A Phase 3 Study Comparing Carelizumab Plus Nab-paclitaxel and Apatinib, Carelizumab Plus Nab-paclitaxel, and Nab-paclitaxel in Patients With Advanced Triple Negative Breast Cancer.
Primary Purpose
Breast Cancer, Triple Negative Breast Cancer
Status
Terminated
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Carelizumab
Nab-paclitaxel
Apatinib
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer focused on measuring SHR-1210, PD-1
Eligibility Criteria
Inclusion Criteria:
- ECOG Performance Status of 0-1.
- Expected lifetime of not less than three months
- Metastatic or locally advanced, histologically documented TNBC (absence of HER2, ER, and PR expression)
- Cancer stage: locally advanced or metastatic breast cancer; Locally advanced breast cancer not amenable to radical resection.
- No prior systemic antitumor therapy for metastatic triple-negative breast cancer.
- Adequate hematologic and organ function
- Measurable disease according to Response Evaluation Criteria in Solid Tumors v1.1 (RECIST v1.1)
Exclusion Criteria:
- Known central nervous system (CNS) disease.
- Previously received anti-VEGFR small molecule tyrosine kinase inhibitors or anti-PD-1/PD-L1 antibody.
- A history of bleeding, any serious bleeding events.
- Uncontrolled pleural effusion, pericardial effusion.
- Malignancies other than TNBC within 5 years prior to randomisation, or ascites requiring recurrent drainage procedures
- History of interstitial pneumonitis.
- Severe chronic or active infections in need of systemic antibacterial, antifungal, or antiviral treatment, including TB, etc.
- Prior allogeneic stem cell or solid organ transplantation.
- History of autoimmune disease
- Active hepatitis B or hepatitis C
- Pregnancy or lactation.
- Peripheral neuropathy grade ≥2.
- Participants with poor blood pressure control;
- Myocardial infarction incident within 6 months prior to randomisation;
- Treatment with systemic immunostimulatory agents within 4 weeks prior to randomisation
- Treatment with systemic immunosuppressive medications within 2 weeks prior to randomisation
Sites / Locations
- Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Experimental A
Experimental B
Comparator C
Arm Description
Subjects receive Carelizumab in combination with Nab-paclitaxel plus Apatinib,each 4-week cycle
Subjects receive Carelizumab in combination with Nab-paclitaxel,each 4-week cycle
Subjects receive nab-paclitaxel intravenously each 4-week cycle.
Outcomes
Primary Outcome Measures
Progression-free Survival (PFS)
Progression-free survival (PFS) as determined by the IRC according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) in PD-L1 positive / ITT population
Secondary Outcome Measures
Progression Free Survival (PFS)
Progression Free Survival (PFS) as determined by the investigator According to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 (v1.1) in PD-L1 positive/ITT population
Overall Survival (OS) in PD-L1 positive/ITT population
Objective response rate (ORR) in the PD-L1-positive/ITT population
Clinical benefit rate (CBR), defined as the proportion of patients with a CR or a PR or stable disease as determined by the investigator according to RECIST 1.1
Percentage of Participants with Adverse Events (AEs)
Serum concentration of SHR-1210 and plasma concentration of apatinib
Proportion of anti-SHR-1210 antibody (ADA) and neutralizing antibody (Nab) formed during the study from baseline
Full Information
NCT ID
NCT04335006
First Posted
March 31, 2020
Last Updated
May 4, 2023
Sponsor
Jiangsu HengRui Medicine Co., Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT04335006
Brief Title
A Phase 3 Study Comparing Carelizumab Plus Nab-paclitaxel and Apatinib, Carelizumab Plus Nab-paclitaxel, and Nab-paclitaxel in Patients With Advanced Triple Negative Breast Cancer.
