A Phase 2 interventional study of Amrubicin in Metastatic Breast Cancer, sponsored by Celgene Corporation. Withdrawn at 28 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2008-09-23.
Sponsored by Celgene Corporation · Phase 2, Interventional, and Treatment
The purpose of the study is to evaluate the incidence of cardiac toxicity of amrubicin when administered to patients with metastatic breast cancer.
12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.
This study's planned enrollment of 66 is close to the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.
Browse Breast Neoplasms studies →Celgene Corporation is the lead sponsor of 50 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Adequate organ function including the following:
Exclusion Criteria:
Incidence of cardiac toxicity
Objective tumor response rate according to RECIST criteria measured every 2 cycles (every 6 weeks)
Duration of overall response
Time to tumor progression
Progression free survival
Toxicity profile
This study is withdrawn, as verified in Sep 2008. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Celgene Corporation