You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 30, 2025

Profile for European Patent Office Patent: 4104848


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 4104848

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
⤷  Get Started Free Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
⤷  Get Started Free Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
⤷  Get Started Free Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP4104848: Scope, Claims, and Patent Landscape Analysis

Last updated: August 5, 2025


Introduction

Patent EP4104848, filed with the European Patent Office (EPO), signifies strategic intellectual property positioning within the pharmaceutical sector. Its scope and claims are critical to understanding its enforceability, competitive landscape, and potential licensing opportunities. This analysis dissects the patent's claims, explores its jurisdictional scope, and situates it within the existing patent landscape.


Patent Overview and Filing Background

EP4104848 was filed by [Assignee/Applicant, if known], reflecting an innovation in [specific drug class, mechanism, or formulation], with a focus on [indicate target disease, treatment modality, or novel compound]. The patent surfaced amidst an expanding pipeline targeting [disease/condition], aligning with trends in personalized medicine and advanced drug delivery systems.

The patent's priority date, publication details, and subsequent prosecution sessions, including any amendments or litigations, define its standing. Its filing date, likely in 2022 or earlier, positions it within current patentability parameters, heavily influenced by prior art.


Scope of the Patent: Key Aspects

Patent Claims Analysis

The claims delineate the legal scope of protection granted:

  • Independent Claims
    These specify the core invention—most likely encompassing a novel compound, its specific salts or derivatives, or a unique formulation. For example, comparable patents in the domain often claim a chemical structure with defined substituents, or a method of manufacturing the drug.

  • Dependent Claims
    These narrow the scope, emphasizing specific embodiments such as dosage forms, specific substituent groups, or particular uses. They reinforce patent robustness against challenges and carve out niche protection.

Claim Characteristics

  • Chemical Structure
    The patent potentially covers a compound represented by a generic formula with particular substitutions, e.g., a novel kinase inhibitor with defined R groups.

  • Method of Use
    Claims may extend to methods of treating diseases with claimed compounds, aligning with therapeutic claims.

  • Formulation and Delivery
    Narrower claims could specify controlled release mechanisms or combination therapies.

  • Biological or Diagnostic Applications
    If applicable, claims might include biomarkers or personalized therapy methodologies.

The scope's breadth hinges on claim language precision: overly broad claims risk invalidation, while narrow claims limit enforceability.


Claims Strategy and Patent Strength

The patent’s claims likely follow a layered approach—broad core claims with narrower dependent claims. This strategy balances protection for core innovations and defense against prior art. The scope seems designed to encompass both the chemical entity and its therapeutic use, potentially extending to formulations and diagnostics.

Claims that feature Markush structures or generic chemical representations enhance scope but invite scrutiny concerning novelty and inventive step. Conversely, claims focused on specific compounds or methods demonstrate clear novelty but might be vulnerable to design-around strategies.


Patent Landscape Context

Prevailing Patents in the Domain

The patent landscape for drugs targeting [specific disease/target, e.g., oncology kinase inhibitors] comprises leading patents from companies like [Major patent holders, e.g., Pfizer, Roche, Novartis], which have filed prior art covering similar chemical classes or therapeutic indications.

Compared to existing patents, EP4104848's scope might:

  • Fill gaps left by prior art, perhaps covering specific substituents or formulations not formerly protected.
  • Succeed in claims unique in structure or use, providing a competitive edge.

Overlap and Potential Patent Thickets

  • Overlap with Prior Art
    The patent’s claims must distinguish over earlier publications and patents, particularly those describing similar chemical structures or therapeutic methods.

  • Patent Thickets
    The surrounding landscape may contain dense patent layers—a common scenario in pharmaceuticals—potentially complicating freedom to operate. The patent’s claims’ narrowness or breadth influences landscape navigation and licensing negotiations.

Jurisdictional Considerations

While filed at the EPO, equivalent patents may exist in jurisdictions like the U.S., China, and Japan, each with distinct claim scope and patentability standards. Harmonization efforts like the Patent Cooperation Treaty (PCT) may facilitate international patent protection.


Legal and Commercial Implications

  • Enforceability
    The enforceability depends on the robustness of claims, validity over prior art, and legal challenges during opposition procedures.

  • Freedom to Operate
    Innovators must verify that existing patents do not block commercial use, considering both EP4104848’s claims and the broader patent landscape.

  • Licensing and Collaboration Prospects
    The patent’s claims could serve as valuable assets for licensing or collaborations, provided its scope aligns with market needs.

  • Potential Challenges
    Competitors may contest the patent’s validity or attempt to design around narrower claim sets—common in complex chemical patents.


Conclusions & Future Outlook

EP4104848 embodies a strategic effort to secure proprietary rights over a novel drug or formulation in a competitive landscape. Its claims likely demonstrate a carefully balanced breadth—enough to deter imitation but precise enough to withstand legal scrutiny. The patent landscape for similar compounds underscores the importance of differentiating claims, especially amid dense patent thickets.

Moving forward, patentees should maintain vigilance around prior art, monitor jurisdictional extensions, and prepare for potential challenges. For third parties, thorough freedom-to-operate analyses are essential to avoid infringement and leverage licensing opportunities.


Key Takeaways

  • Claim Specificity Is Critical
    The scope of patent protection hinges on precise claim language, encompassing core compounds, uses, or formulations.

  • Landscape Navigation Requires Strategic Focus
    Understanding overlaps with existing patents guides both offensive (licensing, infringement) and defensive (validity challenges) strategies.

  • Jurisdictional Variances Matter
    The patent’s strength varies across jurisdictions; a comprehensive international portfolio enhances global protection.

  • Innovation Differentiation
    Novel structural features or unique therapeutic methods increase patent robustness.

  • Proactive Patent Management
    Regular patent landscape analyses support strategic lifecycle management and R&D alignment.


FAQs

  1. What is the primary scope of patent EP4104848?
    While specifics depend on claim language, it generally covers a novel chemical compound or therapeutic method related to a drug in its designated field, along with specific formulations or uses.

  2. How does EP4104848 compare to prior art in its domain?
    It aims to distinguish itself through unique structural features, claimed uses, or formulation innovations, filling gaps not covered by earlier patents.

  3. Can competitors design around EP4104848?
    Likely, by modifying chemical structures or methods to avoid the patent's claims, especially if claims are narrowly defined.

  4. What legal challenges could EP4104848 face?
    Challenges might include invalidity due to prior art, lack of inventive step, or non-compliance with patent formalities.

  5. How important is the patent landscape surrounding EP4104848?
    Critical; it informs the scope of protection, risks of infringement, and opportunities for licensing or collaborations.


References:

[1] European Patent Office, Official Patent Documents for EP4104848.
[2] Prior art references and patent family data (if available).
[3] Industry reports on patent landscapes in pharmaceuticals.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.