This is a phase 1 open label multicentre study of AZD9496 administered orally in patients with advanced ER+ HER2 negative breast cancer. The study design allows an escalation of dose with intensive safety monitoring to ensure the safety of patients. The study will determine the maximum tolerated dose. In addition, expansion cohort(s) at potential therapeutic dose(s) in patients with or without ESR1 mutations will be enrolled to further determine the safety, tolerability, pharmacokinetics and biological activity of AZD9496
A Phase I, Open-Label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of Ascending Doses of AZD9496 in Women with Estrogen Receptor Positive HER-2 Negative Advanced Breast Cancer
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
45
Florida Cancer Specialists
Sarasota, Florida, United States
Research Site
New York, New York, United States
Sarah Cannon
Nashville, Tennessee, United States
Seoul National Univ. Hospital
Seoul, South Korea
Safety and tolerability
Safety and tolerability in terms of adverse events, serious adverse events (including death) and safety measures: ECG, physical examination, vital signs and laboratory variables. Definition of maximum tolerated dose (MTD) or maximum feasible dose (MFD) by measuring the number of evaluable patients with dose-limiting toxicities.Time frame DLT period 28 days
Time frame: Routine safety assessments, throughout the period that patients receive AZD9496 up to 28 days following discontinuation of last dose of study treatment.
Single and multiple dose pharmacokinetics of AZD9496
measurement of plasma levels of AZD9496 at pre-defined intervals in order to establish pharmacokinetic parameters
Time frame: 12 weeks
4β-hydroxycholesterol concentration in blood
Understanding of the CYP3A4 induction potential of AZD9496 by measuring 4β-hydroxycholesterol concentration in blood samples at pre-defined intervals
Time frame: 12 weeks
Antitumour activity
Antitumour activity by evaluation of tumour response assessments using Response Evaluation Criteria in Solid Tumours (RECIST 1.1)
Time frame: every 8 weeks for 24 weeks and then every 12 weeks thereafter until disease progression
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Research Site
Cambridge, United Kingdom
Christie
Manchester, United Kingdom