Phase
Condition
Breast Cancer
Cancer
Treatment
DECLARAN cream
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Women and men ≥18 years old
Patients with diagnosis of breast cancer with stage I-III radically operated withresidual disease post neoadjuvant treatment or stage IV
Patients candidated for capecitabine in a post-neoadjuvant or metastatic settingtreated with 2000-2500 mg/m2 d1-14 q21, or 1500 mg daily continuously (metronomicschedule)
Patients who provided written informed consent
Exclusion
Exclusion Criteria:
Patients previously treated with drugs that may have induced HFS
Assessed by the investigator to be unable or unwilling to comply with therequirements of the protocol
Pregnant, lactating, or breastfeeding, or intending to become pregnant during thestudy or within 60 days after the final dose of study treatmen
Study Design
Study Description
Connect with a study center
Centro di Riferimento Oncologico (CRO) di Aviano - IRCCS
Aviano, Pordenone 33081
ItalyActive - Recruiting
Azienda Sanitaria Universitaria del Friuli Centrale (ASUFC)
Udine, 33100
ItalySite Not Available
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