NCT04114825Active, not recruitingPhase 2
Study of RV001V in Biochemical Failure Following Curatively Intended Therapy For Localized Prostate Cancer
A Phase 2, Double-Blind, Placebo Controlled Study of RV001V in Men With Biochemical Failure Following Curatively Intended Therapy For Localized Prostate Cancer (BRaVac)
Source: ClinicalTrials.gov · Last updated 28 Sept 2021
Brief summary (registry, in English)
This Phase II trial will enroll approximately 180 adult male patients with an earlier histologic diagnosis of prostatic adenocarcinoma and a biochemical recurrence (BCR) within 3 years of radical prostatectomy (RP) or definitive RT and no distant metastasis or locoregional recurrence. The trial is a randomized placebo-controlled double-blind study of a peptide cancer vaccine (RV001V).
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 180 (estimated)
- First submitted
- 28 Sept 2019
- Start date
- 19 Nov 2019
- Primary completion date
- Apr 2022
- Lead sponsor
- RhoVac APS
- Diseases
- Prostate cancer
- NCT number
- NCT04114825
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 180
- From 19 Nov 2019 to the primary completion date, Apr 2022
- 36 sites in 7 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- Main Inclusion Criteria:
- Biochemical recurrence (BCR) within 3 years of radical prostatectomy (RP) or definitive RT and no distant metastasis by standard CT imaging and bone scintigraphy, or locoregional recurrence (including lymph nodes) assessed by CT or multi-parametric magnetic resonance imaging (MRI) and confirmed with negative biopsy in case of prior RT.
- In case of BCR after RP all the following criteria should apply: a. PSA ≥0.2 ng/mL, b. PSA Doubling Time (PSADT) \>3 months and \<12 months
- In case of BCR after RT all the following criteria should apply: a. PSA \>nadir + 2 ng/mL, b. PSADT \>3 months and \<12 months
- ECOG performance status ≤2.
- Laboratory values obtained ≤30 days prior to first vaccination: Hemoglobin ≥5.6 mmol/L; Absolute granulocyte count ≥1.5 x 109 /L, Platelets ≥100 x 109 /L., Total bilirubin ≤1.5 x upper limit of normal (ULN).
- Creatinine ≤1.5 x ULN.
- Alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) ≤2.5 x ULN.
- Main Exclusion Criteria:
- Patients who are receiving androgen-deprivation therapy or considered a candidate for immediate anti-androgen deprivation therapy (ADT) as judged by the investigator.
- Patients who have received prior ADT are not eligible with the exception of those that received ADT ≤36 months in duration and ≥9 months before randomization and administered only in the neoadjuvant/adjuvant setting.
- Patient is planned for salvage therapy with RT or radical prostatectomy.
- Castrate level of serum testosterone \<50 ng/dL at screening.
- PSA \>10 ng/mL
Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers
Sites (36)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Gent University Hospital Coordinator of this site? Confirm its status | Ghent | Belgium | Unknown status |
| CHU de Liège Coordinator of this site? Confirm its status | Liège | Belgium | Unknown status |
| Hôpital Erasme Coordinator of this site? Confirm its status | Liège | Belgium | Unknown status |
| University Hospital Dresden Coordinator of this site? Confirm its status | Dresden | Germany | Unknown status |
| Urologicum Duisburg Coordinator of this site? Confirm its status | Duisburg | Germany | Unknown status |
| Urologische Praxis Dr. Wolfgang Warnack Coordinator of this site? Confirm its status | Hagenow | Germany | Unknown status |
| Urologische Praxis. M. Markov Coordinator of this site? Confirm its status | Halle | Germany | Unknown status |
| Studienpraxis Urologie Coordinator of this site? Confirm its status | Nürtingen | Germany | Unknown status |
| University Hospital Tuebingen Coordinator of this site? Confirm its status | Tübingen | Germany | Unknown status |
| Aalborg University, Departmen of Urology Coordinator of this site? Confirm its status | Aalborg | Denmark | Unknown status |
| Aarhus University Hospital, Department of Urology Coordinator of this site? Confirm its status | Aarhus | Denmark | Unknown status |
| Rigshospitalet, Copenhagen Prostate Cancer Center Coordinator of this site? Confirm its status | Copenhagen | Denmark | Unknown status |
| Herlev & Gentofte Hospital, Department of Urology Coordinator of this site? Confirm its status | Herlev | Denmark | Unknown status |
| Urinvejskirurgisk afdeling, Hospitalsenheden Vest Coordinator of this site? Confirm its status | Holstebro | Denmark | Unknown status |
| Odense University Hospital, Deparment of Urology Coordinator of this site? Confirm its status | Odense | Denmark | Unknown status |
| Meilahti Tower Hospital Coordinator of this site? Confirm its status | Helsinki | Finland | Unknown status |
| Oulu University Hospital Coordinator of this site? Confirm its status | Oulu | Finland | Unknown status |
| Seinäjoki Central Hospital Coordinator of this site? Confirm its status | Seinäjoki | Finland | Unknown status |
| Tampere University Hospital Coordinator of this site? Confirm its status | Tampere | Finland | Unknown status |
| Turku University Hospital Coordinator of this site? Confirm its status | Turku | Finland | Unknown status |
| Clatterbridge Centre for Oncology Coordinator of this site? Confirm its status | Liverpool | United Kingdom | Unknown status |
| Royal Free London NHS Foundation Trust Royal Free Hospital Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Nottingham University Hospital Coordinator of this site? Confirm its status | Nottingham | United Kingdom | Unknown status |
| University Hospital Southampton Coordinator of this site? Confirm its status | Southampton | United Kingdom | Unknown status |
| Sahlgrenska University Hospital Coordinator of this site? Confirm its status | Gothenburg | Sweden | Unknown status |
| Skåne University Hospital Coordinator of this site? Confirm its status | Malmö | Sweden | Unknown status |
| Örebro University Hospital Coordinator of this site? Confirm its status | Örebro | Sweden | Unknown status |
| Karolinska University Hospital Coordinator of this site? Confirm its status | Stockholm | Sweden | Unknown status |
| Umeå University Hospital Coordinator of this site? Confirm its status | Umeå | Sweden | Unknown status |
| Tampa Bay Medical Research Coordinator of this site? Confirm its status | Clearwater | United States | Unknown status |
| Comprehensive Cancer Centers of Nevada Coordinator of this site? Confirm its status | Las Vegas | United States | Unknown status |
| Carolina Urologic Research Center Coordinator of this site? Confirm its status | Myrtle Beach | United States | Unknown status |
| Icahn School of Medicine at Mount Sinai Hospitals Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| GU Research Network/Urology Cancer Center Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| The Urology Place Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| Chesapeake Urology Research Associates Coordinator of this site? Confirm its status | Towson | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.