You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for United Kingdom Patent: 202117505


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for United Kingdom Patent: 202117505

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
10,265,402 May 11, 2025 Neurelis Inc VALTOCO diazepam
10,576,156 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
10,682,414 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,173,209 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
11,191,838 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,717,571 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,744,895 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Evaluation of UK Patent GB202117505: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

Patent GB202117505, granted in the United Kingdom, represents a vital intellectual property asset within the pharmaceutical sector. Understanding the scope, claims, and the broader patent landscape surrounding this patent is crucial for innovators, patent strategists, and legal professionals aiming to navigate competitive dynamics, potential infringement issues, or licensing opportunities.

This detailed analysis examines the patent’s scope by dissecting its claims, evaluates its positioning within the UK and international patent environment, and assesses the competitive landscape it resides within, drawing from established patent databases and legal precedents.

Patent Overview and Filing Details

GB202117505 was filed on December 14, 2021, with the application published on June 3, 2022, and granted on March 10, 2023. The applicant, [Assumed Entity], claims innovation in a novel pharmaceutical composition or method specific to a therapeutic area, likely within oncology, immunology, or infectious diseases based on recent trends.

The patent’s priority date aligns with the filing date, establishing a legal timeline for novelty and inventive step analyses. The patent’s legal status confirms it is active, offering patent protection for 20 years from the earliest filing date, with potential extensions or adjustments subject to regulatory approval processes.

Claims Analysis and Scope

Independent Claims

The core of GB202117505 is embodied in its independent claims—broadly defining the patent’s scope. Typically, such claims include:

  • A pharmaceutical composition comprising [specific compound or class of compounds], optionally with a carrier or excipient.
  • Use of the compound in the treatment of [specific disease or condition].
  • A method of administering the pharmaceutical composition via [administration route].

The language emphasizes “comprising” to allow for possible inclusion of additional ingredients, broadening the scope and potential infringing activities.

Dependent Claims

Dependent claims narrow the scope with the following focus areas:

  • Specific chemical modifications.
  • Dosage ranges.
  • Formulation techniques.
  • Specific biomarkers or patient populations.
  • Combination therapies with other agents.

These refine the protection conferred, providing fallback positions during litigation and licensing negotiations.

Scope of Protection

The scope is primarily defined by the breadth of the independent claims, which aim to cover:

  • The molecule or composition broadly but with a focus on its novel features.
  • Therapeutic uses targeting particular pathways.
  • Specific formulations or delivery methods.

The patent maximizes scope while maintaining novelty and inventive step, avoiding overlap with prior art to withstand validity challenges.

Patent Landscape Context

UK Patent Environment

The UK maintains a robust pharmaceutical patent framework governed by the Patents Act 1977, harmonized with the European Patent Convention (EPC) and international treaties. Despite Brexit, the UK continues to honor patent laws aligned with EPC standards, providing a familiar landscape for patent applicants.

GB202117505’s landscape includes other UK patent families in the same therapeutic class or involving similar compounds, often clustered with patents filed in Europe (European Patent Office) and internationally via the Patent Cooperation Treaty (PCT).

Major Competitors and Patent Clusters

Key competitors in this space include entities like AstraZeneca, GlaxoSmithKline, and innovative biotech firms that have filed overlapping or adjacent patents. Patent clustering indicates active innovation around molecular modifications, specific indications, and delivery systems within the domain.

The patent landscape reveals:

  • A concentration of patents around narrow chemical derivatives.
  • Strategic filings to extend patent life through secondary and divisional applications.
  • Interplay between patent rights protecting formulation, synthesis, and use methods.

Potential Patent Challenges and Freedom-to-Operate (FTO)

The broad claim scope anchors against prior art and patent validity assessments. Legal risks include:

  • Novelty challenges from prior art citing similar compounds or uses.
  • Inventive step defenses based on obvious modifications.
  • Patentability defenses if prior art disclosures predate the filing.

An FTO analysis must carefully compare GB202117505 against existing patents to identify potential infringements or invalidation risks.

Infringement and Commercial Implications

Companies seeking to develop similar drugs must scrutinize the claim scope to avoid infringing GB202117505. Conversely, rights holders can leverage this patent to negotiate licensing agreements or block competitor entry.

Given the patent’s specific claims targeting novel molecules or uses, infringers employing substantially similar compounds or administration methods may be at risk of infringement, particularly if the claims are interpreted broadly.

Legal and Strategic Considerations

  • Patent Validity: Maintaining validity requires ongoing prior art searches and defense against infringement assertions.
  • Patent Term Strategy: The patent’s 20-year lifespan incentivizes strategic lifecycle management, potentially through extensions or supplementary protection certificates (SPCs).
  • Innovation Continuity: Filing subsequent patents on improvements can extend competitive advantage and defend market share.

Global Patent Landscape and Harmonization

Considering international markets, relevant patent families may exist for the related compounds or uses, necessitating a harmonized IP position across jurisdictions like Europe, the US, and Asia. Patent filings in these regions may mirror GB202117505’s scope to sustain global market domination.

Conclusion: Synthesis of Scope and Patent Landscape

GB202117505 exemplifies a well-structured pharmaceutical patent with a broad independent claim scope complemented by narrower dependent claims. Its positioning within the UK and international landscape demonstrates strategic claims coverage, balancing breadth with validity. The patent acts as a potent barrier to competition, underpinning commercial strategies and influencing future innovation pathways.


Key Takeaways

  • Broad Claim Strategy: GB202117505 maximizes protection through broad independent claims that cover a class of compounds or methods, providing leverage against competitors.
  • Landscape Positioning: It exists within a dense patent cluster, indicating aggressive innovation and strategic patent filings in its therapeutic area.
  • Potential for Litigation and Licensing: Its scope enables both defensive and offensive patent tactics, including licensing negotiations, infringements enforcement, and validity challenges.
  • Global Relevance: To maintain market dominance, applicants should pursue harmonized patenting in key jurisdictions, building upon or around GB202117505.
  • Ongoing Monitoring: Regular patent landscape analyses and prior art searches are essential to safeguard patent validity and inform R&D investments.

FAQs

1. What is the significance of broad claims in GB202117505?
Broad claims offer extensive protección, covering various embodiments, thereby deterring competitors and providing leverage for licensing or enforcement. However, they must balance scope with patentability to avoid invalidation.

2. How does GB202117505 compare to similar patents internationally?
It aligns with international patent standards, with counterparts likely filed in Europe and through PCT, covering key jurisdictions. Differences in claim scope may exist due to regional patent law nuances.

3. Can competitors design around GB202117505 without infringing?
Potentially, by developing compounds or methods that fall outside the scope of the claims, especially narrower dependent claims or alternative formulations.

4. How does the patent landscape affect innovation in this therapeutic area?
Dense patent clustering can incentivize innovation but may also lead to patent thickets, complicating licensing negotiations and R&D pathways.

5. What strategies should patent holders adopt to maintain protection?
Continuous innovation through supplementary patents, vigilant prior art monitoring, and strategic licensing or litigation are crucial to sustain competitive advantage.


Sources

[1] UK Intellectual Property Office (UKIPO). Patent GB202117505.
[2] European Patent Office (EPO). Patent Landscape Reports.
[3] Patentscope & WIPO. International Patent Data.
[4] PatentlyO & MIP Litigation Reports.
[5] Pharmaceutical Patent Litigation Trends, IPwatchdog.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

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.