The aim of this study is to evaluate the efficacy and safety of ESG401 as first-line treatment in patients with unresectable recurrent or metastatic triple-negative breast cancer.
This is a randomized, open-label, multicenter Phase 3 study to evaluate ESG401 versus Investigator's Choice Chemotherapy (ICC) as first-line treatment in subjects with unresectable recurrent or metastatic triple-negative breast cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
504
IV infusion on day 1,8, and 15 of each 28 day cycle
Paclitaxel, Nab-paclitaxel, Capecitabine, Eribulin, or Carboplatin
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Beijing, China
RECRUITINGProgression Free Survival (PFS) assessed by Blinded Independent Central Review (BICR)
Defined as the time from randomization to the first documented disease progression per RECIST 1.1 based on BICR or death due to any cause, whichever occurs first.
Time frame: Randomization up to approximately 28 months
Overall Survival (OS)
Defined as the time from randomization until the date of death due to any cause.
Time frame: Randomization up to approximately 41 months
Progression-Free Survival (PFS) assessed by Investigator
Defined as the time from randomization to the first documented disease progression per RECIST 1.1 based on investigator or death due to any cause, whichever occurs first.
Time frame: Randomization up to approximately 28 months
Objective Response Rate (ORR) assessed by Blinded Independent Central Review (BICR)
Defined as the percentage of patients who achieve complete response(CR) or partial response (PR), as assessed by BICR per RECIST 1.1
Time frame: Randomization up to approximately 28 months
Disease control rate (DCR) assessed by Blinded Independent Central Review (BICR)
Defined as the percentage of patients who achieve CR, PR or stable disease (SD), as assessed by BICR per RECIST 1.1
Time frame: Randomization up to approximately 28 months
Duration of Response (DoR) assessed by Blinded Independent Central Review (BICR)
Defined as the time from the date of first documented CR or PR until date of documented disease progression per RECIST 1.1, as assessed by BICR or death due to any cause, whichever occurs first.
Fei Ma, PhD
CONTACT
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Time frame: Randomization up to approximately 28 months
Time to Response (TTR) assessed by Blinded Independent Central Review (BICR)
Defined as the time from the date of randomization until the first documentation of CR or PR as assessed by BICR per RECIST 1.1.
Time frame: Randomization up to approximately 28 months
Objective Response Rate (ORR) assessed by Investigator
Defined as the percentage of patients who achieve complete response(CR) or partial response (PR), as assessed by investigator per RECIST 1.1
Time frame: Randomization up to approximately 28 months
Disease control rate (DCR) assessed by Investigator
Defined as the percentage of patients who achieve CR, PR or stable disease (SD), as assessed by investigator per RECIST 1.1
Time frame: Randomization up to approximately 28 months
Duration of Response (DoR) assessed by Investigator
Defined as the time from the date of first documented CR or PR until date of documented disease progression per RECIST 1.1, as assessed by investigator or death due to any cause, whichever occurs first.
Time frame: Randomization up to approximately 28 months
Time to Response (TTR) assessed by Investigator
Defined as the time from the date of randomization until the first documentation of CR or PR as assessed by investigator per RECIST 1.1.
Time frame: Randomization up to approximately 28 months
Quality of life evaluated using the NCC-BC-A scale
To assess the impact of ESG401 on disease related symptoms and quality of life of patients using the NCC-BC-A scale
Time frame: Randomization up to approximately 28 months
Adverse events(AEs) and severe adverse events (SAEs)
Incidence and severity of AEs and SAEs (per CTCAE 5.0), and clinically significant abnormal laboratory findings
Time frame: From signing the ICF up to last dose plus 30 days
Clearance
Mean population clearance will be derived from pooled data of drug concentrations. Covariates of influence on drug clearance will be incorporated within a population pharmacokinetic model.
Time frame: Randomization up to approximately 28 months
Volume of distribution
Mean population volume of distribution will be derived from pooled data of drug concentrations. Covariates of influence on volume of distribution will be incorporated within a population pharmacokinetic model.
Time frame: Randomization up to approximately 28 months
Anti-drug Antibodies
Incidence of anti-drug antibodies.
Time frame: Randomization up to approximately 28 months