The purpose of this study is to determine whether DCVAC/PCa added onto Standard of Care therapy can improve survival times for patients with Metastatic Castration Resistant Prostate Cancer
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
DCVAC/PCa is the experimental therapy added on to Docetaxel
Docetaxel is Standard of Care First Line Chemotherapy
Unnamed facility
Brno, Czechia
Unnamed facility
Hradec Králové, Czechia
Unnamed facility
Jihlava, Czechia
Unnamed facility
Liberec, Czechia
Survival rate
Time frame: 135 weeks
Radiographic Progression Free Survival
Time frame: 135 weeks
Duration to Prostate Specific Antigen (PSA) Progression
Time frame: 135 weeks
Changes in Quality of Life (QOL) assessed by European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30
Time frame: 0, 10, 22, 37, 53, 65 weeks
Changes in Pain assessed by EORTC QLQ-C30
Time frame: 0, 10, 22, 37, 53, 65 weeks
Incidence of Adverse Events
Time frame: 135 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Nová Ves pod Pleší, Czechia
Unnamed facility
Olomouc, Czechia
Unnamed facility
Ostrava, Czechia
Unnamed facility
Prague, Czechia
Unnamed facility
Ústí nad Labem, Czechia
Unnamed facility
Zlín, Czechia