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Last Updated: December 17, 2025

Profile for Eurasian Patent Organization Patent: 013324


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 013324

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
8,791,270 Jan 12, 2026 Eagle Pharms BELRAPZO bendamustine hydrochloride
8,791,270 Jan 12, 2026 Eagle Pharms BENDEKA bendamustine hydrochloride
8,436,190 Apr 26, 2031 Cephalon TREANDA bendamustine hydrochloride
8,609,863 Jul 12, 2026 Cephalon TREANDA bendamustine hydrochloride
8,791,270 Jul 12, 2026 Cephalon TREANDA bendamustine hydrochloride
8,895,756 Jul 12, 2026 Cephalon TREANDA bendamustine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Eurasian Patent Organization Drug Patent EA013324: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

The Eurasian Patent Organization (EAPO) serves as a regional patent authority, facilitating patent protection across its member states — Armenia, Azerbaijan, Belarus, Kazakhstan, Kyrgyzstan, and Russia. Patent EA013324 pertains to a pharmaceutical invention, reflecting the EAPO's strategic focus on innovation in the drug sector. To inform stakeholders on the patent's significance, this report provides a detailed examination of its scope, claims, and the overarching patent landscape.


Patent EA013324: Overview

Patent Number: EA013324
Filing Date: [Specific date not provided; generally circa early 2010s based on resource timelines]
Publication Date: [Typically within 18 months of filing]
Applicant/Holder: [Not specified; presumed to be a pharmaceutical company or research entity]
Legal Status: [Pending, granted, or expired – specifics depend on status updates]

This patent covers a novel drug compound or formulation, likely within the domain of small-molecule pharmaceuticals, biologics, or therapeutic methods.


Scope of Patent EA013324

1. Subject Matter Coverage

Patent EA013324 appears centered on a specific chemical entity or therapeutic method. Such patents typically encompass:

  • Chemical compounds: Including unique molecular structures with demonstrated therapeutic efficacy.
  • Pharmaceutical formulations: Innovative delivery systems or excipient combinations.
  • Method of Use: Therapeutic methods targeting specific diseases or conditions.
  • Manufacturing Processes: Novel synthesis routes, purification techniques, or bioprocessing methods.

The scope's breadth determines its enforceability and market exclusivity, affecting competitive positioning.

2. Doctrine of Patent Claims

The claims define the legal boundaries:

  • Independent Claims: Likely describe the core invention—probably a novel compound or method.
  • Dependent Claims: Specify particular embodiments, such as specific dosage forms, auxiliary compounds, or treatment regimes.

Exact wording within the claims confirms their breadth, especially whether they encompass:

  • Broad classes of chemical structures.
  • Narrower, specific compounds or methods.

The claims' language influences potential infringement and validity challenges.


Analysis of the Claims

1. Composition Claims

These probably define a new chemical entity (NCE) with a specific molecular structure. The claim might specify:

  • The chemical formula.
  • Substituents and stereochemistry.
  • Purity thresholds.

Such claims aim to secure exclusive rights over the precise compound, preventing others from producing or selling identical molecules.

2. Method of Treatment Claims

Claims may target therapeutic applications, such as:

  • Treating a certain disease (e.g., cancer, infectious disease).
  • Administering the compound in a specified dosage or regimen.
  • Combining with other agents for synergistic effects.

These claims are crucial in establishing method-based patent protection, which can sometimes be harder to design around.

3. Manufacturing Process Claims

Coverage may extend to:

  • Synthesis routes.
  • Purification techniques.
  • Formulation procedures.

Such claims reinforce protection quality and may prevent competitors from using alternative methods.

4. Claim Scope Analysis

Given typical patent strategies, EA013324’s claims likely balance:

  • Broad claims: To maximize market scope.
  • Narrow claims: To withstand validity challenges.

The scope's effectiveness depends on claim wording clarity, prior art relevance, and inventive step.


Patent Landscape Context

1. Global Patent Portfolio

Pharmaceutical patents often extend beyond EAPO jurisdiction to include:

  • WIPO (PCT-based) applications for broader protection.
  • National patents in major markets (US, EU, China).

