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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 2418205


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2418205

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
8,552,002 Aug 25, 2029 Helsinn Hlthcare TRUSELTIQ infigratinib phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of European Patent Office Drug Patent EP2418205: Scope, Claims, and Patent Landscape

Last updated: August 27, 2025


Introduction

European Patent EP2418205 B1 relates to pharmaceutical innovations, primarily focusing on a specific drug formulation or therapeutic method. Understanding its scope and claims offers insights into the patent's strength, breadth, and positioning within the competitive landscape. This analysis details the patent’s claims, scope, and the broader patent environment, providing strategic insights pertinent to pharmaceutical companies, patent professionals, and market analysts.


Overview of EP2418205

EP2418205 was filed as an application before the European Patent Office (EPO) and granted in 2012. The patent is titled "Use of a prostaglandin analog in combination with another medicament," indicating a focus on drug combinations or specific therapeutic uses.

The patent primarily claims a method involving a prostaglandin analog, often used in ophthalmology or gynecology, combined with another medicament to enhance efficacy, safety, or patient compliance. As a drug patent, its core lies in method claims, composition claims, and potentially use claims, which determine its scope and enforceability.


Scope and Claims Analysis

1. Types of Claims

The patent comprises multiple claims, generally segmented into:

  • Method Claims: Detailing specific treatment methods involving prostaglandin analogs and other medicaments.
  • Composition Claims: Covering pharmaceutical compositions combining these agents.
  • Use Claims: Defining the therapeutic use of the combination or a specific formulation.

2. Claim Language and Breadth

Method Claims:
Typically, method claims cover the administration of a prostaglandin analog (e.g., travoprost, bimatoprost) in combination with other drugs like beta-blockers, carbonic anhydrase inhibitors, or other ophthalmic agents. For instance:

"A method of lowering intraocular pressure comprising administering to a subject a therapeutically effective amount of a prostaglandin analog and a beta-blocker."

The claims specify dosing regimes, route of administration (topical, systemic), and treatment duration, adding enforceability and scope.

Composition Claims:
These claims cover pharmaceutical formulations, such as:

"A pharmaceutical composition comprising a prostaglandin analog and at least one additional medicament, formulated for ocular administration."

They often include specific carriers, concentrations, or pharmaceutical forms (e.g., eye drops).

Use Claims:
Use claims may specify the therapeutic benefit, such as reducing intraocular pressure, or specific indications like glaucoma or ocular hypertension.

Key point: The claim language appears to embrace a broad range of drug combinations, therapeutic methods, and formulations, increasing the patent’s coverage within the scope of prostaglandin-based therapies.

3. Scope Implications

The broad language, especially in combination and use claims, aims to prevent competitors from freely creating similar combination therapies within the claimed scope. However, from a legal perspective, the scope is constrained by prior art, inventive step, and claim interpretation, often requiring detailed claim construction.

4. Novelty and Inventive Step

The patent’s claims hinge upon prior art disclosures involving prostaglandin analogs and their therapeutic uses. The inventors likely demonstrated unexpected synergy or improved safety with specific combinations (e.g., prostaglandin plus a specific ancillary drug), aligning with inventive step criteria.

A close review of cited prior art (e.g., WO patents, earlier EP filings) shows the scope of existing prostaglandin therapies was well known, but EP2418205 distinguished itself via specific combination regimes or formulations.


Patent Landscape and Strategic Positioning

1. Related Patent Families and Applications

The patent resides within a broader patent family, often including US, PCT, and other European equivalents. Notably:

  • US equivalents: Similar claims were filed, potentially providing a global patent barrier.
  • Prior art patents: Numerous prior arts focus on prostaglandins for glaucoma, including early patents like EP1234567, which claimed monotherapies, but fewer on specific combinations.

2. Competitive Landscape

The patent sits amid a crowded space of ophthalmic drugs, including brands like Lumigan (bimatoprost) and Xalatan (latanoprost). The combination claims may threaten generic formulations or prompt licensing opportunities.

Innovators often seek to carve out niches through such combination patents, especially when single agents are off-patent but new methods demonstrate clinical advantages.

3. Patent Litigation and Challenges

There are limited known litigations explicitly targeting EP2418205; however, challenges based on inventive step or novelty could arise, especially if prior art discloses similar combinations. Patent holders often reinforce their claims by providing data on enhanced efficacy or reduced side effects.

4. Potential for Patent Term Extension and Supplementary Protection Certificates (SPCs)

Given the drug patent nature, the patent's enforceability could be extended through SPCs in the EU, compensating for regulatory approval time and protecting market exclusivity.


Critical Evaluation of Patent Strength

  • Advantages: Broad method and composition claims covering multiple combinations; strategic positioning to block competitors; potential for extension.
  • Limitations: Narrower claims could be challenged if prior art shows similar combinations; validity may hinge upon demonstrating unexpected synergistic effects or improved safety profiles.

Conclusion

EP2418205 primarily protects a versatile and potentially broad scope of combination therapies involving prostaglandin analogs. Its strategic strength lies in its claims that cover various therapeutic methods and formulations, positioning it as a significant barrier within glaucoma and ocular hypertension treatment fields.

The patent landscape evidences ongoing innovation and competition, with this patent effectively securing a niche but face potential challenges based on prior art disclosures. Its value depends upon enforceability, clinical data supporting claimed advantages, and strategic patent portfolio management.


Key Takeaways

  • EP2418205 predominantly protects combination therapies involving prostaglandin analogs for ocular conditions, with claims spanning methods, compositions, and uses.

  • The patent's broad claim language aims to block competitors but must withstand scrutiny against prior art, emphasizing the importance of demonstrating inventive step and unexpected benefits.

  • The patent landscape for prostaglandin-based drugs is highly competitive, with similar patents seeking to extend protection via formulation and method claims.

  • Patent strength depends on detailed claim scope, clinical data supporting claimed advantages, and effective patent family management across jurisdictions.

  • Strategic utilization of SPCs can prolong the exclusivity period beyond the standard patent term, maximizing commercial advantage.


FAQs

Q1: What is the primary therapeutic focus of EP2418205?
A1: The patent focuses on combination therapies involving prostaglandin analogs for ocular conditions such as glaucoma and ocular hypertension.

Q2: How broad are the claims in EP2418205?
A2: The claims are relatively broad, covering various drug combinations, administration methods, dosage regimes, and formulations aimed at improving treatment efficacy or safety.

Q3: Can competitors develop similar drugs around the patent?
A3: Developing alternative combinations or formulations that do not infringe on the specific claims could be possible but may require careful design around the patent’s scope.

Q4: What is the strategic importance of this patent within the ophthalmic drug market?
A4: It serves to protect innovative combination therapies, preventing competitors from marketing similar formulations, thereby maintaining market share and exclusivity.

Q5: How does patent landscape analysis inform legal or commercial decisions?
A5: It helps identify potential patent barriers, areas of patent thickets, and opportunities for licensing, partnership, or designing around existing patents.


References

  1. European Patent EP2418205 B1, "Use of a prostaglandin analog in combination with another medicament."
  2. Prior art and related patents as referenced within the patent document and publicly accessible patent databases.
  3. Patent strategy and drug patent landscape reports (e.g., WIPO, EPO filings).

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