Official Title
A Multicentre, Open-parallel, Randomized, Controlled Phase Ⅲ Study Comparing Carelizumab Plus Nab-paclitaxel and Apatinib, Carelizumab Plus Nab-paclitaxel, and Nab-paclitaxel in Patients With Unresectable Locally Advanced or Metastatic Triple Negative Breast Cancer.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Terminated
Why Stopped
Sponsor R & D Strategy Adjustment
Study Start Date
July 14, 2020 (Actual)
Primary Completion Date
April 14, 2023 (Actual)
Study Completion Date
April 14, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jiangsu HengRui Medicine Co., Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This randomized, open-label phase 3 study will evaluate the safety and efficacy of Carelizumab (an engineered anti-programmed death-ligand 1 [PD-1] antibody) in combination with Nab-paclitaxel and Apatinib, carelizumab plus nab-paclitaxel, and Nab-paclitaxel in Patients with Unresectable Locally Advanced or Metastatic Triple Negative Breast Cancer. Participants will be randomized in a 1:1:1 ratio to Arm A (Carelizumab + Nab-paclitaxel + Apatinib), Arm B (Carelizumab + Nab-paclitaxel), or Arm C (Nab-paclitaxel).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Triple Negative Breast Cancer
Keywords
SHR-1210, PD-1
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Experimental A
Arm Type
Experimental
Arm Description
Subjects receive Carelizumab in combination with Nab-paclitaxel plus Apatinib,each 4-week cycle
Arm Title
Experimental B
Arm Type
Experimental
Arm Description
Subjects receive Carelizumab in combination with Nab-paclitaxel,each 4-week cycle
Arm Title
Comparator C
Arm Type
Active Comparator
Arm Description
Subjects receive nab-paclitaxel intravenously each 4-week cycle.
Intervention Type
Drug
Intervention Name(s)
Carelizumab
Other Intervention Name(s)
SHR-1210
Intervention Description
Participants receive SHR-1210 intravenously (IV)
Intervention Type
Drug
Intervention Name(s)
Nab-paclitaxel
Intervention Description
administered intravenously every 4-week cycle
Intervention Type
Drug
Intervention Name(s)
Apatinib
Intervention Description
administered orally every 4-week cycle
Primary Outcome Measure Information:
Title
Progression-free Survival (PFS)
Description
Progression-free survival (PFS) as determined by the IRC according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) in PD-L1 positive / ITT population
Time Frame
Randomisation to the first occurrence of disease progression or death (through the end of study, approximately 42 months)
Secondary Outcome Measure Information:
Title
Progression Free Survival (PFS)
Description
Progression Free Survival (PFS) as determined by the investigator According to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 (v1.1) in PD-L1 positive/ITT population
Time Frame
Up to approximately 42 months
Title
Overall Survival (OS) in PD-L1 positive/ITT population
Time Frame
Up to approximately 42 months
Title
Objective response rate (ORR) in the PD-L1-positive/ITT population
Time Frame
Up to approximately 42 months
Title
Clinical benefit rate (CBR), defined as the proportion of patients with a CR or a PR or stable disease as determined by the investigator according to RECIST 1.1
Time Frame
Up to approximately 42 months
Title
Percentage of Participants with Adverse Events (AEs)
Time Frame
Up to approximately 42 months
Title
Serum concentration of SHR-1210 and plasma concentration of apatinib
Time Frame
Up to approximately 42 months
Title
Proportion of anti-SHR-1210 antibody (ADA) and neutralizing antibody (Nab) formed during the study from baseline
Time Frame
Up to approximately 42 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ECOG Performance Status of 0-1.
Expected lifetime of not less than three months
Metastatic or locally advanced, histologically documented TNBC (absence of HER2, ER, and PR expression)
Cancer stage: locally advanced or metastatic breast cancer; Locally advanced breast cancer not amenable to radical resection.
No prior systemic antitumor therapy for metastatic triple-negative breast cancer.
Adequate hematologic and organ function
Measurable disease according to Response Evaluation Criteria in Solid Tumors v1.1 (RECIST v1.1)
Exclusion Criteria:
Known central nervous system (CNS) disease.
Previously received anti-VEGFR small molecule tyrosine kinase inhibitors or anti-PD-1/PD-L1 antibody.
A history of bleeding, any serious bleeding events.
Uncontrolled pleural effusion, pericardial effusion.
Malignancies other than TNBC within 5 years prior to randomisation, or ascites requiring recurrent drainage procedures
History of interstitial pneumonitis.
Severe chronic or active infections in need of systemic antibacterial, antifungal, or antiviral treatment, including TB, etc.
Prior allogeneic stem cell or solid organ transplantation.
History of autoimmune disease
Active hepatitis B or hepatitis C
Pregnancy or lactation.
Peripheral neuropathy grade ≥2.
Participants with poor blood pressure control;
Myocardial infarction incident within 6 months prior to randomisation;
Treatment with systemic immunostimulatory agents within 4 weeks prior to randomisation
Treatment with systemic immunosuppressive medications within 2 weeks prior to randomisation
Facility Information:
Facility Name
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
A Phase 3 Study Comparing Carelizumab Plus Nab-paclitaxel and Apatinib, Carelizumab Plus Nab-paclitaxel, and Nab-paclitaxel in Patients With Advanced Triple Negative Breast Cancer.
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