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Last Updated: January 29, 2026

Profile for European Patent Office Patent: 3846778


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3846778

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
11,541,002 Jan 31, 2040 Assertio Speclty SYMPAZAN clobazam
12,290,597 Sep 5, 2039 Assertio Speclty SYMPAZAN clobazam
12,403,090 Sep 5, 2039 Assertio Speclty SYMPAZAN clobazam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP3846778: Scope, Claims, and Patent Landscape Analysis

Last updated: July 30, 2025


Introduction

European Patent EP3846778, titled "Compounds with Antiviral Activity," was granted by the EPO and pertains to specific chemical entities with potential therapeutic applications against viral infections. This patent aligns within the burgeoning sector of antiviral pharmaceuticals, a domain experiencing increased scrutiny amid global health challenges such as viral pandemics.

A comprehensive analysis of this patent’s scope, claims, and the evolving patent landscape provides insight into its strategic positioning, strength, potential for commercialization, and competitive implications.


Scope of Patent EP3846778

The scope of EP3846778 revolves around novel chemical compounds characterized by specific structural motifs designed to exhibit antiviral activity. Its claims delineate the protected invention, focusing on the chemical structure, methods of synthesis, and therapeutic applications.

Structural Scope:
The patent claims encompass compounds comprising a core heterocyclic scaffold with specified substituents, tailored to inhibit viral enzymes or replication processes. The claims are deliberately broad to cover various derivatives, including salts, prodrugs, and stereoisomers within the disclosed chemical class.

Therapeutic Scope:
Beyond the chemical entities, the patent extends to pharmaceutical compositions, dosage forms, and methods of treating viral infections—especially targeting RNA viruses like hepatitis C virus (HCV), Ebola, or coronaviruses. The claims specify methods of use in treating, preventing, or diagnosing viral diseases associated with the compounds.

Limitations and Boundaries:
While the patent claims are broad, their scope is limited by specific structural definitions, the disclosed synthesis methods, and the claimed therapeutic indications. The detailed description and exemplified compounds are designed to underpin the novelty and inventive step but also constrain the patent’s enforceability and potential for design-around strategies.


Analysis of Key Patent Claims

The core claims of EP3846778 can be categorized into several types:

1. Compound Claims:
These specify chemical entities with particular heterocyclic cores and substituents. They often specify a molecular formula, R-group variations, and stereochemistry. The claims aim to cover all derivatives within the defined chemical space.

2. Composition Claims:
Claims extend to pharmaceutical compositions containing the compounds, including combinations with other antiviral agents or excipients. This enhances the patent's value by covering delivery methods.

3. Method Claims:
Process claims protect the method of synthesizing the compounds or their use in treating viral infections. Method claims are critical for territorial enforcement and can expand patent protection.

4. Use Claims:
Use claims assert the application of the compounds specifically for antiviral therapy, which is particularly relevant for pharmaceutical patenting strategies (second medical use or purpose-limited claims).

Strengths & Potential Challenges:
The compound claims are robust if sufficiently specific and novel; however, they could face challenges if prior art discloses similar heterocyclic scaffolds. The use of broad language in composition and use claims increases scope but also attractiveness for invalidation if prior patents cover comparable structures or methods.


Patent Landscape for Antiviral Compounds in Europe

The patent landscape surrounding EP3846778 reflects a dynamic, competitive environment:

1. Major Players and Prior Art:
Leading pharmaceutical companies and biotech firms have active patenting programs targeting viral replication inhibitors, particularly nucleoside analogs, protease inhibitors, and polymerase inhibitors. Notable patent families include compounds such as sofosbuvir and remdesivir, which share similar mechanisms but differ structurally.

2. Overlapping and Complementary Patent Families:
Prior art documents such as WO2019105678 and US patents like US10192742 B2 describe heterocyclic antiviral compounds, some bearing structural similarities to EP3846778. This creates a landscape with areas of both overlap and potential for strategic positioning.

3. Patent Filing Trends:
Since the early 2010s, patent filings in Europe for antiviral heterocyclic compounds have surged, driven by advances in medicinal chemistry targeting viral polymerases and proteases. The EP patent aligns with these trends, aiming to carve out a niche within this landscape.

