Titre A Phase 3, Randomized Study of Adjuvant Cretostimogene Grenadenorepvec Versus Observation for the Treatment of Intermediate Risk Non-Muscle Invasive Bladder Cancer (IR-NMIBC) Following Transurethral Resection of Bladder Tumor (TURBT)
Protocole ID PIVOT-006
ClinicalTrials.gov ID NCT06111235
Type(s) de cancer Vessie/urothélial
Phase Phase III
Type étude Clinique
Médicament Cretostimogene Grenadenorepvec Versus Observation
Institution CENTRE UNIVERSITAIRE DE SANTE MCGILL
   SITE GLEN
      1001 boul. Décarie , Montréal, QC, H4A 3J1
Ville Montréal
Investigateur(trice) principal(e) Dr Wassim Kassouf
Coordonnateur(trice) Karla Jauregui Sanchez
 514-934-1934
Statut Actif en recrutement
Date d'activation 10-06-2024
Critètes d'éligibilité
  • Pathologically confirmed IR-NMIBC, per American Urologic Association/Society of Urologic Oncology/National Comprehensive Cancer Network guidelines, within 90 days of participant randomization:
    • Recurrent LG Ta within 12 months of prior LG or HG (HG Ta ≤ 3 cm) tumor
    • Solitary LG Ta >3 cm tumor
    • Multifocal LG Ta tumors
    • Primary and solitary HG Ta ≤3 cm tumor
    • LG T1 tumor
  • All visible disease removed by TURBT within 12 weeks of study randomization
  • Acceptable baseline organ function
Critètes d'exclusion
  • High-risk NMIBC (e.g., HG T1, Recurrent or multifocal HG Ta>3cm tumor(s), CIS)
  • Low-Risk NMIBC (e.g., solitary LG Ta ≤3 cm tumor)
  • Disease in the prostatic urethra at any time or in the upper genitourinary tract within 24 months of randomization
  • Muscle-invasive bladder cancer, locally advanced or metastatic bladder cancer
  • Prior treatment with any human adenovirus serotype 5 based therapy (e.g., Ad-interferon or Adstiladrin)