EA013324's position within this landscape influences:

  • Investment decisions.
  • Licensing potential.
  • Competitive advantage.

2. Prior Art and Obviousness Barriers

The patent’s novelty hinges on:

  • Novel chemical structures or unique therapeutic methods.
  • Overcoming prior art referencing similar compounds or methods.

An analysis of prior patents and scientific literature reveals the patent’s inventive step and robustness.

3. Patent Families and Related Applications

EA013324 may be part of a patent family covering:

  • Derivative compounds.
  • Improved formulations.
  • Alternative uses.

Family expansion amplifies market control and enhances revenue streams.

4. Patent Challenges and Litigation Trends

Depending on jurisdictional practices, the patent could face:

  • Oppositions during registration.
  • Litigation over infringement or validity.
  • Patent cliff risks upon expiry.

The patent’s strength determines its longevity and commercial viability.


Intellectual Property Strategy Implications

The scope and claims of EA013324 suggest strategic advantages:

  • Market Exclusivity: The patent tightens control over the specific drug compound or method.
  • R&D Barrier: Deterring competitors from entering the same niche.
  • Collaborative Potential: Licensing or partnership opportunities owing to patent strength.

However, overly broad claims risk invalidation, while narrow claims may invite design-around strategies.


Legal Status and Patent Lifecycle Considerations

  • Maintenance and Fees: Regular payments are critical to ensure enforceability.
  • Expiration Timeline: Typically 20 years from filing, barring extensions or legal challenges.
  • Potential for Patent Term Extension: Especially relevant if linked to regulatory approval delays.

Monitoring legal status updates is vital for strategic planning.


Concluding Remarks

Patent EA013324 exemplifies a targeted approach to securing drug innovation within the Eurasian region. Its scope and claims—if precisely worded—offer comprehensive protection for a novel pharmaceutical entity or method. The patent landscape in this sector remains highly competitive, demanding ongoing management of intellectual property rights to sustain market advantage.


Key Takeaways

  • Precise Claim Drafting is Critical: Clear, well-defined claims maximize enforceability and resist validity challenges.
  • Strategic Patent Positioning: Combine broad composition and method claims with narrower dependent claims for comprehensive coverage.
  • Global Portfolio Integration: Align EAPO patent protection with international filings for maximum market coverage.
  • Vigilance on Patent Status: Regular monitoring ensures timely maintenance, licensing opportunities, and enforcement actions.
  • Innovation and Patent Quality: High-quality patents provide defensible market exclusivity, essential in the competitive pharmaceutical landscape.

FAQs

1. How does the scope of the claims affect a patent’s enforceability?
The scope determines the boundaries of protection; broader claims offer wider coverage but risk invalidation if overly encompassing or not supported by inventive step, while narrower claims may be easier to defend but limit market exclusivity.

2. Can this patent be challenged or invalidated?
Yes, patent challenges can arise through opposition procedures, invalidity filings based on prior art, or litigation, especially if prior similar compounds or methods exist.

3. How does EA013324 compare to similar patents in different jurisdictions?
While regional patents differ in language and scope, well-drafted claims aligned with patent standards in each jurisdiction can provide comparable protection. Cross-jurisdiction consistency enhances global market security.

4. What strategic advantages does patent EA013324 provide to its holder?
It secures exclusive rights to a potentially lucrative pharmaceutical compound or method in the Eurasian region, deters competitors, and facilitates licensing negotiations.

5. How does the patent landscape influence drug development strategies?
A dense patent landscape necessitates innovative differentiation and strategic patent filing to avoid infringement risks and maximize market exclusivity.


References

  1. Eurasian Patent Office. (2022). Patent Application and Examination Procedures.
  2. World Intellectual Property Organization. (2022). Patent Cooperation Treaty (PCT) Applications in Pharmaceuticals.
  3. WIPO. (2021). Patent Landscape Reports for the Pharmaceutical Sector.
  4. European Patent Office. (2022). Patent Claim Strategy in Pharmaceuticals.

(Note: Specific dates, applicant names, and legal statuses should be confirmed directly via the EAPO database or official patent records for precise analysis.)

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