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Study identifier: NCT06861192 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Clinical Study of Fasudil Hydrochloride and PD1 Inhibitor Combined With Androgen Deprivation in Neoadjuvant Therapy of Prostate Cancer

Condition: Prostate CA  ·  Sponsor: baotai Liang

PhasePhase 2/Phase 3
Planned participants83
Who can joinMale, 18 Years to 85 Years
Healthy volunteersNo

About this study

The high incidence of prostate cancer is one of the important diseases that threaten the health of old men in our country. Although androgen deprivation therapy is an important treatment option for prostate cancer, although neoadjuvant androgen deprivation therapy combined with radical prostatectomy reduced the positive rate of surgical margins, it did not show statistically significant improvement in prostate-specific antigen (PSA). At the same time, few trials reported pathological complete response (pCR) and minimal residual lesion (MRD). The purpose of this project is to verify the therapeutic effect of fasudil hydrochloride and PD1 inhibitor combined with androgen deprivation in patients with locally advanced prostate cancer or oligometastatic prostate cancer before radical prostatectomy through randomized controlled clinical trials, so as to find an effective treatment for locally advanced prostate cancer or oligometastatic prostate cancer.

This description comes directly from the study's public registry record.

Talk to the study team

resident doctor  ·  China+18852069821  ·  2978793353@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Zhongda HospitalNanjing, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06861192