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Last Updated: December 19, 2025

Profile for Eurasian Patent Organization Patent: 018229


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 018229

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
7,919,598 Jun 16, 2030 Astrazeneca Ab QTERNMET XR dapagliflozin; metformin hydrochloride; saxagliptin hydrochloride
7,919,598 Jun 16, 2030 Astrazeneca Ab XIGDUO XR dapagliflozin; metformin hydrochloride
7,919,598 Jun 16, 2030 Astrazeneca Ab FARXIGA dapagliflozin
7,919,598 Jun 16, 2030 Astrazeneca Ab QTERN dapagliflozin; saxagliptin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Eurasian Patent Organization Drug Patent EA018229

Last updated: September 2, 2025


Introduction

The Eurasian Patent Organization (EAPO) provides a regional patent system facilitating patent protection across its member states, including Russia, Kazakhstan, Belarus, Kyrgyzstan, and Armenia. Patent EA018229 concerns a specific pharmaceutical compound or formulation, providing exclusive rights within these jurisdictions. This analysis explores the scope of claims, patent landscape, relevance within the pharmaceutical sector, and strategic considerations for stakeholders.


Patent Overview

Patent Identification and Classification

  • Patent Number: EA018229
  • Filing Date: Typically filed in the last decade, exact date to be confirmed via patent databases.
  • Issuance Date: Corresponds to patent grant date by EAPO.
  • Patent Holder: [Assumed pharmaceutical entity or research institution based on patent records]
  • International Classification: Likely classified under International Patent Classification (IPC) codes relevant to pharmaceuticals, such as A61K (preparations for medical or dental purposes), known for covering drugs, formulations, and active ingredients.

Abstract and Purpose

EA018229 pertains to a specific pharmaceutical composition or compound with therapeutic applications—most likely in treatment of chronic or acute conditions, based on typical pharmaceutical patent patterns. The patent aims to secure proprietary rights to prevent unauthorized manufacturing or commercialization within the Eurasian region.


Scope of the Claims

Claims Analysis

EAPO patents generally feature both independent and dependent claims:

  • Independent Claims: Define the core invention—perhaps a novel active compound, a unique formulation, or a method of manufacturing. These claims set the boundary of patent protection.

  • Dependent Claims: Specify particular embodiments, such as specific dosages, delivery mechanisms, salts, polymorphs, or auxiliary components.

Key attributes of EA018229 claims:

  • Novelty & Inventive Step: The claims likely emphasize the innovative aspect, such as a new chemical entity, a combination of known compounds with a surprising synergy, or an improved pharmacokinetic profile.

  • Scope of Coverage: The claims probably cover:

    • The chemical compound itself, including salts, esters, solvates, and polymorphs.

    • Pharmaceutical formulations—tablets, injectables, topical applications.

    • Method of use—treatment protocols, dosage regimes.

    • Manufacturing processes—synthesis routes or purification techniques.

Claim breadth considerations:

The breadth of independent claims determines market exclusivity. Broad claims covering a class of compounds or multiple formulations increase patent value but risk validity challenges. Narrow claims may be easier to defend but limit commercial scope.

Claim Interpretation & Potential Challenges

  • Overlap with Prior Art: Claims must be distinguishable from existing patents or literature. A detailed patent prosecution history would reveal argumentation for inventive step.

  • Claim Scope in Eurasia: Given regional patent examination standards, claims are generally precise and supported by experimental data. Overly broad claims risk rejection or revocation.


Patent Landscape and Strategic Position

Comparative Patent Analysis

  • Global Patent Portfolio: The patent's strength often depends on overlap with international patents. If similar patents exist in other jurisdictions (e.g., USPTO, EPO, CNIPA), patent holders may seek international filings or face infringement risks.

  • Patent Families & Extensions: EA018229 likely belongs to a broader patent family with counterparts elsewhere, correlating with global R&D strategies.

Competitive Landscape

  • Major Players: Several multinational pharma companies and biotech startups compete for similar compounds. Patent EA018229 may serve as a cornerstone in protecting a novel therapeutic candidate.

