Actively Recruiting

Age: 40Years - 75Years
All Genders
Healthy Volunteers
NCT06717295

The CCANED-CIPHER Study: Early Cancer Detection and Treatment Response Monitoring Using AI-Based Platelet and Immune Cell Transcriptomic Profiling

Led by Javier Toledo · Updated on 2026-01-02

6000

Participants Needed

4

Research Sites

136 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of the CCANED-CIPHER study is to develop and validate an AI-based blood test for early cancer detection and to monitor treatment effectiveness in cancer patients. This two-phase, multi-center observational study aims to identify specific transcriptomic biomarkers in platelets and immune cells that distinguish cancer patients from healthy individuals and correlate with treatment outcomes. By analysing blood samples using artificial intelligence, the study seeks to create a safe, non-invasive method to enhance cancer diagnosis and monitor treatment responses over time.

CONDITIONS

Official Title

The CCANED-CIPHER Study: Early Cancer Detection and Treatment Response Monitoring Using AI-Based Platelet and Immune Cell Transcriptomic Profiling

Who Can Participate

Age: 40Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 40 years or older
  • Confirmed diagnosis of Non-Small Cell Lung Cancer, Glioblastoma Multiforme, Colorectal Cancer, Hepatocellular Carcinoma, Breast Cancer, Prostate Cancer, Ovarian Cancer, or Pancreatic Cancer (Phase 1)
  • Adults aged 40 years or older
  • Confirmed diagnosis of Hepatocellular Carcinoma or Non-Small Cell Lung Cancer
  • Willingness to provide blood samples at baseline, 6 weeks, and 6 months post-therapy initiation (Phase 2)
Not Eligible

You will not qualify if you...

  • Currently pregnant
  • Presence of any active infectious diseases
  • Use of anticoagulant or antiplatelet drugs within the past 2 weeks
  • Any medical or psychological conditions affecting ability to comply with study procedures
  • Presence of another malignancy unless in remission for at least 5 years (Phase 2)
  • Significant uncontrolled co-morbid conditions interfering with study participation or outcomes (Phase 2)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Various Cancer Centres

Rosario, Argentina

Active, Not Recruiting

2

NSIA- Lagos University Teaching Hospital Cancer Centre

Lagos, Nigeria

Actively Recruiting

3

Babraham Research Institute

Cambridge, United Kingdom, CB22 3AT

Enrolling by Invitation

4

Dysplasia Diagnostics Limited

London, United Kingdom, W1W 7LT

Actively Recruiting

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Research Team

J

Javier Toledo, Medical Degree

CONTACT

O

Osagie Izuogu, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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