Pilot Study Using Molecular Profiling to Find Potential Targets & Select Treatments for Pts With Met br ca

Completed · Early Phase 1

Conditions studied: Metastatic Breast Cancer

In brief

The purpose of this study is to determine the response rate, that is the % of patients with non-progression of their metastatic breast cancer after 4 months on treatment that was selected by molecular testing and proteomics.

Key facts

Study ID

NCT01074814

Run by

Translational Drug Development

People needed

28

Starts

2010-03-01

Expected to finish

2012-07-01

Last updated by the study team

2023-09-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have a life expectancy of greater than 3 months
• metastatic breast cancer, with measurable or evaluable non-measurable disease
• Have progressed on at least 3 prior chemotherapeutic or biological regimens
• Be defined as refractory to the last line of therapy according to the following criteria: Documented disease progression under the last treatment or within two months of the last treatment dosing AND Have received ≥ 30 days of the last treatment AND Have discontinued for progression by RECIST 1.1 criteria
• ≥18 years of age
• ECOG 0-1
• willing to undergo a biopsy or surgical procedure to obtain tissue
• Must have been off their prior regimen for ≥ 3 weeks or 5 x half life of drug
• Have adequate organ and bone marrow function as defined below:
• Female patients of child-bearing potential must have a negative pregnancy test and agree to use at least one form of contraception during the study and for at least one month after treatment discontinuation. For the purposes of this study, child-bearing potential is defined as: all female patients unless they are post-menopausal for at least one year or are surgically sterile
• Male patients must use a form of barrier contraception approved by the Investigator during the study and for at least one month after treatment discontinuation.

You may not qualify if…

• Tumor biopsy intended for use in the current study which was performed more than 2 months prior
• Frozen material is not available/obtained
• Metastatic lesion is not accessible to biopsy
• Patients with > 6 months treatment under the last line of therapy
• Patients with symptomatic CNS metastasis. Patients with a history of CNS metastases who have been treated must be stable without symptoms for 4 weeks after completion of treatment, with image documentation required, and must be either off steroids or on a stable dose of steroids for ≥ 2 weeks prior to enrollment
• Any previous history of another malignancy (other than cured basal cell carcinoma of the skin or cured in-situ carcinoma of the cervix) within 5 years of study entry
• Uncontrolled concurrent illness including, but not limited to, ongoing or active serious infection, symptomatic congestive heart failure, unstable angina pectoris, unstable cardiac arrhythmias, psychiatric illness, or situations that would limit compliance with the study requirements or the ability to willingly give written informed consent
• Known HIV, HBV, HCV infection
• Pregnant or breast-feeding patients or any patient with childbearing potential not using adequate contraception.

Where it is running

• Tgen Clinical Research Services — Scottsdale, Arizona, United States
• Fairfax North Virginia Hematology Oncology — Fairfax, Virginia, United States
• Evergreen Hematology and Oncology — Spokane, Washington, United States

Full record on ClinicalTrials.gov

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