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A Non-Interventional Real-World Study of Revilutamide in Metastatic Hormone-Sensitive Prostate Cancer

A Non-Interventional Real-World Study of Revilutamide in Metastatic Hormone-Sensitive Prostate Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084348
Enrollment
Unknown
Registered
2024-05-15
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

prostate cancer

Interventions

observation group:Included patients in the treatment with revalutamide

Sponsors

Cancer Hospital Affiliated to Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1) Age= 18 years old 2) Patients diagnosed with metastatic hormone-sensitive prostate cancer 3) Investigator assessment that revilutamide can be used, or has received or is receiving revilutamide therapy; 4) Signed informed consent and voluntarily joined this study 5) Male patients whose partner is a female of childbearing potential should be surgically sterile or agree to use an effective method of contraception during the trial and for 3 months after the last administration of study drug.

Exclusion criteria

Exclusion criteria: 1: Participating in other drug intervention clinical studies; 2: Other conditions judged by the investigator to be inappropriate for inclusion in the study

Design outcomes

Primary

MeasureTime frame
safety analysis;

Secondary

MeasureTime frame
Duration of medication;Time to start the first follow-up anti-prostate cancer therapy;rPFS(Investigator evaluation);MFS;OS;Objective response rate of soft tissue lesions;SSE;Until the pain progresses;pharmacoeconomics;PSA;

Countries

China

Contacts

Public ContactBiXing

Cancer Hospital Affiliated to Xinjiang Medical University

44272603@qq.com+86 138 0995 2707

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026