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

NCT05720026 | Recruiting Phase 3

• 1 other identifier: SYSA1901-002
• Study Type: interventional
• Target: 560
• Locations: 1 country
• Sites: 1

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.

Conditions

HER2-positive Breast Cancer

Outcome Measures

Primary Outcomes (1)

• Total pathologic complete response (tpCR) assessed by Independent Review Committee（IRC）

  The tpCR is defined as the histological evidence of no malignancy of lymph nodes in the regions of primary lesion and metastasis of breast cancer (i.e., ypT0/is, ypN0 in accordance with the AJCC staging system)

  Up to 5 months

Secondary Outcomes (7)

• Percentage of patients with tpCR as assessed by the investigator

  Up to 5 months

• Breast pathologic complete response (bpCR) assessed by IRC

  Up to 5 months

• Breast pathologic complete response (bpCR) assessed by the investigator

  Up to 5 months

• Percentage of patients with an objective response (BORR)

  Prior to surgery

• Incidence of adverse event

  Up to approximately 30 months after randomization

Study Arms (2)

Treatment group

EXPERIMENTAL

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

Drug: SYSA1901; Drug: Trastuzumab; Drug: Docetaxel

Control group

ACTIVE COMPARATOR

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

Drug: Pertuzumab; Drug: Trastuzumab; Drug: Docetaxel

Interventions

SYSA1901 DRUG

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

Also known as: pertuzumab biosimilar

Treatment group

Pertuzumab DRUG

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

Also known as: Perjeta®

Control group

Trastuzumab DRUG

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

Also known as: Herceptin®

Control group; Treatment group

Docetaxel DRUG

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

Also known as: Docetaxel injection

Control group; Treatment group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Voluntary agreement to provide written informed consent;
• Age ≥ 18 years;
• 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);
• Eastern Cooperative Oncology Group (ECOG) performance status: 0-1;
• HER2 positive, defined as immunohistochemistry (IHC) 3+, or IHC 2+ with In Situ Hybridization (ISH) positive;
• Estrogen receptor (ER) and progestin receptor (PR) negative; ER and PR negative is defined as \< 1% nuclear staining;
• Agree to receive surgical treatment of breast cancer at the participating unit when the surgical criteria are met after neoadjuvant therapy;
• Primary tumor size of \> 2 cm in diameter;
• Left ventricular ejection fraction (LVEF)≥ 55% measured by echocardiography (ECHO) or multiple gated acquisition (MUGA) scan;
• 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;
• Women of childbearing age must have a negative pregnancy test prior to the first dose;
• 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.

You may not qualify if:

• Stage IV (metastatic) breast cancer, inflammatory breast cancer, and bilateral breast cancer;
• Previous severe allergic reactions to any drug or its components in this trial (NCI-CTCAE 5.0 grade greater than 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);
• Major surgery and incomplete recovery within 4 weeks prior to the first dose of study drug;
• Patients have received other clinical trial drugs within 4 weeks before the first dose of study drug;
• 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);
• History of immunodeficiency diseases, including human immunodeficiency virus (HIV) positive, active syphilis;
• 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;
• Any uncontrollable complication, infection, or other condition that may affect study compliance or interfere with efficacy evaluation;
• History of drug abuse, or alcoholism, drug addicts;
• History of neurological or psychiatric disorders and poor compliance, such as epilepsy and dementia;
• Pregnant and breastfeeding women;
• 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.

Sponsors & Collaborators

• CSPC ZhongQi Pharmaceutical Technology Co., Ltd.: lead

Study Sites (1)

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

RECRUITING

MeSH Terms

Interventions

pertuzumab; Trastuzumab; Docetaxel

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins; Taxoids; Cyclodecanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Hydrocarbons; Organic Chemicals; Diterpenes; Terpenes

Study Officials

• Shao Zhimin, Professor

  Fudan University

  STUDY CHAIR

Central Study Contacts

Shao Zhimin, Professor

CONTACT

+86-021-64175590-88603; szm@163.com

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 25, 2022
• First Posted: February 9, 2023
• Study Start: January 9, 2023
• Primary Completion: August 29, 2025
• Study Completion: February 21, 2026
• Last Updated: February 9, 2023

Record last verified: 2023-02

Locations

CN (1)