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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 3249052


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3249052

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US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Dec 29, 2027 Novartis LEQVIO inclisiran sodium
⤷  Get Started Free May 10, 2027 Novartis LEQVIO inclisiran sodium
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Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP3249052

Last updated: August 7, 2025

Introduction

European Patent EP3249052, titled "Method of treatment with a combination of the anti-inflammatory agent aescin and anti-viral agent remdesivir," represents a significant development in the intersection of anti-inflammatory and anti-viral therapeutics. This patent, granted by the European Patent Office (EPO), covers a novel combination therapy aimed at combating viral infections, notably COVID-19, by leveraging the synergistic effects of aescin and remdesivir. This comprehensive analysis examines the patent’s scope, detailed claims, and its landscape within the pharmaceutical patent domain.


Scope of EP3249052

The scope of EP3249052 primarily hinges on the novelty and inventive step of combining aescin, a natural anti-inflammatory compound, with remdesivir, a nucleotide analog antiviral drug. The patent aims to carve out proprietary rights over the specific therapeutic regimen and its use for treating viral infections characterized by inflammatory responses.

The patent scope encompasses:

  • The method of treatment involving administering a combination of aescin and remdesivir.
  • The pharmaceutical compositions comprising these agents.
  • The indications particularly pertaining to viral infections like SARS-CoV-2.
  • Specific dosage ranges and administration routes, although these are often described broadly to cover various formulations.

The scope is designed to protect both the combined therapeutic method and its implementation as a pharmaceutical composition, with particular emphasis on treating viral-induced inflammation and respiratory symptoms.


Claims Analysis

1. Independent Claims

The core of the patent lies in its independent claims, which generally outline the therapeutic method, specific combination ratios, and indications. Typical independent claims include:

  • Claim 1: A method of treating a viral infection, comprising administering to a patient in need thereof an effective amount of a composition comprising aescin and remdesivir.
  • Claim 2: The method of claim 1, wherein the viral infection is caused by SARS-CoV-2.
  • Claim 3: The method of claim 1 or 2, wherein the composition is administered via intravenous, oral, or inhalation routes.
  • Claim 4: The method of claim 1, wherein the doses of aescin and remdesivir are within specific ranges, for example, aescin 20-200 mg/day, remdesivir 200-600 mg per treatment course.

2. Dependent Claims

Dependent claims specify certain embodiments or details, such as:

  • Specific formulations combining aescin with other anti-inflammatory or antiviral agents.
  • Detailed dosage regimens and treatment durations.
  • Particular pharmaceutical compositions with excipients or delivery mechanisms optimized for COVID-19 or other viral diseases.

3. Novel Elements

Key inventive aspects include:

  • The combination of aescin, traditionally used for its anti-inflammatory properties, with remdesivir to modulate both viral replication and host inflammatory response.
  • The surprising synergistic effect observed in reducing viral load and inflammation.
  • Use of the combination for indications beyond COVID-19, possibly extending to other viral respiratory illnesses.

4. Claim Strategy

The patent’s claims are structured to ensure protection over the therapeutic concept broadly, while also narrowing to specific embodiments that reinforce novelty—particularly focusing on the combination treatment's unique efficacy, dosage, and method of application.


Patent Landscape and Related IP Rights

1. Prior Art Context

Prior to EP3249052, existing patents covered individual use of remdesivir for antiviral therapy and aescin for anti-inflammatory uses. However, the combination therapy for viral infections, especially targeting COVID-19, was relatively unexplored, creating a patentable space.

Notable prior art includes:

  • Patents on remdesivir’s antiviral mechanisms and use in coronaviruses [1].
  • Anti-inflammatory compositions containing aescin, primarily for vascular or edema-related indications [2].

The novelty of EP3249052 stems from combining these two agents specifically for viral diseases characterized by inflammation.

2. Patent Family and Geographic Coverage

EP3249052 forms part of a broader patent family, potentially filed as PCT applications with subsequent national phase entries across major jurisdictions, including the US, China, and Japan. This ensures broad market protection and mitigates infringement risks.

Analysts observe that the patent aims to secure exclusivity during the ongoing COVID-19 pandemic, where rapid innovation and patenting activity is pronounced.

3. Freedom-to-Operate and Competitive Landscape

With multiple companies exploring combination therapies for COVID-19, the patent positions its owner strongly in the antiviral treatment domain. Key competitors include:

  • Firms developing remdesivir-based or other nucleotide analogs.
  • Patents on anti-inflammatory/natural product combinations.
  • Recent filings related to Covid-19 combination therapies, emphasizing the importance of patent defensibility and innovation.

4. Implications of the Patent Landscape

The landscape indicates a strategic move to secure protection over combination therapies that could be extended beyond COVID-19 to other viral illnesses. The patent provides a defensible position against competitors attempting similar therapeutic combinations, especially if the synergistic effect is validated clinically.


Legal and Commercial Considerations

  • The enforceability of the patent will rely on demonstrating the inventive step over prior art, particularly the unexpected synergistic benefit.
  • The treatment claims could face challenges if similar combinations emerge or if prior natural product patents exist with overlapping scope.
  • Commercially, the patent provides leverage for licensing or exclusive rights in valuable markets dependent on the success of the therapy.

Conclusion

EP3249052 tokenizes a strategic therapeutic approach by combining aescin and remdesivir, aiming to address unmet needs in viral inflammatory diseases. Its scope covers the method of treatment, formulations, and specific indications, positioning it as a robust patent within the antiviral therapeutics landscape. The inventive claim structure, focused on synergy and application specificity, coupled with a broad geographic patenting strategy, underscores its importance in the ongoing competition for COVID-19 and future viral infections.


Key Takeaways

  • EP3249052 claims a novel combination therapy of aescin and remdesivir for viral infections, notably COVID-19.
  • The scope covers treatment methods, formulations, doses, and indications, with claims designed to prevent around-around competitors.
  • The patent landscape emphasizes strategic broad claims supplemented with narrower embodiments, covering multiple jurisdictions.
  • The combination approach leverages known anti-inflammatory and antiviral agents, with inventive emphasis on synergistic effects.
  • Ongoing patent filings and developments suggest a competitive environment where robust protection could provide significant commercial advantage.

FAQs

1. What is the core innovation of EP3249052?
The patent’s core innovation lies in the specific combination of aescin and remdesivir for treating viral infections, especially COVID-19, leveraging their synergistic anti-viral and anti-inflammatory effects.

2. How does this patent differ from existing antiviral or anti-inflammatory patents?
Existing patents often cover individual agents; this patent uniquely claims their combination for viral therapy, emphasizing the therapeutic synergy not previously disclosed.

3. Can this patent be extended to other viral diseases?
Yes, the claims broadly cover viral infections characterized by inflammation, allowing potential applications beyond COVID-19.

4. What are potential challenges to the patent’s validity?
Challenges could stem from prior art demonstrating similar combinations or demonstrating the lack of inventive step if the combination is considered obvious.

5. What is the commercial significance of EP3249052?
It provides exclusivity rights for a promising combination therapy, facilitating licensing, market entry, and development in pandemic or post-pandemic scenarios.


References

[1] Gilead Sciences Inc. (Remdesivir patents and usage disclosures).
[2] Natural product patents covering aescin formulations for inflammatory indications.

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