Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Mary Crowley Medical Research Center
This study is being conducted to assess and monitor immune response in patients with minimally symptomatic or asymptomatic hormone refractory prostate cancer who will be receiving Provenge® (Sipuleucel-T) therapy as part of their standard of care treatment regimen. The trial only involves the collection of additional blood samples for the purposes of monitoring immune response. These samples will be taken at 7 time points before, during and after patients receive Provenge® (Sipuleucel-T). There will be no other study-specific procedures performed (other than the blood draws) nor any use of investigational agents in this study.
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients who plan to receive standard of care Provenge® (Sipuleucel-T) at their primary physican's office.
You may not be if
None
Clareo Health | Blood for Immune Response to Provenge® in HRPC
