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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04126525
Other study ID # KY2019-023
Secondary ID
Status Active, not recruiting
Phase Phase 2
First received
Last updated
Start date June 18, 2019
Est. completion date November 2026

Study information

Verified date November 2023
Source RenJi Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective, open label study to evaluate the efficacy and safety of neoadjuvant pyrotinib in early breast cancer patients.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 53
Est. completion date November 2026
Est. primary completion date October 28, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Female, Aged =18 and =70 years - Histologically confirmed invasive HER2 positive breast cancer, early disease(Stage ?A-?) - Subjects with at least one evaluable lesion - ECOG 0-1 - Adequate organ function Exclusion Criteria: - Metastatic disease (Stage IV) - Subjects that are unable to swallow tablets, or dysfunction of gastrointestinal absorption - Treated or treating with T-DM1, lapatinib and neratinib before study entry - History of immunodeficiency, including HIV-positive, suffering from other acquired, congenital immunodeficiency disease, or history of organ transplantation - Subjects had any heart disease, including: (1) angina; (2) requiring medication or clinically significant arrhythmia; (3) myocardial infarction; (4) heart failure; (5) Any heart diseases judged by investigator as unsuitable to participate in the trial - Female patients who are pregnancy, lactation or women who are of childbearing potential tested positive in baseline pregnancy test. Female patients of childbearing age that are reluctant to take effective contraceptive measures throughout the trial period - Evidence of significant medical illness that in the investigator's judgment will substantially increase the risk associated with the subject's participation in and completion of the study

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Pyrotinib
dual HER2 blockade in the neoadjuvant setting

Locations

Country Name City State
China Renji Hospital Shanghai

Sponsors (1)

Lead Sponsor Collaborator
RenJi Hospital

Country where clinical trial is conducted

China, 

References & Publications (1)

Yin W, Wang Y, Wu Z, Ye Y, Zhou L, Xu S, Lin Y, Du Y, Yan T, Yang F, Zhang J, Liu Q, Lu J. Neoadjuvant Trastuzumab and Pyrotinib for Locally Advanced HER2-Positive Breast Cancer (NeoATP): Primary Analysis of a Phase II Study. Clin Cancer Res. 2022 Sep 1;2 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary pCR pathological complete response 1-2 weeks after surgery
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