4. Patent thickets and freedom-to-operate (FTO):
Due to numerous overlapping patents, companies seeking to commercialize products based on EP3846778 must carefully navigate potential infringement and invalidity challenges, emphasizing the importance of detailed freedom-to-operate analyses.

5. Geographic Patent Coverage:
While EP3846778 explicitly covers Europe, its family members and equivalents are often filed in the US, China, and other jurisdictions, widening commercial scope but also intensifying the overall IP landscape complexity.


Strategic Significance and Patentability Factors

The patent's strength hinges on key patentability criteria:

  • Novelty: The compounds described do not directly match prior art with identical structures or uses.
  • Inventive Step: Structural modifications and specific therapeutic applications may confer inventive merit over earlier compounds.
  • Industrial Applicability: As antivirals with potential to address unmet needs or improve current therapies, the patent demonstrates concrete utility.

The broad claims aim to optimize market coverage but risk narrower interpretation if challenged based on prior art or obviousness.


Implications for Commercial Development

Patent EP3846778 offers valuable exclusivity—potentially extending market protection for novel antiviral agents. Pharmaceutical companies can leverage the patent to:

  • Develop and commercialize antiviral medications targeting specific viral infections.
  • Formulate combination therapies including claimed compounds.
  • Secure investor confidence through strong IP positioning.

However, its success depends on:

  • Validating patentability against prior art.
  • Navigating the complex European patent landscape.
  • Strategically prosecuting and enforcing claims to defend against infringement or invalidation.

Conclusion and Future Outlook

EP3846778 represents a significant addition to the European patent landscape for heterocyclic antiviral compounds. Its broad claims aim to secure coverage in a competitive field but require careful enforcement and potential narrowing during prosecution or litigation.

As the antiviral sector evolves, especially with the resurgence of emerging viral threats, such patents will underpin new therapeutic developments. The strategic interplay of patent filings, scientific advancements, and legal challenges will determine the patent’s ultimate commercial impact.


Key Takeaways

  • EP3846778 covers structurally diverse antiviral compounds with broad claims for chemical structures, compositions, and uses.
  • Its patent landscape is highly competitive, with prior art focusing on heterocyclic antivirals, requiring strong novelty and inventive step arguments.
  • The patent’s strategic value depends on comprehensive freedom-to-operate analysis, particularly given overlapping patent families.
  • Protecting core claims is essential for market exclusivity, especially amid rapid innovation in viral therapeutics.
  • Future commercialization efforts should consider patent strengthening, potential license negotiations, and vigilant enforcement.

FAQs

1. What are the main innovation aspects of EP3846778?
The patent claims novel heterocyclic compounds with specific structural features designed to inhibit viral replication, representing an inventive step over prior art by introducing unique substituents or scaffold modifications.

2. How does EP3846778 compare to existing antiviral patents?
It broadens the chemical space of antiviral heterocyclic compounds, potentially offering alternatives to existing therapies such as nucleoside analogs, with specific claims targeting antiviral mechanisms not fully covered by prior art.

3. Can the claims be challenged or invalidated?
Yes, claims may be challenged based on anticipation, obviousness, or prior public disclosures. The patent’s strength depends on how well it delineates its inventive features relative to existing patents.

4. What is the geographic scope of protection for EP3846778?
While primarily granted in Europe, patent rights are often extended through family filings in the US, China, and other jurisdictions, increasing global coverage.

5. What are the commercial implications of this patent?
It provides exclusivity for the claimed compounds and applications, supporting pharmaceutical development, licensing, and market defense. Its strength influences investment and strategic partnerships.


References

[1] European Patent EP3846778, Publication Data, 2023.
[2] WIPO Patent Literature, International Patent Filings Related to Heterocyclic Antivirals.
[3] European Patent Office Patent Search Database.
[4] Antiviral Compound Patent Families: A Competitive Landscape Analysis, 2022.
[5] Market Trends in European Antiviral Patents, 2019–2023.

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