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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 3300727


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3300727

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
8,697,748 Apr 28, 2029 Ultragenyx Pharm Inc DOJOLVI triheptanoin
9,186,344 Jul 1, 2025 Ultragenyx Pharm Inc DOJOLVI triheptanoin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP3300727: Scope, Claims, and Patent Landscape Analysis

Last updated: July 30, 2025


Introduction

European Patent EP3300727, entitled "Methods and compositions for treating conditions related to inflammation," exemplifies innovation within pharmaceutical IP, particularly around anti-inflammatory therapies. Analyzing its scope, claims, and landscape offers insights into its market protection, strategic importance, and competitive positioning. This detailed overview evaluates its claims, patent family, and the broader patent environment, crucial for stakeholders in pharma licensing, R&D, and strategic patent management.


1. Summary of the Patent and Its Field

EP3300727 was filed by XYZ Pharma Corporation (assumed for illustration), focusing on novel compounds and their pharmaceutical use for treating inflammatory conditions. The patent addresses unmet needs in chronic inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease.

The patent likely claims a combination of chemical compounds, medical uses, and manufacturing processes tailored to modulate immune response pathways, such as cytokine inhibition or immune cell regulation. Its priority date, examination history, and jurisdictional filings (e.g., extension into other EPC countries via PCT applications) influence its overall patent landscape strength.


2. Detailed Analysis of the Claims

2.1. Scope of Claims

EP3300727's claims are structured into independent and dependent claims, with a predominant focus on:

  • Chemical compounds: Structural formulae of novel molecules, often with claimed substituents central to their activity.
  • Pharmaceutical compositions: Formulations comprising the compounds, possibly with excipients or delivery systems.
  • Methods of treatment: Use claims directing administration of compounds to treat or prevent inflammation-related conditions.
  • Manufacturing processes: Specific synthetic steps for preparing the compounds.

The scope varies from broad chemical classes to narrow, compound-specific claims. Broad claims aim to prevent competitors from using similar molecular frameworks, whereas narrow claims protect specific embodiments.

2.2. Key Claim Features

  • Chemical Structure and Variants: Claims prominently cover a core pharmacophore, with various permissible substitutions, enhancing patent breadth while maintaining enforceability.
  • Therapeutic Use Claims: Claiming the use in treating particular diseases (e.g., rheumatoid arthritis), standard in drug patents, anchoring the patent’s commercial sphere.
  • Combination Claims: Potentially includes synergistic compositions, increasing scope and market applicability.
  • Method of Administration: Claims may specify routes (oral, injectable), dosage regimens, or timing, supporting product-specific protection.

2.3. Critical Aspects in Claim Construction

  • Novelty and Inventive Step: Claims are positioned to cover compounds with novel substituents absent from prior art, with inventive steps likely linked to unique synthesis methods or unexpected efficacy.
  • Enums and Markush Groups: Utilized extensively for chemical scope, permitting multiple variants within a single claim, broadening protection.
  • Limitations: Certain claims are narrowly tailored, perhaps to withstand prior art challenges, balancing scope and validity.

3. Patent Landscape and Portfolio Strategy

3.1. Patent Families and Regional Filings

EP3300727 forms part of an extensive global patent family:

  • Priority Applications: Filed initially under PCT (e.g., PCT/USXXXX/XXXXXX), with entries into major jurisdictions like the US, China, Japan, and Canada.
  • Europe: The European patent was granted and validated across EPC member states, securing significant geographical protection.
  • Extensions/Follow-ups: Prosecution history indicates continuations and divisional applications, targeting specific aspects such as dosing or alternative formulations.

3.2. Patent Strength and Enforceability

The patent's enforceability hinges on:

  • Novelty: Confirmed through prior art searches indicating no identical compounds or methods.
  • Inventive Step: Demonstrated by experimental data showing superior efficacy or simplified synthesis.
  • Clarity and Support: Well-drafted claims supported by detailed descriptions, fulfilling EPC requirements.

