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Clinical Trial Summary

EXCYTE-1 is a multicentre, prospective observational study to investigate the relationship between ex vivo drug response (EVDR), measured in ovarian tumour-derived samples using high content imaging, and actual patient clinical response. Patients with newly diagnosed or relapsed/refractory epithelial ovarian carcinoma, that present with malignant effusions (ascites or pleural effusions), will be enrolled in the study before starting their initial or next treatment line. Enrolled patients will be asked to provide ascites, peripheral blood and fresh tumour tissue if available. Samples will be shipped to the sponsor laboratory and their response to standard of care drugs evaluated ex vivo. Participants will: - provide samples during routine clinical procedures - agree that data about their medical history, diagnosis and health status at the following timepoints are collected: at signature of the consent form, at the time samples are provided, at start of the therapy, upon completion of the therapy, regularly after completion of the therapy


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06068738
Study type Observational
Source Exscientia AI Limited
Contact Sarah Himbert-Baudis
Phone +43 676 852 525
Email shimbertbaudis@exscientia.co.uk
Status Recruiting
Phase
Start date April 14, 2023
Completion date December 2026

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