Clinical Trials

This phase 3 study will evaluate the efficacy and safety of GDC-0077 in combination with palbociclib and fulvestrant in patients with PIK3CA-mutant, ER+, HER2-negative locally advanced or metastatic breast cancer.
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This study aims to screen patients with advanced cancer and unmet clinical needs for actionable biomarkers to be used to guide therapy.
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This trial will investigate if using an immunotherapy drug alone prior to the combination of immunotherapy and standard chemotherapy is safe and effective in treating breast cancer before surgery.
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This study will evaluate the pharmacodynamics, pharmacokinetics, safety, and biologic activity of GDC-9545 in participants with Stage I-III operable ER+, HER2- untreated breast cancer.
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This study is assessing the benefits of prescribed exercise in clinical populations, including people with breast cancer.
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The aim of the POSNOC trial is to find out if further axillary treatment is of benefit in women with macrometastases found in one or two lymph nodes.
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This study will evaluate the safety and efficacy of targeted therapies or immunotherapy in participants with have inoperable tumours that have a genetic mutation.
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This study evaluates the efficacy and safety of adjuvant atezolizumab or placebo and trastuzumab emtansine for HER2-positive breast cancer at high risk of recurrence following preoperative therapy
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This study will look at the effect of intravenous iron on anaemia and anaemia-related symptoms during chemotherapy and up to 12 months after chemotherapy treatment.
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This study aims to find out if receiving intravenous iron ferric carboxymaltose will reduce the incidence of anaemia while patients are receiving adjuvant chemotherapy for breast cancer, and whether this is associated with an improvement in quality of life and exercise tolerance.
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This trial is evaluating a new online service for managing self-reported symptoms by people with advanced breast cancer.
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This study that will determine whether pantoprazole, an approved PPI, affects capecitabine absorption, and as a result, affects cancer survival outcomes.
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This study is comparing capecitabine with capecitabine and oral cyclophosphamide in patients with advanced breast cancer.
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A randomised clinical trial of adjuvant radiation therapy versus observation following breast conserving surgery and endocrine therapy in patients with molecularly characterised luminal A low risk early breast cancer.
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New Zealand Clinical Research is calling for male volunteers in Auckland and Christchurch to participate in two large trials looking at potential new treatments for breast cancer.
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This study looks at using a magnetic tracer verses a standard technique for sentinel node biopsy in breast cancer.
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This study will look at an e-health lifestyle intervention to improve health-related quality of life and prevent or modify the risk of chronic disease in New Zealand women previously treated for breast cancer.
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This is an observational study of the frequency and causes of impaired liver metabolism of cyclophosphamide in breast cancer.
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This phase 2 clinical trial is looking into lymph node grafting for upper limb lymphoedema following breast cancer treatment.
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This study aims to combat endocrine related cognitive problems in breast cancer by increasing magnesium levels.
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This study will compare if StrataXRT gel is adequate compared with Mepitel film in decreasing the number of women who develop radiation-induced skin reactions during or immediately after radiation for breast cancer.
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The purpose of this study is to assess the efficacy and safety of pembrolizumab (MK-3475) versus placebo in combination with neoadjuvant (pre-surgery) chemotherapy and adjuvant (post-surgery) endocrine therapy in the treatment of adults who have high-risk early-stage estrogen receptor-positive, human epidermal growth factor receptor 2-negative (ER+/HER2-) breast cancer.
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The New Zealand Familial Breast Cancer Study commenced in 2013 with the key goal of better-understanding DNA sequence changes in genes that alter the risk of developing breast cancer
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This is an observational cohort study of toxicity in female patients treated for early breast cancer with Adriamycin and Cyclophosphamide chemotherapy.
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The PantoCIN trial will test the ability of a cheap, widely available drug to prevent two of chemotherapy’s most unpleasant side-effects: delayed nausea and vomiting.
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This study is assessing the benefits of prescribed exercise in clinical populations, including people with breast cancer.
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This study aims to reduce inflammation in post-menopausal women with breast cancer through the use of asprin.
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THYmine2 is an observational study to assess whether the thymine loading test can prospectively categorize patients who cannot tolerate 5-FU treatment (e.g. FOLFOX, CapeOx, FLOX). This treatment is commonly used in breast cancer treatment. Reactions occur in approximately 10% of patients and can result in life-threatening events.
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This study looks at using a magnetic tracer verses a standard technique for sentinel node biopsy in breast cancer.
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This study will introduce participants to a supervised, personalised exercise programme from point-of-diagnosis through to week 12 of chemotherapy in individuals receiving treatment for early-stage breast cancer.
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The primary purpose of this study is to investigate whether it is effective and feasible to treat post cancer related fatigue (CRF) using acupuncture.
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The primary purpose of this study is to develop and evaluate a new low literacy decision aid relating to fertility preservation for younger women with early stage breast cancer.
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This study will determine whether SAR439859 per os improves progression free survival (PFS) when compared with a endocrine monotherapy of the choice of the physician, in participants with metastatic or locally advanced breast cancer.
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This study will investigate the effect of stereotactic radiotherapy to see whether it helps women with ER+, HER2- advanced breast cancer continue CDK 4/6 treatment for longer.
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The purpose of this study is to see if a program of manual drainage and use of a compression bra can improve outcomes for breast cancer patients experiencing post-treatment oedema (accumulation of fluid under the skin).
