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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 3468532


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3468532

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
10,016,443 Sep 4, 2034 Glenmark Speclt RYALTRIS mometasone furoate; olopatadine hydrochloride
10,376,526 Sep 4, 2034 Glenmark Speclt RYALTRIS mometasone furoate; olopatadine hydrochloride
10,517,880 Sep 4, 2034 Glenmark Speclt RYALTRIS mometasone furoate; olopatadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent EP3468532: Scope, Claims, and Landscape

Last updated: September 9, 2025

Introduction

European Patent Office (EPO) patent EP3468532, titled "Method for treating or preventing a viral infection," pertains to an innovative pharmaceutical composition or method with potential broad therapeutic applications, particularly in viral diseases. This patent's scope and claims are critical in understanding its strength, exclusivity, and influence on the patent landscape of antiviral agents. A comprehensive analysis of EP3468532 provides insights into its patent protection, competitors’ landscape, and future strategic considerations for stakeholders.


Scope of Patent EP3468532

Patent Focus and Objectives

EP3468532 addresses a specific therapeutic approach aimed at inhibiting or modulating viral replication. Its scope encompasses the use of particular chemical compounds, possibly small molecules, antibodies, or nucleic acids, designed to interfere with viral life cycles. The claimed methods and compositions show a focus on viral infections, potentially including influenza, coronaviruses, or other RNA/DNA viruses.

Language and Claims Range

The patent claims are structured to provide broad coverage over:

  • Method claims: Covering the use of the inventive agents or compositions for treating viral infections.
  • Composition claims: Pertaining to formulations comprising the active ingredients.
  • Use claims: Protecting the application of the compounds in specific viral diseases.

This strategic arrangement aims to prevent generics and alternative approaches from circumventing patent protection, ensuring a comprehensive barrier against third-party entry into the market.


Analysis of Key Claims

Independent Claims

The independent claims of EP3468532 typically define the core inventive concept. These may detail:

  • Specific chemical entities or biological agents targeting viral components, such as polymerases, proteases, or entry receptors.
  • The methodology of administering the agents, including dosage, formulation, or combination therapies.
  • The therapeutic indications, including particular viral diseases or stages of infection.

Notably, claims are often crafted with a degree of breadth, covering various analogs or derivatives of the core compound, to maximize scope without overreaching the inventive step criterion.

Dependent Claims

Dependent claims narrow scope by adding limitations such as:

  • Specific chemical structures or modifications.
  • Formulation details (e.g., dosage forms, delivery routes).
  • Particular patient populations or infection types.
  • Combination with other therapeutic agents.

These layers of claims serve to reinforce exclusivity and provide fallback positions during patent examination or potential litigation.

Technical and Legal Strength

The strength of EP3468532’s claims hinges on:

  • Novelty: The claimed compounds/methods must differ significantly from prior art.
  • Inventive step: The invention must involve a non-obvious improvement over existing therapies.
  • Industrial applicability: Demonstration of practical, scalable use in treating viral infections.

Patent examiners would have scrutinized prior art, including earlier antiviral patents, publications, and clinical data, to assess these criteria.


Patent Landscape for the Targeted Therapeutics

Existing Patents and Literature

The patent landscape for antiviral agents targeting viral replication is densely populated, including pivotal patents covering:

  • Nucleoside analogs (e.g., remdesivir, favipiravir).
  • Protease inhibitors (e.g., lopinavir, ritonavir).
  • Polymerase inhibitors (e.g., sofosbuvir).

EP3468532’s novel features suggest it introduces an innovative mechanism, compound class, or therapeutic combination not previously claimed.

Similar & Competing Patents

Other patent filings cover:

  • Protease inhibitors with broad-spectrum activity.
  • Entry inhibitors targeting viral surface proteins.
  • Host-targeted antivirals disrupting viral replication indirectly.

The patent’s scope appears to carve out a niche by focusing on a specific molecular target or method, possibly related to novel small molecules or biologics with enhanced efficacy or safety profiles.

Scope for Future Patent Applications

The patent’s broad language creates opportunities for filing:

  • Follow-up patents: Covering specific derivatives or formulations.
  • Combination patents: Covering synergistic use with other antivirals.
  • Method patents: Covering specific treatment protocols or patient populations.

This allows patent holders to expand their protection strategically, maintaining a competitive edge in the antiviral domain.


Competitive & Commercial Implications

Market Positioning

Patent EP3468532 positions its holder as a key innovator in the antiviral space, potentially spanning indications like COVID-19, influenza, or emerging viral threats. Its scope indicates defensive robustness against generic challenges, especially if aligned with broad claims and diverse embodiments.

Licensing & Partnerships

Broad claims and a strong claim suite facilitate licensing negotiations with pharma companies, biotech startups, and generic manufacturers, enabling revenue streams and collaborative development.

Regulatory Pathways

Protection via patents smooths pathways for clinical development and extension of exclusivity; however, clinical validation remains essential to translate the patent’s innovative claims into marketable therapies.


Patent Landscape Summary

  • Density: The antiviral patent landscape is saturated, but novel mechanisms or compounds such as those claimed in EP3468532 can carve out new niches.
  • Strength: The combination of broad independent claims and detailed dependent claims enhances enforceability.
  • Risks: Prior art and obviousness challenges remain, particularly if similar compounds or methods exist.

Concluding Remarks

EP3468532 embodies a strategic patent with comprehensive claims targeting a significant antiviral therapeutic approach. Its broad scope offers competitive advantages, but maintaining robust patent prosecution and vigilant monitoring of the evolving landscape are essential. Future innovations, such as derivative compounds or combination therapies, can leverage this patent’s foundations, fostering ongoing R&D and commercialization efforts.


Key Takeaways

  • Broad Claim Strategy: EP3468532 claims a wide range of compositions and methods, safeguarding extensive antiviral applications.
  • Innovative Focus: Its novelty likely resides in a unique molecular target or method, pivotal for differentiating from prior art.
  • Landscape Position: It exists within a competitive but evolving antiviral patent environment, with opportunities for expansion via follow-up filings.
  • Commercial Leverage: Strong patent protection can facilitate licensing, partnership, and market exclusivity.
  • Ongoing Monitoring: Regular patent landscape assessments are critical to adapt to emerging threats and innovations.

FAQs

1. What is the primary therapeutic focus of patent EP3468532?
It centers on methods and compositions for treating or preventing viral infections, likely targeting specific viral replication mechanisms with novel agents.

2. How does EP3468532 compare to existing antiviral patents?
It claims a potentially distinct molecular target or approach, offering broader or alternative protective coverage compared to existing patents on nucleoside analogs, protease, or polymerase inhibitors.

3. Can the patent be challenged on the grounds of obviousness?
Yes, given the crowded antiviral landscape, opponents might argue the claims are obvious improvements. However, the patent’s specificity and molecular novelty serve as defenses.

4. Will the scope of EP3468532 protect against future similar innovations?
Broad independent claims provide strong initial protection; yet, ongoing innovation may require further patent filings or claims to maintain exclusivity.

5. What should licensors or licensees consider when negotiating around this patent?
They should evaluate the patent’s claims scope, validity, and potential for infringement, while strategizing for supplemental or follow-up patents to extend protection.


Sources
[1] European Patent Register, EP3468532.
[2] WIPO Patent Scope and Examination Guidelines.
[3] Patent landscape reports on antiviral agents (2022).

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