Actively Recruiting

Phase 2
Age: 18Years - 85Years
MALE
NCT07163910

Homoharringtonine Plus Androgen Deprivation Therapy in the Neoadjuvant Treatment of Prostate Cancer: A Single-Arm Clinical Study

Led by baotai Liang · Updated on 2025-11-18

93

Participants Needed

1

Research Sites

139 weeks

Total Duration

On this page

Sponsors

B

baotai Liang

Lead Sponsor

T

The Affiliated Tumor Hospital of Nantong University, Nantong, Jiangsu Province, China

Collaborating Sponsor

AI-Summary

What this Trial Is About

The project aims to verify the therapeutic effect of neoadjuvant homoharringtonine combined with androgen deprivation therapy in patients with localized high-risk/very high-risk, regional lymph node-metastatic, or metastatic prostate cancer before radical prostatectomy through clinical trials, thereby identifying an effective treatment for patients with advanced prostate cancer.

CONDITIONS

Official Title

Homoharringtonine Plus Androgen Deprivation Therapy in the Neoadjuvant Treatment of Prostate Cancer: A Single-Arm Clinical Study

Who Can Participate

Age: 18Years - 85Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years to 85 years
  • Histologically or cytologically confirmed prostate cancer
  • Localized high-risk/very high-risk prostate cancer defined by clinical stage T3-T4, Gleason score 8, primary Gleason pattern 5, or PSA > 20 ng/mL, without local lymph node or distant metastasis
  • Prostate cancer with local lymph node metastasis but no distant metastasis
  • Metastatic prostate cancer confirmed by imaging
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1
  • Able to voluntarily sign informed consent and adhere to treatment and follow-up
Not Eligible

You will not qualify if you...

  • Any previous or ongoing prostate cancer treatment including radiotherapy, chemotherapy, or androgen deprivation therapy
  • History of previous prostatectomy
  • Severe underlying medical, psychiatric, or psychological diseases affecting treatment as judged by investigator
  • Known allergy to study drugs
  • Refusal to undergo radical prostatectomy
  • Deemed ineligible for the clinical trial by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Zhongda Hospital

Nanjing, Jiangsu, China, 210009

Actively Recruiting

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Research Team

R

resident doctor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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