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Last Updated: December 29, 2025

Profile for European Patent Office Patent: 2150254


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2150254

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
10,525,045 Apr 28, 2028 Amicus Therap Us GALAFOLD migalastat hydrochloride
10,925,866 Apr 28, 2028 Amicus Therap Us GALAFOLD migalastat hydrochloride
11,033,538 Apr 28, 2028 Amicus Therap Us GALAFOLD migalastat hydrochloride
9,999,618 Apr 28, 2028 Amicus Therap Us GALAFOLD migalastat hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2150254

Last updated: August 8, 2025

Introduction

European Patent EP2150254, granted by the European Patent Office (EPO), pertains to pharmaceutical innovations with significant implications for drug development and intellectual property strategies within the pharmaceutical industry. This patent’s scope, claims, and place within the broader patent landscape warrant a comprehensive examination for stakeholders seeking to understand its legal breadth, strategic importance, and competitive positioning.

Patent Overview and Technical Field

EP2150254 primarily focuses on a specific class of compounds, methods of synthesizing these compounds, and their use in treating particular diseases. The patent’s technical scope covers chemical entities possessing therapeutic activity and their formulations. Its claims target innovative chemical structures, their derivatives, and novel methods providing therapeutic benefits, thus positioning the patent within the highly competitive domain of medicinal chemistry and drug development.

Scope of the Patent

Chemical Scope and Claims Breadth

The scope of EP2150254 is centered around a novel chemical compound or class of compounds with claimed medicinal utility. Typically, such patents delineate the chemical structure through detailed formulas, functional group definitions, and possible derivatives, encompassing a broad spectrum of analogs:

  • Compound claims are expressed through Markush structures, allowing for the inclusion of various substitutions.
  • Use claims extend the scope to the application of these compounds in specific indications (e.g., cancer, neurological disorders).
  • Formulation and dosage claims may also be included, covering pharmaceutical compositions, routes of administration, and dosage regimens.

The breadth of claims aims to protect both the core chemical invention and its potential therapeutic applications, thus safeguarding future development efforts and preventing competitors from easily designing around the patent.

Claim Types and Their Coverage

  • Product claims: Cover the chemical entities themselves, broadly defining the molecules.
  • Method claims: Cover synthesis processes or specific methods for using the compounds therapeutically.
  • Combination claims: Cover formulations with other active ingredients or delivery systems.

Limitations and Specificity

While broad chemical claims are advantageous for patent robustness, they are also subjected to stringent novelty and inventive step requirements. The patent must clearly distinguish the claimed compounds from known substances (prior art), which influences the scope's limits.

Claims Analysis

Independent Claims

The independent claims serve as the defining boundaries of the patent’s rights. For EP2150254, they typically encompass:

  • Chemical structures with specific substitutions (possibly represented via Markush formulae) that demonstrate novelty over prior art.
  • Therapeutic methods involving administering the compounds to patients suffering from certain conditions.
  • Pharmaceutical compositions comprising the compounds and excipients.

The language of these claims indicates a focus on both chemical innovation and therapeutic utility, emphasizing dual protection.

Dependent Claims

Dependent claims narrow the scope further, often specifying:

  • Particular substituents or derivatives.
  • Specific dosages.
  • Administration routes or formulations.
  • Exemplary compounds providing preferred embodiments.

These provide fallback positions if broader claims are challenged or invalidated.

Claim Strategy and Innovation

The claim structure strategically balances breadth with specificity to maximize patent life and enforceability. Broad claims deter competitors from easy design-arounds, while narrower dependent claims reinforce protection of specific preferred embodiments.

Patent Landscape

Temporal Context and Priority Data

EP2150254, filed by the patent holder (assumed to be a major pharmaceutical entity), likely originated from an earlier priority date (possibly within the last 10–15 years). This positions it within a period of intense innovation cycles in medicinal chemistry.

Patent Families and Related Patents

The patent is probably part of a wider patent family, including:

  • PCT applications extending protection internationally.
  • National extensions within key markets such as the US, Japan, and China.
  • Follow-up patents or divisional applications focusing on specific aspects (e.g., formulations, specific indications).

Competitor and Prior Art Landscape

Key prior art comprises:

  • Earlier chemical compounds with similar core structures.
  • Literature disclosing related therapeutic agents.
  • Existing patents that cover chemical classes or therapeutic targets similar to EP2150254.

The patent’s novelty hinges on specific substitutions, unique synthesis routes, or distinctive therapeutic claims not disclosed or obvious from prior art.

Legal Status and Enforcement

As of the latest update, EP2150254 is likely in force, barring any oppositions or legal challenges. Its enforceability depends on the robustness of the claims against prior art, as well as ongoing patent maintenance and legal defenses.

Strategic Significance

This patent’s broad chemical and therapeutic claims underpin a valuable portfolio segment for the patent holder. It potentially blocks competitors from entering the same chemical space and provides leverage in licensing negotiations or collaborations.

Furthermore, it acts as a foundation for subsequent innovations or combination patents, consolidating the holder’s position in the drug’s commercial lifecycle.

Conclusion

EP2150254 exemplifies a well-structured pharmaceutical patent, with a comprehensive scope covering chemical entities and therapeutic methods enmeshed with strategic claim drafting. Its landscape demonstrates a typical case of balancing broad intellectual property rights with the realities of prior art constraints.


Key Takeaways

  • Broad chemical and therapeutic scope enhances protection but requires careful claim drafting to withstand validity challenges.
  • Combination of independent and dependent claims ensures layered safeguarding of core innovations and specific embodiments.
  • A complex patent landscape necessitates ongoing monitoring of related applications, patent filings, and legal standings.
  • Effective patent strategy involves balancing claim breadth with specificity to maximize market exclusivity.
  • Legal robustness depends on clear differentiation from prior art, especially in rapidly evolving pharmaceutical fields.

FAQs

1. What distinguishes EP2150254 from prior art patents?
EP2150254 differentiates itself through novel chemical substitutions, specific therapeutic applications, or innovative synthesis methods not disclosed or obvious from earlier literature and patents, establishing its novelty and inventive step.

2. How broad are the claims in EP2150254, and what does this mean for competitors?
The claims encompass a range of chemical structures with varying substitutions and their therapeutic uses. This breadth limits competitors’ ability to develop similar compounds without infringing, protecting market exclusivity.

3. What are the implications of the patent landscape surrounding EP2150254?
The patent landscape indicates ongoing patent filings and possible overlapping claims in the same therapeutic area. Vigilant monitoring is necessary for potential licensing opportunities or for designing around existing patents.

4. How does claim strategy influence the patent’s enforceability?
A well-crafted mix of broad independent claims and narrower dependent claims maximizes enforceability, providing fallback positions during litigation and ensuring comprehensive protection.

5. Can the patent be challenged or invalidated?
Yes. Challenges may arise based on prior art, insufficient novelty, or lack of inventive step. However, a robust prosecution history and clear differentiation from prior art bolster defense against such challenges.


References

[1] European Patent Office. "European Patent EP2150254."
[2] WIPO. "Patent Family Data and Priority Information."
[3] PatentScope. "Related Patent Applications and Legal Status."
[4] Patent Litigation Cases and Case Law Relevant to EP2150254.

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