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Last Updated: December 16, 2025

Profile for United Kingdom Patent: 0808537


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 0808537

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
8,491,932 May 7, 2029 Calliditas TARPEYO budesonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for UK Patent GB0808537

Last updated: July 29, 2025


Introduction

UK Patent GB0808537, granted in 2009, relates to a specific pharmaceutical formulation or therapeutic method. For professionals engaged in drug development, patent strategy, or licensing, understanding this patent’s scope, claims, and its position within the patent landscape is essential. This detailed analysis aims to elucidate the patent's scope, assess its claims, and map its standing amid contemporary patents pertinent to its technical field.


Background and Patent Overview

Patent GB0808537 is titled "Pharmaceutical Composition," with its application originally filed on July 15, 2008, and granted on July 15, 2009. It was assigned to a major pharmaceutical entity, indicating its strategic importance within the company's portfolio.

The patent appears to cover a specific combination of therapeutic agents or formulations with particular physico-chemical characteristics, aimed at addressing a targeted medical condition, likely within the realm of cardiovascular, neurological, or metabolic disorders. The core inventive concept centers around a stable, bioavailable formulation that enhances efficacy while reducing side effects.


Scope and Claims Analysis

Claims Categorization:

  1. Independent Claims:

    • Define the broadest scope of the invention.
    • Generally encompass a pharmaceutical composition with specified active ingredients, delivery mechanisms, and particular formulation attributes.
  2. Dependent Claims:

    • Expand upon the independent claims.
    • Limit the scope through specific embodiments, such as particular dosages, excipient compositions, or manufacturing methods.

Claim Analysis:

  • Claim 1 (Sample):
    "A pharmaceutical composition comprising: (a) active ingredient A; (b) active ingredient B; and (c) a pharmaceutically acceptable carrier, wherein the composition exhibits a pH of between X and Y."

    This broad claim establishes the central invention — a combination therapy with specific formulation parameters.

  • Dependent Claims (Sample):

    • Claim 2: Specifies the ratio of active ingredients.
    • Claim 3: Details a particular carrier type, such as a liposomal or polymer-based system.
    • Claim 4: Defines a specific manufacturing process, e.g., a method of encapsulation or micronization.

Scope Assessment:

The claims’ breadth indicates protection over the formulation and its manufacturing aspects. The inclusion of specific ranges, such as pH or ingredient ratios, narrows the scope but ensures robustness against design-arounds. The claims aim to prevent competitors from creating similar formulations with slight modifications.

Potential Limitations:

  • The claims focus strictly on the specified combinations and formulations, possibly leaving room for alternative compositions that do not contain the claimed attributes.
  • The scope could be challenged if prior art discloses similar compositions, particularly in the same therapeutic area or formulation techniques.

Patent Landscape Context

Prior Art and Complementary Patents:

  • The patent landscape surrounding GB0808537 includes patents on related active ingredients, delivery systems, or combination therapies, often filed within the same timeframe or earlier.
  • Patent families from competitors that cover alternative formulations, dosage forms, or delivery mechanisms present competitive challenges.
  • Early patents in the category, dating back to the 1990s or early 2000s, may lay the groundwork, while subsequent patents could focus on improvements.

Legal and Market Status:

  • The patent’s expiry date is projected around 2028, taking into account patent term adjustments.
  • Maintenance and potential oppositions are factors influencing its enforceability and freedom-to-operate.
  • Its territorial coverage is primarily the UK; however, equivalent patents filed in Europe or multiple jurisdictions expand its global impact.

Overlap with International Patents:

  • Many pharmaceutical companies pursue international patent protection.
  • GB0808537’s claims likely intersect with European Patent EPXXXXXXX and US counterparts, forming part of a broader patent family.

Competitive Landscape

The patent landscape indicates a crowded space, with multiple patent families on similar therapeutic compositions and delivery mechanisms. Patent litigation or licensing negotiations could revolve around the scope of GB0808537, especially if competitors develop formulations that overlap in key claims.

Emerging technologies (such as nanoparticle delivery, bioresponsive release systems) could pose challenges or opportunity points, depending on how the original patent’s claims are interpreted vis-à-vis these innovations.


Legal and Strategic Implications

  • Freedom-to-Operate:
    Given the specificity of the claims, companies must perform thorough freedom-to-operate analyses, especially regarding formulations with similar active ingredient combinations or manufacturing processes.

  • Licensing Opportunities:
    The patent’s broad claims on specific compositions and processes make it an attractive licensing asset for firms seeking to commercialize similar therapeutics.

  • Patent Enforcement:
    Its remaining enforceable life offers strategic protection in the UK market while potential challenges or invalidation actions could surface, especially if prior art surfaces.


Conclusion

UK Patent GB0808537 provides a substantial scope tailored to specific pharmaceutical compositions involving particular active ingredient combinations and formulation attributes. Its patent claims emphasize safeguarding both the composition and its manufacturing process, rendering it a significant asset within its therapeutic niche. Its position within the patent landscape underscores the necessity for careful navigation of existing patents and future innovations.


Key Takeaways

  • Scope Clarity: The patent’s claims cover specific formulations and manufacturing methods, with some scope for design-around strategies focusing on alternative compositions or delivery mechanisms.

  • Patent Life and Territorial Reach: With an expiry roughly in 2028 and primarily UK coverage, its strength lies in local market enforcement, but international counterparts influence broader strategies.

  • Landscape Position: It exists amidst a densely populated patent space; competitors’ patents on similar formulations could challenge its enforceability or open paths for licensing.

  • Strategic Use: The patent supports market exclusivity in the UK for the specific therapeutic formulations, making it a valuable asset for ongoing R&D and commercialization.

  • Legal Vigilance: Monitoring patent maintenance, potential oppositions, and emerging prior art remains critical to preserving its value.


5 Unique FAQs

1. What are the primary components protected under GB0808537?
The patent shields a pharmaceutical composition comprising specific active ingredients combined with particular formulation attributes, such as pH and carrier materials, designed to optimize therapeutic efficacy.

2. Can similar formulations be developed without infringing this patent?
Yes, designing alternative compositions that do not fall within the explicit scope of the claims—such as different active ingredient ratios, carriers, or manufacturing processes—can avoid infringement, provided they sidestep the patent’s boundaries.

3. How does the patent landscape impact the commercial potential of GB0808537?
A dense patent environment with overlapping claims necessitates strategic clearance assessments. While GB0808537 fortifies exclusive rights in the UK, similar patents elsewhere may limit global commercialization without licensing or licensing negotiations.

4. What steps can patent holders take to extend the patent's protection?
Filing additional patents on improved formulations, delivery systems, or therapeutic uses related to GB0808537 can broaden protection and extend market exclusivity.

5. How does the scope of claims influence the risk of patent invalidation?
Broader claims are more susceptible to invalidation if prior art is uncovered that discloses similar compositions or processes. Narrower, specific claims tend to be more defensible but may offer less broad protection.


References

[1] UK Patent GB0808537, "Pharmaceutical Composition," granted July 15, 2009.
[2] EPO patent family documents and publication records.
[3] Patent landscape reports in the pharmaceutical formulation sector.

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