A Phase III Study of ESG401 for Unresectable Recurrent or Metastatic Triple-Negative Breast Cancer
A Randomized, Open-label, Phase III Study of ESG401 Versus Investigator's Choice Chemotherapy as First-line Treatment in Patients With Unresectable Recurrent or Metastatic Triple-Negative Breast Cancer
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 3
Contacts and Locations
Study Contact
Study Contact
- Name: Fei Ma, PhD
Study Contact Backup
- Name: Xiaoyan Xing, PhD
- Phone Number: +86 21 5855 6098
- Email: xingxiaoyan@escugen.com
Study Locations
-
-
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Beijing, China
- Recruiting
- Cancer Institute and Hospital, Chinese Academy of Medical Sciences
-
Contact:
- Fei Ma, PhD
- Phone Number: 8610-8778-8120
- Email: drmafei@126.com
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Key Inclusion Criteria:
- Males or females aged ≥ 18 years ;
- Histologically and/or cytologically confirmed TNBC;
- De novo metastatic or relapsed ≥ 6 months post completion of treatment with curative intent;
- No prior systemic anti-cancer therapy for unresectable recurrent or metastatic disease;
- Participants whose tumours are PD-L1-negative, or Participants whose tumours are PD-L1-positive and have relapsed after prior PD-1/PD-L1 inhibitor therapy for early-stage breast cancer, or comorbidities precluding PD-1/PD-L1 inhibitor therapy;
- Eligible for the chemotherapy options listed as investigator's choice chemotherapy (paclitaxel, nab-paclitaxel, capecitabine, eribulin, or carboplatin) as assessed by the investigator;
- At least one measurable lesion per RECIST v1.1;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 with no worsening within 2 weeks prior to randomization;
- A life expectancy of at least 12 weeks;
- Adequate organ and bone marrow function.
Key Exclusion Criteria:
- Use of any investigational anti-cancer drug within 28 days or 5 half-lives before the first investigational product administration.
- Toxicities from prior anti-tumor therapy not recovering to ≤ Grade 1.
- Prior topoisomerase I inhibitor therapy, including antibody-drug conjugate(ADC) therapy, or prior TROP2 targeted therapy.
- New thromboembolic events, intestinal obstruction, gastrointestinal bleeding or perforation within 6 months.
- Subjects with symptomatic or untreated CNS metastases, or those requiring ongoing treatment for CNS metastases.
- Patients with Primary CNS malignancy, or patients with other malignancies within 3 years prior to the first dose.
- Patients with uncontrollable systemic diseases.
- Patients with gastrointestinal diseases (such as chronic gastritis, chronic enteritis or gastric ulcers), or with a previous history of severe or chronic diarrhea.
- Subjects with clinically significant cardiovascular disease.
- Human Immunodeficiency Virus (HIV) infection.
- Active hepatitis B or hepatitis C.
- Known immediate or delayed hypersensitivity reaction to irinotecan or other camptocampin derivatives such as topotecan or to have had grade≥3 gastrointestinal reactions associated with irinotecan, or allergies, or to any investigational drug or excipient ingredient.
- Pregnant or lactating women.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: ESG401 for injection
IV infusion on day 1, 8 and15 of each 28 day cycle
|
IV infusion on day 1,8, and 15 of each 28 day cycle
|
|
Active Comparator: Investigator's Choice Chemotherapy
If no prior taxane, or prior taxane in the (neo)adjuvant setting and disease-free interval (DFI) >12 months: paclitaxel or nab-paclitaxel.
Note: If subjects are intolerant or contraindicated to receive paclitaxel or albumin-paclitaxel, the investigator may choose other chemotherapy options listed in the study protocol) If prior taxane and DFI ≤ 12 months: capecitabine, eribulin.
If known BRCA1/2 mutation: carboplatin
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Paclitaxel, Nab-paclitaxel, Capecitabine, Eribulin, or Carboplatin
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Progression Free Survival (PFS) assessed by Blinded Independent Central Review (BICR)
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Overall Survival (OS)
Time Frame: Randomization up to approximately 41 months
|
Defined as the time from randomization until the date of death due to any cause.
|
Randomization up to approximately 41 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adverse events(AEs) and severe adverse events (SAEs)
Time Frame: From signing the ICF up to last dose plus 30 days
|
Incidence and severity of AEs and SAEs (per CTCAE 5.0), and clinically significant abnormal laboratory findings
|
From signing the ICF up to last dose plus 30 days
|
|
Progression-Free Survival (PFS) assessed by Investigator
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Objective Response Rate (ORR) assessed by Blinded Independent Central Review (BICR)
Time Frame: Randomization up to approximately 28 months
|
Defined as the percentage of patients who achieve complete response(CR) or partial response (PR), as assessed by BICR per RECIST 1.1
|
Randomization up to approximately 28 months
|
|
Disease control rate (DCR) assessed by Blinded Independent Central Review (BICR)
Time Frame: Randomization up to approximately 28 months
|
Defined as the percentage of patients who achieve CR, PR or stable disease (SD), as assessed by BICR per RECIST 1.1
|
Randomization up to approximately 28 months
|
|
Duration of Response (DoR) assessed by Blinded Independent Central Review (BICR)
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Time to Response (TTR) assessed by Blinded Independent Central Review (BICR)
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Objective Response Rate (ORR) assessed by Investigator
Time Frame: Randomization up to approximately 28 months
|
Defined as the percentage of patients who achieve complete response(CR) or partial response (PR), as assessed by investigator per RECIST 1.1
|
Randomization up to approximately 28 months
|
|
Disease control rate (DCR) assessed by Investigator
Time Frame: Randomization up to approximately 28 months
|
Defined as the percentage of patients who achieve CR, PR or stable disease (SD), as assessed by investigator per RECIST 1.1
|
Randomization up to approximately 28 months
|
|
Duration of Response (DoR) assessed by Investigator
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Time to Response (TTR) assessed by Investigator
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Quality of life evaluated using the NCC-BC-A scale
Time Frame: Randomization up to approximately 28 months
|
To assess the impact of ESG401 on disease related symptoms and quality of life of patients using the NCC-BC-A scale
|
Randomization up to approximately 28 months
|
|
Clearance
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Volume of distribution
Time Frame: Randomization up to approximately 28 months
|
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.
|
Randomization up to approximately 28 months
|
|
Anti-drug Antibodies
Time Frame: Randomization up to approximately 28 months
|
Incidence of anti-drug antibodies.
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Randomization up to approximately 28 months
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Fei Ma, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Estimated)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- ESG401-302
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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