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Study identifier: NCT07148154 Synced from ClinicalTrials.gov · August 06, 2026
● Study status: Recruiting

Development of a Non-invasive IVD for Endometrial Cancer Screening on High-risk Populations

Condition: Endometrial Cancer  ·  Sponsor: MiMARK Diagnostics, S.L.

PhaseN/A
Planned participants3000
Who can joinFemale, 40 Years to no upper limit
Healthy volunteersYes

About this study

CYTOMARK, a non-invasive in vitro diagnostic (IVD) test measuring a defined panel of protein biomarkers in cervical fluid, can accurately detect endometrial cancer in both symptomatic and asymptomatic women at high risk for the disease. The aim of the study consists in validating CYTOMARK's ELISA test, creating and freezing an algorithm detect EC in post-menopausal women with abnormal uterine bleeding (AUB).

This description comes directly from the study's public registry record.

Talk to the study team

Antonio Gil-Moreno, MD, PhD  ·  934893066  ·  antonio.gil@vallhebron.cat

Eva Colás, PhD  ·  934893066  ·  eva.colas@mimark.es

Always discuss trial participation with your own doctor first.

Locations (2)

Hospital Universitari de BellvitgeL'Hospitalet de Llobregat, Barcelona, SpainRecruiting
Hospital Universitari Campus Vall d'HebronBarcelona, SpainRecruiting

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