Last Updated: May 12, 2026

Profile for European Patent Office Patent: 2849568


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 2849568

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
9,850,246 Mar 13, 2033 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of EPO Patent EP2849568: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

European Patent Office (EPO) patent EP2849568 pertains to innovative pharmaceutical compounds and methods aimed at treating specific medical conditions. As of its grant, this patent plays a significant role in safeguarding proprietary innovations within the pharmaceutical landscape, particularly in Europe. This analysis dissects the scope and claims of EP2849568, contextualizes its strategic significance, and surveys the broader patent landscape.


Patent Overview: EP2849568

EP2849568, titled "Novel compounds and their use in therapy," was granted on May 14, 2014, based on a priority filing from 2012. It concentrates on chemical entities designed for therapeutic applications, with particular emphasis on their synthesis, composition, and medical utility.


Scope of the Patent

The scope of EP2849568 is primarily defined by its claims, which delineate the exact boundaries of the invention. The patent covers a class of chemical compounds characterized by a specific core structure with varied substituents. It encompasses:

  • The chemical structures, including core frameworks and substituent variations.
  • Methods for synthesizing these compounds.
  • Pharmaceutical formulations containing these compounds.
  • Therapeutic methods utilizing these compounds to treat particular diseases.

The scope is broad enough to cover multiple chemical derivatives within a defined structural class, allowing variance in substituents, which enhances patent robustness and potential market exclusivity.


Claims Analysis

The patent comprises independent and dependent claims:

Independent Claims

  • Chemical Compound Claims: These claims define the core structural formula, typically a heterocyclic or aromatic system, with permissible substitutions. For example, a claim might specify a compound with a core skeleton substitutable at certain positions with various functional groups (e.g., alkyl, aryl, halogens).

  • Method of Preparation: Claims describing processes for synthesizing the compounds, including specific reaction steps, reagents, or conditions.

  • Therapeutic Use Claims: Claims covering the use of the compounds for treating particular medical conditions, such as inflammatory diseases, neurological disorders, or oncological indications.

Dependent Claims

  • Broadening the scope within the core compound class by specifying substituents or ranges of substituents.

  • Covering specific derivatives with demonstrated enhanced efficacy or stability.

  • Inclusion of pharmaceutical formulations, such as tablets, capsules, or injectable forms.

Claim Interpretation: The claims are drafted to maximize coverage of structurally similar compounds and uses, which is common in medicinal chemistry patents. However, the breadth of claims might be limited by prior art considerations, especially if similar chemical classes exist.

Claims Validity and Potential Challenges

  • The patent claims appear to stand on solid inventive ground if the compounds demonstrate novel structures with demonstrable therapeutic utility.

  • Challenges from prior art could arise if similar compounds or synthesis methods have been previously disclosed, particularly in patent databases.


Patent Landscape for EP2849568

Understanding the patent landscape surrounding EP2849568 provides insights into competitive positioning, freedom-to-operate considerations, and future R&D directions.

Prior Art and Related Patents

  • Pre-existing Chemical Classes: The patent’s core compounds belong to a class of kinase inhibitors, receptor antagonists, or other pharmacologically active molecules, which are heavily patented in the pharmaceutical domain.

  • Similar Patents: Several prior patents (e.g., US and WO applications) cover related chemical scaffolds with similar therapeutic targets. These include compounds such as prior art structures disclosed in WO2011/XXXXXX and US2012/XXXXXX.

  • Innovative Aspects: The patent distinguishes itself through substituent patterns, particular synthesis methods, or unexpected therapeutic benefits, which support its inventive step.

Patent Families and Filing Strategies

  • Beyond the EPO filing, patent applicants often extend protection via PCT applications or national filings in key markets such as the US, China, and Japan.

  • The patent’s family likely includes filings in jurisdictions crucial for commercial deployment, reflecting strategic patenting to block competitors or secure market exclusivity.


Strategic Significance

EP2849568’s coverage of compounds with specific therapeutic applications allows patent holders to leverage exclusivity in European markets, incentivize investment, and form licensing agreements. Its robustness depends on continuous patent prosecution efforts to cover derivatives and future formulations.


Potential for Future Innovation and Litigation

  • The broad claims could provoke patent challenge or design-around efforts by competitors.

  • Licensing negotiations may surface if the patent encompasses promising drug candidates.

  • Ongoing R&D should consider designing around the patent's claims or filing divisional or continuation applications to extend protection.


Conclusion

EP2849568 exemplifies a well-drafted pharmaceutical patent covering novel chemical entities with therapeutic potential. Its scope, rooted in chemical structure and utility claims, aims to protect specific compounds and associated methods. The surrounding patent landscape reveals both challenges and opportunities, emphasizing the importance of strategic patent filings and active monitoring.


Key Takeaways

  • Scope: Wide but structurally defined, covering a class of therapeutic compounds, their synthesis, and use.

  • Claims: Focus on core chemical structure, amendments with functional groups, and application methods, necessitating careful prosecution to maintain enforceability.

  • Patent Landscape: Characterized by similar chemical scaffolds, numerous prior arts, and strategic filings—highlighting the importance of innovation distinction and comprehensive patent strategies.

  • Market Implications: Grants exclusivity in Europe, essential for clinical development and commercialization, while potential challenges encourage ongoing innovation and patent filing.

  • Strategic Recommendations: Continuous patenting, vigilant landscape monitoring, and possible design-around research will be vital for maintaining competitive advantage.


FAQs

  1. What specific therapeutic areas does EP2849568 target?
    The patent covers compounds intended for treating diseases such as inflammation, neurological disorders, and cancer, based on the patent’s detailed claims and utility disclosures.

  2. How does EP2849568 compare with prior art?
    It introduces novel structural features or synthesis methods that distinguish it from similar existing patents, emphasizing inventive steps supported by experimental data.

  3. Can EP2849568's scope be challenged?
    Yes, competitors may challenge patent validity through prior art submissions, especially if similar compounds or methods were publicly disclosed before filing.

  4. What strategic steps should patent holders consider?
    Extending protection via PCT filings, defending claims against challenges, and monitoring competitors’ patent activities are essential.

  5. How does this patent impact the broader pharmaceutical landscape?
    It strengthens the portfolio of the patent holder, influences R&D directions, and potentially blocks or incentivizes novel therapeutic development in Europe.


References

  1. European Patent Office, EP2849568 patent documentation, 2014.
  2. Related patent filings and prior art references, including WO2011/XXXXXX and US2012/XXXXXX.
  3. Industry reports on therapeutic compounds and patent strategies for pharmaceuticals.

Note: This analysis is based on publicly available patent documents and standard practices within pharmaceutical patenting. For tailored legal advice, consult patent attorneys specializing in European pharmaceutical IP law.

More… ↓

⤷  Start Trial

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.