Evaluation of a Diagnostic Test to Identify the Best Drugs for Treatment of Metastatic Colorectal Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorOncosyne AS

About this trial

DSEE-CRC is a top-tier Norwegian and Swedish public-private partnership for the development of µCAN, a unique patient-centric, therapy-guiding in vitro diagnostic test to improve cancer treatment outcomes for metastatic colorectal cancer patients. µCAN takes a cancer biopsy sample as input and combines proprietary patient-derived tumoroid culturing conditions with state of-the-art machine learning, and computer-vision guided fluorescence high- content drug screening and analysis, to identify the best therapeutical approach for clinical practice. DSEE-CRC will have a positive societal and financial impact and directly contributes to the Good Health and Well-being Sustainable Development Goals by delivering patient-tailored treatments, concurrently increasing cancer survivability rates, improving patients' quality of care, and reducing cancer treatment costs for healthcare providers.

Eligibility criteria

Qualifiers

Willing and able to give written informed consent (for each part of the study) for participation in the clinical performance study.

Male or female patients, ≥18 years of age, with Eastern Cooperative Oncology Group (ECOG) performance status 0-1, who have metastatic lesions in the liver or peritoneum (or lymph nodes) that are radiologically assessable and can be biopsied, and who have recently failed 1st line systemic therapy (2nd line for patients with three standard therapy lines) for unresectable metastatic disease and will shortly commence a new line of standard therapy.

Patient is eligible for another line of tumour directed therapy on failure of the SoC.

Haemoglobin at least 10.0 g/dL.

Disqualifiers

Life expectancy < 3 months.

Planned treatment or treatment with another investigational drug or investigational device within 3 months prior to the day of the tumour sampling procedure.

Patients who are pregnant, or currently breastfeeding.

Investigator considers the patient unlikely to comply with clinical performance study procedures, restrictions and requirements.

Trial design

Treatments tested in this trial

  • µCAN drug screen test
  • Standard-of-Care Therapy

Treatment groups

75 Participants
are divided into 2 treatment groups

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Akershus University HospitalRecruiting1478, Lørenskog, AkershusNorwayNorway

Sponsors and collaborators

Oncosyne AS

Lead sponsor

University Hospital, Akershus

Collaborator

CTC Clinical Trial Consultants AB

Collaborator