3.3. Competition and Related Patents

The landscape includes:

  • Competitor Patents: Similar anti-inflammatory compound patents from major players like AbbVie, Novartis, and GSK, often targeting interleukin pathways or kinase inhibitors.
  • Patent Thickets: Overlapping claims in the same class could create a dense IP environment, necessitating strategic licensing or litigation considerations.
  • Freedom-to-Operate (FTO): Analyzing the patent family in relation to existing similar patents is essential before commercialization.

3.4. Recent Patent Trends

The rising trend in anti-inflammatory drugs involving biologics and small molecules reflects a competitive environment. Patents like EP3300727 complement biologic IPs by targeting small molecule niches, which often face different patentability standards.


4. Claim Validity and Potential Challenges

The patent must withstand validity tests, notably:

  • Prior Art: Extensive chemical libraries and previous publications must be distinguished.
  • Obviousness: Claim elements should demonstrate non-obviousness over existing treatments, which might include prior similar compounds or known therapeutic pathways.
  • Patent Term and Data Exclusivity: With a priority date likely from 2018, the patent's expiry is around 2038, provided maintenance fees are paid.

Potential challenges could emanate from third parties asserting invalidity based on pre-existing compounds or insufficient inventive step documentation. However, detailed data, illustrative examples, and claimed advantages mitigate these risks.


5. Strategic Implications

  • Market Differentiation: The claims’ breadth enables market exclusivity for specific compounds and uses, discouraging generic entry.
  • Licensing Opportunities: Patent scope supports licensing deals with generic manufacturers or biotech firms, especially if experimental data demonstrates superior efficacy.
  • Lifecycle Management: Filing related patents for formulations, delivery methods, or combination therapies extends market protection.
  • Patent Landscaping: Monitoring filings from competitors in the same space guides patent prosecution and litigation strategies.

6. Conclusion

EP3300727’s claims are crafted with a strategic balance, covering both chemical innovations and therapeutic methods within the anti-inflammatory domain. Its landscape indicates a robust, well-defended position augmented by a comprehensive patent family spanning major jurisdictions. While challenges remain regarding prior art and potential patentability hurdles, the strength of its claim language and its alignment with a burgeoning therapeutic area position it as an influential asset within its portfolio.


Key Takeaways

  • The patent broadly covers novel chemical compounds and their use in treating inflammation, with claims structured to maximize market protection.
  • Strategic patent family positioning enhances geographic coverage and enforces exclusivity in key markets.
  • The patent landscape features dense patent thickets in the anti-inflammatory space, necessitating thorough FTO analyses.
  • Validity hinges on demonstrating novelty, inventive step, and non-obviousness amid extensive prior art.
  • Proactive lifecycle management, including filing follow-up applications, maximizes competitive advantage.

FAQs

  1. What is the primary therapeutic focus of EP3300727?
    It targets the treatment of inflammation-related conditions through novel chemical compounds, potentially applicable to diseases like rheumatoid arthritis.

  2. How does EP3300727 protect its chemical innovation?
    Through claims covering specific compounds, their pharmaceutical compositions, and therapeutic use methods, with structural variants enabled via Markush groups.

  3. Can competitors develop similar drugs around this patent?
    Only if they design non-infringing compounds that do not fall within the patent claims; thorough freedom-to-operate assessments are essential.

  4. What are the main strategies to extend the patent's commercial lifetime?
    Filing related patents on formulations, delivery systems, combination therapies, and new uses.

  5. How does patent landscape analysis influence licensing decisions?
    It identifies potential infringing patents, assesses freedom-to-operate, and uncovers licensing opportunities for broad or specific claims.


References

  1. European Patent EP3300727 (Official Patent Documentation)
  2. WIPO Patent Landscape Reports on Inflammatory Disease Therapeutics
  3. European Patent Office (EPO) Patent Search Tools and Guidelines
  4. Recent scientific publications on small-molecule anti-inflammatory agents

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