Name | No. | For Patients with | Purpose |
---|---|---|---|
CAMBRIA-2 | 23-06 | ER+/HER2- early breast cancer with intermediate-high or high risk of recurrence |
The purpose of this study is to measure the safety and demonstrate the superiority of camizestrant +/- abemaciclib as compared to standard endocrine therapy +/- abemaciclib by assessment of invasive breast cancer-free survival |
DSSG Group: Breast
PREcoopERA
Name | No. | For Patients with | Purpose |
---|---|---|---|
PREcoopERA | 23-13 | Premenopausal patients with ER-positive/HER2-negative early breast cancer |
A Window-of-Opportunity trial of giredestrant +/- triptorelin vs. anastrozole + triptorelin in premenopausal patients with ER-positive/HER2-negative early breast cancer. |
TREAT ctDNA study
Name | No. | For Patients with | Purpose |
---|---|---|---|
TREAT ctDNA study | 23-06 | ER+/HER2- early-stage breast cancer with ctDNA relapse. |
To evaluate whether elacestrant can delay occurrence of distant metastasis or death when compared to standard endocrine therapy in ER+/HER2- patients with ctDNA relapse. |
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: |
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. |
EXPERT
Name | No. | For Patients with | Purpose |
---|---|---|---|
EXPERT | 19-03 | Patients with luminal A early breast cancer who had breast conserving surgery and endocrine therapy |
The purpose of this study is to see whether a genomic test (looking at specific genes) of breast cancer tissue can be used to select women who can safely avoid radiation therapy because they have a low risk of the cancer coming back. |
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. |