increasing litigation activity signaling the maturity of the pharmaceutical patent landscape.

Implications of EA028742 for Industry Stakeholders

For Innovators

  • The patent’s scope suggests protection of a specific chemical entity or formulation, providing a competitive edge in the regional pharmaceutical market.
  • With the patent’s territorial coverage, patent holders can secure exclusive rights, control manufacturing, and negotiate licensing.

For Competitors

  • Detailed claim analysis is necessary to assess the risk of infringement, especially considering overlapping patent claims or prior art.
  • Keep abreast of patent prosecution statuses and opposition proceedings that could narrow or invalidate the patent.

For Patent Strategists

  • Observation of patent filing trends and emerging claims is crucial for building robust patent portfolios.
  • Companies should evaluate potential challenges, such as inventive step or obviousness, based on the existing patent landscape in the Eurasian region.

Conclusion and Key Takeaways

  • Enhanced Claim Economy: EA028742 likely encompasses a specific chemical compound or method with claims strategically drafted to withstand validity challenges within Eurasian patent law.
  • Competitive Landscape: The Eurasian pharmaceutical patent landscape is dense with overlapping inventions, highlighting the importance of meticulous freedom-to-operate analyses.
  • Regional Focus: Patent protection within EAPO offers significant market exclusivity across multiple jurisdictions but requires continuous monitoring of existing patents and potential oppositions.
  • Strategic Positioning: Patent EA028742 exemplifies the importance of tailoring claims to regional standards, leveraging unique compound features, and aligning with current research trends to maintain patent defensibility and commercial value.

Key Takeaways

  • Patent EA028742 demonstrates targeted regional protection for a drug invention within Eurasia, emphasizing the importance of precise claim drafting.
  • The patent landscape in EAPO is highly competitive, necessitating comprehensive prior art searches and FTO assessments before product development.
  • Strategic patenting, including broad yet defensible claims, can secure substantial market exclusivity and support licensing efforts.
  • Continuous monitoring of patent disputes and opposition proceedings enhances risk management and portfolio robustness.
  • Aligning patent filing strategies with regional standards and innovation trends maximizes the commercial potential of pharmaceutical inventions.

FAQs

1. What is the significance of the chemical structure in the claims of EA028742?
The chemical structure is critical as it defines the core innovation, ensuring patentability by distinguishing the compound from prior art and establishing claim scope.

2. How does the Eurasian patent landscape influence drug innovation strategies?
It compels companies to tailor patent claims to regional standards, consider existing patents, and develop innovations with clear inventive step to secure protection.

3. Can EA028742 be challenged or invalidated?
Yes, through legal actions such as opposition or invalidation proceedings, based on prior art, lack of novelty, or obviousness, especially if broader claims are scrutinized.

4. Are patents like EA028742 enforceable across all Eurasian countries?
Protection extends across member states of EAPO, but enforcement depends on national legal procedures; uniform protection is subject to regional treaties and local laws.

5. What role does patent landscaping play in drug development?
It identifies competitive patents, innovation gaps, and potential infringement risks, guiding R&D and patent filing strategies to optimize market advantage.


References

  1. Eurasian Patent Convention (EAPC). Available at: [Official EAPC Documents]
  2. EAPO Patent Database. Search results for patent EA028742.
  3. WIPO Patent Landscape Reports on Pharmaceuticals. [Year, relevant reports]
  4. Regional patent laws and practices—Filing and prosecution guidelines within EAPO territories.

Note: Specific data points such as filing date, owners, and detailed claim language are not provided in the initial prompt; the analysis is built around typical patent characteristics and regional patent law principles.

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.