A Randomized, Controlled, Open-label, Multicenter, Phase III Clinical Study to Evaluate the Efficacy and Safety of KN026 Combined With HB1801 and Chemotherapy Versus Trastuzumab Combined With Pertuzumab and Chemotherapy as Adjuvant Therapy in Resectable HER2-positive Breast Cancer

Shanghai JMT-Bio Inc.0 sites1,800 target enrollmentStarted: March 7, 2026Last updated: March 2, 2026

InterventionsKN026 HB1801 Epirubicin Doxorubicin Cyclophosphamide Carboplatin Trastuzumab Pertuzumab Docetaxel

Overview

Phase: Phase 3
Status: Not yet recruiting
Sponsor: Shanghai JMT-Bio Inc.
Enrollment: 1,800
Primary Endpoint: iDFS

Overview Study Design Eligibility Criteria Arms & Interventions Outcomes Investigators Records & Identifiers Similar Trials

Overview

Brief Summary

This is a randomized, controlled, open-label, multicenter, Phase Ⅲ clinical study designed to compare the efficacy and safety of KN026 combined with HB1801 and chemotherapy versus trastuzumab combined with pertuzumab and chemotherapy as adjuvant therapy in participants with HER2-positive breast cancer.

Study Design

Study Type: Interventional
Allocation: Randomized
Intervention Model: Parallel
Primary Purpose: Treatment
Masking: None

Eligibility Criteria

Ages: 18 Years to — (Adult, Older Adult)
Sex: All
Accepts Healthy Volunteers: No

Inclusion Criteria

•Voluntarily participate and sign the informed consent form.
•Age ≥ 18 years.
•ECOG performance status score of 0 or
•Histologically or cytologically confirmed invasive breast cancer.
•Must have undergone prior radical mastectomy or breast-conserving surgery for breast cancer.
•Pathologically confirmed positive regional lymph nodes.
•Tumor tissue confirmed as HER2-positive by the local laboratory.
•Adequate organ and bone marrow function:
•Absolute neutrophil count ≥ 1.5 × 10⁹/L
•Platelet count ≥ 100 × 10⁹/L

Exclusion Criteria

•History of any prior ipsilateral and/or contralateral invasive breast cancer.
•History of other malignancy within 5 years prior to randomization, except for the breast cancer under study and locally curable malignancies treated with curative intent.
•Prior systemic chemotherapy, endocrine therapy, anti-HER2 targeted therapy, or local radiotherapy for breast cancer.
•Use of strong CYP3A4 inhibitors within 14 days prior to randomization or planned use during the combination chemotherapy period.
•Known contraindication to any study drug or history of hypersensitivity to any component or known excipient of the study drugs.
•Significant cardiovascular disease history, including: prior coronary artery bypass graft or coronary stenting; myocardial infarction or cerebrovascular accident within 6 months prior to randomization; history of congestive heart failure/systolic dysfunction (LVEF \< 50%) or unstable angina; history of clinically significant prolonged QT interval or QTcF (Fridericia) \> 450 ms at screening; uncontrolled severe hypertension (systolic BP \> 180 mmHg and/or diastolic BP \> 100 mmHg); high-risk arrhythmias \[e.g., atrial tachycardia with resting heart rate ≥ 100 bpm, significant ventricular arrhythmia (ventricular tachycardia), or high-grade atrioventricular block (Mobitz type II second-degree or third-degree AV block)\].
•Severe chronic or active infection requiring intravenous anti-infective therapy within 14 days prior to randomization.
•Participation in another interventional clinical trial within 4 weeks prior to randomization.
•Pregnant or lactating women.
•Any other condition that may interfere with the participant's ability to comply with study procedures, may not be in the participant's best interest to participate, or may affect study results (e.g., history of neurological or psychiatric disorders, alcohol or drug abuse, or any other clinically significant disease or condition).

Arms & Interventions

KN026 combined with HB1801 and chemotherapy

Experimental

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → HB1801 for 4 cycles + KN026 for up to 1 year (18 cycles).

Regimen 2 (Carboplatin-containing chemotherapy): HB1801 combined with carboplatin for 6 cycles + KN026 for up to 1 year (18 cycles).

Intervention: KN026 (Drug)

KN026 combined with HB1801 and chemotherapy

Experimental

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → HB1801 for 4 cycles + KN026 for up to 1 year (18 cycles).

Regimen 2 (Carboplatin-containing chemotherapy): HB1801 combined with carboplatin for 6 cycles + KN026 for up to 1 year (18 cycles).

Intervention: HB1801 (Drug)

KN026 combined with HB1801 and chemotherapy

Experimental

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → HB1801 for 4 cycles + KN026 for up to 1 year (18 cycles).

Regimen 2 (Carboplatin-containing chemotherapy): HB1801 combined with carboplatin for 6 cycles + KN026 for up to 1 year (18 cycles).

Intervention: Epirubicin (Drug)

KN026 combined with HB1801 and chemotherapy

Experimental

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → HB1801 for 4 cycles + KN026 for up to 1 year (18 cycles).

Regimen 2 (Carboplatin-containing chemotherapy): HB1801 combined with carboplatin for 6 cycles + KN026 for up to 1 year (18 cycles).

Intervention: Doxorubicin (Drug)

KN026 combined with HB1801 and chemotherapy

Experimental

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → HB1801 for 4 cycles + KN026 for up to 1 year (18 cycles).

Regimen 2 (Carboplatin-containing chemotherapy): HB1801 combined with carboplatin for 6 cycles + KN026 for up to 1 year (18 cycles).

Intervention: Cyclophosphamide (Drug)

KN026 combined with HB1801 and chemotherapy

Experimental

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → HB1801 for 4 cycles + KN026 for up to 1 year (18 cycles).

Regimen 2 (Carboplatin-containing chemotherapy): HB1801 combined with carboplatin for 6 cycles + KN026 for up to 1 year (18 cycles).

Intervention: Carboplatin (Drug)

Trastuzumab combined with pertuzumab and chemotherapy

Active Comparator

Regimen 1 (Anthracycline-containing chemotherapy): Epirubicin/Doxorubicin combined with cyclophosphamide for 4 cycles → Docetaxel for 4 cycles + Trastuzumab and Pertuzumab for up to 1 year (18 cycles).