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Spots Global Cancer Trial Database for Study of Xyotax (CT-2103) in Patients With Metastatic Breast Cancer

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Study of Xyotax (CT-2103) in Patients With Metastatic Breast Cancer

Official Title: Phase II Study of CT-2103 in Patients With Metastatic Breast Cancer

Study ID: NCT00148707

Interventions

CT-2103 (Xyotax)

Study Description

Brief Summary: The purpose of this study is to collect information on what effects (good or bad) CT-2103 (Xyotax) has on breast cancer as well as any side effects the drug may cause.

Detailed Description: * Patients will be given CT-2103 intravenously every 3 weeks. One week after the first dose of CT-2103 a physical exam, blood work and assessment of any side effects will be performed. * Prior to each injection of CT-2103, a physical exam, blood work and assessment of any side effects will be performed (every 3 weeks). * Every 6 weeks the patient's cancer will be re-evaluated with either a CT scan or MRI to determine whether the treatment is working. * Additional blood work will be performed once per week after the first two doses of CT-2103. * The participation in this study will last at least 2 cycles (6 weeks), however patients may remain on the study as long as there is no disease progression, and they are able to tolerate the study drug without severe side effects.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Contact Details

Name: Lawrence N. Shulman, MD

Affiliation: Dana-Farber Cancer Institute

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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