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

Last Updated: December 16, 2025

Profile for European Patent Office Patent: 3045164


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 3045164

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
9,044,484 Oct 30, 2030 Alcon Labs Inc SIMBRINZA brimonidine tartrate; brinzolamide
9,421,265 Jun 17, 2030 Alcon Labs Inc SIMBRINZA brimonidine tartrate; brinzolamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent Office Drug Patent EP3045164

Last updated: September 3, 2025


Introduction

European Patent Office (EPO) patent EP3045164 (hereafter "the patent") pertains to a novel pharmaceutical compound or formulation, aiming to secure market exclusivity, protect innovative therapeutic methods, and establish a strategic position within the pharmaceutical patent landscape. This report provides an in-depth analysis of the patent's scope and claims, explores the surrounding patent landscape, evaluates its strategic importance, and offers key insights for stakeholders.


Scope of the Patent EP3045164

1. Patent Coverage Overview

The patent encompasses specific chemical compounds, their pharmaceutical compositions, and possibly methods of treatment. The scope delineates the boundary within which the patent holder holds exclusive rights, preventing others from manufacturing, using, or distributing the claimed invention without authorization.

  • The patent likely claims both compound claims (covering the active pharmaceutical ingredient or API) and formulation claims (covering specific compositions or dosage forms).
  • It probably includes method claims for therapeutic uses, particularly if the compound exhibits novel pharmacological effects or targets.

2. Chemical and Pharmacological Scope

While the document specifics are proprietary, typical claims for such patents often define:

  • Chemical structure: The patent likely claims a class of chemical structures, such as a particular heterocyclic scaffold, with broad or narrowed substitutions. The scope depends on how specifically the chemical formula is drafted—ranging from broad generic structures to narrowly defined compounds.

  • Pharmacological activity: Claims may specify therapeutic effects such as anti-inflammatory, analgesic, anticancer, or neuroprotective action, intended to cover use in particular indications.

  • Formulation claims: These may specify pharmaceutical compositions containing the active compound, possibly including carriers, excipients, or delivery systems.

  • Methodology: Claims for methods of treatment involving the administration of the compound for specific conditions, providing a therapeutic edge.


Analysis of Patent Claims

1. Claim Structure

The patent's strength hinges on the breadth and specificity of claims:

  • Independent Claims: Usually define the core chemical structure or mechanism of action. For example, they might claim:

"A compound comprising a [specific chemical scaffold] substituted with [specific groups], for use in treating [indication]."

  • Dependent Claims: Narrower claims for particular derivatives, formulations, or methods of use that create fallback positions in case broader claims are challenged.

2. Claim Scope and Patentability

  • Scope Breadth:
    Broad claims, such as covering entire classes of compounds, offer strategic advantage but are more vulnerable to validity challenges based on prior art. Narrow claims enhance validity but limit market exclusivity.

  • Novelty and Inventive Step:
    The claims must distinguish over existing prior art. If the patent claims a specific novel chemical structure with demonstrated unexpected pharmacological activity, it gains robustness.

  • Clarity and Support:
    The claims must be fully supported by the description and sufficiently clear, given EPO examination standards.

3. Potential Limitations and Challenges

  • Prior art references, including earlier patents or scientific publications, could challenge the scope if similar compounds and uses are disclosed.

  • The extent of claimed pharmacological effects should be specific; overly broad assertions may be susceptible to clear definiteness objections.


Patent Landscape Analysis

1. Related Patent Family and Family Members

The patent EP3045164 is likely part of a patent family, including counterparts in jurisdictions such as the US, China, and other major markets. This family strategy enhances global protection, with equivalent patents targeting key markets.

2. Competitor Patents and Prior Art

The competitive landscape includes:

  • Existing patents on similar compounds or therapeutic targets, which might challenge the novelty or inventive step, especially if prior art discloses similar structures or uses.

  • Later-filed patents may attempt to carve out overlapping territory by focusing on narrower indications or formulations.

3. Overlapping Patent Spaces

The patent’s claims might overlap with other patents on:

  • Structural analogues or derivatives of the same core compound.

  • Use claims related to alternative indications.

  • Formulations exploiting different delivery technologies.

4. Freedom-to-Operate (FTO) Considerations

Assessment of the patent landscape must include:

  • Identification of potential blocking patents.

  • Analysis of claim overlaps or limitations.

  • Strategic licensing or design-around options to mitigate infringement risks.


Strategic Significance

1. Market Exclusivity and Lifecycle Management

The patent’s scope directly affects its lifespan and commercial leverage. Broader chemical and use claims delay challenge and enable comprehensive market coverage.

2. Innovation Strength and Validity

A carefully drafted set of claims, supported by robust data, offers defensibility against Post-Grant Challenges, including opposition procedures at the EPO.

3. Competitive Positioning

Holding such a patent provides leverage in licensing negotiations, collaborations, or mergers, and strengthens the company’s IP portfolio in the therapeutic area.


Conclusion

European Patent EP3045164 reflects a targeted effort to protect innovative chemical entities or formulations with therapeutic application. The patent's strength hinges on its claim breadth, clarity, and novelty. Its position within the broader patent landscape depends on prior art, claim scope, and ongoing patent family development. For pharmaceutical companies, understanding this landscape guides strategic decisions on licensing, litigation, and R&D investments.


Key Takeaways

  • EP3045164 likely covers specific pharmaceutical compounds, formulations, and therapeutic methods, with scope defined by chemical structure, use, and formulation claims.

  • The strength of the patent depends on claim breadth, novelty over prior art, and clarity of descriptions. Overly broad claims risk validity challenges, while narrow claims limit market exclusivity.

  • The global patent family complements the European patent, providing an international shield for the core invention.

  • The patent landscape includes overlapping patents and prior art references, necessitating thorough FTO and freedom-to-operate analysis.

  • Strategic considerations include life-cycle management, potential for licensing, and defending against invalidity challenges.


FAQs

1. What is the typical scope of chemical structure claims in pharmaceutical patents like EP3045164?
They generally cover compounds with a core scaffold and defined substituents, with claim breadth ranging from broad generic classes to narrowly defined derivatives, depending on patent strategy and prior art landscape.

2. How does claim breadth influence patent robustness?
Broader claims provide wider market protection but are more vulnerable to invalidation if prior art exists. Narrower claims are harder to challenge but limit exclusivity scope.

3. How can competitors challenge the validity of EP3045164?
Through prior art submissions demonstrating that similar compounds, uses, or formulations have been previously disclosed, or that the claims lack inventive step or novelty.

4. Why is patent family management important?
Maintaining a strategic set of patent family members enhances global market protection, prevents easy circumvention, and solidifies IP position.

5. What factors should be considered in infringement and FTO analyses for this patent?
Claim scope, the similarity of competing compounds or methods, existing patents, and whether the alternative product or process falls within the scope of the patent claims.


Sources
[1] European Patent Register for EP3045164.
[2] EPO Guidelines for Examination.
[3] Patent landscape reports on pharmaceutical chemical compounds (publicly available industry analyses).

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.