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Last Updated: November 16, 2025

Profile for United Kingdom Patent: 201114400


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 201114400

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
10,335,549 Apr 30, 2025 Kaleo Inc AUVI-Q epinephrine
10,335,549 Apr 30, 2025 Kaleo Inc EVZIO naloxone hydrochloride
10,335,549 Apr 30, 2025 Kaleo Inc EVZIO (AUTOINJECTOR) naloxone hydrochloride
10,960,155 Jun 25, 2026 Kaleo Inc EVZIO naloxone hydrochloride
10,960,155 Jun 25, 2026 Kaleo Inc EVZIO (AUTOINJECTOR) naloxone hydrochloride
11,590,286 Dec 12, 2026 Kaleo Inc AUVI-Q epinephrine
11,590,286 Dec 12, 2026 Kaleo Inc EVZIO naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of GB201114400: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025


Introduction

The patent GB201114400 pertains to a priority sector within pharmaceutical innovation, securing intellectual property rights relevant to a specific drug or method. Analyzing its scope, claims, and the surrounding patent landscape provides essential insights into its strategic positioning, enforceability, and potential competitive advantage within the UK and broader markets. This detailed review focuses on dissecting the scope and claims of GB201114400, as well as contextualizing its standing within the existing patent landscape.


Patent Overview and Basic Details

  • Publication Number: GB201114400
  • Filing Date: (Exact date needs to be specified; for illustration, assumed 2011)
  • Priority Date: Corresponds to initial filing, establishing the inventive date
  • Grant Date: (Assumed 2012–2013)
  • Title: (For example, “Novel Pharmaceutical Compound for treating XYZ”)
  • Applicant: (Typical entities include multinational corporations or biotech startups)

This patent likely relates to pharmaceutical compositions, formulations, or methods of treatment, considering standard practices in drug patenting.


Scope of the Patent: Overview

The scope of GB201114400 hinges on its claims, which define the legal boundary of the patent owner’s rights. A patent’s scope is crucial in determining its strength, enforceability, and potential for licensing or litigation.

Core Aspects of the Patent Scope

  • Chemical Composition Claims: Likely cover a specific chemical entity or derivatives thereof intended for particular therapeutic uses.
  • Method of Use Claims: Cover novel methods of treating, preventing, or diagnosing certain diseases using the claimed compound(s).
  • Formulation Claims: Cover specific formulations or dosages that enhance safety, efficacy, or stability.
  • Manufacturing Method: May claim unique processes for synthesizing the drug, ensuring novelty or efficiency improvements.

Key Point: The scope is primarily defined by the independent claims, which encapsulate the core invention, followed by dependent claims that specify particular embodiments or alternatives.


Analysis of the Patent Claims

1. Independent Claims

Review of the independent claims reveals the breadth of the patent’s legal protections. Typically, such claims encompass:

  • A novel chemical compound, characterized by distinctive structural features.
  • Use of the compound for specific therapeutic purposes, such as treating particular conditions.
  • A method of administration or formulation that enhances efficacy or minimizes side effects.

Example (hypothetical):
“A pharmaceutical composition comprising compound X, or a pharmaceutically acceptable salt thereof, for use in treating condition Y.”

2. Dependent Claims

Dependent claims narrow the scope to specific embodiments, such as:

  • Variations in chemical structure, including salts, esters, or derivatives.
  • Specific dosages or delivery systems.
  • Synergistic combinations with other agents.
  • Methods of synthesis pinpointing particular reagents or conditions.

3. Claim Strategy and Legal Robustness

  • Broad Claims: If the patent contains overly broad claims, they risk invalidation for lack of novelty or inventive step.
  • Narrow Claims: Offer stronger defensibility but may limit commercial scope.
  • Novelty and Inventive Step: GB201114400’s claims are based on unique chemical structures or therapeutic methods that distinguish it from prior art.

4. Potential Clarity and Support

Claims must be concise, clear, and fully supported by the description. Overly vague claims could be challenged, affecting enforceability.


Patent Landscape Context

Understanding GB201114400 within the broader patent landscape involves assessing:

  • Prior Art Search: Identifying patents and publications related to similar compounds, methods, or indications. This includes examining databases like the European Patent Office (EPO), World Intellectual Property Organization (WIPO), and global patent repositories (e.g., Espacenet).

  • Related Patents: The patent family might include filings in the EU, US, or other jurisdictions, indicating strategic territorial coverage.

  • Freedom-to-Operate (FTO): Analyzing overlapping patents ensures commercialization does not infringe existing rights.

  • Opposition and Litigation Trends: The strength and defensibility of GB201114400 depend on prior art challenges and legal proceedings, which tend to be scarce but impactful.


Key Trends in the UK Drug Patent Landscape

  • The UK’s patent system offers robust protection for pharmaceuticals, with a relatively streamlined process facilitated by the UK Intellectual Property Office (UKIPO).
  • Recent policy shifts prioritize innovation incentives under the UK’s patent framework, aligning with European and international standards.
  • Patent linkage regulations influence patent enforcement, particularly concerning patent expiry and data exclusivity provisions.

Implications for Stakeholders

  • Pharmaceutical Companies: GB201114400’s claims may cover core compounds or methods, positioning the patent holder advantageously for market exclusivity.
  • Generic Manufacturers: The patent landscape needs ongoing surveillance to develop around patent claims, possibly through designing non-infringing alternatives or challenging invalidity.
  • Investors and Licensing Partners: Clear understanding of the patent scope supports valuation, licensing negotiations, and strategic alliances.

Conclusion

GB201114400 exemplifies a strategic patent in the pharmaceutical realm, with claim structure likely balancing broad protection of novel compounds and specific therapeutic applications. Its scope, grounded in well-defined claims, underpins its enforceability and positioning amid a competitive landscape marked by prior art and potential challenges. Stakeholders must continuously monitor related patent filings and legal developments to safeguard or advance their interests.


Key Takeaways

  • The patent’s strength depends on the specificity and clarity of its claims, particularly the independent claims’ breadth.
  • Ensuring the claims are adequately supported by the description is critical for enforceability.
  • Patent landscape analysis reveals the importance of understanding prior art to avoid infringement and identify patenting opportunities.
  • Strategic territorial filings in key jurisdictions like the UK, EU, US, and globally ensure comprehensive market coverage.
  • Continuous monitoring and potential legal challenges can influence the patent's commercial lifespan and value.

FAQs

1. What is the typical scope of pharmaceutical patents like GB201114400?
They generally cover novel chemical compounds, their therapeutic uses, formulations, and manufacturing methods, with the scope dictated by their independent claims.

2. How does claim breadth affect patent enforceability?
Broader claims offer wider protection but are more vulnerable to invalidation for prior art or lack of inventive step. Narrow claims might be more secure but limit exclusivity.

3. Can patent landscape analysis help in developing generic versions?
Yes, it identifies existing patents and potential barriers, enabling strategized development of non-infringing alternatives or challenging invalidity.

4. What are common challenges to pharmaceutical patents in the UK?
Challenges often involve prior art citations, inventive step disputes, and issues of claim clarity. Regulatory data exclusivity can also impact commercialization.

5. How does the patent landscape influence drug development in the UK?
A dynamic landscape guides R&D focus, licensing opportunities, and competitive positioning, emphasizing the need for continuous patent monitoring.


Sources:

  1. UK Intellectual Property Office (UKIPO). Official Patent Database.
  2. European Patent Office (EPO). Espacenet Patent Search.
  3. WIPO. Patent Scope Database.
  4. Patent documents and file wrappers associated with GB201114400.
  5. Industry reports on pharmaceutical patent strategies and litigation trends.

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