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This observational study will see if a breast magnetic resonance imaging (MRI) of women recently diagnosed with breast cancer impacts on their treatment planning and cancer outcomes.
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BRCA-P is an international breast cancer prevention clinical trial open to women with a confirmed BRCA1 gene mutation who have not had a diagnosis of breast cancer.
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A study assessing the efficacy and safety of capivasertib + fulvestrant versus placebo + fulvestrant as treatment for locally advanced or metastatic HR+/HER2- breast cancer following recurrence or progression on or after treatment with an aromatase inhibitor
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This trial will investigate if treatment with a PI3K inhibitor (alpelisib), in combination with fulvestrant, will improve outcomes for patients with metastatic breast cancer when compared with standard treatment.
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A study evaluating the efficacy and safety of nivolumab versus placebo in combination with neoadjuvant (pre-surgery) chemotherapy and adjuvant (post-surgery) endocrine therapy in participants with high-risk ER+, HER2- early stage breast cancer.
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This study aims to assess the efficacy and safety of cryotherapy in preventing CIPN in patients receiving taxanes for breast or gynaecological cancer.
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This study aims to find out if the combination of anti-HER2 therapy with PD-L1 inhibitor and CTLA4 inhibitor will reactivate anti-tumour immune response and improve clinical outcomes in trastuzumab-resistant, advanced HER2+ breast cancer.
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This study will see if the study drug LY3484356 alone or in combination with abemaciclib is safe and effective in participants with advanced or metastatic breast cancer.
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This study is testing olaparib, in homologous recombination (HR) deficient metastatic breast cancer in patients who do not have hereditary mutations in BRCA1 and BRCA2.
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This study will determine whether treatment with alpelisib in combination with abraxane is safe and effective in subjects with advanced triple negative breast cancer (aTNBC) who carry either a PIK3CA mutation or have PTEN loss without PIK3CA mutation.
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The purpose of this study is to see if a handheld imaging device (MEprobe) can accurately detect the microscopic presence of cancer in breast surgery patients.
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Lifepool is a research resource for study into breast cancer and women's health. It aims to recruit 100,000 Australian women. This will establish one of the largest cohorts in the world, providing research tools to answer critical questions about breast cancer. Lifepool aims to gather information on health and lifestyle, mammogram data and asks permission to track the health of each participant through linkage with other health databases.
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This study is investigating the safety, tolerability and pharmacokinetic (PK) profile of LYT-100 in healthy volunteers and in those with breast cancer-related lymphoedema (BCRL).
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This study will investigate the feasibility of using oestradiol vaginal tablets for women on adjuvant aromatase inhibitors for breast cancer.
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This study is investigating the combination of palbociclib, letrozole and venetoclax in ER and BCL-2 positive locally advanced or metastatic breast cancer.
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This interventional study will look at the effect of self-directed physical activity and motivational interviewing on quality of life, psychological health and immune outcomes in female breast cancer survivors
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The purpose of this study is to determine whether a structured peer support program can improve exercise adherence and health outcomes in breast cancer survivors.
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This study will investigate whether delivering radiation therapy while patients are in a prone position can help minimise skin toxicities ahead of surgery.
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The purpose of this study is to investigate whether it is possible for blood samples to be used to monitor whether the correct dose of cancer medicines are being provided to patients.
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This trial is investigating the efficacy and feasibility of a personalised risk assessment for breast and ovarian cancer, through offering a polygenic risk score.
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This trial is investigating the efficacy of providing neuropsychological feedback in addressing self-reported cognitive impairment in breast cancer survivors.
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This study will assess the safety and effectiveness of an investigational agent (MSH2TR) used to detect lymph node spread of cancer in patients with HER2+ breast cancer.
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This dose escalation and expansion study will investigate the use of spartalizumab + LAG525 in combination with NIR178, capmatinib, MCS110, or canakinumab in patients with advanced or metastatic triple negative breast cancer.
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This is an open-label, multicenter, global phase 2 basket study of entrectinib (RXDX-101) for the treatment of patients with solid tumors that harbor an NTRK1/2/3 or ROS1 gene fusion.
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This study aims to assess the impact of a computerised cognitive training program on the neurotoxic effects of chemotherapy on cognition in breast cancer patients.
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The purpose of this study is to determine if breast cancer genetic material (known as circulating tumour DNA (ctDNA) can be detected in the bloodstream. It is hoped that this research will demonstrate the utility of this circulating material as an early marker of residual or recurrent breast cancer activity after treatment
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An open-label, randomized, window of opportunity study between diagnosis and definite surgery, to assess the effect of antiestrogen therapies, alone and in combination with microionized progesterone (prometrium) in patients with newly diagnosed ER+PR+ breast cancer.
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This trial aims to determine feasibility and preliminary efficacy of a 12-week online yoga program in women with breast cancer-related lymphoedema, and to evaluate its impact on coping skills and quality of life.
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The purpose of this study is to determine the effect of an online yoga exercise on mental health in women diagnosed with breast or gynaecological cancer.
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This study looks at how to manage the fear of cancer recurrence/progression in women with breast and ovarian cancer.
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This study examines the impact of a fertility decision aid developed using health literacy principles on decision-related outcomes in younger women with breast cancer.
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