CADY Sub-Study

Name No. For Patients with Purpose
CADY Sub-Study 08-01

No new patients will be recruited to this study. The original study involved patients with breast cancer treated with Trastuzumab.If you participated in the CTRIAL-IE (ICORG) 08-01 CADY study on cardiac dysfunction in HER-2 positive breast cancer patients, please read this important data protection notice. Cancer Trials Ireland, in collaboration with Abbott Laboratories, is conducting a follow-up sub-study to re-test stored biological samples using advanced biomarker technology and review medical records for cardiovascular outcomes. This research aims to improve early detection of heart risks in breast cancer patients treated with Trastuzumab. Your data remains securely stored and protected, with strict access controls. If you wish to learn more, withdraw consent, or exercise your data rights, click here to read the full notice.

The study aims to:
(1) Evaluate the predictive capability of chosen cardiac biomarkers in forecasting cardiac dysfunction in breast cancer patients treated with Trastuzumab.
(2) Develop a predictive model using machine learning techniques based on the most accurate and sensitive combination of biomarkers.


EMBER-4

Name No. For Patients with Purpose
EMBER-4 24-07

Estrogen receptor positive (ER+), human epidermal receptor 2 negative (HER2-) early-stage, resected, invasive breast cancer without evidence of distant metastasis.

To measure how well imlunestrant works compared to standard hormone therapy in patients with early-stage breast cancer that is ER+ and HER2-.


Exosomes in TNBC

Name No. For Patients with Purpose
Exosomes in TNBC 22-21

Early or metastatic triple negative breast cancer (TNBC)

The main purpose of this study is to profile exosomes isolated from the plasma of women diagnosed with TNBC during routine treatment and follow up in the oncology clinic using Nanoparticle tracking analysis (NTA) and Raman/infra-red spectroscopy.


UCARE

Name No. For Patients with Purpose
UCARE 24-21

Female patients diagnosed with stage I-III breast cancer.

The main purpose of the study is to evaluate pathways for identifying, managing, and overcoming side effects of cancer therapies that can negatively impact quality-of-life and overall outcomes for women during and after cancer treatment.


Wavelia

Name No. For Patients with Purpose
Wavelia 24-22

Female patients with an investigator-assessed discrete breast abnormality of size > 1cm.

The main purpose of this study is to determine whether a microwave imaging system (Wavelia #2) can be used for the detection of breast cancer.


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.


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.