BKM120 For Triple Negative Breast Cancer
Completed · Phase 2
Conditions studied: Breast Cancer
In brief
Triple negative breast cancer (TNBC) has an aggressive phenotype and poor prognosis. This tumor type characterized by lack of expression of estrogen receptor (ER), progesterone receptor (PR) and no amplification of the human epidermal growth factor 2 (HER2) accounts for 15% of breast cancers. Limited treatment options exist in the clinic as hormonal therapies and HER2-trageted agents have proven ineffective. BKM120 is a drug that works by blocking a protein called phosphatidylinositol-3-kinase (PI3K) which may contribute to cancer growth. This drug has been used in experiments in the laboratory and information from these research studies suggests that BKM120 may help to prevent cancer cells from growing. In this research study, the investigators are looking to see if BKM120 works to stop breast cancer cells from growing.
Key facts
- Study ID
- NCT01790932
- Run by
- Dana-Farber Cancer Institute
- People needed
- 50
- Starts
- 2012-06-01
- Expected to finish
- 2015-09-01
- Last updated by the study team
- 2019-01-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Pathologically and radiologically confirmed metastatic triple negative breast cancer
- Up to two prior lines of chemotherapy for metastatic breast cancer
- Availability of a representative tumor specimen
- At least one measurable lesion
You may not qualify if…
- Have received previous treatment with PI3K inhibitors
- Symptomatic central nervous system (CNS) metastases (controlled and asymptomatic CNS metastases are acceptable)
- Concurrent malignancy or has a malignancy within 3 years of study enrollment
- Any of the following mood disorders: active major depressive episode, bipolar disorder, obsessive-compulsive disorder, schizophrenia, history of suicidal attempt or ideation, homicidal ideation, greater than or equal to Common Toxicity Criteria for Adverse Events (CTCAE) grade 3 anxiety
- Concurrently using other approved or investigational antineoplastic agent and/or chemotherapy within 21 days prior to enrollment in this study
- Has received radiation therapy within 28 days prior to enrollment in this study or has not recovered from side effects of such therapy
- Major surgery within 28 days of starting therapy or has not recovered from major side effects of a previous surgery
- Poorly controlled diabetes mellitus
- History of cardiac dysfunction
- Currently receiving treatment with QT prolonging medication and the treatment cannot be discontinued or switched to a different medication
- Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of BKM120
- Receiving chronic treatment with steroids or another immunosuppressive agent
- Other concurrent severe and/or uncontrolled medical condition that would contraindicate participation in this study
- History of non-compliance to a medical regimen
- Currently being treated with drugs known to be moderate or strong inhibitors or inducers of isoenzyme Cytochrome P450, family 3, subfamily A (CYP3A)
- Known history of human immunodeficiency virus (HIV)
- Pregnant or breastfeeding
- Unwilling to observe total abstinence or to use double barrier method for birth control throughout trial
Where it is running
- Dana-Farber Cancer Institute at Faulkner Hospital — Boston, Massachusetts, United States
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
- Brigham and Women's Hospital — Boston, Massachusetts, United States
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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