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Last Updated: December 11, 2025

Profile for European Patent Office Patent: 3185911


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3185911

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 Jul 28, 2035 Telix Innovations GOZELLIX gallium ga-68 gozetotide
⤷  Get Started Free Jul 28, 2035 Telix ILLUCCIX gallium ga-68 gozetotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP3185911: Scope, Claims, and Patent Landscape Analysis

Last updated: August 3, 2025


Introduction

European Patent EP3185911 pertains to innovative pharmaceutical technology, with its core focus on the treatment of specific medical conditions possibly linked to novel formulations or therapeutic methods. Understanding the scope, claims, and patent landscape surrounding EP3185911 is paramount for stakeholders, including competitors, licensing entities, and R&D institutions, to navigate the intellectual property (IP) environment effectively.

This analysis dissects the patent's claims, scope, and its position within the broader patent landscape, emphasizing how EP3185911 advances or intersects with existing patents, and its strategic significance within the pharmaceutical IP domain.


Scope and Claims of EP3185911

1. Overview of the Patent Claims

The core strength of any patent resides in its claims, which precisely delineate the invention's legal boundaries. EP3185911's claims encompass:

  • Method Claims: Covering specific therapeutic methods, possibly including administration protocols, dosage regimes, or targeted patient populations.
  • Formulation Claims: Detailing particular chemical compositions, drug delivery vehicles, or inert carriers that enhance efficacy, stability, or bioavailability.
  • Device or Delivery System Claims: If applicable, protection extends to novel drug delivery systems or medical device integrations facilitating administration.

Example of Claims Breakdown:

  • Claim 1: A pharmaceutical composition comprising a specific active ingredient (e.g., a new compound or a known compound in a novel form) combined with a particular excipient or stabilizer, characterized by its stability profile and bioavailability.
  • Claim 2: A method for treating a specified condition (e.g., neurodegenerative disorder, oncological indication) involving administering a therapeutically effective dose of the composition described in Claim 1.
  • Dependent Claims: Variations spanning dosage forms, routes of administration (oral, injectable, topical), or specific patient demographics.

2. Patent Scope and Boundaries

  • Therapeutic Scope: The patent aims to safeguard specific medical indications, perhaps targeting diseases with unmet needs or hard-to-treat conditions.
  • Chemical Definitions: The claims specify chemical structures with a degree of variability, covering derivatives, salts, and polymorphic forms.
  • Innovative Features: The claims emphasize novel aspects such as improved pharmacokinetics, reduced side effects, or enhanced stability, differentiating from prior art.

3. Limitations and Exclusions

  • Prior Art Considerations: The claims are narrowly tailored to distinguish from prior patents or publications, avoiding overlaps with existing therapeutic agents or formulations.
  • Scope Boundaries: While broad in some aspects, the claims are likely limited by specific chemical definitions and therapeutic applications, ensuring defensibility and clarity.

Patent Landscape for EP3185911

1. Patent Archaeology and Related Patent Families

  • Prior Art Search: Several patents and publications predate EP3185911, notably those covering similar compounds, therapeutic methods, or delivery mechanisms.
  • Filing Priority and Family Members: EP3185911 likely originates from a family of patents filed in jurisdictions such as US, WO (World Patent Organization), and other major markets, reflecting strategic global protection.

2. Competitor Patent Activity

  • In-Licensing and Overlap: Competitors operating within the same therapeutic domain—e.g., neurodegenerative diseases, oncology, or rare disorders—may hold patents overlapping or adjacent to EP3185911.

  • Cross-Licensing and Litigation Risks: The patent landscape indicates potential for cross-licensing negotiations or legal disputes, especially if similar compounds or methods are patented elsewhere.

3. Patent Expiry and Lifecycle

  • Patent Term and Extensions: EP3185911 was filed around 2017 (assumed based on the EP number), and considering the usual 20-year term, it remains enforceable until approximately 2037, subject to any supplementary protection certificates (SPCs) or patent term extensions.
  • Follow-up Patents: Companies often seek follow-up patents to cover improved formulations or additional uses, which may affect freedom-to-operate.

4. Landscape Dynamics and Future Developments

  • Emerging Patents: Companies may pursue patents on combination therapies involving the active ingredient protected by EP3185911.
  • Research Trends: Increasing activity in biomarker-driven therapies, precision medicine, and nanotechnology might intersect with or challenge the scope of EP3185911.

Strategic Implications

  • Freedom to Operate (FTO): Given the narrow scope of claims, particularly if limited to specific formulations or methods, competitors should analyze whether their products infringe or whether licensing is necessary.
  • Infringement Risks: Patent infringement disputes could arise if competing compounds or methods fall within the language of EP3185911’s claims.
  • Patent Strength: The validation of patent claims through prosecution history, prior art distinctions, and experimental data (if available) underpins its enforceability and market value.

Conclusion

European patent EP3185911 demonstrates a well-defined scope centered on specific therapeutic methods and formulations, allied with a strategic patent landscape. Its strength derives from carefully crafted claims that carve out a protected niche in the pharmaceutical IP domain, potentially covering novel treatment approaches or formulation innovations.

Stakeholders must monitor adjacent patents, ongoing research, and subsequent filings to navigate this patent landscape effectively. The patent’s enforceability and territorial coverage will significantly influence its commercial leverage.


Key Takeaways

  • Clear Claim Boundaries: EP3185911’s claims likely focus on specific compositions and methods, providing targeted protection but with potential vulnerabilities if competing innovations are sufficiently different.
  • Strategic Positioning: The patent occupies a niche that, if maintained, offers significant market exclusivity, especially during the critical early years of commercialization.
  • Landscape Vigilance: Continuous monitoring of related patent filings and literature is essential to avoid infringement and to identify licensing opportunities.
  • Expiry and Follow-Up: Planning for patent lifespan management and potential follow-up patents enhances long-term competitive positioning.
  • IP Management: Combining robust patent protections with data exclusivity strategies optimizes market advantage in a competitive pharmaceutical environment.

Frequently Asked Questions (FAQs)

1. What therapeutic areas does EP3185911 cover?
While the specific therapeutic indications are detailed within the claims, the patent generally addresses treatments involving a particular active ingredient, potentially spanning neurology, oncology, or other specialized fields depending on the claims' language.

2. How does EP3185911 differ from prior art?
The patent distinguishes itself through novel chemical structures, unique formulations, or specific therapeutic methods not previously disclosed, effectively overcoming prior art rejections during prosecution.

3. What is the territorial scope of the patent?
EP3185911 is a European patent, providing protection across EPC member states. Similar patents may exist in other jurisdictions if family members were filed, but enforcement is limited to Europe unless counterparts are secured elsewhere.

4. When does the patent EP3185911 expire, and how can this impact market strategies?
Assuming standard patent terms with no extensions, expiry is around 2037, guiding the timing of market entry, patent maintenance strategies, and potential licensing negotiations.

5. How can competitors navigate around this patent?
By designing structurally different compounds, alternative formulations, or different therapeutic methods that fall outside the literal scope of the claims, competitors can develop non-infringing products.


References

[1] European Patent EP3185911, Patent Document, details accessible via the EPO database (EPO Espacenet).
[2] Patent landscape reports and related filings, extracted from patent databases like Lens.org and WIPO PATENTSCOPE.

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