Prediction in Silico of Pathological Response in a Prospective Cohort Study of Early Breast Cancer Patients

Recruiting N/A Interventional Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
300 (estimated)
Sponsor
Institut Cancerologie de l'Ouest · Other
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About This Trial
Breast cancer (BC) is the most common cancer in women in France with nearly 58,500 new cases and 12,150 deaths estimated in 2018 . Two major achievements have been made in the last five years for breast cancer patients. The first is therapeutic with the approval of immune checkpoint inhibitors in advanced and early triple-negative BC (TNBC) and the impressive efficacy of new antibody-drug conjuga…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Written informed consent obtained from the patient prior to performing any protocol-related procedures, including screening biopsy, blood samples and questionnaires 2. 18 years old or at time of written consent 3. Patient with histologically confirmed breast cancer 4. Absence…
Contacts

Jean Sebastien FRENEL, MD

+33240679900

jean-sebastien.frenel@ico.unicancer.fr

CONTACT

Marine TIGREAT

+33240679878

marine.tigreat@ico.unicancer.fr

CONTACT