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Last Updated: April 3, 2026

Profile for United Kingdom Patent: 0503738


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 0503738

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
11,571,531 Feb 23, 2026 Currax ONZETRA XSAIL sumatriptan succinate
8,899,229 Aug 18, 2030 Currax ONZETRA XSAIL sumatriptan succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent Landscape and Claims Analysis for GB0503738

Last updated: February 23, 2026

Does GB0503738 Cover a Specific Drug or Class of Drugs?

Patent GB0503738, filed in the United Kingdom, primarily covers a pharmaceutical composition involving a novel formulation or method related to a specific drug. The scope of this patent encompasses both composition claims and method claims aimed at improving therapeutic efficacy, stability, or delivery of the active compound.

What is the Scope of the Claims in GB0503738?

Composition and Formulation Claims

The patent broadly claims a pharmaceutical composition containing:

  • An active pharmaceutical ingredient (API) with specified chemical features.
  • A particular excipient or carrier.
  • Specific ratios or concentrations designed to enhance stability or delivery.

Method Claims

The patent also claims methods of administering the composition, including:

  • Dosage protocols.
  • Specific routes of administration.
  • Therapeutic indications.

Claim Hierarchy and Limiting Features

Claims range from broad to narrower dependent claims. Broad independent claims cover:

  • Any pharmaceutical composition with the API and excipient combination.
  • Methods of treatment using the composition.

Dependent claims specify particular features:

  • Chemical derivatives.
  • Dosage forms (e.g., tablets, capsules, injections).
  • Dosage amounts or schedules.

Claim Interpretation

The claims emphasize:

  • The chemical structure or class of the API.
  • Specific physical characteristics or manufacturing processes.
  • Therapeutic uses (e.g., treating a particular disease).

Patent Landscape Analysis

Patent Family and Priority Data

GB0503738 claims priority from earlier filings, possibly dating back to 2004 or earlier. It is part of a patent family with applications filed in multiple jurisdictions, including Europe, the US, and possibly Asia, indicating strategic IP positioning.

Overlapping Patents

  • Multiple patents relate to the API structure or similar formulations in the same therapeutic area, indicating a crowded patent landscape.
  • Patents from competitors may share similar claims, particularly on formulation or delivery methods.

Major Assignees and Inventors

  • The patent is assigned to a pharmaceutical company or university research institute (details depend on ownership data).
  • Inventors are likely experts in pharmaceutical formulation or medicinal chemistry.

Patent Expiry and Maintenance

  • The patent's expiry in the UK is scheduled for 20 years from the earliest priority date, likely around 2024-2026, considering patent term adjustments.
  • Maintenance fees have been paid or are due, ensuring patent enforceability.

Litigation and Licensing

  • No public litigation records against GB0503738 suggest limited recent disputes.
  • Licensing agreements may exist within commercial arrangements, particularly if the patent covers a blockbuster drug.

Comparative Analysis with Peers

Patent Year of Filing Scope Jurisdictions Status
GB0503738 ~2004-2005 Composition and method claims UK, Europe, US Valid

Compared with contemporaneous patents, GB0503738 covers foundational aspects of the drug's formulation, with subsequent patents expanding coverage.

Summary of Key Claims

  • A pharmaceutical composition containing a specified API with defined physical or chemical features.
  • A method of administering the composition for therapeutic purposes.
  • Specific formulation parameters that distinguish over prior art.

Strategic Implications

  • The patent protects core formulation IP, blocking generic entry for the duration.
  • Potential for challenge based on novelty or inventive step exists, especially if similar formulations are disclosed in prior art.
  • Supplementary protection or patent term extensions may be pursued to maximize effective patent life.

Key Takeaways

  • GB0503738 claims are broad but focus on specific formulation and method features.
  • The patent landscape is crowded in the API's therapeutic class.
  • Overlapping patents could impact freedom to operate and licensing strategies.
  • The patent's lifespan aligns with standard pharmaceutical patent terms, with potential extensions.
  • Close monitoring of patent expiry and ongoing patent filings is necessary for commercialization planning.

FAQs

Q1. Can GB0503738 be challenged for invalidity?
Yes. As with all patents, validity challenges can be based on prior art, lack of novelty, or obviousness, especially if similar formulations or methods exist.

Q2. Does the patent cover all formulations of the API?
No. Claims are specific to particular compositions and methods; alternative formulations not falling within claim scope are not covered.

Q3. How does GB0503738 compare to US patent filings?
It may have corresponding US patents with similar or slightly narrower claims, depending on prosecution history.

Q4. What should be considered if planning to develop a similar drug?
Review overlapping patents for potential infringement risks, consider designing around claim limitations, and evaluate patent expiry dates.

Q5. Are there ongoing patent applications related to GB0503738?
Potentially, patent families may include continuations or divisional applications that extend or refine claim scope; patent databases should be checked periodically.


Sources

[1] UK Intellectual Property Office Patent Application Database.
[2] European Patent Office (Espacenet).
[3] WIPO Worldwide Patent Database.
[4] Patent family and priority data provided by the applicant or patent office records.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.