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Company profile

Ixico PLC

UK company 03131723, incorporated on 28 November 1995.

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IXICO is a premier medical imaging services provider, working with pharma and biotech partners to improve the outcomes of CNS trials.

Company number
03131723
Incorporated
28 Nov 1995
Companies House status
Active

Company identity

Browse spinouts
Founded / incorporated
28 November 1995

Company number 03131723

Verify at Companies House
Legal name
IXICO PLC
Company type
Public Limited Company
Region
London
Registered address
4TH FLOOR, GRIFFIN COURT
15 LONG LANE
LONDON
EC1A 9PN
Insolvency history
No

Company events

Reference milestones and recent Companies House filing stream events.

5 events
31 Mar
2027

Accounts due

Accounts Due

Next accounts due date

15 Oct
2026

Confirmation statement due

Confirmation Due

Next confirmation statement due date

01 Oct
2025

Confirmation statement filed

Confirmation

Last confirmation statement made up date

30 Sep
2025

Accounts filed

Accounts

Last accounts made up date

28 Nov
1995

Incorporated

Inception

Company registered at Companies House

Spinout profile

1 entry

Company description

IXICO plc develops diagnostic medical imaging technology and develops medical image analytics and clinical trials management software platforms.

Project impact

Economic impacts IXICO had a significant impact on the pharmaceutical industry where medical imaging is rapidly becoming an important tool in clinical trials to assess the safety and efficacy of new drugs using imaging biomarkers. IXICO's imaging biomarkers provide several benefits to pharmaceutical companies: In concept trials of AD therapies the developed biomarkers allow pharmaceutical companies to power their studies with fewer subjects. The developed imaging biomarkers do provide evidence of efficacy with around 100 subjects per arm (an "arm" in a clinical trial refers to any of the treatment groups in a randomized trial. Most randomized trials have two "arms", e.g. untreated vs. treated groups) over 12 months rather than 400 or so per arm needed for cognitive testing. Based on a conservative cost estimate of $30k per subject enrolled, this provides a significant cost saving for the companies. Similarly, pharmaceutical companies use the developed imaging biomarkers to enrich their clinical trials. In the context of clinical trials, such enrichment allows the identification of a population of patients in whom a drug effect, if present, is more likely to be demonstrable. In AD trials that use the developed biomarkers, an increase in the conversion rate in a prodromal Alzheimer's trial from 40% to 60% saves 30% off the cost of a pair of pivotal trials that used progression free survival as an endpoint, and which might otherwise cost $800m - $1bn. Impacts on public policy and services The imaging biomarkers developed in the underpinning research have had a significant impact on informing the development of new guidelines for the use of Magnetic Resonance Imaging (MRI) and low hippocampal volume in regulatory clinical trials: It now seems likely that to modify the course of Alzheimer's Disease, it is necessary to start the treatment in the pre-dementia (or prodromal) phase. The identification of patients at this stage can only be done confidently with the help of biomarkers: imaging provides a non-invasive alternative to cerebrospinal fluid (CSF) biomarkers for this purpose. The critical importance of imaging biomarkers in AD trials has been recognised by the CAMD consortium by submitting to regulators an application to qualify low hippocampal volume as a biomarker. This submission - approved by EMA and currently under review by the FDA - incorporates key data obtained using the underpinning research described here: the availability of this technology, with the regulatory qualification, is having global impact on the design of future trials of AD medicines in the pre-dementia population. In particular, the EMA Committee for Medicinal Products for Human Use has issued a positive opinion on the use of MRI to measure hippocampal volume as a tool to enrich recruitment into regulated clinical trials in the pre-dementia stages of Alzheimer's disease, in which the EMA directly refers to IXICO's technology. This was the first imaging-based biomarker to be qualified by a regulatory agency. Impacts on healthcare The imaging biomarkers developed in the underpinning research have been so effective in clinical trials that IXICO has recently decided also to develop products for diagnostic use (Brain Health Centre). IXICO's product for diagnostics directly uses the methods described in reference of the underpinning research and has also been CE marked. It is currently undergoing trials involving 200 patients as part of new NHS brain health centres.

IXICO plc
1995