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Neoadjuvant Study of Navelbine in Patients With HER2 Positive Breast Cancer

U

University of Chinese Academy Sciences

Status and phase

Unknown
Phase 3

Conditions

Breast Cancer

Treatments

Drug: Navelbine
Drug: Docetaxel

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This is a randomized, double-blind multicenter Phase III study for evaluating the efficacy of neoadjuvant Navelbine plus trastuzumab and Pertuzumab versus Docetaxel plus trastuzumab and Pertuzumab given as neoadjuvant treatment in HER2 positive early-stage or locally advanced breast cancer.

Enrollment

50 estimated patients

Sex

Female

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Female patients, 18 years ≤ age ≤ 80 years; Performance Status- Eastern Cooperative Oncology Group (ECOG) 0-1 Histologically confirmed invasive breast cancer(early stage or locally advanced) HER2 positive (HER2+++ by IHC or FISH+) Known hormone receptor status. Cardiovascular: Baseline left ventricular ejection fraction (LVEF)≥55% measured by ECHO Signed informed consent form (ICF)

Exclusion criteria

Metastatic disease (Stage IV) or inflammatory breast cancer Previous or current history of malignant neoplasms, except for curatively treated: Basal and squamous cell carcinoma of the skin, Carcinoma in situ of the cervix.

Clinically relevant cardiovascular disease: Known history of uncontrolled or symptomatic angina, clinically significant arrhythmias, congestive heart failure, transmural myocardial infarction, uncontrolled hypertension ≥180/110); Unable or unwilling to swallow tablets.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

NHP
Experimental group
Description:
Navelbine, Herceptin, Pertuzumab
Treatment:
Drug: Navelbine
THP
Active Comparator group
Description:
Docetaxel, Herceptin, Pertuzumab
Treatment:
Drug: Docetaxel

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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