This is a Phase I, open-label study to assess the safety, tolerability, pharmacokinetics and anti-tumor activity of AZD4635 in Japanese patients with advanced solid malignancies. This study consists of 2 cohorts, Cohort1 and Cohort2. At least 3 or up to 6 evaluable Japanese patients with advanced solid malignancies will be enrolled in Cohort1 and 6 evaluable patients will be enrolled in Cohort2.
Objectives: Primary objective: Investigate the safety and tolerability of AZD4635 monotherapy in Japanese patients Secondary objective: Characterize the single-dose and multiple-dose plasma pharmacokinetic (PK) parameters of AZD4635 monotherapy Determine the preliminary anti-tumor activity of AZD4645 monotherapy Overall design: This is a phase I, open-label study of AZD4635 in Japanese patients with advanced solid malignancies. The study consists of 2 cohorts, Cohort 1 and Cohort 2. At least 3 or up to 6 evaluable Japanese subjects with advanced solid malignancies will be enrolled in Cohort 1 and 6 evaluable patients will be required for Cohort 2 to confirm the tolerability. The total number of evaluable subjects in each cohort will depend upon available data in each cohort and decision of Safety Review Committee(SRC). Study Period: The study is expected to start in June 2019 and end in June 2020. Number of Subjects: 9 to 12 evaluable subjects will be enrolled in this study to confirm the tolerability. Treatments and treatment duration: Subjects will receive AZD4635 once daily (QD). A single dose of AZD4635 will be taken on Cycle 0 Day1 and the subsequent dose of AZD4635 will be taken from Cycle 1 Day 1 until discontinuation criterion is met. A cycle of study treatment will be defined as 21 days of continuous dosing.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
10
AZD4635 taken orally
Research Site
Chūōku, Japan
Research Site
Kashiwa, Japan
The incidence of Adverse event and SAE
Investigate the safety and tolerability of AZD4635
Time frame: From the informed consent to 30 days post last dose
The incidence of Dose-limiting toxicity (DLTs)
Investigate the safety and tolerability of AZD4635
Time frame: 25 days (Cycle0 and Cycle1)
Objective response rate (ORR)
Summarize based on RECIST 1.1 by cohort and overall.
Time frame: Tumor assessment is Cycle 4 Day 1 and then on Day 1 of each even numbered cycle (+/-5 days) until disease progression. Expected to be for up to 6 months.
Maximum plasma concentration (Cmax)
Characterize the single-dose and multiple-dose plasma of AZD4635
Time frame: Samples will be collected at pre-specified time points in the single-dose and multiple-dose portion of the study beginning with Cycle 1 Day 1 until last dose. Expected to be for up to 6 months.
Disease control rate (DCR)
Summarize based on RECIST 1.1 by cohort and overall.
Time frame: Tumor assessment is Cycle 4 Day 1 and then on Day 1 of each even numbered cycle (+/-5 days) until disease progression. Expected to be for up to 6 months.
Area under the plasma concentration-time curve (AUC)
Characterize the single-dose and multiple-dose plasma of AZD4635
Time frame: Samples will be collected at pre-specified time points in the single-dose and multiple-dose portion of the study beginning with Cycle 1 Day 1 until last dose. Expected to be for up to 6 months.
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