This is a multi-center, open-label, phase I/IIa trial, dose-escalation study with a 3 + 3 cohort design to determine the recommended dose of estetrol for the treatment of patients with advanced breast cancer. After completing phase I part of the study (i.e. 4 weeks of treatment), patients will receive further treatment for 8 weeks at their individual phase I dose level (phase IIa part of the study).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
12
Estetrol formulated in tablets, in escalating doses, will be investigated in patients with estrogen receptor positive (ER+) locally advanced or metastatic breast cancer.
Katholisches Klinikum Mainz
Mainz, Germany
Universitatsmedizin Mainz
Mainz, Germany
The number of patients with a dose limiting toxicity (DLT)
Time frame: 4 weeks
Questionnaire on estrogen deficiency symptoms
Quality of Life will be assessed by means of a questionnaire on estrogen deficiency symptoms.
Time frame: 12 weeks
Pharmacokinetics: estetrol trough levels
Time frame: 2 weeks, 4 weeks, 8 weeks
Preliminary anti-tumour response according to RECIST 1.1
Time frame: 12 weeks
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