Titre A Phase 2 Nonrandomized, Open-label, Multisite Study to Evaluate the Safety and Efficacy of Raludotatug Deruxtecan in Participants With Gastrointestinal Cancers
Protocole ID MK-5909-005 (REJOICE-GI01)
ClinicalTrials.gov ID NCT06864169
Type(s) de cancer Colorectal
Estomac
Oesophage
Pancréas
Voies biliaires
Phase Phase II
Type étude Clinique
Médicament Raludotatug Deruxtecan
Institution CENTRE HOSPITALIER DE L'UNIVERSITE DE MONTREAL  
Ville Montréal
Investigateur(trice) principal(e) Dre Francine Aubin
Coordonnateur(trice) Adeline Hamon
 514-890-8000 poste 30737
Statut Actif en recrutement
Date d'activation 19-06-2025
Critètes d'éligibilité The main inclusion criteria include but are not limited to the following:
  • Has one of the following cancers:
    • Unresectable or metastatic pancreatic ductal adenocarcinoma (PDAC)
    • Unresectable or metastatic adenocarcinoma of the biliary tract [intra- or extrahepatic holangiocarcinoma (CCA) or gallbladder cancer (GBC)]
    • Unresectable or metastatic colorectal adenocarcinoma
    • Unresectable or metastatic gastric adenocarcinoma
    • Gastroesophageal junction adenocarcinoma (GEJAC)
    • Esophageal adenocarcinoma (EAC)
  • Has received prior therapy for the cancer
  • Has a life expectancy of at least 3 months
  • If human immunodeficiency virus (HIV) infected, must have well controlled HIV on antiretroviral therapy (ART)
Critètes d'exclusion The main exclusion criteria include but are not limited to the following:
  • Has a history of (noninfectious) interstitial lung disease (ILD)/pneumonitis that required steroids or has current ILD/pneumonitis, and/or suspected ILD/pneumonitis
  • Has clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses
  • Has uncontrolled or significant cardiovascular disease
  • Has a known additional malignancy that is progressing or has required active treatment within the past 3 years
  • Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis
  • Active autoimmune disease that has required systemic treatment in the past 2 years
  • Has not adequately recovered from major surgery or has ongoing surgical complications
  • HIV-infected participants with a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease