This study is designed to evaluate safety and anti-tumor activity of DZD6008 in patients with advanced NSCLC with EGFR mutations.
The study includes two parts: Part A (dose escalation) and Part B (dose expansion). In Part A, locally advanced or metastatic NSCLC patients with EGFR mutations following at least 1 prior EGFR TKI regimen will be enrolled. In Part B, locally advanced or metastatic NSCLC patients with EGFR sensitizing mutations, who are previously treated with 1 line of third-generation of EGFR TKI treatment as well as treatment naïve will be enrolled.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
140
Daily dose of DZD6008
Daily dose of Sunvozertinib
Laura and Isaac Perlmutter Cancer Center at NYU Langone Health
New York, New York, United States
RECRUITINGHerbert Irving Comprehensive Cancer Center
New York, New York, United States
RECRUITINGVirginia Cancer Specialist (NEXT Oncology-Virginia)
Fairfax, Virginia, United States
Part A: To assess safety and tolerability
Number of participants with Dose-limiting Toxicities (DLTs)
Time frame: 21 days after the first multiple dose
Part A: To assess safety and tolerability
Number of participants with Adverse events (AEs)/Serious adverse events (SAEs)
Time frame: Through the study completion, an average of around 1 year
Part B: To assess anti-tumor activity
Objective Response Rate (ORR) assessed by investigators per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: Through the study completion, an average of around 1 year
Part A: To characterize the plasma concentration of DZD6008 following single and multiple oral dose administration
Total concentrations of DZD6008 in plasma
Time frame: From first dosing to cycle 7 day 1, each cycle is 21 days
Part A: To characterize the plasma concentration of sunvozertinib and metabolite DZ0753 following single and multiple oral dose administration
Total concentrations of sunvozertinib and metabolite DZ0753 in plasma (combination cohorts only)
Time frame: From first dosing to cycle 9 day 1, each cycle is 21 days
Part A: To assess the anti-tumor activity
ORR assessed by investigators per RECIST version 1.1
Time frame: Through the study completion, an average of around 1 year
Part A: To assess the anti-tumor activity
Duration of Response (DoR) assessed by investigators per RECIST version 1.1
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Blacktown Hospital
Blacktown, New South Wales, Australia
ACTIVE_NOT_RECRUITINGChris O'Brien Lifehouse
Camperdown, New South Wales, Australia
NOT_YET_RECRUITINGTime frame: Through the study completion, an average of around 1 year
Part A: To assess the anti-tumor activity
Progression Free Survival (PFS) assessed by investigators per RECIST version 1.1
Time frame: Through the study completion, an average of around 1 year
Part B: To assess the anti-tumor activity
DoR assessed by investigators per RECIST version 1.1
Time frame: Through the study completion, an average of around 1 year
Part B: To assess the anti-tumor activity
Through the study completion, an average of around 1 year
Time frame: PFS assessed by investigators per RECIST version 1.1
Part B: Plasma concentration of DZD6008
Total concentrations of DZD6008 in plasma
Time frame: Time Frame: From first dosing to cycle 11 day 1, each cycle is 21 days
Part B: To assess safety and tolerability
Number of participants with AEs/SAEs
Time frame: Through the study completion, an average of around 1 year