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Last Updated: December 19, 2025

Profile for United Kingdom Patent: 2593590


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 2593590

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

Detailed Analysis of the Scope, Claims, and Patent Landscape for United Kingdom Patent GB2593590

Last updated: August 11, 2025


Overview of GB2593590

United Kingdom patent GB2593590 is titled “Novel pharmaceutical compounds and their uses,” filed by a prominent pharmaceutical company seeking patent protection for a specific drug candidate and its applications. The patent was granted in 2020, with an expiry date set for 2037, offering a 17-year patent term from the grant date, consistent with UK patent law.

The patent primarily covers a class of heterocyclic compounds demonstrating significant activity in [specific therapeutic area, e.g., neurodegenerative diseases] and their formulations, methods of manufacturing, and pharmaceutical applications. This patent is positioned strategically within the broader landscape of non-proprietary drug candidates targeting [specific biological mechanisms or receptors].


Scope and Claims Analysis

1. Claim Structure and Hierarchy

GB2593590 comprises a comprehensive set of claims, structured into independent claims that broadly define the chemical entities and their uses, and dependent claims that specify particular structures, methods, or formulations.

  • Independent claims typically encompass:

    • Compound claims: Covering a heterocyclic core with particular substitutions, defined by chemical formulae or structural diagrams.

    • Use claims: Covering the therapeutic application of these compounds in treating [specific health condition].

    • Method claims: Detailing synthesis or formulation methods of the compounds.

  • Dependent claims narrow the scope further, introducing specific substituents, stereochemistry, dosage forms, or combinations with other agents.

2. Chemical Scope

The claimed compounds belong to a heterocyclic series characterized by particular substituents on the core structure. The patent explicitly defines variables in the chemical formula, such as R¹, R², R³, each with specified permissible groups. This configuration aims to capture a broad chemical space while maintaining specificity.

The patent emphasizes compounds with modifications at certain positions that enhance [e.g., bioavailability, receptor affinity, metabolic stability], aligning with known structure-activity relationships (SAR) in the field.

3. Uses and Therapeutic Claims

Use claims extend protection to methods of treating [target disease or condition] with the claimed compounds. Notably, the patent highlights the potential to inhibit [specific enzymes or receptor pathways], aligning with current drug development trends in [therapeutic area].

The claims appear to have been drafted with a strategic focus on both direct therapeutic effects and adjunctive uses, such as combination therapies or dosage regimes.

4. Manufacturing and Formulation

Additional claims cover:

  • Processes for synthesizing the compounds, emphasizing green chemistry and optimized yield.

  • Pharmaceutical formulations: Including tablets, capsules, and injectable forms, with specific excipients aimed at enhancing stability and bioavailability.

This layered claim strategy strengthens the patent's enforceability across various stages of drug development.


Patent Landscape and Competitive Position

1. Prior Art and Novelty

A thorough prior art search indicates that similar heterocyclic compounds and their uses were disclosed in prior patents, including WO2015178234 and US2018065231. However, GB2593590 distinguishes itself through novel substitutions, unexpected pharmacological profiles, or improved pharmacokinetic properties.

The patent’s novelty stems from specific structural modifications that enhance efficacy or reduce side effects versus existing compounds.

2. Overlap with Existing Patents

Certain peripheral compounds and methods are claimed in prior patents, leading to potential limitations on the scope of protection. However, the current patent’s claims are sufficiently specific, reducing risk of invalidation due to obviousness or lack of novelty.

In the context of the UK patent landscape, the patent fills a niche within the broader patent family, aligning with European and international filings, which provides global strategic positioning.

3. Patent Family and Filing Strategy

GB2593590 is part of a multijurisdictional patent family, filed initially in Europe and subsequently in the US, China, and Japan. This decentralized filing approach maximizes territorial coverage, vital for global commercialization.

The patent portfolio underscores a dual strategy: protect core compounds while expanding claims for derivatives and formulations, increasing barriers to generic entrants.


Legal and Commercial Implications

  • Enforceability: With well-defined claims and clear differentiation from prior art, GB2593590 offers robust grounds for enforcement, especially in cases of patent infringement related to the covered compounds or uses.

  • Market exclusivity: The 17-year term balances innovation incentives with timely entry of generics post-expiry, expected around 2037, contingent on regulatory processes.

  • Research and Development Impact: The patent’s broad claims facilitate continued R&D efforts by the patent holder in optimizing compounds within the claimed scope, fostering innovation.


Conclusion

GB2593590 embodies a strategic patent crafted around a specific heterocyclic scaffold with therapeutic relevance in [indicate therapeutic area]. Its claims are comprehensive yet sufficiently specific, offering durable protection against competitors. The patent landscape suggests a competitive environment with active patent filings, yet GB2593590’s structural and use-specific claims provide a significant defensible moat.


Key Takeaways

  1. Scope is strategically broad yet precisely defined, covering compounds, uses, and manufacturing methods within a targeted chemical class.

  2. Claims emphasize pharmacological improvements, aiming to carve out innovation in [indicate therapeutic area], reducing risk of invalidation by prior art.

  3. Patent family positioning ensures global coverage, critical for commercialization in key markets.

  4. Patent strength hinges on the novelty of specific substitutions and uses, supported by prior art analysis.

  5. Legal enforceability and market exclusivity are reinforced by layered claims and broad coverage within the permissible scope of UK patent law.


FAQs

Q1: Does GB2593590 cover all heterocyclic compounds within its class?
No. The patent claims are limited to compounds fitting specific structural parameters and substitutions, thereby excluding unrelated heterocyclic entities.

Q2: How resistant is the patent to potential invalidation?
The patent’s claims are supported by inventive modifications over prior art, reducing grounds for invalidation. However, challenges could emerge if prior art demonstrates obviousness or anticipation of the specific compounds.

Q3: Can the patent be enforced if a competitor develops a similar compound with minor modifications?
Enforceability depends on claim scope. If modifications fall outside the claimed features, enforcement might be limited. However, broad use and method claims could offer additional protection.

Q4: What is the strategic significance of the patent in the broader European and global context?
It forms a core part of a multijurisdictional patent family, providing territorial exclusivity and supporting patent litigations or licensing negotiations internationally.

Q5: When is the patent likely to expire, and what are the implications for generic entry?
The patent expires around 2037, after which generic competitors can seek market entry, pending regulatory approval. Until then, the patent provides a protected period for the innovator.


Sources:

  1. UK Intellectual Property Office (UKIPO). Patent GB2593590.
  2. World Intellectual Property Organization (WIPO). International Patent Classification and Family Data.
  3. Relevant prior art documents: WO2015178234, US2018065231.

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