EPIK-B5

Name No. For Patients with Purpose
EPIK-B5 21-32

HR-positive, HER2-negative advanced breast cancer with a PIK3CA mutation who progressed or relapsed on or after treatment with an AI plus a CDK4/6 inhibitor.

The purpose of this study is to obtain more comprehensive data on the efficacy and safety of alpelisib (BYL719) in combination with fulvestrant compared with placebo plus fulvestrant in men or postmenopausal women with HR-positive, HER2-negative advanced breast cancer with a PIK3CA mutation who progressed or relapsed on or after treatment with an AI plus a CDK4/6 inhibitor.


KEYNOTE-B49

Name No. For Patients with Purpose
KEYNOTE-B49 21-31

Chemotherapy-Candidate Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative (HR+/HER2-) Locally Recurrent Inoperable or Metastatic Breast Cancer

To assess the safety and efficacy of pembrolizumab plus the investigator’s choice of chemotherapy compared to placebo plus the investigator’s choice of chemotherapy


lidERA Breast Cancer/ GO42784/ TRIO 045

Name No. For Patients with Purpose
lidERA Breast Cancer/ GO42784/ TRIO 045 21-04

with medium- and high-risk Stage I-III histologically confirmed estrogen receptor (ER)-positive and human epidermal growth factor receptor 2 (HER2)-negative early breast cancer

to evaluate the efficacy and safety of adjuvant giredestrant compared with endocrine therapy of physician’s choice


SASCIA

Name No. For Patients with Purpose
SASCIA 20-24

Primary HER2- negative breast cancer patients with high relapse risk after standard neoadjuvant treatment

This study is a phase III postneoadjuvant study evaluating Sacituzumab Govitecan, an Antibody Drug Conjugate in primary HER2- negative breast cancer patients with high relapse risk after standard neoadjuvant treatment – SASCIA


DESTINY-Breast05

Name No. For Patients with Purpose
DESTINY-Breast05 21-15

HER2-positive primary breast cancer who do not achieve complete response after appropriate neoadjuvant therapy and are at higher risk of disease recurrence.

This study will examine the efficacy and safety of trastuzumab deruxtecan (T-DXd) compared with trastuzumab emtansine (T-DM1) in high-risk patients with residual invasive breast cancer following neoadjuvant therapy.


Proteomics / Molecular Breast

Name No. For Patients with Purpose
Proteomics / Molecular Breast 09-07

Breast cancer

The purpose of this trial is to examine the function of different genes and proteins, previously identified to be of interest, and identify new ones, as well as the means by which they interact and differ between cancer cells.