The purpose of this study is to assess the safety of the second cycle of DCVAC/PCa in patients who completed the first cycle of DCVAC/PCa in the clinical trial SP003 without an objective progression of the disease.
Same as brief summary
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
DCVAC/PCa Experimental therapy
Unnamed facility
Hradec Králové, Czechia
Unnamed facility
Jablonec nad Nisou, Czechia
Unnamed facility
Nový Jičín, Czechia
Unnamed facility
Olomouc, Czechia
Unnamed facility
Safety evaluation of the second cycle of DCVAC
Safety evaluation of the second cycle of active cellular immunotherapy, which includes a second leukapheresis procedure, who after primary radical prostatectomy completed first cycle of active cellular immunotherapy in clinical trial SP003 without objective disease progression requiring additional anti-tumor therapy.
Time frame: 52 weeks
Time to Prostate Specific Antigen (PSA) Doubling Time
Time frame: 52 weeks
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Prague, Czechia
Unnamed facility
Uherské Hradiště, Czechia
Unnamed facility
Ústí nad Labem, Czechia