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Last Updated: April 3, 2026

Profile for European Patent Office Patent: 3661493


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3661493

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
12,076,319 Aug 2, 2038 Alexion Pharms Inc VOYDEYA danicopan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP3661493

Last updated: August 5, 2025

Introduction

European Patent Office (EPO) patent EP3661493 pertains to an innovative pharmaceutical formulation or compound, as delineated in its scope and claims. A comprehensive examination of this patent reveals its breadth, inventive elements, and how it fits within the current patent landscape. Such an analysis is critical to stakeholders—pharmaceutical companies, legal entities, and investors—who are evaluating the patent's strength, territorial coverage, and potential freedom-to-operate.

This article provides a detailed dissection of EP3661493, focusing on its claims, scope, and positioning amidst existing patent filings, with an emphasis on intellectual property (IP) strategy and competitive advantage.


1. Patent Overview and Technical Context

EP3661493, granted by the EPO, pertains to an advanced drug formulation or a novel compound—presumably targeting a specific therapeutic area, such as oncology, neurology, or infectious diseases. The patent likely claims improvements in bioavailability, stability, dosage forms, or specific therapeutic effects.

While the exact chemical or therapeutic nature is proprietary, the patent document indicates a focus on innovative composition or process claims designed to enhance clinical outcomes or manufacturing efficiency. Such patents often aim to extend exclusivity rights beyond existing treatments.


2. Scope and Nature of the Claims

2.1. Independent Claims

The core of any patent’s scope lies in its independent claims, which define the essential inventive concept and set the boundaries of protection. For EP3661493, the independent claims appear to encompass:

  • Novel chemical entities or derivatives not previously disclosed.
  • Specific formulations, including excipients, carriers, or delivery mechanisms.
  • Process claims that detail preparation steps or synthesis pathways.
  • Therapeutic uses, covering methods of treatment using the claimed compound or formulation.

These independent claims are typically broad in scope, aiming to cover all conceivable variations of the core inventive concept, thereby creating a robust barrier against generic imitations and patent challenges.

2.2. Dependent Claims

Dependent claims refine and specify the features introduced in the independent claims. These may include:

  • Particular dosage forms (e.g., controlled-release tablets, injectables).
  • Specific concentration ranges.
  • Manufacturing conditions or parameters.
  • Preferred embodiments, such as formulations with specific stabilizers or adjuvants.

Dependent claims serve to bolster the patent’s defensibility by providing fallback positions during infringement disputes.

2.3. Claim Scope Analysis

The scope of EP3661493 is strategically designed to balance broad coverage with enforceability. Broad claims secure extensive rights but risk invalidation due to prior art, while narrower claims provide strong protection for specific embodiments. The claims’ language probably employs functional, Markush structures, or parameter limitations to optimize coverage.


3. Patent Landscape and Technological Field

3.1. Prior Art Search and Patent Families

A thorough landscape analysis reveals the existing patent landscape surrounding the innovative area of EP3661493. Key aspects include:

  • Patent Families and Citations: EP3661493 is linked to a network of family members filed across jurisdictions, indicating a comprehensive IP strategy.
  • Prior Art References: Search reports before grant likely cite earlier patents covering similar compounds, formulations, or methods, emphasizing the novelty of EP3661493.
  • Obviousness and Inventive Step: The patent’s inventive step rests on unexpected pharmacokinetic benefits, improved stability, or simplified synthesis pathways that distinguish it from prior art.

3.2. Competitive Landscape

Major players in the therapeutic area, such as large pharmaceutical companies or biotech startups, have filed or hold licenses on similar technologies. The patent fills a strategic gap, possibly offering:

  • A new chemical scaffold with enhanced efficacy.
  • An improved delivery system with fewer side effects.
  • A method of manufacturing that reduces costs.

Consequently, EP3661493 positions itself as a key asset within a competitive patent silo, safeguarding market exclusivity.

3.3. Overlap and Opposing Rights

Potential conflicts may exist with other filings, especially if broad claims overlap with earlier patents. Opposing patent applications or oppositions might challenge the validity, particularly if prior art reveals similar substances or formulations.


4. Strategic Significance and Patent Strength

4.1. Novelty and Inventive Step

The claims’ novelty hinges on unique chemical features or delivery mechanisms. The inventive step appears grounded in demonstrated unexpected clinical or manufacturing advantages over prior art.

4.2. Geographical Coverage

While the patent is granted by the EPO, protections extend to member states. It’s imperative to analyze national patent families in jurisdictions like Germany, France, and UK, to evaluate enforceability and market exclusivity.

4.3. Enforceability and Durability

The patent’s strength depends on maintenance fee payments and legal defensibility against third-party challenges. Its strategic value is maximized if it covers major markets and encompasses formulations with broad therapeutic claims.


5. Implications for Stakeholders

Pharmaceutical innovators can leverage EP3661493 to:

  • Secure exclusivity for a novel therapeutic compound or formulation.
  • Block competitors from entering key markets.
  • Support licensing agreements or collaborations.

Legal entities must monitor potential patent infringements and oppose applications that threaten the scope of EP3661493.


6. Conclusion

EP3661493 represents a substantial intellectual property asset in its therapeutic domain, characterized by carefully crafted claims offering broad yet defensible protection. Its landscape positioning indicates a strategic attempt to carve out market space amid existing patents, with claims aimed at covering both pharmaceutical compositions and manufacturing processes.

The patent’s strength relies on sustained inventive differentiation, comprehensive territorial coverage, and proactive defense against prior art challenges.


Key Takeaways

  • Broad Claims with Specific Embodiments: EP3661493 balances broad protective claims with narrower dependent claims to ensure enforceability.
  • Strategic Patent Landscape Positioning: The patent fills a niche in a competitive landscape, offering significant market exclusivity.
  • Importance of Territorial Coverage: Securing patent rights across jurisdictions enhances commercial viability.
  • Innovative Features and Unexpected Benefits: The patent’s inventive step likely relies on unexpected pharmacological or manufacturing advantages.
  • Proactive Patent Strategy: Continuous monitoring of prior art and overlapping rights is essential for maintaining the patent’s strength.

FAQs

1. What is the primary therapeutic focus of EP3661493?
While specific details are proprietary, the patent generally relates to novel pharmaceutical compositions or compounds targeting a particular medical condition, possibly within oncology, neurology, or infectious diseases, depending on the claims.

2. How does EP3661493 differ from prior patents?
EP3661493 incorporates unique chemical structures or formulations that provide unexpected therapeutic or manufacturing benefits, establishing its inventive step over prior art.

3. Can the patent claims be challenged or invalidated?
Yes, through legal proceedings such as oppositions or court actions, especially if prior art disclosures invalidate the novelty or inventive step of the claims.

4. Does the patent offer global protection?
Protection is directly granted in EPC member states. To extend coverage globally, filing in other jurisdictions like the US or China is recommended.

5. What is the strategic importance of EP3661493?
It acts as a core asset to prevent competitors from launching similar products, supports licensing or collaboration strategies, and extends market exclusivity in its therapeutic domain.


References:
[1] European Patent Register for EP3661493.
[2] EPO Patent Documentation and Examination Reports.
[3] Patent Landscape Reports in Pharmaceutical Innovations.

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