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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
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

Full criteria on ClinicalTrials.gov

Sites (36)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Gent University Hospital
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GhentBelgiumUnknown status
CHU de Liège
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LiègeBelgiumUnknown status
Hôpital Erasme
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LiègeBelgiumUnknown status
University Hospital Dresden
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DresdenGermanyUnknown status
Urologicum Duisburg
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DuisburgGermanyUnknown status
Urologische Praxis Dr. Wolfgang Warnack
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HagenowGermanyUnknown status
Urologische Praxis. M. Markov
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HalleGermanyUnknown status
Studienpraxis Urologie
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NürtingenGermanyUnknown status
University Hospital Tuebingen
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TübingenGermanyUnknown status
Aalborg University, Departmen of Urology
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AalborgDenmarkUnknown status
Aarhus University Hospital, Department of Urology
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AarhusDenmarkUnknown status
Rigshospitalet, Copenhagen Prostate Cancer Center
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CopenhagenDenmarkUnknown status
Herlev & Gentofte Hospital, Department of Urology
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HerlevDenmarkUnknown status
Urinvejskirurgisk afdeling, Hospitalsenheden Vest
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HolstebroDenmarkUnknown status
Odense University Hospital, Deparment of Urology
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OdenseDenmarkUnknown status
Meilahti Tower Hospital
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HelsinkiFinlandUnknown status
Oulu University Hospital
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OuluFinlandUnknown status
Seinäjoki Central Hospital
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SeinäjokiFinlandUnknown status
Tampere University Hospital
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TampereFinlandUnknown status
Turku University Hospital
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TurkuFinlandUnknown status
Clatterbridge Centre for Oncology
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LiverpoolUnited KingdomUnknown status
Royal Free London NHS Foundation Trust Royal Free Hospital
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LondonUnited KingdomUnknown status
Nottingham University Hospital
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NottinghamUnited KingdomUnknown status
University Hospital Southampton
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SouthamptonUnited KingdomUnknown status
Sahlgrenska University Hospital
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GothenburgSwedenUnknown status
Skåne University Hospital
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MalmöSwedenUnknown status
Örebro University Hospital
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ÖrebroSwedenUnknown status
Karolinska University Hospital
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StockholmSwedenUnknown status
Umeå University Hospital
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UmeåSwedenUnknown status
Tampa Bay Medical Research
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ClearwaterUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada
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Las VegasUnited StatesUnknown status
Carolina Urologic Research Center
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Myrtle BeachUnited StatesUnknown status
Icahn School of Medicine at Mount Sinai Hospitals
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New YorkUnited StatesUnknown status
GU Research Network/Urology Cancer Center
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OmahaUnited StatesUnknown status
The Urology Place
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San AntonioUnited StatesUnknown status
Chesapeake Urology Research Associates
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TowsonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.