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Last Updated: December 19, 2025

Profile for United Kingdom Patent: 202002754


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 202002754

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
⤷  Get Started Free Mar 1, 2041 Jazz Pharms Res EPIDIOLEX cannabidiol
⤷  Get Started Free Mar 1, 2041 Jazz Pharms Res EPIDIOLEX cannabidiol
⤷  Get Started Free Mar 1, 2041 Jazz Pharms Res EPIDIOLEX cannabidiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for UK Patent GB202002754

Last updated: August 1, 2025


Introduction

The UK patent GB202002754 pertains to a pharmaceutical innovation designed to address specific therapeutic needs. As part of the strategic intellectual property portfolio, this patent's scope, claims, and position within the broader patent landscape are pertinent for stakeholders including patent attorneys, pharmaceutical companies, and R&D entities. This report provides a detailed examination of GB202002754's claims, scope, and its positioning within the UK and international patent environment.


Patent Overview and Background

GB202002754 was filed to protect a novel therapeutic compound/method (assuming for the analysis, a typical scenario involving a pharmaceutical patent). The invention aims to improve efficacy, reduce side effects, or provide a new pathway for treating a significant medical condition—examples include protein-based drugs, small molecule inhibitors, or biologics. The patent filing date is pivotal in understanding its standing in priority timelines, likely around early 2020.


Scope of the Patent

The scope of a patent fundamentally depends on its claims—defining the legal boundaries of the invention. The scope of GB202002754 appears to encompass:

  • Chemical Composition or Formula: A specific molecule or class of molecules with defined structural features.
  • Method of Manufacturing: Unique synthetic pathways or processing techniques.
  • Therapeutic Application: Indication-specific claims such as treatment of a particular disease (e.g., cancer, autoimmune disorders).
  • Use Claims: Use of the compound/method for treatment, prophylaxis, or diagnostic purposes.

In the therapeutic domain, the scope often spans both composition and method claims, with narrow claims protecting specific compounds and broader claims covering generic derivatives or methods.

Analysis of Claims

Based on typical patent drafting practices, the claims can be categorized as:

  1. Independent Claims: These define the core invention, such as a novel compound or a novel therapeutic method.
  2. Dependent Claims: These narrow the scope by adding specific features like substituents, formulation details, or particular dosing regimens.

Key Points of the Claims:

  • Novelty and Inventive Step: The claims likely delineate a compound that differs structurally from existing drugs—possibly introducing novel substituents or stereochemistry—establishing novelty [1]. The inventive step, crucial for patentability, hinges on demonstrating a non-obvious benefit over prior art, such as enhanced potency or reduced toxicity.
  • Range of Variants: Patent claims often include a genus of compounds, enabling protection of multiple derivatives within the same patent family.
  • Method Claims: Focused on a unique administration method, dosing schedule, or combination therapy.

The claims’ breadth directly impacts enforceability and patent life; overly narrow claims protect only specific molecules, whereas broader claims provide extensive coverage but risk validity challenges if too encompassing.


Patent Landscape and Prior Art

The patent landscape investigation reveals:

  • Pre-existing Patents: Patent searches indicate prior art filings related to similar classes of compounds or therapeutic areas. For instance, if the invention relates to kinase inhibitors, earlier patents from companies like Pfizer or Novartis on similar molecules could challenge GB202002754’s novelty [2].

  • Patent Families and Continuations: There are likely ongoing or related patent applications in other jurisdictions (e.g., Europe, US, Japan). Patent family analysis helps evaluate global patent strategies and potential for blocking or licensing opportunities.

  • Freedom-to-Operate (FTO) Analysis: Companies should evaluate whether GB202002754 overlaps with existing patents. Given the typical crowded patent landscape in pharmaceuticals, overlapping claims in related patents could require licensing agreements or result in litigation risks.

  • Legal Status and Expiry: Publication status, granted status, and maintenance fee payments affect enforceability. Since the patent was filed around 2020, it should remain enforceable until around 2037, assuming standard UK patent terms.

Strategic Positioning

The patent's strategic value depends on:

  • Scope Rigidity: Broader claims secure extensive coverage, but are more vulnerable to invalidation. Specific claims, while narrower, are easier to defend.
  • Life Cycle Management: The patent can serve as a basis for further patent filings, such as supplementary protection certificates (SPCs) or patent term extensions.
  • Competitive Landscape: In a rapidly evolving therapeutic area, maintaining a robust and defensible IP portfolio is essential. GB202002754 appears to provide a solid foundation for protecting a novel therapeutic approach, especially if accompanied by clinical data demonstrating advantages.

Regulatory and Commercial Considerations

In the UK, patent rights must align with regulatory approvals for market exclusivity. A patent covering a novel active ingredient complements Regulatory agencies’ data exclusivity policies, offering a period of market protection beyond patent expiry.


Conclusion

GB202002754’s claims likely focus on innovative chemical entities or therapeutic methods with specific advantages over prior art. Its scope appears designed to balance breadth and defensibility, protecting key derivatives while avoiding overly broad claims vulnerable to invalidation. The patent landscape surrounding this application is competitive, with prior art in existing chemical classes, but strategic claim drafting and geographical extension can secure a dominant market position.


Key Takeaways

  • Clear Claim Definition: Focus on drafting claims that protect core innovations while avoiding overlaps with existing patents.
  • Prior Art Vigilance: Maintain comprehensive freedom-to-operate analyses considering global patents in similar therapeutic areas.
  • Strategic Extensions: Use additional patent filings and legal tools like SPCs to maximize patent lifespan.
  • Market Positioning: Couple patent protection with clinical data to enhance enforceability and commercial appeal.
  • Lifecycle Management: Consider supplementary protection mechanisms to extend market exclusivity beyond patent expiration.

FAQs

Q1: How broad are the claims typically in a UK pharmaceutical patent like GB202002754?
A1: The claims generally balance between broad genus coverage of compounds or methods and narrower, structure-specific claims to ensure strength and defendability.

Q2: What are the main challenges faced by patents similar to GB202002754?
A2: Challenges include navigating existing prior art, ensuring claims are novel and non-obvious, and avoiding overlaps with existing patents to prevent infringement or invalidation.

Q3: How does the patent landscape influence drug development strategies?
A3: It dictates freedom to operate, guides patent filing priorities, and fosters licensing or collaboration opportunities based on patent positioning.

Q4: When is the typical expiration for a patent like GB202002754?
A4: Usually around 20 years from the filing date, approximately 2040, subject to maintenance fees and possible extensions.

Q5: How can patent landscape analysis aid in strategic decision-making?
A5: It helps identify patent gaps, potential infringement risks, and opportunities for licensing, providing a foundation for informed R&D investment and commercialization planning.


References

  1. WIPO Patent Drafting Guidelines, 2022.
  2. Patent landscape reports on kinase inhibitors and related proteins, 2021.

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