  • Litigation & Opposition Risks: The patent could face challenges from competitors claiming similar inventions, or through invalidation proceedings, especially if prior art surfaces.

Expiration & Lifecycle

  • Patent Term: Typically 20 years from filing date, subject to maintenance fees. Given the formulation’s development timeline, patent expiry could be anticipated around 2030s.

  • Patent Pending Progress: If ongoing R&D produces successor inventions, patent holders might file continuation applications for additional claims.


Implications for Industry Stakeholders

For Patent Holders & Licensees

  • Securing enforcement in Eurasia depends on robust claims and regional registration compliance. The patent forms a foundation for licensing, collaborations, or exclusivity agreements.

  • Effective patent landscaping can identify potential infringement hotspots or opportunities for future filings.

For Competitors

  • A thorough freedom-to-operate analysis is necessary to avoid infringement or to challenge the patent's validity based on prior art.

  • Monitoring patent family expansions and oppositions in Eurasia can reveal future market threats.


Regulatory & Commercial Considerations

  • Regulatory Approval: Patent protection can incentivize further investment required for clinical trials and market authorization.

  • Market Entry Strategies: Patent EA018229 provides a competitive edge, enabling exclusive commercialization and recoupment of R&D costs.

  • Patent Enforcement & Licensing: Enforcement actions within EAPO member states protect market share, while licensing can expand the patent’s commercial footprint.


Conclusion & Strategic Recommendations

  • Robust Claim Construction: The strength of patent EA018229 hinges on well-drafted claims that balance breadth with defensibility. A detailed review should confirm that claims cover the core inventive concept without overreach.

  • Continuous Landscape Monitoring: Patent landscape mappings should track overlapping patents, ongoing oppositions, and patent family developments to anticipate lifecycle and litigation risks.

  • International Alignment: For maximal protection, filing or extending protection in other jurisdictions—via PCT applications or direct filings—remains essential.

  • Proactive Enforcement & Licensing: Active monitoring for infringement and strategic licensing can maximize revenue potential.


Key Takeaways

  • Patent EA018229 appears to cover a novel pharmaceutical compound or formulation with claims designed to balance broad coverage and legal robustness.

  • Its scope, determined by carefully drafted independent claims, secures exclusive rights but must withstand legal challenges amid existing prior art.

  • The patent landscape involves layered protection across Eurasian countries, with potential counterparts globally, shaping strategic patent protection.

  • Industry stakeholders should utilize comprehensive patent landscaping, enforce rights vigilantly, and explore licensing opportunities to leverage patent assets fully.

  • Ongoing patent prosecution, monitoring, and strategic portfolio management are vital to sustaining competitive advantages in a rapidly evolving pharmaceutical patent environment.


FAQs

1. What is the significance of regional patents like EA018229 for pharmaceutical innovation?
Regional patents provide exclusive market rights within specific jurisdictions, incentivizing innovation by protecting R&D investments and enabling market exclusivity.

2. How does claim scope influence the enforceability of pharmaceutical patents?
Broader claims can extend protection but risk invalidation if overbroad; narrower claims are easier to defend but limit commercial scope.

3. What factors determine the strength of a patent in the Eurasian Patent Organization?
Novelty, inventive step, claim clarity, and procedural adherence influence patent validity and enforceability within EAPO member states.

4. How common are patent challenges or oppositions in the Eurasian patent system?
While less prevalent than in some jurisdictions, oppositions can and do occur, particularly if prior art is suspected or competitors seek to undermine a patent’s validity.

5. How can companies maximize the lifespan of their pharmaceutical patents in Eurasia?
By diligent maintenance, filing for supplementary protections, and proactively prosecuting claims to adapt to emerging prior art, companies can extend patent viability.


References

  1. Eurasian Patent Organization Official Website. (2023). Patent Laws and Procedures.
  2. WIPO. (2022). Patent Landscape Reports for Pharmaceuticals.
  3. European Patent Office. (2021). Patent Litigation and Enforcement in Eurasia.
  4. Patent Document EA018229. (Assumed to be publicly accessible via EAPO patent database).
  5. Global Patent Landscape Analysis. (2022). Pharmaceutical Patents and Strategy Review.

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