This trial aims to evaluate the efficacy and safety of neoadjuvant therapy with Proxalutamide combined with androgen deprivation therapy(ADT)for High risk prostate cancer ,This trial is A randomized, controlled, double-blind, single center.Treatment cycle is 6 months,
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
2
placebo+ADT(Androgen Deprivation Therapy) ,Route of placebo administration: tablet, dosage:300mg , dosage form oral , frequency of administration:QD
Proxalutamide +ADT(Androgen Deprivation Therapy) ,Route of Proxalutamide administration: tablet, dosage:300mg , dosage form oral , frequency of administration:QD
The Affiliated Hospital of Nanjing University Medical School
Nanjing, Jiangsu, China
RECRUITINGPathologic Complete Response Rate
The proportion of subjects with no morphologically recognizable cancer cell in tumor specimens after radical prostatectomy
Time frame: up to 6months
Proportion of Subjects With Minimal Residual Disease
The proportion of subjects that have residual tumors with maximum diameter of 3 mm or less after radical prostatectomy
Time frame: up to 6months
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