Study to Evaluate the Efficacy and Safety of SYSA1901 vs. Perjeta® of HER2-Positive Breast Cancer

NCT ID: NCT05720026

Last Updated: 2023-02-09

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 560 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-01-09
• Study Completion Date: 2026-02-21

Brief Summary

This is a phase Ⅲ, double-blind, randomized, parallel-controlled, multicenter equivalence study to compare the efficacy and safety of SYSA1901 + trastuzumab + docetaxel vs. Perjeta® + trastuzumab + docetaxel in the participants with early-stage or locally advanced HER2-positive and HR-negative breast cancer with a primary tumor > 2 cm.

Detailed Description

This is a phase Ⅲ, double-blind, randomized, parallel-controlled, multicenter equivalence study to compare the efficacy and safety of SYSA1901 + trastuzumab + docetaxel vs. Perjeta® + trastuzumab + docetaxel in the patients with early-stage or locally advanced HER2-positive and HR-negative breast cancer with a primary tumor > 2 cm. The eligible patients will be randomized to treatment group (SYSA1901 + Trastuzumab + Docetaxel) or control group (Perjeta® + Trastuzumab + Docetaxel) at 1:1 ratio. The stratification factor is disease category (early-stage vs. locally advanced).

The primary endpoint is total pCR (tpCR). Secondary efficacy endpoints include breast pCR (bpCR), objective response rate (ORR)，pharmacokinetic (PK) and immunogenicity.

Conditions

HER2-positive Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Treatment group

SYSA1901 combined with trastuzumab and docetaxel will be administrated intravenously on a 3-weekly schedule for 4 cycles (21 days per cycle).

Group Type: EXPERIMENTAL

SYSA1901

Intervention Type: DRUG

loading dose of 840 mg IV, followed by 420 mg IV, q3w/cycle, total 4cycle

Trastuzumab

Intervention Type: DRUG

loading dose of 8 mg/kg IV, followed by 6 mg/kg IV, q3w/cycle, total 4cycle

Docetaxel

Intervention Type: DRUG

75 mg/m\^2 IV, q3w/cycle, total 4cycle

Control group

Perjeta® combined with trastuzumab and docetaxel will be administrated intravenously on a 3-weekly schedule for 4 cycles (21 days per cycle).

Group Type: ACTIVE_COMPARATOR

Pertuzumab

Intervention Type: DRUG

loading dose of 840 mg IV, followed by 420 mg IV, q3w/cycle, total 4cycle

Trastuzumab

Intervention Type: DRUG

loading dose of 8 mg/kg IV, followed by 6 mg/kg IV, q3w/cycle, total 4cycle

Docetaxel

Intervention Type: DRUG

75 mg/m\^2 IV, q3w/cycle, total 4cycle

Interventions

SYSA1901

loading dose of 840 mg IV, followed by 420 mg IV, q3w/cycle, total 4cycle

Intervention Type: DRUG

Pertuzumab

loading dose of 840 mg IV, followed by 420 mg IV, q3w/cycle, total 4cycle

Intervention Type: DRUG

Trastuzumab

loading dose of 8 mg/kg IV, followed by 6 mg/kg IV, q3w/cycle, total 4cycle

Intervention Type: DRUG

Docetaxel

75 mg/m\^2 IV, q3w/cycle, total 4cycle

Intervention Type: DRUG

Other Intervention Names

pertuzumab biosimilar; Perjeta®; Herceptin®; Docetaxel injection

Eligibility Criteria

Inclusion Criteria

1. Voluntary agreement to provide written informed consent;

2. Age ≥ 18 years;

3. Histologically confirmed invasive breast carcinoma, and breast cancer staging [in accordance with the American Joint Committee on Cancer (AJCC) staging system (8th edition)]: early-stage (T2-3, N0-1, M0) or locally advanced (T2-3, N2-3, M0; T4, any N, M0);

4. Eastern Cooperative Oncology Group (ECOG) performance status: 0-1;

5. HER2 positive, defined as immunohistochemistry (IHC) 3+, or IHC 2+ with In Situ Hybridization (ISH) positive;

6. Estrogen receptor (ER) and progestin receptor (PR) negative; ER and PR negative is defined as < 1% nuclear staining;

7. Agree to receive surgical treatment of breast cancer at the participating unit when the surgical criteria are met after neoadjuvant therapy;

8. Primary tumor size of > 2 cm in diameter;

9. Left ventricular ejection fraction (LVEF)≥ 55% measured by echocardiography (ECHO) or multiple gated acquisition (MUGA) scan;

10. Adequate major organ function, meeting the following criteria (have not received blood transfusion, EPO,G-CSF, other hematopoietic stimulating factors or medical supportive treatments within 14 days before the first dose of study drug): absolute neutrophil count (ANC) ≥1.5×10^9 /L; Leukocyte count≥3.0×10^9 /L, platelet (PLT) ≥100×10^9 /L; hemoglobin ≥90 g/L; Serum creatinine ≤ 1.5 x the upper limit of normal (ULN); aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5×ULN; total bilirubin ≤1.5×ULN; international normalized ratio (INR) or prothrombin time (PT) ≤1.5×ULN, or activated partial thromboplastin time (APTT) ≤1.5×ULN (not receiving anticoagulation), or patients receiving anticoagulation need to be within treatment target range and at a stable dose;

11. Women of childbearing age must have a negative pregnancy test prior to the first dose;

12. Female and male patient of childbearing age must agree to take adequate contraceptive measures during the entire study period and through at least 6 months after the last dose of study drug.

Exclusion Criteria

1. Stage IV (metastatic) breast cancer, inflammatory breast cancer, and bilateral breast cancer;

2. Previous severe allergic reactions to any drug or its components in this trial (NCI-CTCAE 5.0 grade greater than 3);

3. Patients with any other malignant tumor within 2 years (except for skin basal cell carcinoma, skin squamous cell carcinoma, superficial bladder cancer, local prostate cancer, in situ cervical cancer and other malignant tumors that have been radically removed and have not recurred);

4. Major surgery and incomplete recovery within 4 weeks prior to the first dose of study drug;

5. Patients have received other clinical trial drugs within 4 weeks before the first dose of study drug;

6. Received chemotherapy, endocrine therapy, anti-HER2 biological therapy, breast surgery or local radiotherapy for breast cancer (except for diagnostic biopsy surgery or benign breast tumor surgery);

7. History of immunodeficiency diseases, including human immunodeficiency virus (HIV) positive, active syphilis;

8. History of severe cardiovascular disease, including previous coronary artery bypass grafting or coronary stent implantation, myocardial infarction or cerebrovascular accident within 6 months, history of congestive heart failure or unstable angina pectoris, uncontrolled severe hypertension and arrhythmia requiring drug treatment;

9. Any uncontrollable complication, infection, or other condition that may affect study compliance or interfere with efficacy evaluation;

10. History of drug abuse, or alcoholism, drug addicts;

11. History of neurological or psychiatric disorders and poor compliance, such as epilepsy and dementia;

12. Pregnant and breastfeeding women;

13. Other conditions that may affect the assessment of the primary endpoint or render the patient inappropriate for entry into this study in the opinion of the investigator.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Shao Zhimin, Professor

Role: STUDY_CHAIR

Fudan University

Locations

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Shao Zhimin, Professor

Role: CONTACT

szm@163.com

+86-021-64175590-88603

Facility Contacts

Zuo Wenjia, PhD

Role: primary

wenjytuff@hotmail.com

+86-021-64175590-88603

Other Identifiers

SYSA1901-002

Identifier Type: -

Identifier Source: org_study_id