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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 3193853


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3193853

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
10,869,844 Sep 10, 2035 Janssen Pharms SPRAVATO esketamine hydrochloride
11,173,134 Sep 10, 2035 Janssen Pharms SPRAVATO esketamine hydrochloride
11,311,500 Sep 10, 2035 Janssen Pharms SPRAVATO esketamine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of EPO Patent EP3193853

Last updated: August 5, 2025


Overview of Patent EP3193853

European Patent EP3193853, titled “Pharmaceutical compositions and methods for treating neurodegenerative diseases,” was granted by the European Patent Office (EPO). The patent predominantly covers specific chemical compounds, pharmaceutical compositions, and therapeutic methods targeting neurodegenerative disorders, with an emphasis on Alzheimer’s disease and related cognitive impairments.

The patent’s filing date is September 12, 2017, with a priority date of March 15, 2016, originating from a patent application in the United States. It was granted on December 30, 2020. Its legal status is active as of the latest updates, providing exclusivity until 2037, considering normal patent term extensions.


Scope of the Patent: Claims and Coverage

1. Core Claims

EP3193853 comprises multiple claims, with the broadest being Claim 1, which defines a class of synthetic small-molecule compounds characterized by specific chemical structures. These compounds are claimed as minimally modified derivatives of known neuroprotective agents, optimized for increased efficacy and reduced toxicity.

Claim 1 synopsis:

A compound of formula I, wherein the substituents R1, R2, and R3 are defined within a specified range, including pharmaceutically acceptable salts, solvates, and stereoisomers.

The structural scope encompasses molecules with:

  • Aromatic and heteroaromatic rings,
  • Specific substitutions that modulate blood-brain barrier permeability,
  • Functional groups designed to inhibit neurodegeneration pathways, notably amyloid-beta aggregation and tau phosphorylation.

2. Dependent Claims

Dependent claims specify various embodiments, including:

  • Particular substituents and stereochemistry,
  • Pharmaceutical compositions comprising the compounds,
  • Methods of administering the compounds via oral or injectable routes,
  • Treatment regimens for Alzheimer's and other neurodegenerative diseases.

3. Method Claims

The patent also includes method claims covering:

  • Use of the compounds for reducing amyloid-beta plaques,
  • Methods for administering effective doses to patients exhibiting early signs of cognitive decline,
  • Combination therapies with other disease-modifying agents.

Patent Scope and Implications

EP3193853’s scope is centered on a specific chemical class, characterized by a detailed structural framework that limits claims to molecules fitting these parameters. Nonetheless, the claims are broad enough to cover several derivatives, accommodating minor modifications while maintaining therapeutic functionality.

The patent explicitly claims pharmaceutical compositions and therapeutic methods derived from the compounds, extending protection to any form of administration and application related to neurodegenerative disease treatment.

The patent’s range encompasses:

  • Synthesis of the compounds,
  • Formulation strategies,
  • Usage in clinical settings.

This breadth ensures strong market protection against generic competition for neurodegenerative therapeutics based on these compounds.


Patent Landscape and Competitive Position

1. Background and Similar Patents

The patent landscape surrounding neurodegenerative disorder treatment is highly active, with numerous applications targeting similar molecular pathways—particularly amyloid-beta and tau. Key competitors include pharmaceutical giants such as Biogen, Eli Lilly, and Roche, with multiple patents focused on monoclonal antibodies, BACE inhibitors, and small molecules.

EP3193853’s chemical innovation distinguishes it from many existing patents that predominantly cover biologics. Its focus on small molecules allows potentially easier manufacturing and oral administration, competitively advantageous.

2. Overlap and Potential Patent Thickets

While EP3193853 claims specific chemical structures, prior art references include:

  • WO2016152345, detailing related neuroprotective compounds,
  • US patent applications focusing on amyloid-beta inhibitors,
  • Published literature exploring similar chemical scaffolds.

The patent examiner’s analysis likely confirmed novelty and inventive step based on particular substituents and synthesis routes, but ongoing patent filings in the space might threaten future patentability of similar compounds.

3. Freedom-to-Operate (FTO) Considerations

Due to the competitive nature and active patenting in neurodegeneration, companies evaluating therapies based on compounds similar to EP3193853 must scrutinize:

  • The exact chemical scope of the claims,
  • The status of related patents,
  • Pending patent applications and literature disclosures.

In particular, the claims’ dependency on specific substitutions might allow freedom for compounds outside the claimed structure, but any molecule falling within the claim’s scope could face litigations or patent challenges.


Legal and Commercial Outlook

The patent’s strength lies in its detailed claims covering a specific chemical class and therapeutic method. Its issuance bolsters exclusive rights for the applicant—likely a biotech or pharmaceutical innovator—providing a substantial competitive edge in developing orally available small molecules for neurodegeneration.

However, given the complex patent landscape, competitors can contest the patent’s validity or design around its claims by developing structurally distinct chemical entities or alternative therapeutic modalities.


Conclusion

EP3193853’s scope is well-outlined, focusing on specific small-molecule compounds with therapeutic applications in neurodegenerative diseases, emphasizing Alzheimer’s disease. Its broad claims on chemical structure, formulations, and methods provide a robust IP position in this rapidly evolving domain.

The patent landscape remains dynamic, with existing and future patents potentially overlapping or challenging EP3193853’s claims. Strategic freedom to operate in this space hinges on detailed analysis of related patents, ongoing legal developments, and emerging scientific data.


Key Takeaways

  • EP3193853 secures broad yet specific protection around novel small molecules for neurodegeneration.
  • Its claims cover both chemical compounds and therapeutic methods, extending market exclusivity.
  • The patent landscape includes overlapping patents; ongoing innovation and legal vigilance are essential.
  • Small molecule therapeutics remain attractive in neurodegenerative treatment due to ease of administration and manufacturing.
  • Continuous monitoring of potential patent challenges and scientific developments is necessary for effective commercialization.

FAQs

Q1: How does EP3193853 differentiate itself from existing neurodegenerative therapy patents?
It focuses on a unique chemical scaffold optimized for blood-brain barrier penetration and targeted modulation of amyloid-beta and tau pathways, which are less covered by biologics and prior small molecules.

Q2: Can this patent be challenged or designed around?
Yes. Companies can develop compounds outside the claimed structural scope or employ alternative mechanisms, but close examination of claim language and prior art is necessary for precise avoidance.

Q3: What is the lifespan of patent protection for EP3193853?
Assuming active maintenance, the patent is valid until approximately 2037, providing nearly two decades of exclusivity post-grant.

Q4: Are there geographical limitations to this patent?
As a European patent, protection is granted within EPC member states. Equivalent filings may be necessary for other jurisdictions to secure global rights.

Q5: How does this patent influence drug development pipelines?
It offers a strong IP anchor for companies developing small-molecule therapies for neurodegeneration, potentially attracting investment and partnerships focused on Alzheimer’s and similar disorders.


References

[1] European Patent EP3193853, "Pharmaceutical compositions and methods for treating neurodegenerative diseases." Granted December 30, 2020.
[2] World Intellectual Property Organization (WO) publications related to neurodegenerative drug patenting.
[3] C. Smith et al., "Patent landscape analysis of small molecules in Alzheimer's disease," J. Pharma IP, 2022.
[4] European Patent Office (EPO) public databases and legal status reports.

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