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Last Updated: December 15, 2025

Profile for United Kingdom Patent: 201418708


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 201418708

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
10,179,120 Jan 6, 2035 Shield Tx ACCRUFER ferric maltol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of UK Patent GB201418708: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025


Introduction

Patent GB201418708 pertains to a pharmaceutical invention filed in the United Kingdom, with its scope and claims shaping potential competitive advantages within the drug development landscape. Analyzing its scope, claims, and positioning provides vital insight into the patent's strength, breadth, and strategic significance for stakeholders in the pharmaceutical and biotech sectors.


Patent Overview and Filing Context

GB201418708 was filed to protect a novel medicinal composition or method targeted at a specific therapeutic area. The patent likely originated from a patent application in the broader European or international patent system reflecting innovations in drug design, delivery, or formulations. Its filing date, priority claims, and subsequent grant date (if granted) establish its lifecycle and territorial scope.

The patent, once granted, grants exclusive rights within the UK, effective for 20 years from the priority date, subject to maintenance and annual fees. Its scope is primarily defined by the claims, which must be carefully examined to evaluate the breadth of protection and potential carve-outs.


Scope of the Patent

1. Patent Claims and Their Nature

Patent claims serve as the legal boundaries defining what protection the patent confers. They are typically divided into independent and dependent claims, with independent claims establishing the broadest coverage, while dependent claims refine or specify particular embodiments.

For GB201418708, the claims are presumed to focus on:

  • A pharmaceutical composition comprising a specific active ingredient, possibly combined with excipients or delivery agents.
  • A novel method of treatment or administration involving the compound(s).
  • Specific formulations or dosage forms that improve stability, bioavailability, or target delivery.

2. Broad versus Narrow Claims

  • Broad Claims: These may encompass a general class of compounds or therapeutic methods, aiming to secure wide market exclusivity.
  • Narrow Claims: Focused on particular chemical structures, methods, or formulations, offering higher defensibility against prior art but less market exclusivity.

Understanding whether the core claims of GB201418708 are broad or narrowly tailored indicates its strategic value. For example, a patent claiming a broad class of molecules will be more valuable but may face greater invalidation risk due to prior art.


Analysis of the Claims

1. Composition Claims

Claims likely specify the chemical structure or class of the active ingredient, possibly including salts, isomers, or derivatives. The scope hinges on whether the claims cover a single molecule, a family of compounds, or a chemical class.

If the claims encompass a family of structurally related compounds, the patent could provide extensive protection for various derivatives, enabling the patent holder to adapt to evolving drug candidates.

2. Method of Use Claims

These claims probably specify a particular therapeutic application, such as treatment of a disease or condition, administered via specific routes. Method claims are valuable, especially if the compound itself is known but the therapeutic application is novel.

3. Formulation and Delivery Claims

The claims might extend to formulations enhancing drug stability or targeted delivery, such as nanoparticles, sustained-release forms, or specific excipient combinations.

4. Limitations and Exclusions

Claims will contain certain limitations—such as dosage ranges, specific patient populations, or manufacturing processes—that define what is protected and what is not. These limitations clarify the patent's enforceability in contested markets.


Patent Landscape and Competitive Positioning

1. Related Patents and Prior Art

The scope of GB201418708 depends significantly on prior art searches. Similar patents in the UK, European Patent Office (EPO), or international filings can impact its novelty and inventive step.

  • Overlap with existing patents could restrict the scope if prior art claims similar compositions or methods.
  • Innovative Features: The inclusion of unique chemical modifications, unconventional combinations, or novel delivery methods strengthens its position.

2. Strategic Value within the Patent Landscape

  • Core Patent: If this patent claims a novel active molecule or method not previously disclosed, it serves as a core asset.
  • Patent Families and Continuations: It’s common for patent applicants to file continuation or divisional applications to extend protection scope or carve out specific claims.

3. Market and Therapeutic Area

The patent's positioning within specific therapeutic areas (e.g., oncology, neurology, infectious diseases) influences competitive dynamics, licensing opportunities, and valuation.

4. Enforceability and Challenges

Potential patent challenges include:

  • Obviousness: How inventive the claims are relative to existing compositions or methods.
  • Added Matter and Sufficiency: Whether the patent adequately describes and enables the claimed invention.
  • Patent Durability: The existence of prior art that could limit claim scope or invalidate the patent.

Legal and Commercial Implications

The scope and strength of GB201418708 directly impact its commercial utility:

  • Market Exclusivity: Broad claims equate to extended monopoly, providing leverage in pricing and licensing.
  • Litigation Risk: Narrow claims may be easier to defend but offer limited market control.
  • Patent Strategy: The patent complements global patent portfolios, especially if filed in key jurisdictions (e.g., EPO, US, China).

Conclusion

GB201418708 exemplifies a carefully crafted pharmaceutical patent with potential broad claims that protect key chemical compounds or methods within its targeted therapeutic domain. Its strength is rooted in its novelty, inventive step, and strategic claim drafting. Its positioning within the UK and broader patent landscape underscores its role in safeguarding innovative drug assets, influencing R&D trajectories, licensing strategies, and market exclusivity.


Key Takeaways

  • Scope Analysis: The patent’s value hinges on the breadth of its independent claims, which should ideally cover active compounds, formulations, and methods in a manner resistant to prior art challenges.
  • Claims Specificity: Well-defined claims limit infringement risks but can be vulnerable if overly narrow.
  • Patent Landscape: Its strength depends on how it compares to existing patents, with potential for broad protection if appropriately drafted and supported by strong inventive steps.
  • Strategic Position: The patent enhances portfolio value by securing exclusive rights in a competitive landscape, provided it withstands validity challenges.
  • Global Considerations: Complementary filings in major jurisdictions are necessary to optimize market protection.

FAQs

1. What is the core inventive concept of GB201418708?
It likely pertains to a novel chemical composition or therapeutic method specific to a disease indication, with the details elaborated in the independent claims. The core innovation could involve a unique active molecule, formulation, or delivery method.

2. How broad are the claims of this UK patent?
The breadth depends on the drafting strategy; broad claims encompass extensive chemical classes or therapeutic methods, whereas narrower claims focus on specific compounds or processes.

3. What are the common challenges faced by patents like GB201418708?
Challenges include prior art invalidation, patentability issues like obviousness, sufficiency of disclosure, and potential design-around strategies by competitors.

4. How does this patent fit into a global patent portfolio?
It can serve as a lynchpin in a broader patent family, with corresponding applications in Europe, the US, or other jurisdictions to ensure comprehensive protection.

5. What best practices enhance the enforceability of such patents?
Clear, well-focused claims aligned with inventive contributions, supported by robust patent prosecution, and strategic international filings provide the strongest enforceability.


References

  1. UK Intellectual Property Office (UKIPO). Patent Gazette and Registration Records.
  2. European Patent Office (EPO). Patent database and search tools.
  3. WIPO Patent Scope. International patent classifications and applications.
  4. Crystals & Chemicals Ltd. (2018). Patent application GB201418708.
  5. Patent prosecution and litigation case studies relevant to pharmaceutical patents in the UK.

Note: Specific details of GB201418708 are based on typical patent drafting standards for pharmaceutical inventions; for precise claim language and scope, direct access to the full patent document is recommended.

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