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Study identifier: NCT07660627 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Determining Minimal Residual Disease Using ctDNA Deep Sequencing

Condition: Esophageal Adenocarcinoma · Gastric Cancer · Pancreatic Cancer  ·  Sponsor: Masaryk Memorial Cancer Institute

PhaseNA
Planned participants34
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

Preoperative neoadjuvant chemotherapy is the standard treatment for locally advanced gastrointestinal tumours. However, not all patients respond to preoperative treatment. Early identification of progression during neoadjuvant chemotherapy or diagnosis of early disease relapse during adjuvant treatment is essential to modify the treatment strategy. The aim of this project is to validate ctDNA as a biomarker of molecular relapse/progression of disease.

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

Talk to the study team

Martina Lojová, PhD  ·  +420543136232  ·  martina.lojova@mou.cz

Tereza Štěpánková, PhD  ·  +420543136223  ·  tereza.stepankova@mou.cz

Always discuss trial participation with your own doctor first.

Locations (1)

Masaryk Memorial Cancer InstituteBrno, CzechiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07660627