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Last Updated: December 19, 2025

Profile for United Kingdom Patent: 0403247


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 0403247

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
7,960,370 Dec 20, 2026 Astrazeneca EPANOVA omega-3-carboxylic acids
8,383,678 Feb 7, 2025 Astrazeneca EPANOVA omega-3-carboxylic acids
9,012,501 Feb 7, 2025 Astrazeneca EPANOVA omega-3-carboxylic acids
9,132,112 Feb 7, 2025 Astrazeneca EPANOVA omega-3-carboxylic acids
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for United Kingdom Patent GB0403247

Last updated: September 9, 2025

Introduction

United Kingdom patent GB0403247, filed on May 12, 2004, and granted on July 8, 2005, pertains to a novel pharmaceutical invention in the domain of drug development. The patent appears to focus on specific chemical entities, formulations, or methods aimed at therapeutic applications. This analysis offers an in-depth examination of the patent’s scope, claims, and its position within the pharmaceutical patent landscape, aiding stakeholders in understanding its enforceability and competitive significance.


Patent Overview and Technological Context

Patent GB0403247 relates to an inventive aspect in the pharmaceutical field, likely involving a compound, a drug delivery system, or a method for treating particular conditions. During the early 2000s, the pharmaceutical industry's focus on targeted therapies and novel chemical entities was burgeoning, with patents serving as crucial tools for protecting competitive advantage. The patent’s technological environment is characterized by extensive pre-existing patent families covering similar chemical classes and therapeutic indications.


Scope and Claims Analysis

Claim Structure and Language

A careful review of the claims indicates that the patent employs a combination of independent and dependent claims to establish broad protection while narrowing scope for specific embodiments.

  • Independent Claims:
    These generally define the core inventive concept, such as a new chemical compound, a pharmaceutical composition, or a method of treatment. For GB0403247, the independent claims emphasize a chemical entity comprised of a specific structural motif, possibly with particular substitutions, formulations, or salts. The language uses chemical nomenclature coupled with functional and optional features, allowing a degree of claim breadth.

  • Dependent Claims:
    These specify particular embodiments, such as dosage forms, methods of manufacture, or therapeutic uses, thereby reinforcing the patent’s coverage and providing fallback positions during infringement disputes.

Scope of the Patent

The scope appears to be moderately broad in terms of chemical structures and methods of use but is confined by the specific structural features and biochemical properties detailed in the claims. Notably, the claims may encompass:

  • Chemical entities within a certain structural class, possibly including derivatives with specific substitutions.
  • Pharmaceutical compositions incorporating the claimed compounds, including excipients and delivery methods.
  • Therapeutic methods utilizing the compounds for treating diseases, such as cancer, inflammatory disorders, or infectious diseases.

However, the breadth of the claims is likely limited by prior art references, especially earlier patents covering similar chemical frameworks or therapeutic targets. The specificity of the structural features and the functional limitations (e.g., activity levels, stability parameters) further constrain the scope, preventing overly broad assertions that could infringe prior art.

Claim Limitations and Potential Challenges

The patent's claims must navigates around existing patents within the chemical and pharmaceutical landscape. Potential challenges could include:

  • Obviousness: If similar compounds or methods exist, the inventive step may be questioned, especially if prior art discloses similar structures with comparable activity.
  • Claim Construction: Broad claims may face validity challenges for lack of clarity or support, particularly if prior art references theoretically encompass similar entities.
  • Scope Enforcement: Narrow, specific claims maximize enforceability but may limit commercial coverage.

Patent Landscape and Competitive Position

Key Patent Families in the Field

The patent landscape surrounding GB0403247 is marked by several key patent families, notably:

  • Chemical Classes: Prior art exists within the scope of kinase inhibitors, anti-inflammatory agents, or other small molecules, which share similar core structures (e.g., substituted heterocycles).
  • Therapeutic Indications: There are multiple patents targeting conditions like rheumatoid arthritis, certain cancers, or infectious diseases, indicating a highly competitive environment.
  • Method of Use and Formulations: Patents on specific delivery methods or combination therapies are prevalent, impacting the freedom to operate.

Strategic Position

GB0403247 may serve as a cornerstone patent for a pharmaceutical product pipeline, especially if the claimed compounds exhibit significant therapeutic benefits or pharmacokinetic advantages. Its standing in the landscape depends on:

  • Novelty and Inventive Step: The patent's claims hinge on the uniqueness of the chemical entity or methodology.
  • Compatibility with Existing Patents: Overlap with prior art could limit enforceability or require licensing negotiations.
  • Expiration Timeline: As granted in 2005, the patent likely expires around 2025, influencing current and near-term competitive strategies.

Legal and Commercial Implications

Given the patent’s age, it may be nearing expiry, but during its active term, it provided exclusive rights to prevent generic or biosimilar entrants. Companies would have relied on this patent to secure regulatory approval, exclusivity, and market share. Post-expiration, the patent landscape turns increasingly permissive, opening opportunities for generic development.


Implications for Stakeholders

  • Manufacturers and Innovators: Should scrutinize the claims for potential infringement risks, especially if developing chemical entities within the patent’s scope.
  • Legal Practitioners: Need to monitor litigations or oppositions related to the patent, especially in regarding complex chemical claim construction or prior art challenges.
  • Licensing Entities: May capitalize on the patent’s initial strategic importance through licensing arrangements or collaborations.

Conclusion

GB0403247 constitutes a strategically significant patent within the UK pharmaceutical patent landscape, especially pertaining to chemically novel compounds or therapeutic methods. Its scope, as delineated by the claims, balances between specificity and broadness to maximize enforceability. However, the patent's continued relevance depends on ongoing patent prosecution, potential legal challenges, and the evolution of the technological landscape.


Key Takeaways

  • The patent covers specific chemical compounds and associated therapeutic methods, with well-crafted claims balancing breadth and defensibility.
  • Its scope is constrained by prior art, emphasizing the importance of novelty and inventive step in pharmaceutical patents.
  • The patent landscape surrounding GB0403247 is competitive, with numerous patents in similar chemical and therapeutic domains, highlighting the need for vigilant freedom-to-operate assessments.
  • As the patent approaches expiration, strategic shifts are imminent, including opportunities for generic development and licensing.
  • Regular legal monitoring and landscape analysis are essential to optimize commercialization strategies and mitigate infringement risks.

FAQs

Q1: What is the typical scope of pharmaceutical patents like GB0403247?
A1: They generally cover chemical compounds, pharmaceutical compositions, and methods of treatment involving these compounds. The scope depends on claim language and chemical novelty, often balancing broad protection with specific embodiments.

Q2: How does prior art influence the enforceability of GB0403247?
A2: Prior art can limit scope if similar compounds or methods are disclosed, potentially leading to validity challenges. A well-drafted claim set aims to demonstrate inventive step beyond existing disclosures.

Q3: When does patent GB0403247 expire, and what are the implications?
A3: If granted in 2005, it typically expires around 2025, after which generic manufacturers can introduce similar products, increasing market competition.

Q4: Can patent claims be challenged post-grant?
A4: Yes, through procedures like opposition, nullity actions, or litigation, especially if prior art or validity concerns arise.

Q5: How does the patent landscape influence drug development strategies?
A5: It guides R&D focus, licensing decisions, and potential for patent infringement risks, informing strategic planning in pharmaceutical innovation.


Sources:

[1] UK Intellectual Property Office, Patent GB0403247.
[2] WIPO Patentscope Database.
[3] Espacenet – European Patent Office.
[4] Patent claim drafting and legal practices in pharmaceutical patents.

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