Trials / Recruiting
RecruitingNCT05753566
Rezvilutamide in Patients With Biochemical Recurrence After Radical Prostatectomy for Prostate Cancer
Efficacy and Safety of Rezvilutamide in Patients With Biochemical Recurrence After Radical Prostatectomy for Prostate Cancer: A Prospective, Multi-centre Study
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 96 (estimated)
- Sponsor
- The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School · Academic / Other
- Sex
- Male
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the efficacy and safety of rezvilutamide in combination with androgen deprivation therapy(ADT) and standard salvage radiation therapy(SRT) or rezvilutamide in combination with ADT in prostate cancer patients with biochemical recurrence of prostate-specific antigen(PSA) persistence after radical prostatectomy(RP).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rezvilutamide | Specifications of 80 mg; orally, once a day |
| DRUG | Androgen deprivation therapy (ADT) | Androgen deprivation therapy (ADT), the ADT used by each subject will be determined by the investigator, and the dose and frequency of administration will be consistent with the prescription information |
| RADIATION | SRT | SRT according to standard of care (66.6-72 grays will be delivered to the bed of prostate ,\~50.4 grays to the pelvis if needed) |
Timeline
- Start date
- 2023-03-01
- Primary completion
- 2027-03-01
- Completion
- 2028-03-01
- First posted
- 2023-03-03
- Last updated
- 2023-03-06
Locations
2 sites across 1 country: China
Source: ClinicalTrials.gov record NCT05753566. Inclusion in this directory is not an endorsement.